Primary Site >> Stomach Cancer
Gene >> PKN1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000242783 |
| Start | 14471747:14471747(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749748800 |
| CDS Mutation | c.2792C>T |
| AA Mutation | p.Ala931Val(p.A931V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000242783 |
| Start | 14450347:14450347(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.640C>T |
| AA Mutation | p.Arg214Cys(p.R214C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000242783 |
| Start | 14443529:14443529(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374744301 |
| CDS Mutation | c.382G>A |
| AA Mutation | p.Val128Met(p.V128M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000242783 |
| Start | 14469442:14469442(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2078T>C |
| AA Mutation | p.Phe693Ser(p.F693S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000242783 |
| Start | 14443581:14443581(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769391410 |
| CDS Mutation | c.434C>T |
| AA Mutation | p.Ala145Val(p.A145V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000242783 |
| Start | 14450976:14450976(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.837C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000242783 |
| Start | 14463868:14463868(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374706059 |
| CDS Mutation | c.1536C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000242783 |
| Start | 14470628:14470628(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768590761 |
| CDS Mutation | c.2490C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000242783 |
| Start | 14470248:14470248(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368511038 |
| CDS Mutation | c.2379G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |