Primary Site >> Stomach Cancer
Gene >> DHX40
| ID | 1 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000251241 |
| Start | 59577364:59577364(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1072A>G |
| AA Mutation | p.Arg358Gly(p.R358G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000251241 |
| Start | 59607072:59607072(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2240G>C |
| AA Mutation | p.Arg747Thr(p.R747T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000251241 |
| Start | 59573844:59573844(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.651G>T |
| AA Mutation | p.Lys217Asn(p.K217N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000251241 |
| Start | 59577358:59577358(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1066G>A |
| AA Mutation | p.Gly356Arg(p.G356R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000251241 |
| Start | 59587901:59587901(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1430G>A |
| AA Mutation | p.Gly477Asp(p.G477D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000251241 |
| Start | 59602609:59602609(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1894G>C |
| AA Mutation | p.Ala632Pro(p.A632P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000251241 |
| Start | 59602588:59602588(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1873G>A |
| AA Mutation | p.Ala625Thr(p.A625T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000251241 |
| Start | 59577341:59577341(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1049C>T |
| AA Mutation | p.Thr350Met(p.T350M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000251241 |
| Start | 59577352:59577352(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1060A>T |
| AA Mutation | p.Ile354Leu(p.I354L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000251241 |
| Start | 59607042:59607042(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs544885439 |
| CDS Mutation | c.2210C>T |
| AA Mutation | p.Ser737Leu(p.S737L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000251241 |
| Start | 59602545:59602545(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1830C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000251241 |
| Start | 59602593:59602593(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761505328 |
| CDS Mutation | c.1878C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000251241 |
| Start | 59605514:59605514(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375333883 |
| CDS Mutation | c.2040C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000251241 |
| Start | 59579481:59579481(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767404014 |
| CDS Mutation | c.1083A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |