Primary Site >> Stomach Cancer
Gene >> DAG1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000308775 |
| Start | 49533171:49533171(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776025512 |
| CDS Mutation | c.2660G>A |
| AA Mutation | p.Arg887Gln(p.R887Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000308775 |
| Start | 49510683:49510683(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.149T>C |
| AA Mutation | p.Met50Thr(p.M50T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000308775 |
| Start | 49531442:49531442(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.931C>T |
| AA Mutation | p.Arg311Trp(p.R311W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000308775 |
| Start | 49510790:49510790(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.256T>G |
| AA Mutation | p.Leu86Val(p.L86V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000308775 |
| Start | 49532234:49532234(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1723T>C |
| AA Mutation | p.Tyr575His(p.Y575H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000308775 |
| Start | 49510812:49510812(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.278T>G |
| AA Mutation | p.Ile93Ser(p.I93S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000308775 |
| Start | 49531493:49531493(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.982A>G |
| AA Mutation | p.Thr328Ala(p.T328A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000308775 |
| Start | 49531008:49531008(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs556413209 |
| CDS Mutation | c.497C>T |
| AA Mutation | p.Ser166Leu(p.S166L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000308775 |
| Start | 49532829:49532829(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2318T>C |
| AA Mutation | p.Ile773Thr(p.I773T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000308775 |
| Start | 49531479:49531479(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.968C>T |
| AA Mutation | p.Ala323Val(p.A323V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000308775 |
| Start | 49532196:49532196(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761497544 |
| CDS Mutation | c.1685A>G |
| AA Mutation | p.Tyr562Cys(p.Y562C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000308775 |
| Start | 49531154:49531154(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs562046526 |
| CDS Mutation | c.643C>T |
| AA Mutation | p.Arg215Trp(p.R215W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |