Primary Site >> Stomach Cancer
Gene >> AHNAK2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333244 |
| Start | 104954985:104954985(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.623A>G |
| AA Mutation | p.Gln208Arg(p.Q208R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333244 |
| Start | 104949660:104949660(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200253581 |
| CDS Mutation | c.5791G>A |
| AA Mutation | p.Ala1931Thr(p.A1931T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333244 |
| Start | 104938723:104938723(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369118861 |
| CDS Mutation | c.16728G>T |
| AA Mutation | p.Met5576Ile(p.M5576I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333244 |
| Start | 104948810:104948810(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751451433 |
| CDS Mutation | c.6641C>T |
| AA Mutation | p.Ala2214Val(p.A2214V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333244 |
| Start | 104943212:104943212(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.12239T>C |
| AA Mutation | p.Leu4080Pro(p.L4080P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333244 |
| Start | 104940288:104940288(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.15163G>A |
| AA Mutation | p.Gly5055Arg(p.G5055R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333244 |
| Start | 104943788:104943788(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.11663A>C |
| AA Mutation | p.Lys3888Thr(p.K3888T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333244 |
| Start | 104947044:104947044(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777802496 |
| CDS Mutation | c.8407G>A |
| AA Mutation | p.Asp2803Asn(p.D2803N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333244 |
| Start | 104945702:104945702(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.9749G>A |
| AA Mutation | p.Gly3250Asp(p.G3250D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333244 |
| Start | 104946711:104946711(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.8740C>T |
| AA Mutation | p.Pro2914Ser(p.P2914S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333244 |
| Start | 104952869:104952869(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777589450 |
| CDS Mutation | c.2582C>T |
| AA Mutation | p.Pro861Leu(p.P861L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333244 |
| Start | 104945567:104945567(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.9884C>G |
| AA Mutation | p.Ser3295Cys(p.S3295C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333244 |
| Start | 104946062:104946062(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.9389C>G |
| AA Mutation | p.Ser3130Cys(p.S3130C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333244 |
| Start | 104940176:104940176(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.15275T>C |
| AA Mutation | p.Val5092Ala(p.V5092A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333244 |
| Start | 104942045:104942045(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.13406A>G |
| AA Mutation | p.Lys4469Arg(p.K4469R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333244 |
| Start | 104947594:104947594(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7857G>T |
| AA Mutation | p.Gln2619His(p.Q2619H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333244 |
| Start | 104948276:104948276(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778113710 |
| CDS Mutation | c.7175C>T |
| AA Mutation | p.Pro2392Leu(p.P2392L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333244 |
| Start | 104950088:104950088(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5363G>A |
| AA Mutation | p.Ser1788Asn(p.S1788N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333244 |
| Start | 104940770:104940770(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.14681C>A |
| AA Mutation | p.Ser4894Tyr(p.S4894Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333244 |
| Start | 104944440:104944440(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756916033 |
| CDS Mutation | c.11011G>A |
| AA Mutation | p.Asp3671Asn(p.D3671N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333244 |
| Start | 104949518:104949518(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5933A>G |
| AA Mutation | p.Asp1978Gly(p.D1978G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333244 |
| Start | 104952021:104952021(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201025662 |
| CDS Mutation | c.3430C>T |
| AA Mutation | p.Arg1144Trp(p.R1144W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333244 |
| Start | 104952089:104952089(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3362A>G |
| AA Mutation | p.Asp1121Gly(p.D1121G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333244 |
| Start | 104949053:104949053(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs554709190 |
| CDS Mutation | c.6398C>T |
| AA Mutation | p.Ala2133Val(p.A2133V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333244 |
| Start | 104949281:104949281(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs561933027 |
| CDS Mutation | c.6170C>T |
| AA Mutation | p.Pro2057Leu(p.P2057L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333244 |
| Start | 104953134:104953134(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2317C>T |
| AA Mutation | p.Leu773Phe(p.L773F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333244 |
| Start | 104952276:104952276(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369704618 |
| CDS Mutation | c.3175G>A |
| AA Mutation | p.Ala1059Thr(p.A1059T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333244 |
| Start | 104939276:104939276(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.16175C>A |
| AA Mutation | p.Pro5392Gln(p.P5392Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333244 |
| Start | 104944286:104944286(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.11165C>A |
| AA Mutation | p.Pro3722His(p.P3722H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333244 |
| Start | 104944712:104944712(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771418276 |
| CDS Mutation | c.10739G>A |
| AA Mutation | p.Gly3580Asp(p.G3580D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333244 |
| Start | 104945562:104945562(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.9889G>A |
| AA Mutation | p.Ala3297Thr(p.A3297T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333244 |
| Start | 104946057:104946057(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs552120787 |
| CDS Mutation | c.9394G>A |
| AA Mutation | p.Ala3132Thr(p.A3132T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 33 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333244 |
| Start | 104947589:104947589(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7862C>T |
| AA Mutation | p.Pro2621Leu(p.P2621L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 34 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333244 |
| Start | 104953286:104953286(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2165A>G |
| AA Mutation | p.Asp722Gly(p.D722G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 35 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333244 |
| Start | 104940152:104940152(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.15299C>T |
| AA Mutation | p.Ala5100Val(p.A5100V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 36 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333244 |
| Start | 104946437:104946437(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs570457179 |
| CDS Mutation | c.9014C>T |
| AA Mutation | p.Ala3005Val(p.A3005V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 37 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333244 |
| Start | 104949887:104949887(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5564C>T |
| AA Mutation | p.Ala1855Val(p.A1855V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 38 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333244 |
| Start | 104943144:104943144(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.12307G>A |
| AA Mutation | p.Val4103Ile(p.V4103I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 39 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333244 |
| Start | 104945663:104945663(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201088821 |
| CDS Mutation | c.9788C>T |
| AA Mutation | p.Thr3263Met(p.T3263M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 40 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333244 |
| Start | 104946158:104946158(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374657511 |
| CDS Mutation | c.9293C>T |
| AA Mutation | p.Thr3098Met(p.T3098M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 41 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333244 |
| Start | 104949615:104949615(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs544172092 |
| CDS Mutation | c.5836G>A |
| AA Mutation | p.Asp1946Asn(p.D1946N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 42 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333244 |
| Start | 104947976:104947976(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7475C>T |
| AA Mutation | p.Ser2492Leu(p.S2492L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 43 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333244 |
| Start | 104947922:104947922(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370061695 |
| CDS Mutation | c.7529C>T |
| AA Mutation | p.Ala2510Val(p.A2510V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 44 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333244 |
| Start | 104948391:104948391(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7060C>A |
| AA Mutation | p.Leu2354Ile(p.L2354I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 45 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333244 |
| Start | 104941106:104941106(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.14345C>T |
| AA Mutation | p.Ser4782Phe(p.S4782F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 46 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333244 |
| Start | 104939512:104939512(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.15939G>A |
| AA Mutation | p.Met5313Ile(p.M5313I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 47 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333244 |
| Start | 104948555:104948555(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs367959314 |
| CDS Mutation | c.6896G>A |
| AA Mutation | p.Arg2299Gln(p.R2299Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 48 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333244 |
| Start | 104951928:104951928(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3523G>A |
| AA Mutation | p.Ala1175Thr(p.A1175T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 49 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333244 |
| Start | 104953755:104953755(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1696A>G |
| AA Mutation | p.Thr566Ala(p.T566A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 50 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333244 |
| Start | 104947176:104947176(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.8275G>T |
| AA Mutation | p.Asp2759Tyr(p.D2759Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 51 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333244 |
| Start | 104942990:104942990(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201721608 |
| CDS Mutation | c.12461C>T |
| AA Mutation | p.Ala4154Val(p.A4154V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 52 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333244 |
| Start | 104948861:104948861(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6590A>T |
| AA Mutation | p.Lys2197Met(p.K2197M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 53 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333244 |
| Start | 104949628:104949628(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751555786 |
| CDS Mutation | c.5823A>C |
| AA Mutation | p.Glu1941Asp(p.E1941D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 54 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333244 |
| Start | 104942502:104942502(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.12949A>C |
| AA Mutation | p.Ile4317Leu(p.I4317L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 55 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333244 |
| Start | 104949243:104949243(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6208C>T |
| AA Mutation | p.His2070Tyr(p.H2070Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 56 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333244 |
| Start | 104954297:104954297(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374238837 |
| CDS Mutation | c.1154G>A |
| AA Mutation | p.Arg385Gln(p.R385Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 57 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333244 |
| Start | 104941088:104941088(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.14363A>C |
| AA Mutation | p.Glu4788Ala(p.E4788A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 58 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333244 |
| Start | 104946328:104946328(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.9123G>T |
| AA Mutation | p.Gln3041His(p.Q3041H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 59 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333244 |
| Start | 104938542:104938542(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.16909C>T |
| AA Mutation | p.Pro5637Ser(p.P5637S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 60 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333244 |
| Start | 104939888:104939888(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.15563G>A |
| AA Mutation | p.Ser5188Asn(p.S5188N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 61 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333244 |
| Start | 104951501:104951501(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3950C>T |
| AA Mutation | p.Ala1317Val(p.A1317V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 62 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333244 |
| Start | 104943582:104943582(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.11869G>A |
| AA Mutation | p.Ala3957Thr(p.A3957T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 63 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333244 |
| Start | 104944700:104944700(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.10751A>G |
| AA Mutation | p.Asp3584Gly(p.D3584G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 64 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333244 |
| Start | 104947028:104947028(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.8423C>T |
| AA Mutation | p.Ala2808Val(p.A2808V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 65 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333244 |
| Start | 104952564:104952564(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2887A>G |
| AA Mutation | p.Ser963Gly(p.S963G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 66 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333244 |
| Start | 104938928:104938928(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372998948 |
| CDS Mutation | c.16523C>G |
| AA Mutation | p.Thr5508Arg(p.T5508R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 67 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333244 |
| Start | 104943724:104943724(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.11727G>T |
| AA Mutation | p.Lys3909Asn(p.K3909N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 68 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333244 |
| Start | 104953408:104953408(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2043G>T |
| AA Mutation | p.Lys681Asn(p.K681N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 69 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333244 |
| Start | 104945765:104945765(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.9686T>C |
| AA Mutation | p.Leu3229Ser(p.L3229S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 70 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333244 |
| Start | 104946260:104946260(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.9191T>C |
| AA Mutation | p.Leu3064Ser(p.L3064S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 71 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333244 |
| Start | 104942114:104942114(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.13337A>T |
| AA Mutation | p.Glu4446Val(p.E4446V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 72 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333244 |
| Start | 104946662:104946662(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375454064 |
| CDS Mutation | c.8789C>T |
| AA Mutation | p.Ala2930Val(p.A2930V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 73 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333244 |
| Start | 104940644:104940644(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.14807C>T |
| AA Mutation | p.Pro4936Leu(p.P4936L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 74 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333244 |
| Start | 104942426:104942426(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.13025A>G |
| AA Mutation | p.Lys4342Arg(p.K4342R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 75 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333244 |
| Start | 104943467:104943467(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs146136367 |
| CDS Mutation | c.11984C>T |
| AA Mutation | p.Ala3995Val(p.A3995V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 76 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333244 |
| Start | 104940020:104940020(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.15431G>A |
| AA Mutation | p.Ser5144Asn(p.S5144N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 77 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333244 |
| Start | 104946989:104946989(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369899617 |
| CDS Mutation | c.8462C>T |
| AA Mutation | p.Pro2821Leu(p.P2821L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 78 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333244 |
| Start | 104949548:104949548(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs371185338 |
| CDS Mutation | c.5903C>T |
| AA Mutation | p.Ala1968Val(p.A1968V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 79 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333244 |
| Start | 104943197:104943197(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372676751 |
| CDS Mutation | c.12254C>T |
| AA Mutation | p.Ala4085Val(p.A4085V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 80 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333244 |
| Start | 104948304:104948304(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.7147G>T |
| AA Mutation | p.Asp2383Tyr(p.D2383Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 81 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000333244 |
| Start | 104952580:104952580(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs572860937 |
| CDS Mutation | c.2871C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 82 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000333244 |
| Start | 104947600:104947600(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778126939 |
| CDS Mutation | c.7851C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 83 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000333244 |
| Start | 104948146:104948146(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749939034 |
| CDS Mutation | c.7305G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 84 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000333244 |
| Start | 104944006:104944006(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.11445G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 85 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000333244 |
| Start | 104947945:104947945(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375164356 |
| CDS Mutation | c.7506C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 86 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000333244 |
| Start | 104953894:104953894(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760582773 |
| CDS Mutation | c.1557G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 87 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000333244 |
| Start | 104940844:104940844(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751493844 |
| CDS Mutation | c.14607G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 88 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000333244 |
| Start | 104948107:104948107(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs578259727 |
| CDS Mutation | c.7344C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 89 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000333244 |
| Start | 104945161:104945161(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754645832 |
| CDS Mutation | c.10290T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 90 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000333244 |
| Start | 104953264:104953264(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs568401227 |
| CDS Mutation | c.2187C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 91 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000333244 |
| Start | 104953360:104953360(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs188074688 |
| CDS Mutation | c.2091G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 92 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000333244 |
| Start | 104952490:104952490(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs371134105 |
| CDS Mutation | c.2961C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 93 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000333244 |
| Start | 104952481:104952481(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372763281 |
| CDS Mutation | c.2970C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 94 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000333244 |
| Start | 104940250:104940250(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368198892 |
| CDS Mutation | c.15201C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 95 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000333244 |
| Start | 104952829:104952829(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2622G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 96 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000333244 |
| Start | 104946823:104946823(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.8628G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 97 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000333244 |
| Start | 104950090:104950090(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5361C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 98 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000333244 |
| Start | 104948770:104948770(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs371653767 |
| CDS Mutation | c.6681C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 99 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000333244 |
| Start | 104954981:104954981(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs189780647 |
| CDS Mutation | c.627C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 100 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000333244 |
| Start | 104945656:104945656(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755891092 |
| CDS Mutation | c.9795C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 101 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000333244 |
| Start | 104949265:104949265(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs547642658 |
| CDS Mutation | c.6186C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 102 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000333244 |
| Start | 104947567:104947567(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs183423977 |
| CDS Mutation | c.7884G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 103 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000333244 |
| Start | 104950126:104950126(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375331989 |
| CDS Mutation | c.5325G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 104 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000333244 |
| Start | 104945437:104945437(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370496520 |
| CDS Mutation | c.10014G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 105 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000333244 |
| Start | 104950105:104950105(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760125461 |
| CDS Mutation | c.5346G>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 106 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000333244 |
| Start | 104943451:104943451(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs371926103 |
| CDS Mutation | c.12000C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 107 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000333244 |
| Start | 104945998:104945998(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs202104959 |
| CDS Mutation | c.9453G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 108 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000333244 |
| Start | 104941597:104941597(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760948655 |
| CDS Mutation | c.13854C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 109 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000333244 |
| Start | 104953081:104953081(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778257461 |
| CDS Mutation | c.2370C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 110 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000333244 |
| Start | 104946763:104946763(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755980026 |
| CDS Mutation | c.8688G>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |