Primary Site >> Stomach Cancer
Gene >> RASSF6
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000342081 |
| Start | 73576633:73576633(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.916G>A |
| AA Mutation | p.Ala306Thr(p.A306T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000342081 |
| Start | 73576471:73576471(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.973G>A |
| AA Mutation | p.Glu325Lys(p.E325K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000342081 |
| Start | 73582263:73582263(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.691T>C |
| AA Mutation | p.Ser231Pro(p.S231P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000342081 |
| Start | 73611796:73611796(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.96G>T |
| AA Mutation | p.Lys32Asn(p.K32N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000342081 |
| Start | 73581817:73581817(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.817G>A |
| AA Mutation | p.Glu273Lys(p.E273K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000342081 |
| Start | 73576712:73576712(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.837G>C |
| AA Mutation | p.Lys279Asn(p.K279N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000342081 |
| Start | 73587927:73587927(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756955118 |
| CDS Mutation | c.391C>T |
| AA Mutation | p.Arg131Cys(p.R131C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000342081 |
| Start | 73576700:73576700(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs147932445 |
| CDS Mutation | c.849G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |