Primary Site >> Stomach Cancer
Gene >> RFX3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382004 |
| Start | 3330369:3330369(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.364G>A |
| AA Mutation | p.Val122Ile(p.V122I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382004 |
| Start | 3257078:3257078(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1727T>C |
| AA Mutation | p.Val576Ala(p.V576A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382004 |
| Start | 3293131:3293131(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.677G>T |
| AA Mutation | p.Gly226Val(p.G226V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382004 |
| Start | 3262957:3262957(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1583G>A |
| AA Mutation | p.Arg528His(p.R528H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000382004 |
| Start | 3225156:3225156(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs113424988 |
| CDS Mutation | c.2136C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000382004 |
| Start | 3257056:3257056(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1749C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000382004 |
| Start | 3293099:3293099(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757065522 |
| CDS Mutation | c.709C>T |
| AA Mutation | p.Arg237Ter(p.R237*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant;splice_region_variant |
| Transcription ID | ENST00000382004 |
| Start | 3277341:3277342(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.971dupT |
| AA Mutation | p.Leu324PhefsTer14(p.L324Ffs*14) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |