Primary Site >> Stomach Cancer
Gene >> FAT4
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125449198:125449198(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369228145 |
| CDS Mutation | c.8182G>A |
| AA Mutation | p.Val2728Ile(p.V2728I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125319596:125319596(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3185T>G |
| AA Mutation | p.Leu1062Arg(p.L1062R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125449967:125449967(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.8951T>G |
| AA Mutation | p.Leu2984Arg(p.L2984R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125477211:125477211(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.12350C>T |
| AA Mutation | p.Pro4117Leu(p.P4117L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125490830:125490830(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.14008A>C |
| AA Mutation | p.Ser4670Arg(p.S4670R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125449667:125449667(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.8651T>G |
| AA Mutation | p.Leu2884Arg(p.L2884R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125452241:125452241(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.11225C>A |
| AA Mutation | p.Thr3742Lys(p.T3742K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125468674:125468674(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.12062A>T |
| AA Mutation | p.Asp4021Val(p.D4021V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125490228:125490228(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.13406T>A |
| AA Mutation | p.Leu4469His(p.L4469H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125449456:125449456(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.8440G>T |
| AA Mutation | p.Ala2814Ser(p.A2814S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125318309:125318309(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370926669 |
| CDS Mutation | c.1898G>A |
| AA Mutation | p.Arg633His(p.R633H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125450852:125450852(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.9836G>T |
| AA Mutation | p.Cys3279Phe(p.C3279F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125451860:125451860(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746784092 |
| CDS Mutation | c.10844G>A |
| AA Mutation | p.Arg3615Gln(p.R3615Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125452426:125452426(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.11410G>A |
| AA Mutation | p.Asp3804Asn(p.D3804N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125319917:125319917(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs750169762 |
| CDS Mutation | c.3506G>A |
| AA Mutation | p.Arg1169Gln(p.R1169Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125491709:125491709(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.14887G>A |
| AA Mutation | p.Gly4963Ser(p.G4963S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125321515:125321515(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5104G>A |
| AA Mutation | p.Ala1702Thr(p.A1702T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125491545:125491545(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.14723C>A |
| AA Mutation | p.Ala4908Glu(p.A4908E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125490109:125490109(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.13287C>A |
| AA Mutation | p.Asp4429Glu(p.D4429E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125406935:125406935(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5363G>A |
| AA Mutation | p.Arg1788His(p.R1788H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125490749:125490749(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs181607904 |
| CDS Mutation | c.13927C>T |
| AA Mutation | p.Arg4643Cys(p.R4643C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125321345:125321345(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4934G>A |
| AA Mutation | p.Gly1645Asp(p.G1645D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125318122:125318122(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1711A>C |
| AA Mutation | p.Thr571Pro(p.T571P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125451940:125451940(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.10924G>A |
| AA Mutation | p.Asp3642Asn(p.D3642N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125450705:125450705(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373873722 |
| CDS Mutation | c.9689C>T |
| AA Mutation | p.Ala3230Val(p.A3230V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125452058:125452058(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.11042T>C |
| AA Mutation | p.Leu3681Pro(p.L3681P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125481617:125481617(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.12695G>A |
| AA Mutation | p.Ser4232Asn(p.S4232N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125320101:125320101(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3690A>C |
| AA Mutation | p.Leu1230Phe(p.L1230F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125451870:125451870(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.10854G>T |
| AA Mutation | p.Glu3618Asp(p.E3618D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125490750:125490750(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs147961375 |
| CDS Mutation | c.13928G>A |
| AA Mutation | p.Arg4643His(p.R4643H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125468674:125468674(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.12062A>G |
| AA Mutation | p.Asp4021Gly(p.D4021G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125491438:125491438(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.14616A>C |
| AA Mutation | p.Gln4872His(p.Q4872H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 33 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125317487:125317487(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1076C>T |
| AA Mutation | p.Pro359Leu(p.P359L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 34 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125450065:125450065(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.9049T>C |
| AA Mutation | p.Ser3017Pro(p.S3017P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 35 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125451461:125451461(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.10445C>A |
| AA Mutation | p.Ala3482Asp(p.A3482D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 36 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125491508:125491508(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749083638 |
| CDS Mutation | c.14686C>T |
| AA Mutation | p.Arg4896Cys(p.R4896C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 37 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125448955:125448955(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7939C>T |
| AA Mutation | p.Pro2647Ser(p.P2647S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 38 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125319545:125319545(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3134G>A |
| AA Mutation | p.Gly1045Asp(p.G1045D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 39 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125321047:125321047(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755526114 |
| CDS Mutation | c.4636G>A |
| AA Mutation | p.Val1546Ile(p.V1546I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 40 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125408601:125408601(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5727G>T |
| AA Mutation | p.Gln1909His(p.Q1909H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 41 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125451406:125451406(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373744467 |
| CDS Mutation | c.10390G>A |
| AA Mutation | p.Val3464Ile(p.V3464I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 42 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125318074:125318074(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756991867 |
| CDS Mutation | c.1663C>T |
| AA Mutation | p.Arg555Trp(p.R555W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 43 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125318527:125318527(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747065140 |
| CDS Mutation | c.2116A>G |
| AA Mutation | p.Ser706Gly(p.S706G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 44 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125320547:125320547(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4136A>T |
| AA Mutation | p.Asp1379Val(p.D1379V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 45 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125450302:125450302(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.9286G>A |
| AA Mutation | p.Ala3096Thr(p.A3096T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 46 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125451569:125451569(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.10553T>C |
| AA Mutation | p.Met3518Thr(p.M3518T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 47 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125490714:125490714(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771288110 |
| CDS Mutation | c.13892C>T |
| AA Mutation | p.Ser4631Leu(p.S4631L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 48 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125321447:125321447(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5036G>T |
| AA Mutation | p.Arg1679Leu(p.R1679L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 49 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125320769:125320769(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4358G>A |
| AA Mutation | p.Gly1453Asp(p.G1453D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 50 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125448553:125448553(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7537T>A |
| AA Mutation | p.Phe2513Ile(p.F2513I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 51 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125415255:125415255(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6292A>G |
| AA Mutation | p.Ser2098Gly(p.S2098G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 52 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125450815:125450815(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.9799A>G |
| AA Mutation | p.Thr3267Ala(p.T3267A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 53 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125448554:125448554(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.7538T>G |
| AA Mutation | p.Phe2513Cys(p.F2513C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 54 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125321219:125321219(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4808C>A |
| AA Mutation | p.Ala1603Glu(p.A1603E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 55 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125452088:125452088(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.11072G>T |
| AA Mutation | p.Ser3691Ile(p.S3691I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 56 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125490030:125490030(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.13208T>C |
| AA Mutation | p.Ile4403Thr(p.I4403T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 57 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125414991:125414991(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6028A>G |
| AA Mutation | p.Ser2010Gly(p.S2010G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 58 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125415802:125415802(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6839T>G |
| AA Mutation | p.Leu2280Arg(p.L2280R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 59 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125490123:125490123(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760631255 |
| CDS Mutation | c.13301C>T |
| AA Mutation | p.Pro4434Leu(p.P4434L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 60 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125415324:125415324(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6361A>G |
| AA Mutation | p.Thr2121Ala(p.T2121A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 61 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125451065:125451065(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.10049A>C |
| AA Mutation | p.Lys3350Thr(p.K3350T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 62 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125487423:125487423(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.12895G>A |
| AA Mutation | p.Val4299Ile(p.V4299I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 63 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125317314:125317314(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.903G>T |
| AA Mutation | p.Glu301Asp(p.E301D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 64 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125398893:125398893(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5285T>C |
| AA Mutation | p.Leu1762Pro(p.L1762P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 65 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125408747:125408747(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5873C>A |
| AA Mutation | p.Pro1958His(p.P1958H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 66 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125452301:125452301(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.11285T>G |
| AA Mutation | p.Leu3762Arg(p.L3762R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 67 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125451055:125451055(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.10039C>A |
| AA Mutation | p.Gln3347Lys(p.Q3347K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 68 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125415468:125415468(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6505A>G |
| AA Mutation | p.Thr2169Ala(p.T2169A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 69 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125449309:125449309(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.8293G>A |
| AA Mutation | p.Asp2765Asn(p.D2765N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 70 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125415414:125415414(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6451A>C |
| AA Mutation | p.Asn2151His(p.N2151H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 71 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125468606:125468606(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.11994T>G |
| AA Mutation | p.Ile3998Met(p.I3998M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 72 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125434280:125434280(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs147151922 |
| CDS Mutation | c.7054G>A |
| AA Mutation | p.Val2352Ile(p.V2352I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 73 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125491039:125491039(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.14217A>C |
| AA Mutation | p.Gln4739His(p.Q4739H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 74 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125319160:125319160(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs745840096 |
| CDS Mutation | c.2749G>T |
| AA Mutation | p.Ala917Ser(p.A917S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 75 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125416505:125416505(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6901G>T |
| AA Mutation | p.Gly2301Cys(p.G2301C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 76 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125451689:125451689(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.10673T>C |
| AA Mutation | p.Phe3558Ser(p.F3558S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 77 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125468775:125468775(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.12163T>G |
| AA Mutation | p.Ser4055Ala(p.S4055A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 78 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125451653:125451653(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.10637A>C |
| AA Mutation | p.Tyr3546Ser(p.Y3546S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 79 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125319520:125319520(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3109G>A |
| AA Mutation | p.Glu1037Lys(p.E1037K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 80 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125318673:125318673(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2262A>C |
| AA Mutation | p.Glu754Asp(p.E754D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 81 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125449597:125449597(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.8581T>G |
| AA Mutation | p.Phe2861Val(p.F2861V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 82 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125463588:125463588(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.11820T>G |
| AA Mutation | p.Asn3940Lys(p.N3940K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 83 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125449151:125449151(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.8135T>A |
| AA Mutation | p.Met2712Lys(p.M2712K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 84 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125450167:125450167(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.9151T>G |
| AA Mutation | p.Leu3051Val(p.L3051V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 85 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125317358:125317358(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.947G>A |
| AA Mutation | p.Arg316Gln(p.R316Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 86 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125316994:125316994(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.583G>A |
| AA Mutation | p.Gly195Ser(p.G195S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 87 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125320508:125320508(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4097G>A |
| AA Mutation | p.Ser1366Asn(p.S1366N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 88 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125451530:125451530(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.10514A>T |
| AA Mutation | p.Asp3505Val(p.D3505V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 89 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125450680:125450680(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.9664G>C |
| AA Mutation | p.Asp3222His(p.D3222H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 90 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125476189:125476189(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.12226G>A |
| AA Mutation | p.Asp4076Asn(p.D4076N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 91 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125451658:125451658(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.10642T>G |
| AA Mutation | p.Leu3548Val(p.L3548V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 92 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125449981:125449981(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.8965T>C |
| AA Mutation | p.Phe2989Leu(p.F2989L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 93 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125451431:125451431(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.10415C>T |
| AA Mutation | p.Thr3472Ile(p.T3472I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 94 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125318392:125318392(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1981G>A |
| AA Mutation | p.Ala661Thr(p.A661T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 95 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125451564:125451564(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.10548A>C |
| AA Mutation | p.Glu3516Asp(p.E3516D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 96 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125490148:125490148(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.13326G>T |
| AA Mutation | p.Glu4442Asp(p.E4442D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 97 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125316418:125316418(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7T>G |
| AA Mutation | p.Leu3Val(p.L3V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 98 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125416566:125416566(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6962G>A |
| AA Mutation | p.Ser2321Asn(p.S2321N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 99 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125316896:125316896(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.485C>T |
| AA Mutation | p.Ser162Leu(p.S162L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 100 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125317477:125317477(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1066C>T |
| AA Mutation | p.Arg356Cys(p.R356C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 101 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125406991:125406991(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746989506 |
| CDS Mutation | c.5419C>T |
| AA Mutation | p.Arg1807Cys(p.R1807C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 102 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125407105:125407105(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5533G>A |
| AA Mutation | p.Val1845Met(p.V1845M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 103 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125490780:125490780(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.13958G>T |
| AA Mutation | p.Arg4653Met(p.R4653M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 104 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125318044:125318044(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762135802 |
| CDS Mutation | c.1633G>A |
| AA Mutation | p.Ala545Thr(p.A545T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 105 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125451146:125451146(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.10130A>T |
| AA Mutation | p.Asn3377Ile(p.N3377I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 106 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125490195:125490195(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.13373C>A |
| AA Mutation | p.Thr4458Lys(p.T4458K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 107 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125451207:125451207(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.10191T>A |
| AA Mutation | p.Asp3397Glu(p.D3397E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 108 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125319568:125319568(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3157T>C |
| AA Mutation | p.Tyr1053His(p.Y1053H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 109 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125406902:125406902(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5330A>G |
| AA Mutation | p.Tyr1777Cys(p.Y1777C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 110 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125490635:125490635(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.13813A>G |
| AA Mutation | p.Ile4605Val(p.I4605V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 111 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125476231:125476231(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.12268A>C |
| AA Mutation | p.Ser4090Arg(p.S4090R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 112 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125415802:125415802(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6839T>A |
| AA Mutation | p.Leu2280His(p.L2280H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 113 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125451104:125451104(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752591843 |
| CDS Mutation | c.10088G>A |
| AA Mutation | p.Arg3363Gln(p.R3363Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 114 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125451430:125451430(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.10414A>C |
| AA Mutation | p.Thr3472Pro(p.T3472P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 115 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125449211:125449211(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.8195A>G |
| AA Mutation | p.Asp2732Gly(p.D2732G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 116 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125316805:125316805(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.394G>A |
| AA Mutation | p.Ala132Thr(p.A132T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 117 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125319368:125319368(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs192514171 |
| CDS Mutation | c.2957T>C |
| AA Mutation | p.Val986Ala(p.V986A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 118 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125320957:125320957(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4546A>G |
| AA Mutation | p.Thr1516Ala(p.T1516A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 119 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125321447:125321447(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201292031 |
| CDS Mutation | c.5036G>A |
| AA Mutation | p.Arg1679His(p.R1679H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 120 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125448826:125448826(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747229172 |
| CDS Mutation | c.7810G>A |
| AA Mutation | p.Ala2604Thr(p.A2604T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 121 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125491247:125491247(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.14425G>T |
| AA Mutation | p.Asp4809Tyr(p.D4809Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 122 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125318717:125318717(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2306G>A |
| AA Mutation | p.Gly769Asp(p.G769D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 123 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394329 |
| Start | 125446325:125446325(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372786128 |
| CDS Mutation | c.7226C>T |
| AA Mutation | p.Thr2409Met(p.T2409M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 124 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000394329 |
| Start | 125449716:125449716(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.8700T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 125 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000394329 |
| Start | 125490634:125490634(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.13812C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 126 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000394329 |
| Start | 125434279:125434279(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199682494 |
| CDS Mutation | c.7053C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 127 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000394329 |
| Start | 125468741:125468741(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.12129T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 128 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000394329 |
| Start | 125321037:125321037(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4626G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 129 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000394329 |
| Start | 125317077:125317077(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.666G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 130 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000394329 |
| Start | 125320701:125320701(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4290T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 131 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000394329 |
| Start | 125321235:125321235(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4824T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 132 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000394329 |
| Start | 125448945:125448945(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs146157250 |
| CDS Mutation | c.7929C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 133 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000394329 |
| Start | 125318580:125318580(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2169T>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 134 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000394329 |
| Start | 125415671:125415671(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6708C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 135 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000394329 |
| Start | 125317695:125317695(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs546059430 |
| CDS Mutation | c.1284C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 136 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000394329 |
| Start | 125490064:125490064(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.13242G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 137 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000394329 |
| Start | 125318832:125318832(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs554223388 |
| CDS Mutation | c.2421G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 138 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000394329 |
| Start | 125450898:125450898(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.9882T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 139 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000394329 |
| Start | 125479774:125479774(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.12507C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 140 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000394329 |
| Start | 125451903:125451903(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761320064 |
| CDS Mutation | c.10887C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 141 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000394329 |
| Start | 125490994:125490994(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.14172T>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 142 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000394329 |
| Start | 125449659:125449659(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.8643C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 143 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000394329 |
| Start | 125316753:125316753(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.342G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 144 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000394329 |
| Start | 125415629:125415629(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6666C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 145 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000394329 |
| Start | 125319342:125319342(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2931C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 146 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000394329 |
| Start | 125451465:125451465(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.10449T>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 147 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000394329 |
| Start | 125450706:125450706(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142877205 |
| CDS Mutation | c.9690G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 148 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000394329 |
| Start | 125320752:125320752(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4341T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 149 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000394329 |
| Start | 125490196:125490196(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs146914959 |
| CDS Mutation | c.13374G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 150 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000394329 |
| Start | 125415353:125415353(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6390T>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 151 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000394329 |
| Start | 125468783:125468783(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.12171A>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 152 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000394329 |
| Start | 125318304:125318304(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1893C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 153 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000394329 |
| Start | 125490610:125490610(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.13788T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 154 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000394329 |
| Start | 125317260:125317260(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.849G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 155 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000394329 |
| Start | 125491210:125491210(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.14388C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 156 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000394329 |
| Start | 125490097:125490097(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.13275C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 157 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000394329 |
| Start | 125449338:125449338(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.8322T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 158 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000394329 |
| Start | 125320404:125320404(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3993T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 159 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000394329 |
| Start | 125490757:125490757(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.13935C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 160 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000394329 |
| Start | 125316837:125316837(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.426C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 161 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000394329 |
| Start | 125449404:125449404(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.8388T>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 162 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000394329 |
| Start | 125468543:125468543(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.11931T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 163 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000394329 |
| Start | 125477284:125477284(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.12423A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 164 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000394329 |
| Start | 125479798:125479798(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.12531T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 165 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000394329 |
| Start | 125491438:125491438(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761187408 |
| CDS Mutation | c.14616A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |