Primary Site >> Stomach Cancer
Gene >> FOLH1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256999 |
| Start | 49186753:49186753(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.530T>G |
| AA Mutation | p.Val177Gly(p.V177G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256999 |
| Start | 49169201:49169201(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1366A>G |
| AA Mutation | p.Ile456Val(p.I456V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256999 |
| Start | 49154258:49154258(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143235150 |
| CDS Mutation | c.1858C>A |
| AA Mutation | p.Gln620Lys(p.Q620K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256999 |
| Start | 49157998:49157998(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1486A>G |
| AA Mutation | p.Ser496Gly(p.S496G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000256999 |
| Start | 49175859:49175859(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1019A>G |
| AA Mutation | p.Gln340Arg(p.Q340R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256999 |
| Start | 49200391:49200391(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.275T>C |
| AA Mutation | p.Leu92Pro(p.L92P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256999 |
| Start | 49186766:49186766(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778134535 |
| CDS Mutation | c.517G>A |
| AA Mutation | p.Asp173Asn(p.D173N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000256999 |
| Start | 49208386:49208386(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.24C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000256999 |
| Start | 49148718:49148718(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1984A>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000256999 |
| Start | 49157983:49157983(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs764290022 |
| CDS Mutation | c.1501delA |
| AA Mutation | p.Ser501ValfsTer12(p.S501Vfs*12) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |