Primary Site >> Liver Cancer
Gene >> KCNT1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000488444 |
| Start | 135755132:135755132(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.446T>C |
| AA Mutation | p.Leu149Pro(p.L149P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000488444 |
| Start | 135751023:135751023(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.359C>A |
| AA Mutation | p.Pro120Gln(p.P120Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000488444 |
| Start | 135765122:135765122(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1070T>A |
| AA Mutation | p.Leu357Gln(p.L357Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000488444 |
| Start | 135784550:135784550(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2902T>A |
| AA Mutation | p.Tyr968Asn(p.Y968N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000488444 |
| Start | 135770924:135770924(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1780C>G |
| AA Mutation | p.Arg594Gly(p.R594G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000488444 |
| Start | 135768896:135768896(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs750267867 |
| CDS Mutation | c.1412A>G |
| AA Mutation | p.Gln471Arg(p.Q471R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000488444 |
| Start | 135768873:135768873(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1389C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000488444 |
| Start | 135770917:135770917(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1773G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000488444 |
| Start | 135784064:135784067(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2828_2831delTGCC |
| AA Mutation | p.Leu943ArgfsTer22(p.L943Rfs*22) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | splice_donor_variant |
| Transcription ID | ENST00000488444 |
| Start | 135755170:135755170(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.483+1G>T |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | splice_acceptor_variant |
| Transcription ID | ENST00000488444 |
| Start | 135778686:135778686(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2538-2A>C |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |