Primary Site >> Stomach Cancer
Gene >> DCLK2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000296550 |
| Start | 150248353:150248353(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1924G>A |
| AA Mutation | p.Ala642Thr(p.A642T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000296550 |
| Start | 150232389:150232389(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1352A>C |
| AA Mutation | p.Asn451Thr(p.N451T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000296550 |
| Start | 150198035:150198035(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.893C>A |
| AA Mutation | p.Ser298Tyr(p.S298Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000296550 |
| Start | 150102783:150102783(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.727A>G |
| AA Mutation | p.Lys243Glu(p.K243E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000296550 |
| Start | 150249601:150249601(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767593622 |
| CDS Mutation | c.1990G>C |
| AA Mutation | p.Glu664Gln(p.E664Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000296550 |
| Start | 150079133:150079133(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.106A>G |
| AA Mutation | p.Ser36Gly(p.S36G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000296550 |
| Start | 150102784:150102784(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.728A>G |
| AA Mutation | p.Lys243Arg(p.K243R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000296550 |
| Start | 150102713:150102713(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.657G>C |
| AA Mutation | p.Lys219Asn(p.K219N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000296550 |
| Start | 150193208:150193208(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.827A>G |
| AA Mutation | p.Tyr276Cys(p.Y276C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000296550 |
| Start | 150079249:150079249(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.222G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000296550 |
| Start | 150220741:150220741(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775714892 |
| CDS Mutation | c.1095C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |