Primary Site >> Stomach Cancer
Gene >> FAT3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000525166 |
| Start | 92797878:92797878(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4415T>A |
| AA Mutation | p.Ile1472Asn(p.I1472N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000525166 |
| Start | 92355224:92355224(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2662C>T |
| AA Mutation | p.Leu888Phe(p.L888F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000525166 |
| Start | 92799156:92799156(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5693A>G |
| AA Mutation | p.Glu1898Gly(p.E1898G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000525166 |
| Start | 92844375:92844375(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.10558C>T |
| AA Mutation | p.Arg3520Trp(p.R3520W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000525166 |
| Start | 92774113:92774113(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3818C>T |
| AA Mutation | p.Ala1273Val(p.A1273V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000525166 |
| Start | 92800641:92800641(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7178G>A |
| AA Mutation | p.Arg2393Gln(p.R2393Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000525166 |
| Start | 92800958:92800958(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7495G>A |
| AA Mutation | p.Asp2499Asn(p.D2499N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000525166 |
| Start | 92801321:92801321(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs558485124 |
| CDS Mutation | c.7858C>T |
| AA Mutation | p.Arg2620Cys(p.R2620C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000525166 |
| Start | 92355089:92355089(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201896979 |
| CDS Mutation | c.2527C>T |
| AA Mutation | p.Arg843Cys(p.R843C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000525166 |
| Start | 92867168:92867168(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.11636C>T |
| AA Mutation | p.Pro3879Leu(p.P3879L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000525166 |
| Start | 92806404:92806404(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752304278 |
| CDS Mutation | c.8686A>G |
| AA Mutation | p.Lys2896Glu(p.K2896E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000525166 |
| Start | 92354985:92354985(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs76869520 |
| CDS Mutation | c.2423T>C |
| AA Mutation | p.Leu808Pro(p.L808P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000525166 |
| Start | 92353743:92353743(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1181G>A |
| AA Mutation | p.Arg394Lys(p.R394K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000525166 |
| Start | 92354406:92354406(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1844T>C |
| AA Mutation | p.Ile615Thr(p.I615T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000525166 |
| Start | 92799087:92799087(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5624A>C |
| AA Mutation | p.Lys1875Thr(p.K1875T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000525166 |
| Start | 92844394:92844394(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.10577C>T |
| AA Mutation | p.Ala3526Val(p.A3526V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000525166 |
| Start | 92761932:92761932(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3296A>G |
| AA Mutation | p.Asp1099Gly(p.D1099G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000525166 |
| Start | 92890983:92890983(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768827430 |
| CDS Mutation | c.13190C>T |
| AA Mutation | p.Ser4397Leu(p.S4397L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000525166 |
| Start | 92801691:92801691(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs548024174 |
| CDS Mutation | c.8228T>C |
| AA Mutation | p.Val2743Ala(p.V2743A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000525166 |
| Start | 92799023:92799023(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5560G>A |
| AA Mutation | p.Val1854Ile(p.V1854I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000525166 |
| Start | 92866805:92866805(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770021927 |
| CDS Mutation | c.11273C>T |
| AA Mutation | p.Ser3758Leu(p.S3758L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000525166 |
| Start | 92355365:92355365(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2803G>A |
| AA Mutation | p.Gly935Ser(p.G935S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000525166 |
| Start | 92857336:92857336(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.11038G>A |
| AA Mutation | p.Gly3680Arg(p.G3680R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000525166 |
| Start | 92801720:92801720(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.8257T>G |
| AA Mutation | p.Ser2753Ala(p.S2753A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000525166 |
| Start | 92355272:92355272(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2710G>C |
| AA Mutation | p.Glu904Gln(p.E904Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000525166 |
| Start | 92883352:92883352(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.12446G>A |
| AA Mutation | p.Cys4149Tyr(p.C4149Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000525166 |
| Start | 92353007:92353007(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780987790 |
| CDS Mutation | c.445G>A |
| AA Mutation | p.Glu149Lys(p.E149K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000525166 |
| Start | 92353227:92353227(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.665T>C |
| AA Mutation | p.Val222Ala(p.V222A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000525166 |
| Start | 92354780:92354780(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374699170 |
| CDS Mutation | c.2218G>A |
| AA Mutation | p.Asp740Asn(p.D740N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000525166 |
| Start | 92774089:92774089(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3794T>C |
| AA Mutation | p.Ile1265Thr(p.I1265T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000525166 |
| Start | 92799594:92799594(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6131C>A |
| AA Mutation | p.Ser2044Tyr(p.S2044Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000525166 |
| Start | 92844645:92844645(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763689983 |
| CDS Mutation | c.10828G>A |
| AA Mutation | p.Asp3610Asn(p.D3610N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 33 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000525166 |
| Start | 92800527:92800527(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7064T>C |
| AA Mutation | p.Val2355Ala(p.V2355A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 34 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000525166 |
| Start | 92857226:92857226(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368909373 |
| CDS Mutation | c.10928C>T |
| AA Mutation | p.Pro3643Leu(p.P3643L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 35 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000525166 |
| Start | 92836684:92836684(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.9755A>C |
| AA Mutation | p.Lys3252Thr(p.K3252T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 36 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000525166 |
| Start | 92805159:92805159(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.8453A>G |
| AA Mutation | p.Asn2818Ser(p.N2818S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 37 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000525166 |
| Start | 92798091:92798091(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4628T>A |
| AA Mutation | p.Ile1543Asn(p.I1543N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 38 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000525166 |
| Start | 92801306:92801306(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7843A>T |
| AA Mutation | p.Ile2615Phe(p.I2615F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 39 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000525166 |
| Start | 92883150:92883150(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.12244G>A |
| AA Mutation | p.Val4082Met(p.V4082M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 40 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000525166 |
| Start | 92844069:92844069(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.10252G>T |
| AA Mutation | p.Gly3418Trp(p.G3418W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 41 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000525166 |
| Start | 92883117:92883117(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749339528 |
| CDS Mutation | c.12211G>A |
| AA Mutation | p.Val4071Ile(p.V4071I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 42 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000525166 |
| Start | 92800527:92800527(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7064T>G |
| AA Mutation | p.Val2355Gly(p.V2355G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 43 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000525166 |
| Start | 92354683:92354683(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766425087 |
| CDS Mutation | c.2121C>A |
| AA Mutation | p.Asp707Glu(p.D707E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 44 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000525166 |
| Start | 92762063:92762063(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3427T>A |
| AA Mutation | p.Tyr1143Asn(p.Y1143N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 45 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000525166 |
| Start | 92866984:92866984(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.11452C>T |
| AA Mutation | p.Arg3818Cys(p.R3818C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 46 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000525166 |
| Start | 92355395:92355395(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774427780 |
| CDS Mutation | c.2833G>A |
| AA Mutation | p.Asp945Asn(p.D945N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 47 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000525166 |
| Start | 92883364:92883364(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.12458G>A |
| AA Mutation | p.Arg4153Gln(p.R4153Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 48 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000525166 |
| Start | 92799121:92799121(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5658G>T |
| AA Mutation | p.Gln1886His(p.Q1886H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 49 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000525166 |
| Start | 92867087:92867087(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.11555G>A |
| AA Mutation | p.Arg3852His(p.R3852H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 50 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000525166 |
| Start | 92844697:92844697(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769645043 |
| CDS Mutation | c.10880C>T |
| AA Mutation | p.Pro3627Leu(p.P3627L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 51 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000525166 |
| Start | 92798478:92798478(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5015A>G |
| AA Mutation | p.Lys1672Arg(p.K1672R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 52 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000525166 |
| Start | 92798348:92798348(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4885A>C |
| AA Mutation | p.Ser1629Arg(p.S1629R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 53 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000525166 |
| Start | 92353864:92353864(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1302G>T |
| AA Mutation | p.Gln434His(p.Q434H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 54 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000525166 |
| Start | 92801763:92801763(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.8300T>A |
| AA Mutation | p.Ile2767Lys(p.I2767K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 55 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000525166 |
| Start | 92800797:92800797(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7334A>G |
| AA Mutation | p.Asp2445Gly(p.D2445G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 56 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000525166 |
| Start | 92800517:92800517(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757504785 |
| CDS Mutation | c.7054G>A |
| AA Mutation | p.Val2352Ile(p.V2352I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 57 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000525166 |
| Start | 92800229:92800229(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6766T>G |
| AA Mutation | p.Leu2256Val(p.L2256V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 58 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000525166 |
| Start | 92880884:92880884(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.11831C>T |
| AA Mutation | p.Thr3944Met(p.T3944M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 59 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000525166 |
| Start | 92352866:92352866(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.304C>A |
| AA Mutation | p.Leu102Ile(p.L102I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 60 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000525166 |
| Start | 92355296:92355296(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774197887 |
| CDS Mutation | c.2734G>A |
| AA Mutation | p.Val912Met(p.V912M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 61 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000525166 |
| Start | 92761922:92761922(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3286G>T |
| AA Mutation | p.Asp1096Tyr(p.D1096Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 62 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000525166 |
| Start | 92354970:92354970(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2408C>A |
| AA Mutation | p.Thr803Asn(p.T803N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 63 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000525166 |
| Start | 92354843:92354843(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776104026 |
| CDS Mutation | c.2281G>C |
| AA Mutation | p.Glu761Gln(p.E761Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 64 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000525166 |
| Start | 92354561:92354561(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1999C>A |
| AA Mutation | p.Leu667Met(p.L667M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 65 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000525166 |
| Start | 92799963:92799963(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6500A>G |
| AA Mutation | p.Glu2167Gly(p.E2167G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 66 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000525166 |
| Start | 92354255:92354255(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1693T>G |
| AA Mutation | p.Phe565Val(p.F565V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 67 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000525166 |
| Start | 92354435:92354435(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1873A>G |
| AA Mutation | p.Asn625Asp(p.N625D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 68 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000525166 |
| Start | 92798348:92798348(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4885A>G |
| AA Mutation | p.Ser1629Gly(p.S1629G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 69 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000525166 |
| Start | 92810002:92810002(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.8957A>G |
| AA Mutation | p.Tyr2986Cys(p.Y2986C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 70 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000525166 |
| Start | 92857241:92857241(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.10943C>A |
| AA Mutation | p.Pro3648His(p.P3648H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 71 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000525166 |
| Start | 92844208:92844208(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.10391G>C |
| AA Mutation | p.Gly3464Ala(p.G3464A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 72 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000525166 |
| Start | 92880838:92880838(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.11785G>C |
| AA Mutation | p.Gly3929Arg(p.G3929R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 73 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000525166 |
| Start | 92798478:92798478(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5015A>C |
| AA Mutation | p.Lys1672Thr(p.K1672T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 74 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000525166 |
| Start | 92697405:92697405(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3179G>T |
| AA Mutation | p.Arg1060Met(p.R1060M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 75 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000525166 |
| Start | 92353385:92353385(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370637047 |
| CDS Mutation | c.823C>T |
| AA Mutation | p.Arg275Trp(p.R275W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 76 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000525166 |
| Start | 92799777:92799777(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6314A>G |
| AA Mutation | p.Lys2105Arg(p.K2105R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 77 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000525166 |
| Start | 92353913:92353913(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1351T>G |
| AA Mutation | p.Ser451Ala(p.S451A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 78 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000525166 |
| Start | 92836593:92836593(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.9664C>T |
| AA Mutation | p.Pro3222Ser(p.P3222S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 79 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000525166 |
| Start | 92774170:92774170(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3875C>T |
| AA Mutation | p.Ala1292Val(p.A1292V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 80 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000525166 |
| Start | 92353675:92353675(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1113T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 81 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000525166 |
| Start | 92882930:92882930(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.12024C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 82 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000525166 |
| Start | 92809916:92809916(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.8871C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 83 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000525166 |
| Start | 92797870:92797870(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4407C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 84 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000525166 |
| Start | 92810069:92810069(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.9024C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 85 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000525166 |
| Start | 92524848:92524848(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3057G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 86 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000525166 |
| Start | 92354080:92354080(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1518T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 87 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000525166 |
| Start | 92883266:92883266(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768838868 |
| CDS Mutation | c.12360G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 88 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000525166 |
| Start | 92866893:92866893(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.11361C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 89 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000525166 |
| Start | 92353411:92353411(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749840160 |
| CDS Mutation | c.849G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 90 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000525166 |
| Start | 92797960:92797960(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4497G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 91 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000525166 |
| Start | 92798620:92798620(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5157C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 92 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000525166 |
| Start | 92806475:92806475(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.8757T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 93 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000525166 |
| Start | 92798408:92798408(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4945C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 94 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000525166 |
| Start | 92890741:92890741(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.12948G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 95 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000525166 |
| Start | 92524731:92524731(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2940C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 96 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000525166 |
| Start | 92800291:92800291(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6828T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 97 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000525166 |
| Start | 92866869:92866869(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.11337G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 98 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000525166 |
| Start | 92800708:92800708(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7245A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 99 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000525166 |
| Start | 92353354:92353354(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.792T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 100 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000525166 |
| Start | 92353288:92353288(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.726T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 101 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000525166 |
| Start | 92880828:92880828(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.11775C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 102 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000525166 |
| Start | 92354266:92354266(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1704T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 103 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000525166 |
| Start | 92354884:92354884(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2322T>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 104 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000525166 |
| Start | 92797978:92797978(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4515A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 105 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000525166 |
| Start | 92354371:92354371(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs114589936 |
| CDS Mutation | c.1809C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 106 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000525166 |
| Start | 92857257:92857257(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770522223 |
| CDS Mutation | c.10959G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 107 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000525166 |
| Start | 92355313:92355313(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2751T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 108 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000525166 |
| Start | 92799598:92799598(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6135C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 109 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000525166 |
| Start | 92800693:92800693(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7230G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 110 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000525166 |
| Start | 92844674:92844674(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.10857G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 111 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000525166 |
| Start | 92801281:92801281(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs773384938 |
| CDS Mutation | c.7818C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 112 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000525166 |
| Start | 92761873:92761873(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3237T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 113 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000525166 |
| Start | 92797867:92797867(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762238087 |
| CDS Mutation | c.4404G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |