Primary Site >> Stomach Cancer
Gene >> KRT5
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252242 |
| Start | 52516676:52516676(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs60271599 |
| CDS Mutation | c.1400T>C |
| AA Mutation | p.Ile467Thr(p.I467T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252242 |
| Start | 52520194:52520194(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374017172 |
| CDS Mutation | c.103G>A |
| AA Mutation | p.Val35Met(p.V35M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252242 |
| Start | 52520110:52520110(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776667863 |
| CDS Mutation | c.187C>T |
| AA Mutation | p.Arg63Trp(p.R63W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252242 |
| Start | 52517691:52517691(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs61297109 |
| CDS Mutation | c.991C>T |
| AA Mutation | p.Arg331Cys(p.R331C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252242 |
| Start | 52519069:52519069(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.647A>T |
| AA Mutation | p.Glu216Val(p.E216V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252242 |
| Start | 52519067:52519067(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.649C>T |
| AA Mutation | p.Pro217Ser(p.P217S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000252242 |
| Start | 52517197:52517197(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs367665298 |
| CDS Mutation | c.1128C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |