Primary Site >> Stomach Cancer
Gene >> BCLAF1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000531224 |
| Start | 136278318:136278318(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.563A>G |
| AA Mutation | p.Lys188Arg(p.K188R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000531224 |
| Start | 136278163:136278163(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.718T>C |
| AA Mutation | p.Ser240Pro(p.S240P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000531224 |
| Start | 136277988:136277988(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs140335385 |
| CDS Mutation | c.893G>A |
| AA Mutation | p.Arg298Gln(p.R298Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000531224 |
| Start | 136269455:136269455(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2201A>C |
| AA Mutation | p.Lys734Thr(p.K734T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000531224 |
| Start | 136276339:136276339(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1186G>T |
| AA Mutation | p.Asp396Tyr(p.D396Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000531224 |
| Start | 136278706:136278706(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768427687 |
| CDS Mutation | c.175C>T |
| AA Mutation | p.Arg59Cys(p.R59C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000531224 |
| Start | 136279863:136279863(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4G>A |
| AA Mutation | p.Gly2Ser(p.G2S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000531224 |
| Start | 136278177:136278177(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.704C>T |
| AA Mutation | p.Pro235Leu(p.P235L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000531224 |
| Start | 136276137:136276137(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1388A>G |
| AA Mutation | p.Glu463Gly(p.E463G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000531224 |
| Start | 136278643:136278643(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142177067 |
| CDS Mutation | c.238T>C |
| AA Mutation | p.Tyr80His(p.Y80H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000531224 |
| Start | 136278170:136278170(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.711T>G |
| AA Mutation | p.Ser237Arg(p.S237R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000531224 |
| Start | 136278372:136278372(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.509A>G |
| AA Mutation | p.Glu170Gly(p.E170G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000531224 |
| Start | 136277965:136277965(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749571754 |
| CDS Mutation | c.916G>A |
| AA Mutation | p.Ala306Thr(p.A306T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000531224 |
| Start | 136275627:136275627(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768982507 |
| CDS Mutation | c.1757G>A |
| AA Mutation | p.Arg586Gln(p.R586Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000531224 |
| Start | 136276341:136276341(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757818777 |
| CDS Mutation | c.1184A>G |
| AA Mutation | p.Asn395Ser(p.N395S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000531224 |
| Start | 136273111:136273111(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1929T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000531224 |
| Start | 136279858:136279858(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.9C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000531224 |
| Start | 136268206:136268206(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2353G>T |
| AA Mutation | p.Glu785Ter(p.E785*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000531224 |
| Start | 136278406:136278406(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs140155621 |
| CDS Mutation | c.475C>T |
| AA Mutation | p.Arg159Ter(p.R159*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |