Primary Site >> Stomach Cancer
Gene >> SLC22A2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366953 |
| Start | 160258360:160258360(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771411024 |
| CDS Mutation | c.398C>T |
| AA Mutation | p.Ser133Leu(p.S133L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366953 |
| Start | 160258511:160258511(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs750937051 |
| CDS Mutation | c.247G>A |
| AA Mutation | p.Glu83Lys(p.E83K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366953 |
| Start | 160258603:160258603(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767569658 |
| CDS Mutation | c.155G>A |
| AA Mutation | p.Arg52Gln(p.R52Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366953 |
| Start | 160258435:160258435(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.323C>A |
| AA Mutation | p.Ala108Asp(p.A108D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366953 |
| Start | 160249366:160249366(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774295115 |
| CDS Mutation | c.692G>A |
| AA Mutation | p.Arg231Gln(p.R231Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000366953 |
| Start | 160249287:160249287(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs147817271 |
| CDS Mutation | c.771C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000366953 |
| Start | 160258587:160258587(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775546553 |
| CDS Mutation | c.171C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000366953 |
| Start | 160258740:160258740(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs139039970 |
| CDS Mutation | c.18C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |