Primary Site >> Stomach Cancer
Gene >> CHFR
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000432561 |
| Start | 132851630:132851630(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746554223 |
| CDS Mutation | c.1516G>A |
| AA Mutation | p.Ala506Thr(p.A506T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000432561 |
| Start | 132859143:132859143(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.872C>T |
| AA Mutation | p.Ala291Val(p.A291V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000432561 |
| Start | 132843051:132843051(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1912G>A |
| AA Mutation | p.Gly638Ser(p.G638S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000432561 |
| Start | 132859129:132859129(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.886G>C |
| AA Mutation | p.Asp296His(p.D296H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000432561 |
| Start | 132861535:132861535(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs150995074 |
| CDS Mutation | c.719C>T |
| AA Mutation | p.Ala240Val(p.A240V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000432561 |
| Start | 132851637:132851637(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142511371 |
| CDS Mutation | c.1509G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000432561 |
| Start | 132859079:132859079(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.936C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000432561 |
| Start | 132859166:132859166(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747517165 |
| CDS Mutation | c.849C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000432561 |
| Start | 132872326:132872327(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.301dupG |
| AA Mutation | p.Asp101GlyfsTer11(p.D101Gfs*11) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |