Primary Site >> Stomach Cancer
Gene >> NLGN4X
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000275857 |
| Start | 5903653:5903653(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1025C>T |
| AA Mutation | p.Pro342Leu(p.P342L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000275857 |
| Start | 5893184:5893184(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2084C>T |
| AA Mutation | p.Ala695Val(p.A695V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000275857 |
| Start | 6151361:6151361(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.106T>G |
| AA Mutation | p.Phe36Val(p.F36V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000275857 |
| Start | 5903470:5903470(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1208T>C |
| AA Mutation | p.Val403Ala(p.V403A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000275857 |
| Start | 5893140:5893140(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763458960 |
| CDS Mutation | c.2128C>T |
| AA Mutation | p.Arg710Cys(p.R710C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000275857 |
| Start | 6151362:6151362(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs398124363 |
| CDS Mutation | c.105G>T |
| AA Mutation | p.Lys35Asn(p.K35N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000275857 |
| Start | 5903660:5903660(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1018T>A |
| AA Mutation | p.Phe340Ile(p.F340I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000275857 |
| Start | 5892867:5892867(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2401G>A |
| AA Mutation | p.Gly801Arg(p.G801R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000275857 |
| Start | 5909112:5909112(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.753T>G |
| AA Mutation | p.Phe251Leu(p.F251L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000275857 |
| Start | 6151066:6151066(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.401C>G |
| AA Mutation | p.Thr134Ser(p.T134S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000275857 |
| Start | 5893461:5893461(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1807A>G |
| AA Mutation | p.Ile603Val(p.I603V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000275857 |
| Start | 6151001:6151001(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.466G>A |
| AA Mutation | p.Glu156Lys(p.E156K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000275857 |
| Start | 5893316:5893316(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1952A>T |
| AA Mutation | p.Lys651Met(p.K651M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000275857 |
| Start | 5893312:5893312(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1956C>A |
| AA Mutation | p.Asp652Glu(p.D652E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000275857 |
| Start | 5909206:5909206(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.659G>A |
| AA Mutation | p.Gly220Asp(p.G220D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000275857 |
| Start | 6029394:6029394(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.511T>C |
| AA Mutation | p.Tyr171His(p.Y171H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000275857 |
| Start | 5903680:5903680(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.998C>T |
| AA Mutation | p.Pro333Leu(p.P333L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000275857 |
| Start | 5903756:5903756(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.922A>G |
| AA Mutation | p.Met308Val(p.M308V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000275857 |
| Start | 6029411:6029411(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.494A>C |
| AA Mutation | p.Lys165Thr(p.K165T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000275857 |
| Start | 5893145:5893145(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2123A>G |
| AA Mutation | p.His708Arg(p.H708R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000275857 |
| Start | 5903794:5903794(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.884A>C |
| AA Mutation | p.Lys295Thr(p.K295T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000275857 |
| Start | 6151181:6151181(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.286T>C |
| AA Mutation | p.Ser96Pro(p.S96P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000275857 |
| Start | 5903086:5903086(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1592C>T |
| AA Mutation | p.Ala531Val(p.A531V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000275857 |
| Start | 5893157:5893157(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2111G>A |
| AA Mutation | p.Arg704His(p.R704H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000275857 |
| Start | 5893596:5893596(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1672G>A |
| AA Mutation | p.Ala558Thr(p.A558T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000275857 |
| Start | 5903305:5903305(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1373A>G |
| AA Mutation | p.Asp458Gly(p.D458G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000275857 |
| Start | 5892938:5892938(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2330A>T |
| AA Mutation | p.Asn777Ile(p.N777I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000275857 |
| Start | 5893179:5893179(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2089T>C |
| AA Mutation | p.Tyr697His(p.Y697H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000275857 |
| Start | 5903115:5903115(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs144614029 |
| CDS Mutation | c.1563C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000275857 |
| Start | 6151107:6151107(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.360G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000275857 |
| Start | 5903088:5903088(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778867539 |
| CDS Mutation | c.1590C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000275857 |
| Start | 5903643:5903643(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749255933 |
| CDS Mutation | c.1035C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 33 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000275857 |
| Start | 5903535:5903535(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764507720 |
| CDS Mutation | c.1143C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 34 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000275857 |
| Start | 5893183:5893183(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755736361 |
| CDS Mutation | c.2085G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 35 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000275857 |
| Start | 5903307:5903307(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1371C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 36 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000275857 |
| Start | 5903457:5903457(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1221C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 37 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000275857 |
| Start | 5909078:5909078(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.787T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 38 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000275857 |
| Start | 5903133:5903133(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772619986 |
| CDS Mutation | c.1545C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |