Primary Site >> Stomach Cancer
Gene >> DEAF1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382409 |
| Start | 686886:686886(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.776C>T |
| AA Mutation | p.Ala259Val(p.A259V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382409 |
| Start | 674690:674690(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751558688 |
| CDS Mutation | c.1349C>T |
| AA Mutation | p.Pro450Leu(p.P450L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382409 |
| Start | 688050:688050(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.525G>C |
| AA Mutation | p.Gln175His(p.Q175H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382409 |
| Start | 679753:679753(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368901164 |
| CDS Mutation | c.1061C>T |
| AA Mutation | p.Thr354Met(p.T354M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382409 |
| Start | 688031:688031(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.544G>A |
| AA Mutation | p.Ala182Thr(p.A182T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382409 |
| Start | 687961:687961(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.614T>C |
| AA Mutation | p.Val205Ala(p.V205A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382409 |
| Start | 679801:679801(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1013C>T |
| AA Mutation | p.Ser338Leu(p.S338L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382409 |
| Start | 688355:688355(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.493G>T |
| AA Mutation | p.Gly165Cys(p.G165C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382409 |
| Start | 687959:687959(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs773963410 |
| CDS Mutation | c.616C>T |
| AA Mutation | p.Arg206Trp(p.R206W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000382409 |
| Start | 687963:687963(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747584307 |
| CDS Mutation | c.612C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000382409 |
| Start | 678719:678719(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs140525006 |
| CDS Mutation | c.1230G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000382409 |
| Start | 688398:688398(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs773559333 |
| CDS Mutation | c.450C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000382409 |
| Start | 686948:686948(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372643492 |
| CDS Mutation | c.714C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000382409 |
| Start | 644595:644595(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142320326 |
| CDS Mutation | c.1653C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000382409 |
| Start | 674758:674758(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200163005 |
| CDS Mutation | c.1281G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |