Primary Site >> Stomach Cancer
Gene >> BRF1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000546474 |
| Start | 105228880:105228880(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs587707880 |
| CDS Mutation | c.728G>A |
| AA Mutation | p.Arg243Lys(p.R243K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000546474 |
| Start | 105219007:105219007(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1506G>T |
| AA Mutation | p.Lys502Asn(p.K502N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000546474 |
| Start | 105272721:105272721(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.439C>T |
| AA Mutation | p.His147Tyr(p.H147Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000546474 |
| Start | 105217692:105217692(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs371981699 |
| CDS Mutation | c.1624G>A |
| AA Mutation | p.Val542Met(p.V542M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000546474 |
| Start | 105241316:105241316(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.643A>C |
| AA Mutation | p.Lys215Gln(p.K215Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000546474 |
| Start | 105286353:105286353(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.208G>C |
| AA Mutation | p.Gly70Arg(p.G70R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000546474 |
| Start | 105217761:105217761(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1555A>G |
| AA Mutation | p.Ser519Gly(p.S519G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000546474 |
| Start | 105211211:105211211(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1907A>G |
| AA Mutation | p.Tyr636Cys(p.Y636C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000546474 |
| Start | 105241288:105241288(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759137877 |
| CDS Mutation | c.671G>A |
| AA Mutation | p.Arg224His(p.R224H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000546474 |
| Start | 105226670:105226670(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs765277183 |
| CDS Mutation | c.879G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000546474 |
| Start | 105217654:105217654(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368636007 |
| CDS Mutation | c.1662G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000546474 |
| Start | 105221757:105221757(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200689064 |
| CDS Mutation | c.1206C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |