Primary Site >> Stomach Cancer
Gene >> FGFR2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358487 |
| Start | 121520025:121520025(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.893G>A |
| AA Mutation | p.Gly298Asp(p.G298D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358487 |
| Start | 121565524:121565524(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.290C>T |
| AA Mutation | p.Ala97Val(p.A97V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358487 |
| Start | 121515208:121515208(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1196G>A |
| AA Mutation | p.Arg399Gln(p.R399Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358487 |
| Start | 121488013:121488013(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1964A>G |
| AA Mutation | p.Asp655Gly(p.D655G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358487 |
| Start | 121565545:121565545(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.269A>C |
| AA Mutation | p.Glu90Ala(p.E90A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358487 |
| Start | 121515295:121515295(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1109C>A |
| AA Mutation | p.Thr370Lys(p.T370K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358487 |
| Start | 121565632:121565632(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199575491 |
| CDS Mutation | c.182G>A |
| AA Mutation | p.Arg61His(p.R61H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358487 |
| Start | 121487408:121487408(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2003A>C |
| AA Mutation | p.Lys668Thr(p.K668T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358487 |
| Start | 121496687:121496687(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1708G>C |
| AA Mutation | p.Gly570Arg(p.G570R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358487 |
| Start | 121517444:121517444(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.959C>T |
| AA Mutation | p.Thr320Met(p.T320M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358487 |
| Start | 121515260:121515260(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs121913474 |
| CDS Mutation | c.1144T>C |
| AA Mutation | p.Cys382Arg(p.C382R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358487 |
| Start | 121515296:121515296(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1108A>G |
| AA Mutation | p.Thr370Ala(p.T370A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358487 |
| Start | 121517398:121517398(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1005G>T |
| AA Mutation | p.Glu335Asp(p.E335D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000358487 |
| Start | 121485484:121485484(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs794727163 |
| CDS Mutation | c.2106G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000358487 |
| Start | 121520162:121520162(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs138769323 |
| CDS Mutation | c.756G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000358487 |
| Start | 121551333:121551333(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.581delA |
| AA Mutation | p.Asn194ThrfsTer39(p.N194Tfs*39) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000358487 |
| Start | 121515209:121515209(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1195C>T |
| AA Mutation | p.Arg399Ter(p.R399*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |