Primary Site >> Stomach Cancer
Gene >> GPR161
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367835 |
| Start | 168085608:168085608(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1513A>G |
| AA Mutation | p.Ser505Gly(p.S505G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367835 |
| Start | 168096571:168096571(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764952468 |
| CDS Mutation | c.1036C>T |
| AA Mutation | p.Arg346Trp(p.R346W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367835 |
| Start | 168085716:168085716(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1405G>T |
| AA Mutation | p.Ala469Ser(p.A469S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367835 |
| Start | 168085704:168085704(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199866265 |
| CDS Mutation | c.1417G>A |
| AA Mutation | p.Glu473Lys(p.E473K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367835 |
| Start | 168096815:168096815(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.792C>G |
| AA Mutation | p.Asn264Lys(p.N264K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367835 |
| Start | 168096961:168096961(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.646A>G |
| AA Mutation | p.Arg216Gly(p.R216G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367835 |
| Start | 168096612:168096612(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779202531 |
| CDS Mutation | c.995G>A |
| AA Mutation | p.Arg332His(p.R332H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367835 |
| Start | 168104776:168104776(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.75C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367835 |
| Start | 168096737:168096737(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.870C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367835 |
| Start | 168090598:168090598(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771035075 |
| CDS Mutation | c.1170G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |