Primary Site >> Stomach Cancer
Gene >> ALB
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000295897 |
| Start | 73413488:73413488(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761031075 |
| CDS Mutation | c.912A>T |
| AA Mutation | p.Glu304Asp(p.E304D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000295897 |
| Start | 73417541:73417541(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs78575701 |
| CDS Mutation | c.1300C>T |
| AA Mutation | p.Arg434Cys(p.R434C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000295897 |
| Start | 73419628:73419628(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1774T>G |
| AA Mutation | p.Phe592Val(p.F592V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000295897 |
| Start | 73413439:73413439(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.863T>A |
| AA Mutation | p.Ile288Asn(p.I288N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000295897 |
| Start | 73413458:73413458(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143665140 |
| CDS Mutation | c.882G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | frameshift_variant;splice_region_variant |
| Transcription ID | ENST00000295897 |
| Start | 73415036:73415036(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1064delT |
| AA Mutation | p.Leu355CysfsTer17(p.L355Cfs*17) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |