Primary Site >> Stomach Cancer
Gene >> NUTM1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333756 |
| Start | 34356943:34356943(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2851G>A |
| AA Mutation | p.Glu951Lys(p.E951K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333756 |
| Start | 34348341:34348341(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.389C>T |
| AA Mutation | p.Ala130Val(p.A130V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333756 |
| Start | 34348328:34348328(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.376C>A |
| AA Mutation | p.Leu126Ile(p.L126I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333756 |
| Start | 34357478:34357478(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200540515 |
| CDS Mutation | c.3386G>A |
| AA Mutation | p.Arg1129His(p.R1129H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333756 |
| Start | 34348391:34348391(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.439G>T |
| AA Mutation | p.Ala147Ser(p.A147S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333756 |
| Start | 34353756:34353756(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.875A>G |
| AA Mutation | p.Glu292Gly(p.E292G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333756 |
| Start | 34355049:34355049(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1307T>G |
| AA Mutation | p.Leu436Arg(p.L436R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333756 |
| Start | 34350790:34350790(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.812C>T |
| AA Mutation | p.Thr271Ile(p.T271I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333756 |
| Start | 34354481:34354481(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1027G>C |
| AA Mutation | p.Ala343Pro(p.A343P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333756 |
| Start | 34348428:34348428(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746914938 |
| CDS Mutation | c.476C>T |
| AA Mutation | p.Pro159Leu(p.P159L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333756 |
| Start | 34354617:34354617(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1163C>T |
| AA Mutation | p.Ser388Leu(p.S388L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000333756 |
| Start | 34355961:34355961(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1869T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000333756 |
| Start | 34356153:34356153(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2061C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000333756 |
| Start | 34348429:34348429(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768665655 |
| CDS Mutation | c.477G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |