Primary Site >> Stomach Cancer
Gene >> SMO
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000249373 |
| Start | 129210478:129210478(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1582A>G |
| AA Mutation | p.Thr528Ala(p.T528A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000249373 |
| Start | 129206503:129206503(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1180T>C |
| AA Mutation | p.Tyr394His(p.Y394H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000249373 |
| Start | 129205222:129205222(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.557A>C |
| AA Mutation | p.Lys186Thr(p.K186T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000249373 |
| Start | 129205731:129205731(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775852783 |
| CDS Mutation | c.869G>A |
| AA Mutation | p.Arg290His(p.R290H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000249373 |
| Start | 129205638:129205638(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.776C>T |
| AA Mutation | p.Ser259Leu(p.S259L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000249373 |
| Start | 129209375:129209375(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755295928 |
| CDS Mutation | c.1444C>T |
| AA Mutation | p.Arg482Cys(p.R482C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000249373 |
| Start | 129203557:129203557(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.505T>G |
| AA Mutation | p.Cys169Gly(p.C169G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000249373 |
| Start | 129203548:129203548(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.496T>C |
| AA Mutation | p.Phe166Leu(p.F166L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000249373 |
| Start | 129211750:129211750(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1916T>C |
| AA Mutation | p.Val639Ala(p.V639A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000249373 |
| Start | 129209333:129209333(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1402A>G |
| AA Mutation | p.Ser468Gly(p.S468G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000249373 |
| Start | 129205369:129205369(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142599757 |
| CDS Mutation | c.704C>T |
| AA Mutation | p.Ala235Val(p.A235V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000249373 |
| Start | 129206548:129206548(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1225G>A |
| AA Mutation | p.Gly409Ser(p.G409S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000249373 |
| Start | 129211104:129211104(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1792G>T |
| AA Mutation | p.Gly598Trp(p.G598W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000249373 |
| Start | 129205628:129205628(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.766T>C |
| AA Mutation | p.Trp256Arg(p.W256R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000249373 |
| Start | 129206190:129206190(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.961G>A |
| AA Mutation | p.Val321Met(p.V321M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000249373 |
| Start | 129206266:129206266(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1037T>G |
| AA Mutation | p.Leu346Arg(p.L346R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000249373 |
| Start | 129206363:129206363(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1134G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000249373 |
| Start | 129205244:129205244(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199916953 |
| CDS Mutation | c.579C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000249373 |
| Start | 129210390:129210390(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1494G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000249373 |
| Start | 129205733:129205733(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.871C>T |
| AA Mutation | p.Arg291Ter(p.R291*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000249373 |
| Start | 129212263:129212263(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372847405 |
| CDS Mutation | c.2176C>T |
| AA Mutation | p.Arg726Ter(p.R726*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000249373 |
| Start | 129205629:129205629(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753152001 |
| CDS Mutation | c.767G>A |
| AA Mutation | p.Trp256Ter(p.W256*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |