Primary Site >> Stomach Cancer
Gene >> HDAC3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000305264 |
| Start | 141630090:141630090(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748543297 |
| CDS Mutation | c.317G>A |
| AA Mutation | p.Arg106His(p.R106H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000305264 |
| Start | 141634914:141634914(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.178C>T |
| AA Mutation | p.Arg60Cys(p.R60C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000305264 |
| Start | 141625280:141625280(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1145C>T |
| AA Mutation | p.Ala382Val(p.A382V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000305264 |
| Start | 141636775:141636775(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.16G>A |
| AA Mutation | p.Ala6Thr(p.A6T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000305264 |
| Start | 141626276:141626276(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.838G>A |
| AA Mutation | p.Val280Ile(p.V280I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000305264 |
| Start | 141634890:141634890(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.202G>A |
| AA Mutation | p.Asp68Asn(p.D68N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000305264 |
| Start | 141625746:141625746(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.998C>T |
| AA Mutation | p.Ala333Val(p.A333V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000305264 |
| Start | 141628590:141628590(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs141006049 |
| CDS Mutation | c.660C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000305264 |
| Start | 141625288:141625288(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747001778 |
| CDS Mutation | c.1137C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000305264 |
| Start | 141626213:141626213(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.901C>T |
| AA Mutation | p.Arg301Ter(p.R301*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |