Primary Site >> Liver Cancer
Gene >> FGFR2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358487 |
| Start | 121517373:121517373(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1030G>T |
| AA Mutation | p.Ala344Ser(p.A344S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358487 |
| Start | 121515181:121515181(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1223A>G |
| AA Mutation | p.Asp408Gly(p.D408G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358487 |
| Start | 121565519:121565519(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.295C>T |
| AA Mutation | p.Pro99Ser(p.P99S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000358487 |
| Start | 121517371:121517371(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs121918491 |
| CDS Mutation | c.1032G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | inframe_deletion |
| Transcription ID | ENST00000358487 |
| Start | 121551395:121551415(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.499_519delCATGCTGTGCCTGCGGCCAAC |
| AA Mutation | p.His167_Asn173del(p.H167_N173del) |
| Mutation Classification | In_Frame_Del |
| Feature Type | Transcript |