Primary Site >> Stomach Cancer
Gene >> CHRNA4
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370263 |
| Start | 63349726:63349726(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200750362 |
| CDS Mutation | c.1685C>T |
| AA Mutation | p.Pro562Leu(p.P562L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370263 |
| Start | 63350732:63350732(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.679G>A |
| AA Mutation | p.Ala227Thr(p.A227T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370263 |
| Start | 63350584:63350584(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs796052323 |
| CDS Mutation | c.827C>T |
| AA Mutation | p.Thr276Met(p.T276M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370263 |
| Start | 63346823:63346823(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752686095 |
| CDS Mutation | c.1799G>A |
| AA Mutation | p.Arg600His(p.R600H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370263 |
| Start | 63349711:63349711(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs76895198 |
| CDS Mutation | c.1700C>T |
| AA Mutation | p.Ala567Val(p.A567V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370263 |
| Start | 63350560:63350560(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs28931591 |
| CDS Mutation | c.851C>T |
| AA Mutation | p.Ser284Leu(p.S284L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370263 |
| Start | 63349795:63349795(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375524982 |
| CDS Mutation | c.1616C>T |
| AA Mutation | p.Ser539Leu(p.S539L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370263 |
| Start | 63359596:63359596(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.180C>A |
| AA Mutation | p.Asp60Glu(p.D60E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370263 |
| Start | 63350617:63350617(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.794T>C |
| AA Mutation | p.Phe265Ser(p.F265S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370263 |
| Start | 63350521:63350521(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766414326 |
| CDS Mutation | c.890C>T |
| AA Mutation | p.Pro297Leu(p.P297L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370263 |
| Start | 63350263:63350263(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762374374 |
| CDS Mutation | c.1148G>A |
| AA Mutation | p.Arg383His(p.R383H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370263 |
| Start | 63350405:63350405(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs56175056 |
| CDS Mutation | c.1006C>T |
| AA Mutation | p.Arg336Cys(p.R336C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370263 |
| Start | 63350404:63350404(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs281865068 |
| CDS Mutation | c.1007G>A |
| AA Mutation | p.Arg336His(p.R336H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000370263 |
| Start | 63350304:63350304(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1107G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000370263 |
| Start | 63349776:63349776(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs121912283 |
| CDS Mutation | c.1635G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000370263 |
| Start | 63349968:63349968(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1443C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000370263 |
| Start | 63350790:63350790(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs149407396 |
| CDS Mutation | c.621C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000370263 |
| Start | 63359638:63359638(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200705061 |
| CDS Mutation | c.138C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |