Primary Site >> Stomach Cancer
Gene >> ALLC
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252505 |
| Start | 3702444:3702444(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1057G>T |
| AA Mutation | p.Val353Phe(p.V353F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252505 |
| Start | 3701628:3701628(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.967G>C |
| AA Mutation | p.Val323Leu(p.V323L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252505 |
| Start | 3681694:3681694(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.359A>C |
| AA Mutation | p.Glu120Ala(p.E120A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252505 |
| Start | 3695809:3695809(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs190283526 |
| CDS Mutation | c.604G>A |
| AA Mutation | p.Ala202Thr(p.A202T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252505 |
| Start | 3678534:3678534(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.151A>C |
| AA Mutation | p.Thr51Pro(p.T51P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252505 |
| Start | 3682951:3682951(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.388G>C |
| AA Mutation | p.Asp130His(p.D130H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252505 |
| Start | 3701625:3701625(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.964C>T |
| AA Mutation | p.Pro322Ser(p.P322S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000252505 |
| Start | 3697401:3697401(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.795A>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000252505 |
| Start | 3682950:3682950(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372636443 |
| CDS Mutation | c.387C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000252505 |
| Start | 3696300:3696300(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372774798 |
| CDS Mutation | c.693G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000252505 |
| Start | 3678535:3678536(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.152_153insTCTG |
| AA Mutation | p.Arg52LeufsTer51(p.R52Lfs*51) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |