Primary Site >> Stomach Cancer
Gene >> PMS1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000441310 |
| Start | 189877296:189877296(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2659C>G |
| AA Mutation | p.Gln887Glu(p.Q887E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000441310 |
| Start | 189877285:189877285(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs377603311 |
| CDS Mutation | c.2648G>A |
| AA Mutation | p.Arg883His(p.R883H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000441310 |
| Start | 189854596:189854596(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1324A>C |
| AA Mutation | p.Ser442Arg(p.S442R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000441310 |
| Start | 189795808:189795808(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772427166 |
| CDS Mutation | c.172G>A |
| AA Mutation | p.Gly58Arg(p.G58R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000441310 |
| Start | 189854650:189854650(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1378A>C |
| AA Mutation | p.Ser460Arg(p.S460R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000441310 |
| Start | 189867903:189867903(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2447A>G |
| AA Mutation | p.Asn816Ser(p.N816S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000441310 |
| Start | 189795844:189795844(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.208G>A |
| AA Mutation | p.Ala70Thr(p.A70T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000441310 |
| Start | 189867826:189867826(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762377532 |
| CDS Mutation | c.2370C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |