Primary Site >> Stomach Cancer
Gene >> FGFR3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260795 |
| Start | 1801924:1801924(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.829G>A |
| AA Mutation | p.Val277Met(p.V277M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260795 |
| Start | 1801889:1801889(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779284979 |
| CDS Mutation | c.794C>T |
| AA Mutation | p.Ala265Val(p.A265V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260795 |
| Start | 1803747:1803747(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.986T>C |
| AA Mutation | p.Val329Ala(p.V329A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260795 |
| Start | 1806914:1806914(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2254C>T |
| AA Mutation | p.Leu752Phe(p.L752F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000260795 |
| Start | 1805669:1805669(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1645G>A |
| AA Mutation | p.Gly549Arg(p.G549R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260795 |
| Start | 1805810:1805810(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs146672976 |
| CDS Mutation | c.1706C>T |
| AA Mutation | p.Ala569Val(p.A569V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260795 |
| Start | 1799362:1799362(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.218T>C |
| AA Mutation | p.Val73Ala(p.V73A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260795 |
| Start | 1805842:1805842(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761196249 |
| CDS Mutation | c.1738G>A |
| AA Mutation | p.Asp580Asn(p.D580N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000260795 |
| Start | 1805841:1805841(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200589145 |
| CDS Mutation | c.1737C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |