Primary Site >> Stomach Cancer
Gene >> WRN
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000298139 |
| Start | 31068277:31068277(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs62506077 |
| CDS Mutation | c.674G>A |
| AA Mutation | p.Arg225Gln(p.R225Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000298139 |
| Start | 31124542:31124542(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771294955 |
| CDS Mutation | c.2651G>A |
| AA Mutation | p.Arg884His(p.R884H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000298139 |
| Start | 31120391:31120391(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2597T>G |
| AA Mutation | p.Val866Gly(p.V866G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000298139 |
| Start | 31111624:31111624(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2098G>A |
| AA Mutation | p.Val700Ile(p.V700I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000298139 |
| Start | 31087874:31087874(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs149565907 |
| CDS Mutation | c.1530A>T |
| AA Mutation | p.Glu510Asp(p.E510D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000298139 |
| Start | 31090872:31090872(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1759T>C |
| AA Mutation | p.Tyr587His(p.Y587H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000298139 |
| Start | 31150360:31150360(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3592G>T |
| AA Mutation | p.Val1198Leu(p.V1198L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000298139 |
| Start | 31124557:31124557(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374262282 |
| CDS Mutation | c.2666G>A |
| AA Mutation | p.Arg889Gln(p.R889Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000298139 |
| Start | 31111765:31111765(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2239C>A |
| AA Mutation | p.Leu747Ile(p.L747I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000298139 |
| Start | 31081172:31081172(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1145A>C |
| AA Mutation | p.Lys382Thr(p.K382T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000298139 |
| Start | 31157429:31157429(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs146861737 |
| CDS Mutation | c.3881C>T |
| AA Mutation | p.Ala1294Val(p.A1294V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000298139 |
| Start | 31111650:31111650(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2124T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000298139 |
| Start | 31067146:31067146(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.618T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000298139 |
| Start | 31141594:31141594(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775952540 |
| CDS Mutation | c.3132G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000298139 |
| Start | 31120419:31120419(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2625A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000298139 |
| Start | 31120314:31120314(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2520T>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000298139 |
| Start | 31100856:31100856(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201982706 |
| CDS Mutation | c.1989G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000298139 |
| Start | 31143616:31143616(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs778872619 |
| CDS Mutation | c.3382delA |
| AA Mutation | p.Ser1128ValfsTer34(p.S1128Vfs*34) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000298139 |
| Start | 31081132:31081132(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs17847577 |
| CDS Mutation | c.1105C>T |
| AA Mutation | p.Arg369Ter(p.R369*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |