Primary Site >> Stomach Cancer
Gene >> CDK6
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265734 |
| Start | 92725703:92725703(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.460A>T |
| AA Mutation | p.Thr154Ser(p.T154S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000265734 |
| Start | 92618206:92618206(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.700G>A |
| AA Mutation | p.Val234Met(p.V234M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265734 |
| Start | 92774805:92774805(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761377867 |
| CDS Mutation | c.260G>A |
| AA Mutation | p.Arg87Gln(p.R87Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265734 |
| Start | 92671531:92671531(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.542T>A |
| AA Mutation | p.Val181Asp(p.V181D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265734 |
| Start | 92833148:92833148(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.176T>A |
| AA Mutation | p.Ile59Asn(p.I59N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265734 |
| Start | 92725659:92725659(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771163287 |
| CDS Mutation | c.504C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |