Primary Site >> Stomach Cancer
Gene >> UNC5B
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000335350 |
| Start | 71299147:71299147(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772181278 |
| CDS Mutation | c.2708C>T |
| AA Mutation | p.Thr903Met(p.T903M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000335350 |
| Start | 71286836:71286836(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751397139 |
| CDS Mutation | c.700C>T |
| AA Mutation | p.Arg234Cys(p.R234C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000335350 |
| Start | 71290993:71290993(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1178C>T |
| AA Mutation | p.Ala393Val(p.A393V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000335350 |
| Start | 71287693:71287693(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs566257491 |
| CDS Mutation | c.829G>A |
| AA Mutation | p.Ala277Thr(p.A277T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000335350 |
| Start | 71293479:71293479(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763600986 |
| CDS Mutation | c.1847G>A |
| AA Mutation | p.Arg616His(p.R616H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000335350 |
| Start | 71296666:71296666(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2414A>G |
| AA Mutation | p.Glu805Gly(p.E805G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000335350 |
| Start | 71288631:71288631(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770198176 |
| CDS Mutation | c.965G>A |
| AA Mutation | p.Arg322His(p.R322H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000335350 |
| Start | 71297949:71297949(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2531G>A |
| AA Mutation | p.Gly844Asp(p.G844D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000335350 |
| Start | 71291482:71291482(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs141795100 |
| CDS Mutation | c.1345G>A |
| AA Mutation | p.Ala449Thr(p.A449T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000335350 |
| Start | 71295940:71295940(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2305A>G |
| AA Mutation | p.Lys769Glu(p.K769E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000335350 |
| Start | 71299262:71299262(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368414601 |
| CDS Mutation | c.2823C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000335350 |
| Start | 71287725:71287725(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771064404 |
| CDS Mutation | c.861C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |