Primary Site >> Stomach Cancer
Gene >> FAT2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261800 |
| Start | 151505818:151505818(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.12797C>A |
| AA Mutation | p.Pro4266His(p.P4266H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261800 |
| Start | 151544901:151544901(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6226T>C |
| AA Mutation | p.Tyr2076His(p.Y2076H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261800 |
| Start | 151568721:151568721(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.211T>C |
| AA Mutation | p.Tyr71His(p.Y71H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261800 |
| Start | 151521714:151521714(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.10879C>A |
| AA Mutation | p.Leu3627Met(p.L3627M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261800 |
| Start | 151551489:151551489(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4274G>A |
| AA Mutation | p.Gly1425Glu(p.G1425E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261800 |
| Start | 151521510:151521510(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs61743252 |
| CDS Mutation | c.11083G>A |
| AA Mutation | p.Glu3695Lys(p.E3695K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261800 |
| Start | 151542933:151542933(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.8194C>G |
| AA Mutation | p.Pro2732Ala(p.P2732A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261800 |
| Start | 151567274:151567274(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1658A>T |
| AA Mutation | p.Gln553Leu(p.Q553L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261800 |
| Start | 151525782:151525782(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.10492C>G |
| AA Mutation | p.Gln3498Glu(p.Q3498E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261800 |
| Start | 151537822:151537822(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200557129 |
| CDS Mutation | c.9164C>T |
| AA Mutation | p.Ala3055Val(p.A3055V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261800 |
| Start | 151521648:151521648(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142359154 |
| CDS Mutation | c.10945C>T |
| AA Mutation | p.Arg3649Trp(p.R3649W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261800 |
| Start | 151505953:151505953(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.12662G>A |
| AA Mutation | p.Gly4221Asp(p.G4221D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261800 |
| Start | 151568582:151568582(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.350T>G |
| AA Mutation | p.Leu117Arg(p.L117R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261800 |
| Start | 151521921:151521921(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.10672C>G |
| AA Mutation | p.Arg3558Gly(p.R3558G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261800 |
| Start | 151542330:151542330(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778219876 |
| CDS Mutation | c.8797G>A |
| AA Mutation | p.Ala2933Thr(p.A2933T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261800 |
| Start | 151553216:151553216(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs773412435 |
| CDS Mutation | c.4117G>A |
| AA Mutation | p.Val1373Ile(p.V1373I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261800 |
| Start | 151566173:151566173(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2759A>G |
| AA Mutation | p.Asp920Gly(p.D920G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261800 |
| Start | 151525898:151525898(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs745811126 |
| CDS Mutation | c.10376G>C |
| AA Mutation | p.Gly3459Ala(p.G3459A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261800 |
| Start | 151522001:151522001(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.10592C>A |
| AA Mutation | p.Ala3531Asp(p.A3531D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261800 |
| Start | 151568675:151568675(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.257A>C |
| AA Mutation | p.Glu86Ala(p.E86A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261800 |
| Start | 151550742:151550742(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4426G>A |
| AA Mutation | p.Asp1476Asn(p.D1476N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261800 |
| Start | 151567287:151567287(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759730487 |
| CDS Mutation | c.1645T>C |
| AA Mutation | p.Ser549Pro(p.S549P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261800 |
| Start | 151568645:151568645(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.287G>T |
| AA Mutation | p.Arg96Ile(p.R96I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261800 |
| Start | 151565705:151565705(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772579836 |
| CDS Mutation | c.3227G>T |
| AA Mutation | p.Gly1076Val(p.G1076V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261800 |
| Start | 151521417:151521417(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.11176C>T |
| AA Mutation | p.Pro3726Ser(p.P3726S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261800 |
| Start | 151543349:151543349(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.7778C>T |
| AA Mutation | p.Ser2593Phe(p.S2593F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261800 |
| Start | 151545317:151545317(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs145637545 |
| CDS Mutation | c.5810G>A |
| AA Mutation | p.Arg1937Gln(p.R1937Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261800 |
| Start | 151553264:151553264(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4069A>G |
| AA Mutation | p.Thr1357Ala(p.T1357A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261800 |
| Start | 151528064:151528064(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.10096C>A |
| AA Mutation | p.Leu3366Ile(p.L3366I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261800 |
| Start | 151507597:151507597(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs538316910 |
| CDS Mutation | c.12074C>T |
| AA Mutation | p.Ala4025Val(p.A4025V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261800 |
| Start | 151521900:151521900(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.10693A>G |
| AA Mutation | p.Thr3565Ala(p.T3565A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261800 |
| Start | 151542956:151542956(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.8171A>G |
| AA Mutation | p.Tyr2724Cys(p.Y2724C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 33 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261800 |
| Start | 151521647:151521647(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201335279 |
| CDS Mutation | c.10946G>A |
| AA Mutation | p.Arg3649Gln(p.R3649Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 34 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261800 |
| Start | 151542293:151542293(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.8834A>T |
| AA Mutation | p.Tyr2945Phe(p.Y2945F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 35 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261800 |
| Start | 151567073:151567073(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1859C>T |
| AA Mutation | p.Ser620Phe(p.S620F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 36 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261800 |
| Start | 151529353:151529353(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.9851G>A |
| AA Mutation | p.Ser3284Asn(p.S3284N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 37 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261800 |
| Start | 151568801:151568801(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.131A>C |
| AA Mutation | p.Glu44Ala(p.E44A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 38 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261800 |
| Start | 151544918:151544918(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6209T>A |
| AA Mutation | p.Phe2070Tyr(p.F2070Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 39 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261800 |
| Start | 151542945:151542945(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201629483 |
| CDS Mutation | c.8182C>T |
| AA Mutation | p.Arg2728Trp(p.R2728W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 40 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261800 |
| Start | 151549334:151549334(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368074191 |
| CDS Mutation | c.4750C>T |
| AA Mutation | p.Arg1584Trp(p.R1584W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 41 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261800 |
| Start | 151566050:151566050(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775693755 |
| CDS Mutation | c.2882G>A |
| AA Mutation | p.Arg961Gln(p.R961Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 42 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261800 |
| Start | 151542486:151542486(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776351095 |
| CDS Mutation | c.8641G>A |
| AA Mutation | p.Gly2881Arg(p.G2881R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 43 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261800 |
| Start | 151543361:151543361(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.7766A>C |
| AA Mutation | p.Glu2589Ala(p.E2589A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 44 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261800 |
| Start | 151568652:151568652(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.280T>G |
| AA Mutation | p.Phe94Val(p.F94V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 45 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261800 |
| Start | 151554593:151554593(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3714T>A |
| AA Mutation | p.Asn1238Lys(p.N1238K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 46 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261800 |
| Start | 151534520:151534520(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.9316G>C |
| AA Mutation | p.Val3106Leu(p.V3106L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 47 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261800 |
| Start | 151512321:151512321(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756607776 |
| CDS Mutation | c.11749G>A |
| AA Mutation | p.Val3917Met(p.V3917M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 48 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261800 |
| Start | 151566284:151566284(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs147663319 |
| CDS Mutation | c.2648G>A |
| AA Mutation | p.Arg883His(p.R883H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 49 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261800 |
| Start | 151505929:151505929(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.12686C>T |
| AA Mutation | p.Pro4229Leu(p.P4229L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 50 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261800 |
| Start | 151537883:151537883(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.9103G>A |
| AA Mutation | p.Ala3035Thr(p.A3035T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 51 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261800 |
| Start | 151507539:151507539(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.12132G>T |
| AA Mutation | p.Trp4044Cys(p.W4044C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 52 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261800 |
| Start | 151568745:151568745(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201874812 |
| CDS Mutation | c.187G>A |
| AA Mutation | p.Ala63Thr(p.A63T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 53 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261800 |
| Start | 151529249:151529249(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.9955C>T |
| AA Mutation | p.Pro3319Ser(p.P3319S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 54 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261800 |
| Start | 151521740:151521740(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.10853A>G |
| AA Mutation | p.Tyr3618Cys(p.Y3618C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 55 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261800 |
| Start | 151531635:151531635(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.9763G>A |
| AA Mutation | p.Val3255Met(p.V3255M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 56 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261800 |
| Start | 151521848:151521848(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771778319 |
| CDS Mutation | c.10745C>T |
| AA Mutation | p.Ala3582Val(p.A3582V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 57 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261800 |
| Start | 151565780:151565780(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3152T>C |
| AA Mutation | p.Val1051Ala(p.V1051A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 58 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261800 |
| Start | 151521372:151521372(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.11221G>C |
| AA Mutation | p.Val3741Leu(p.V3741L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 59 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261800 |
| Start | 151566533:151566533(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2399A>G |
| AA Mutation | p.Lys800Arg(p.K800R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 60 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261800 |
| Start | 151512486:151512486(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747251482 |
| CDS Mutation | c.11584G>A |
| AA Mutation | p.Ala3862Thr(p.A3862T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 61 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261800 |
| Start | 151568502:151568502(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.430C>A |
| AA Mutation | p.Leu144Met(p.L144M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 62 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261800 |
| Start | 151505932:151505932(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.12683T>C |
| AA Mutation | p.Phe4228Ser(p.F4228S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 63 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261800 |
| Start | 151566030:151566030(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs149531804 |
| CDS Mutation | c.2902G>A |
| AA Mutation | p.Ala968Thr(p.A968T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 64 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261800 |
| Start | 151517730:151517730(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759922777 |
| CDS Mutation | c.11353C>T |
| AA Mutation | p.Arg3785Trp(p.R3785W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 65 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261800 |
| Start | 151545232:151545232(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5895C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 66 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261800 |
| Start | 151545714:151545714(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5413T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 67 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261800 |
| Start | 151507506:151507506(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760967696 |
| CDS Mutation | c.12165C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 68 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261800 |
| Start | 151567084:151567084(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs79269043 |
| CDS Mutation | c.1848C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 69 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261800 |
| Start | 151534485:151534485(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.9351C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 70 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261800 |
| Start | 151531909:151531909(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754876966 |
| CDS Mutation | c.9489C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 71 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261800 |
| Start | 151545190:151545190(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5937G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 72 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261800 |
| Start | 151506045:151506045(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.12570C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 73 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261800 |
| Start | 151568010:151568010(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.922C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 74 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261800 |
| Start | 151553307:151553307(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs150507279 |
| CDS Mutation | c.4026G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 75 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261800 |
| Start | 151543180:151543180(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.7947G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 76 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261800 |
| Start | 151567546:151567546(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1386C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 77 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261800 |
| Start | 151554653:151554653(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3654G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 78 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261800 |
| Start | 151507179:151507179(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.12492G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 79 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261800 |
| Start | 151553250:151553250(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4083G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 80 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261800 |
| Start | 151521343:151521343(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776869049 |
| CDS Mutation | c.11250G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 81 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261800 |
| Start | 151505583:151505583(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.13032T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 82 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261800 |
| Start | 151529193:151529193(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.10011T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 83 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261800 |
| Start | 151512313:151512313(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs138511375 |
| CDS Mutation | c.11757C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 84 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261800 |
| Start | 151544941:151544941(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6186T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 85 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261800 |
| Start | 151544677:151544677(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372798111 |
| CDS Mutation | c.6450G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 86 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261800 |
| Start | 151550797:151550797(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4371T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 87 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261800 |
| Start | 151537824:151537824(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.9162G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 88 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261800 |
| Start | 151521934:151521934(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374245805 |
| CDS Mutation | c.10659C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 89 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261800 |
| Start | 151506003:151506003(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142209223 |
| CDS Mutation | c.12612G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 90 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000261800 |
| Start | 151566924:151566925(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2007_2008delAT |
| AA Mutation | p.Cys670Ter(p.C670*) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 91 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000261800 |
| Start | 151507233:151507233(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.12438delC |
| AA Mutation | p.Arg4147AspfsTer52(p.R4147Dfs*52) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 92 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000261800 |
| Start | 151525891:151525891(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.10383delC |
| AA Mutation | p.Tyr3462ThrfsTer16(p.Y3462Tfs*16) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 93 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000261800 |
| Start | 151528036:151528036(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.10124delA |
| AA Mutation | p.Lys3375ArgfsTer20(p.K3375Rfs*20) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 94 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000261800 |
| Start | 151566992:151566992(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.1940delA |
| AA Mutation | p.Asn647ThrfsTer8(p.N647Tfs*8) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 95 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000261800 |
| Start | 151510151:151510151(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757978010 |
| CDS Mutation | c.11929C>T |
| AA Mutation | p.Gln3977Ter(p.Q3977*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 96 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000261800 |
| Start | 151507232:151507233(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.12438dupC |
| AA Mutation | p.Arg4147GlnfsTer12(p.R4147Qfs*12) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 97 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000261800 |
| Start | 151540751:151540752(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.8854dupC |
| AA Mutation | p.Leu2952ProfsTer12(p.L2952Pfs*12) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 98 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000261800 |
| Start | 151543795:151543796(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.7331dupA |
| AA Mutation | p.His2445AlafsTer14(p.H2445Afs*14) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 99 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000261800 |
| Start | 151525890:151525891(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs747011618 |
| CDS Mutation | c.10383dupC |
| AA Mutation | p.Tyr3462LeufsTer26(p.Y3462Lfs*26) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |