Primary Site >> Stomach Cancer
Gene >> SUGP1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000247001 |
| Start | 19280259:19280259(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1276G>A |
| AA Mutation | p.Gly426Arg(p.G426R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000247001 |
| Start | 19279297:19279297(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200366547 |
| CDS Mutation | c.1444G>A |
| AA Mutation | p.Gly482Ser(p.G482S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000247001 |
| Start | 19276662:19276662(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1924C>T |
| AA Mutation | p.Arg642Trp(p.R642W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000247001 |
| Start | 19303820:19303820(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775710080 |
| CDS Mutation | c.566G>A |
| AA Mutation | p.Arg189Gln(p.R189Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000247001 |
| Start | 19297000:19297000(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1232C>T |
| AA Mutation | p.Ser411Leu(p.S411L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000247001 |
| Start | 19303773:19303773(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs150375001 |
| CDS Mutation | c.613G>A |
| AA Mutation | p.Glu205Lys(p.E205K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000247001 |
| Start | 19302346:19302346(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.806A>G |
| AA Mutation | p.Lys269Arg(p.K269R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000247001 |
| Start | 19280218:19280218(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375092440 |
| CDS Mutation | c.1317C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |