Primary Site >> Stomach Cancer
Gene >> DDX11
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000545668 |
| Start | 31091839:31091839(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1210G>A |
| AA Mutation | p.Gly404Ser(p.G404S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000545668 |
| Start | 31096661:31096661(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758908151 |
| CDS Mutation | c.1546G>A |
| AA Mutation | p.Gly516Arg(p.G516R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000545668 |
| Start | 31097948:31097948(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1826T>C |
| AA Mutation | p.Val609Ala(p.V609A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000545668 |
| Start | 31103838:31103838(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2718G>C |
| AA Mutation | p.Met906Ile(p.M906I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000545668 |
| Start | 31091827:31091827(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756846997 |
| CDS Mutation | c.1198G>A |
| AA Mutation | p.Asp400Asn(p.D400N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000545668 |
| Start | 31091753:31091753(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751663827 |
| CDS Mutation | c.1124C>T |
| AA Mutation | p.Ala375Val(p.A375V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000545668 |
| Start | 31092878:31092878(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1275C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000545668 |
| Start | 31091748:31091748(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764305418 |
| CDS Mutation | c.1119G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000545668 |
| Start | 31094801:31094801(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1461C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000545668 |
| Start | 31101097:31101097(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2019A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000545668 |
| Start | 31101868:31101868(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779746853 |
| CDS Mutation | c.2088C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |