Primary Site >> Stomach Cancer
Gene >> SLC16A3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000392339 |
| Start | 82238968:82238968(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1390A>G |
| AA Mutation | p.Ser464Gly(p.S464G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000392339 |
| Start | 82237561:82237561(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.791C>T |
| AA Mutation | p.Ala264Val(p.A264V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000392339 |
| Start | 82237830:82237830(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1060A>G |
| AA Mutation | p.Ser354Gly(p.S354G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000392339 |
| Start | 82237527:82237527(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781158081 |
| CDS Mutation | c.757G>A |
| AA Mutation | p.Ala253Thr(p.A253T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000392339 |
| Start | 82237467:82237467(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs186654805 |
| CDS Mutation | c.697G>A |
| AA Mutation | p.Val233Met(p.V233M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000392339 |
| Start | 82236729:82236729(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.224G>A |
| AA Mutation | p.Gly75Asp(p.G75D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000392339 |
| Start | 82237425:82237425(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.655G>A |
| AA Mutation | p.Asp219Asn(p.D219N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000392339 |
| Start | 82237652:82237652(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs571273730 |
| CDS Mutation | c.882C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000392339 |
| Start | 82236131:82236131(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.123C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000392339 |
| Start | 82238961:82238961(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs377133474 |
| CDS Mutation | c.1383G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |