Primary Site >> Stomach Cancer
Gene >> SLC43A2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000301335 |
| Start | 1616764:1616764(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.166G>A |
| AA Mutation | p.Val56Ile(p.V56I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000301335 |
| Start | 1585941:1585941(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200971388 |
| CDS Mutation | c.1189G>A |
| AA Mutation | p.Glu397Lys(p.E397K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000301335 |
| Start | 1616751:1616751(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.179C>T |
| AA Mutation | p.Thr60Ile(p.T60I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000301335 |
| Start | 1575701:1575701(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1613A>G |
| AA Mutation | p.Tyr538Cys(p.Y538C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000301335 |
| Start | 1591359:1591359(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.841A>G |
| AA Mutation | p.Ser281Gly(p.S281G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000301335 |
| Start | 1583307:1583307(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs745538583 |
| CDS Mutation | c.1247G>A |
| AA Mutation | p.Arg416Gln(p.R416Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000301335 |
| Start | 1615001:1615001(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374321900 |
| CDS Mutation | c.402G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |