Primary Site >> Stomach Cancer
Gene >> FGFR1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000447712 |
| Start | 38418235:38418235(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1423C>T |
| AA Mutation | p.Arg475Trp(p.R475W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000447712 |
| Start | 38414625:38414625(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1982G>A |
| AA Mutation | p.Arg661Gln(p.R661Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000447712 |
| Start | 38418234:38418234(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747333248 |
| CDS Mutation | c.1424G>A |
| AA Mutation | p.Arg475Gln(p.R475Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000447712 |
| Start | 38424603:38424603(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.842G>A |
| AA Mutation | p.Ser281Asn(p.S281N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000447712 |
| Start | 38424697:38424697(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.748C>T |
| AA Mutation | p.Arg250Trp(p.R250W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000447712 |
| Start | 38421806:38421806(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774768179 |
| CDS Mutation | c.1072G>A |
| AA Mutation | p.Val358Ile(p.V358I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000447712 |
| Start | 38418250:38418250(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781310679 |
| CDS Mutation | c.1408C>T |
| AA Mutation | p.Arg470Cys(p.R470C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000447712 |
| Start | 38421823:38421823(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1055A>G |
| AA Mutation | p.His352Arg(p.H352R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000447712 |
| Start | 38414598:38414598(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2009A>G |
| AA Mutation | p.Glu670Gly(p.E670G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000447712 |
| Start | 38429801:38429801(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201055054 |
| CDS Mutation | c.239G>A |
| AA Mutation | p.Arg80His(p.R80H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000447712 |
| Start | 38421905:38421905(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.973G>A |
| AA Mutation | p.Val325Met(p.V325M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000447712 |
| Start | 38424592:38424592(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.853C>T |
| AA Mutation | p.Pro285Ser(p.P285S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000447712 |
| Start | 38413992:38413992(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2218G>A |
| AA Mutation | p.Val740Met(p.V740M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000447712 |
| Start | 38414010:38414010(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2200C>T |
| AA Mutation | p.Arg734Trp(p.R734W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000447712 |
| Start | 38415990:38415990(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1734C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000447712 |
| Start | 38417958:38417958(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1464C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000447712 |
| Start | 38413945:38413945(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2265C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000447712 |
| Start | 38421807:38421807(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746072842 |
| CDS Mutation | c.1071C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |