Primary Site >> Stomach Cancer
Gene >> DVL2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000005340 |
| Start | 7230766:7230766(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.226G>A |
| AA Mutation | p.Ala76Thr(p.A76T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000005340 |
| Start | 7227237:7227237(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1396G>A |
| AA Mutation | p.Val466Met(p.V466M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000005340 |
| Start | 7228003:7228003(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1076C>A |
| AA Mutation | p.Pro359His(p.P359H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000005340 |
| Start | 7229598:7229598(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.737G>A |
| AA Mutation | p.Arg246His(p.R246H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000005340 |
| Start | 7225902:7225902(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767490193 |
| CDS Mutation | c.2174T>C |
| AA Mutation | p.Met725Thr(p.M725T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000005340 |
| Start | 7230144:7230144(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.422C>A |
| AA Mutation | p.Ser141Tyr(p.S141Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000005340 |
| Start | 7227159:7227159(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780644904 |
| CDS Mutation | c.1474G>A |
| AA Mutation | p.Val492Ile(p.V492I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000005340 |
| Start | 7227236:7227236(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1397T>C |
| AA Mutation | p.Val466Ala(p.V466A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000005340 |
| Start | 7229894:7229894(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs150085753 |
| CDS Mutation | c.570C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000005340 |
| Start | 7227168:7227168(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1465C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000005340 |
| Start | 7230371:7230371(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.324A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000005340 |
| Start | 7229388:7229388(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780064157 |
| CDS Mutation | c.807G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000005340 |
| Start | 7226101:7226101(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1975C>T |
| AA Mutation | p.Arg659Ter(p.R659*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |