Primary Site >> Stomach Cancer
Gene >> SNRPN
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000346403 |
| Start | 24975481:24975481(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.127T>C |
| AA Mutation | p.Cys43Arg(p.C43R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000346403 |
| Start | 24976935:24976935(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.326C>A |
| AA Mutation | p.Ala109Glu(p.A109E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000346403 |
| Start | 24976949:24976949(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370688371 |
| CDS Mutation | c.340G>T |
| AA Mutation | p.Val114Leu(p.V114L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000346403 |
| Start | 24975509:24975509(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.155A>C |
| AA Mutation | p.Lys52Thr(p.K52T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000346403 |
| Start | 24978427:24978427(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.706C>T |
| AA Mutation | p.Arg236Cys(p.R236C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000346403 |
| Start | 24978230:24978230(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.597G>T |
| AA Mutation | p.Met199Ile(p.M199I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000346403 |
| Start | 24977805:24977805(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.448G>A |
| AA Mutation | p.Val150Ile(p.V150I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000346403 |
| Start | 24978271:24978271(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.638T>C |
| AA Mutation | p.Ile213Thr(p.I213T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000346403 |
| Start | 24976316:24976316(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs571239725 |
| CDS Mutation | c.167C>T |
| AA Mutation | p.Ala56Val(p.A56V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000346403 |
| Start | 24977827:24977827(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775190561 |
| CDS Mutation | c.470C>T |
| AA Mutation | p.Ala157Val(p.A157V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |