Primary Site >> Liver Cancer
Gene >> KCNH2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262186 |
| Start | 150974758:150974758(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199473495 |
| CDS Mutation | c.260T>C |
| AA Mutation | p.Leu87Pro(p.L87P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000262186 |
| Start | 150946877:150946877(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3330G>T |
| AA Mutation | p.Gln1110His(p.Q1110H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262186 |
| Start | 150952675:150952675(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199472901 |
| CDS Mutation | c.1307C>T |
| AA Mutation | p.Thr436Met(p.T436M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262186 |
| Start | 150945442:150945442(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781369850 |
| CDS Mutation | c.3403C>T |
| AA Mutation | p.Arg1135Cys(p.R1135C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262186 |
| Start | 150951719:150951719(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs554855472 |
| CDS Mutation | c.1674G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262186 |
| Start | 150947021:150947021(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3186T>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262186 |
| Start | 150948994:150948994(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs72549418 |
| CDS Mutation | c.2454G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |