Primary Site >> Stomach Cancer
Gene >> FANCC
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000289081 |
| Start | 95107131:95107131(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1468C>T |
| AA Mutation | p.Leu490Phe(p.L490F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000289081 |
| Start | 95126559:95126559(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.866C>A |
| AA Mutation | p.Ala289Asp(p.A289D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000289081 |
| Start | 95125127:95125127(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.955A>G |
| AA Mutation | p.Thr319Ala(p.T319A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000289081 |
| Start | 95240729:95240729(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.265delA |
| AA Mutation | p.Ile89PhefsTer2(p.I89Ffs*2) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | frameshift_variant;splice_region_variant |
| Transcription ID | ENST00000289081 |
| Start | 95172038:95172038(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.455delA |
| AA Mutation | p.Asn152IlefsTer6(p.N152Ifs*6) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | stop_gained;splice_region_variant |
| Transcription ID | ENST00000289081 |
| Start | 95171080:95171080(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781542763 |
| CDS Mutation | c.520C>T |
| AA Mutation | p.Arg174Ter(p.R174*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000289081 |
| Start | 95101721:95101721(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370974124 |
| CDS Mutation | c.1663C>T |
| AA Mutation | p.Arg555Ter(p.R555*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |