Primary Site >> Stomach Cancer
Gene >> FGFR4
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000292408 |
| Start | 177092353:177092353(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754633250 |
| CDS Mutation | c.760G>A |
| AA Mutation | p.Gly254Arg(p.G254R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000292408 |
| Start | 177091709:177091709(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.628G>A |
| AA Mutation | p.Val210Met(p.V210M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000292408 |
| Start | 177091803:177091803(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.722T>C |
| AA Mutation | p.Val241Ala(p.V241A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000292408 |
| Start | 177095650:177095650(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs138800021 |
| CDS Mutation | c.1748C>T |
| AA Mutation | p.Pro583Leu(p.P583L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000292408 |
| Start | 177097545:177097545(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2278A>G |
| AA Mutation | p.Thr760Ala(p.T760A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000292408 |
| Start | 177093544:177093544(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770012793 |
| CDS Mutation | c.1390C>T |
| AA Mutation | p.Arg464Trp(p.R464W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000292408 |
| Start | 177096168:177096168(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1933A>G |
| AA Mutation | p.Lys645Glu(p.K645E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000292408 |
| Start | 177090486:177090486(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.188G>A |
| AA Mutation | p.Gly63Asp(p.G63D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000292408 |
| Start | 177090593:177090593(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.295T>C |
| AA Mutation | p.Tyr99His(p.Y99H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000292408 |
| Start | 177093460:177093460(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754621505 |
| CDS Mutation | c.1306G>A |
| AA Mutation | p.Val436Met(p.V436M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000292408 |
| Start | 177093158:177093158(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766591955 |
| CDS Mutation | c.1078G>A |
| AA Mutation | p.Ala360Thr(p.A360T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000292408 |
| Start | 177090536:177090536(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772536234 |
| CDS Mutation | c.238C>T |
| AA Mutation | p.Arg80Trp(p.R80W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000292408 |
| Start | 177090962:177090962(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201257476 |
| CDS Mutation | c.461G>A |
| AA Mutation | p.Arg154His(p.R154H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000292408 |
| Start | 177090589:177090589(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.291C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000292408 |
| Start | 177097325:177097325(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770001903 |
| CDS Mutation | c.2187G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000292408 |
| Start | 177097577:177097577(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs574277502 |
| CDS Mutation | c.2310C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000292408 |
| Start | 177095558:177095558(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs528265762 |
| CDS Mutation | c.1656C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000292408 |
| Start | 177091708:177091708(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.627C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000292408 |
| Start | 177093702:177093702(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1446A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000292408 |
| Start | 177095334:177095334(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs150885537 |
| CDS Mutation | c.1524C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000292408 |
| Start | 177093277:177093277(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1201delC |
| AA Mutation | p.Arg401AlafsTer50(p.R401Afs*50) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |