Primary Site >> Stomach Cancer
Gene >> FICD
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000552695 |
| Start | 108519399:108519399(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1301C>T |
| AA Mutation | p.Thr434Ile(p.T434I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000552695 |
| Start | 108519456:108519456(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372450332 |
| CDS Mutation | c.1358C>T |
| AA Mutation | p.Thr453Met(p.T453M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000552695 |
| Start | 108518855:108518855(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767630290 |
| CDS Mutation | c.757G>A |
| AA Mutation | p.Val253Met(p.V253M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000552695 |
| Start | 108519349:108519349(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1251C>A |
| AA Mutation | p.Phe417Leu(p.F417L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000552695 |
| Start | 108519309:108519309(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1211A>G |
| AA Mutation | p.Glu404Gly(p.E404G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000552695 |
| Start | 108519047:108519047(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770607435 |
| CDS Mutation | c.949G>A |
| AA Mutation | p.Gly317Arg(p.G317R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000552695 |
| Start | 108519008:108519008(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763250722 |
| CDS Mutation | c.910G>A |
| AA Mutation | p.Val304Met(p.V304M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000552695 |
| Start | 108518744:108518744(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs151147125 |
| CDS Mutation | c.646C>T |
| AA Mutation | p.Arg216Cys(p.R216C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000552695 |
| Start | 108519335:108519335(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1237C>T |
| AA Mutation | p.Pro413Ser(p.P413S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000552695 |
| Start | 108517101:108517101(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201767952 |
| CDS Mutation | c.129G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000552695 |
| Start | 108519205:108519205(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs536678902 |
| CDS Mutation | c.1107C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000552695 |
| Start | 108518788:108518788(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751598998 |
| CDS Mutation | c.690A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000552695 |
| Start | 108519409:108519409(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368029472 |
| CDS Mutation | c.1311G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000552695 |
| Start | 108519007:108519007(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs750760178 |
| CDS Mutation | c.909C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |