Primary Site >> Stomach Cancer
Gene >> UBA2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000246548 |
| Start | 34431864:34431864(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.226G>A |
| AA Mutation | p.Ala76Thr(p.A76T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000246548 |
| Start | 34466975:34466975(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1702A>T |
| AA Mutation | p.Asn568Tyr(p.N568Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000246548 |
| Start | 34438712:34438712(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.527G>A |
| AA Mutation | p.Arg176His(p.R176H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000246548 |
| Start | 34452057:34452057(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.948G>T |
| AA Mutation | p.Lys316Asn(p.K316N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000246548 |
| Start | 34445060:34445060(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.710G>A |
| AA Mutation | p.Arg237His(p.R237H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000246548 |
| Start | 34438705:34438705(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.520A>G |
| AA Mutation | p.Thr174Ala(p.T174A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000246548 |
| Start | 34428503:34428503(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.71G>T |
| AA Mutation | p.Gly24Val(p.G24V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000246548 |
| Start | 34458893:34458893(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1370A>C |
| AA Mutation | p.His457Pro(p.H457P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000246548 |
| Start | 34443865:34443865(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.603T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000246548 |
| Start | 34451991:34451991(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs146405147 |
| CDS Mutation | c.882G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000246548 |
| Start | 34445016:34445016(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.666C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000246548 |
| Start | 34438680:34438680(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772883163 |
| CDS Mutation | c.495G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |