Primary Site >> Stomach Cancer
Gene >> SHKBP1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000291842 |
| Start | 40580348:40580348(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774556159 |
| CDS Mutation | c.425G>A |
| AA Mutation | p.Arg142Gln(p.R142Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000291842 |
| Start | 40583622:40583622(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1070G>A |
| AA Mutation | p.Arg357His(p.R357H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000291842 |
| Start | 40580877:40580877(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.785C>T |
| AA Mutation | p.Ala262Val(p.A262V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000291842 |
| Start | 40583431:40583431(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.994G>A |
| AA Mutation | p.Ala332Thr(p.A332T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000291842 |
| Start | 40580920:40580920(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759277424 |
| CDS Mutation | c.828C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000291842 |
| Start | 40583650:40583650(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs114170090 |
| CDS Mutation | c.1098C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |