Primary Site >> Stomach Cancer
Gene >> HDAC6
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000334136 |
| Start | 48820182:48820182(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2264C>T |
| AA Mutation | p.Ser755Leu(p.S755L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000334136 |
| Start | 48822786:48822786(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199596944 |
| CDS Mutation | c.2504G>A |
| AA Mutation | p.Arg835Gln(p.R835Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000334136 |
| Start | 48816146:48816146(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1499A>G |
| AA Mutation | p.His500Arg(p.H500R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000334136 |
| Start | 48805494:48805494(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.368G>A |
| AA Mutation | p.Gly123Asp(p.G123D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000334136 |
| Start | 48823361:48823361(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2962G>A |
| AA Mutation | p.Ala988Thr(p.A988T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000334136 |
| Start | 48814981:48814981(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1079C>T |
| AA Mutation | p.Pro360Leu(p.P360L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000334136 |
| Start | 48820211:48820211(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2293C>A |
| AA Mutation | p.Leu765Met(p.L765M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000334136 |
| Start | 48815417:48815417(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs147989097 |
| CDS Mutation | c.1183G>A |
| AA Mutation | p.Val395Ile(p.V395I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000334136 |
| Start | 48816178:48816178(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1531A>G |
| AA Mutation | p.Met511Val(p.M511V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000334136 |
| Start | 48808309:48808309(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.789C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000334136 |
| Start | 48803151:48803151(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs202245023 |
| CDS Mutation | c.246A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |