Primary Site >> Stomach Cancer
Gene >> KRT18
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000388835 |
| Start | 52952819:52952819(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1270G>T |
| AA Mutation | p.Asp424Tyr(p.D424Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000388835 |
| Start | 52951620:52951620(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.797A>T |
| AA Mutation | p.Glu266Val(p.E266V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000388835 |
| Start | 52949396:52949396(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.223G>A |
| AA Mutation | p.Gly75Arg(p.G75R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000388835 |
| Start | 52951595:52951595(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.772G>A |
| AA Mutation | p.Glu258Lys(p.E258K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000388835 |
| Start | 52949295:52949295(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.122G>A |
| AA Mutation | p.Gly41Asp(p.G41D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000388835 |
| Start | 52950858:52950858(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752822458 |
| CDS Mutation | c.609C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |