Primary Site >> Stomach Cancer
Gene >> UBASH3B
| ID | 1 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000284273 |
| Start | 122783054:122783054(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.603A>C |
| AA Mutation | p.Glu201Asp(p.E201D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000284273 |
| Start | 122789169:122789169(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.841A>G |
| AA Mutation | p.Ile281Val(p.I281V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000284273 |
| Start | 122799007:122799007(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs550761105 |
| CDS Mutation | c.1423G>A |
| AA Mutation | p.Val475Ile(p.V475I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000284273 |
| Start | 122808124:122808124(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1760T>C |
| AA Mutation | p.Leu587Pro(p.L587P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000284273 |
| Start | 122779564:122779564(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.470A>C |
| AA Mutation | p.Lys157Thr(p.K157T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000284273 |
| Start | 122808093:122808093(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777116957 |
| CDS Mutation | c.1729G>A |
| AA Mutation | p.Ala577Thr(p.A577T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000284273 |
| Start | 122808172:122808172(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1808G>A |
| AA Mutation | p.Arg603Gln(p.R603Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000284273 |
| Start | 122789224:122789224(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766138790 |
| CDS Mutation | c.896C>T |
| AA Mutation | p.Thr299Met(p.T299M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000284273 |
| Start | 122779692:122779692(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.598A>T |
| AA Mutation | p.Thr200Ser(p.T200S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000284273 |
| Start | 122809807:122809807(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1871T>G |
| AA Mutation | p.Leu624Arg(p.L624R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000284273 |
| Start | 122779639:122779639(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.545C>T |
| AA Mutation | p.Ala182Val(p.A182V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000284273 |
| Start | 122789237:122789237(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766919387 |
| CDS Mutation | c.909C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000284273 |
| Start | 122783213:122783213(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.762T>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000284273 |
| Start | 122779601:122779601(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs140669282 |
| CDS Mutation | c.507G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |