Primary Site >> Stomach Cancer
Gene >> HHAT
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261458 |
| Start | 210623553:210623553(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs367896407 |
| CDS Mutation | c.1273C>T |
| AA Mutation | p.Arg425Cys(p.R425C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261458 |
| Start | 210464519:210464519(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.871G>A |
| AA Mutation | p.Ala291Thr(p.A291T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261458 |
| Start | 210587978:210587978(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1124T>C |
| AA Mutation | p.Val375Ala(p.V375A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261458 |
| Start | 210464627:210464627(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753743106 |
| CDS Mutation | c.979A>G |
| AA Mutation | p.Thr327Ala(p.T327A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261458 |
| Start | 210404648:210404648(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.653C>A |
| AA Mutation | p.Pro218His(p.P218H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261458 |
| Start | 210418218:210418218(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs148639278 |
| CDS Mutation | c.749G>A |
| AA Mutation | p.Arg250His(p.R250H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261458 |
| Start | 210513168:210513168(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1023A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261458 |
| Start | 210404511:210404511(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs111463628 |
| CDS Mutation | c.516G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000261458 |
| Start | 210587901:210587901(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1047T>G |
| AA Mutation | p.Tyr349Ter(p.Y349*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000261458 |
| Start | 210348985:210348985(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779025178 |
| CDS Mutation | c.10C>T |
| AA Mutation | p.Arg4Ter(p.R4*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |