Primary Site >> Stomach Cancer
Gene >> KRT23
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000209718 |
| Start | 40936479:40936479(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.125G>A |
| AA Mutation | p.Arg42His(p.R42H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000209718 |
| Start | 40936458:40936458(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.146C>T |
| AA Mutation | p.Thr49Met(p.T49M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000209718 |
| Start | 40936549:40936549(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758942765 |
| CDS Mutation | c.55G>A |
| AA Mutation | p.Gly19Arg(p.G19R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000209718 |
| Start | 40936383:40936383(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.221C>T |
| AA Mutation | p.Ala74Val(p.A74V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000209718 |
| Start | 40925379:40925379(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs575192650 |
| CDS Mutation | c.1117C>T |
| AA Mutation | p.Arg373Trp(p.R373W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000209718 |
| Start | 40936239:40936239(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201868895 |
| CDS Mutation | c.365A>G |
| AA Mutation | p.Tyr122Cys(p.Y122C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000209718 |
| Start | 40936297:40936297(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.307C>T |
| AA Mutation | p.Arg103Cys(p.R103C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000209718 |
| Start | 40936364:40936364(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.240C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000209718 |
| Start | 40936580:40936580(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.24C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000209718 |
| Start | 40930041:40930041(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370055839 |
| CDS Mutation | c.535C>T |
| AA Mutation | p.Arg179Ter(p.R179*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000209718 |
| Start | 40936484:40936485(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs748265990 |
| CDS Mutation | c.119dupG |
| AA Mutation | p.Ala41SerfsTer76(p.A41Sfs*76) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000209718 |
| Start | 40936439:40936440(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.164dupC |
| AA Mutation | p.Gly56TrpfsTer61(p.G56Wfs*61) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |