Primary Site >> Stomach Cancer
Gene >> NSMF
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371475 |
| Start | 137453787:137453787(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.866G>A |
| AA Mutation | p.Arg289Gln(p.R289Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371475 |
| Start | 137453153:137453153(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776985530 |
| CDS Mutation | c.950C>T |
| AA Mutation | p.Thr317Met(p.T317M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371475 |
| Start | 137450005:137450005(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1337G>A |
| AA Mutation | p.Arg446His(p.R446H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371475 |
| Start | 137449967:137449967(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1375C>A |
| AA Mutation | p.His459Asn(p.H459N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371475 |
| Start | 137452565:137452565(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1153G>A |
| AA Mutation | p.Glu385Lys(p.E385K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371475 |
| Start | 137453073:137453073(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs570925575 |
| CDS Mutation | c.1030G>A |
| AA Mutation | p.Val344Met(p.V344M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371475 |
| Start | 137453084:137453084(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200107765 |
| CDS Mutation | c.1019C>T |
| AA Mutation | p.Thr340Ile(p.T340I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371475 |
| Start | 137453129:137453129(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.974T>C |
| AA Mutation | p.Leu325Pro(p.L325P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371475 |
| Start | 137455281:137455281(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.737A>G |
| AA Mutation | p.Lys246Arg(p.K246R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000371475 |
| Start | 137449472:137449472(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778638506 |
| CDS Mutation | c.1515G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |