Primary Site >> Stomach Cancer
Gene >> KRT39
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355612 |
| Start | 40958677:40958677(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749011755 |
| CDS Mutation | c.1400A>G |
| AA Mutation | p.Glu467Gly(p.E467G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355612 |
| Start | 40963670:40963670(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.665C>T |
| AA Mutation | p.Ser222Phe(p.S222F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355612 |
| Start | 40958762:40958762(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1315T>G |
| AA Mutation | p.Ser439Ala(p.S439A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355612 |
| Start | 40966778:40966778(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.79A>G |
| AA Mutation | p.Thr27Ala(p.T27A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000355612 |
| Start | 40960466:40960466(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1032G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000355612 |
| Start | 40966812:40966812(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.45A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000355612 |
| Start | 40960337:40960337(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1161C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000355612 |
| Start | 40966502:40966502(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.355C>T |
| AA Mutation | p.Arg119Ter(p.R119*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000355612 |
| Start | 40966514:40966514(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760470392 |
| CDS Mutation | c.343C>T |
| AA Mutation | p.Arg115Ter(p.R115*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |