Primary Site >> Pancreatic Cancer
Gene >> STAB1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000321725 |
| Start | 52521942:52521942(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs144247661 |
| CDS Mutation | c.6262G>A |
| AA Mutation | p.Val2088Met(p.V2088M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000321725 |
| Start | 52517580:52517580(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4594G>A |
| AA Mutation | p.Gly1532Arg(p.G1532R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000321725 |
| Start | 52504049:52504049(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1044G>T |
| AA Mutation | p.Glu348Asp(p.E348D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000321725 |
| Start | 52505340:52505340(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777086203 |
| CDS Mutation | c.1540G>A |
| AA Mutation | p.Ala514Thr(p.A514T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000321725 |
| Start | 52506849:52506849(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1988C>T |
| AA Mutation | p.Ala663Val(p.A663V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000321725 |
| Start | 52508301:52508301(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2177G>A |
| AA Mutation | p.Gly726Glu(p.G726E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000321725 |
| Start | 52516702:52516702(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4297G>A |
| AA Mutation | p.Asp1433Asn(p.D1433N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000321725 |
| Start | 52520023:52520023(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369575212 |
| CDS Mutation | c.5315G>A |
| AA Mutation | p.Arg1772Gln(p.R1772Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000321725 |
| Start | 52522650:52522650(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374832817 |
| CDS Mutation | c.6706G>A |
| AA Mutation | p.Val2236Ile(p.V2236I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000321725 |
| Start | 52522932:52522932(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs184802643 |
| CDS Mutation | c.6902G>A |
| AA Mutation | p.Arg2301His(p.R2301H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000321725 |
| Start | 52520536:52520536(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749031768 |
| CDS Mutation | c.5636G>A |
| AA Mutation | p.Arg1879Gln(p.R1879Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000321725 |
| Start | 52509309:52509309(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2335C>T |
| AA Mutation | p.Gln779Ter(p.Q779*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |