Primary Site >> Stomach Cancer
Gene >> MVP
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000357402 |
| Start | 29847296:29847296(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2365G>A |
| AA Mutation | p.Glu789Lys(p.E789K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000357402 |
| Start | 29841745:29841745(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1341G>T |
| AA Mutation | p.Gln447His(p.Q447H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000357402 |
| Start | 29835734:29835734(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755247776 |
| CDS Mutation | c.608C>T |
| AA Mutation | p.Ala203Val(p.A203V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000357402 |
| Start | 29844657:29844657(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1799G>A |
| AA Mutation | p.Arg600His(p.R600H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000357402 |
| Start | 29834012:29834012(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753938190 |
| CDS Mutation | c.523C>T |
| AA Mutation | p.Arg175Trp(p.R175W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000357402 |
| Start | 29841973:29841973(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1495T>C |
| AA Mutation | p.Ser499Pro(p.S499P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000357402 |
| Start | 29831008:29831008(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754161146 |
| CDS Mutation | c.256G>A |
| AA Mutation | p.Ala86Thr(p.A86T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000357402 |
| Start | 29845896:29845896(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs149725123 |
| CDS Mutation | c.2055C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000357402 |
| Start | 29841921:29841921(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1443C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000357402 |
| Start | 29841942:29841942(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs537113581 |
| CDS Mutation | c.1464G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000357402 |
| Start | 29834047:29834047(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772883962 |
| CDS Mutation | c.558C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000357402 |
| Start | 29835723:29835723(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766590067 |
| CDS Mutation | c.597C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000357402 |
| Start | 29844775:29844775(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747731704 |
| CDS Mutation | c.1917C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000357402 |
| Start | 29836949:29836949(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747145264 |
| CDS Mutation | c.900C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000357402 |
| Start | 29830579:29830579(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.35delC |
| AA Mutation | p.Pro12HisfsTer40(p.P12Hfs*40) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000357402 |
| Start | 29834030:29834030(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.541G>T |
| AA Mutation | p.Glu181Ter(p.E181*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | splice_acceptor_variant |
| Transcription ID | ENST00000357402 |
| Start | 29847195:29847195(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2266-2A>G |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |