Primary Site >> Stomach Cancer
Gene >> CHRM3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000255380 |
| Start | 239908947:239908947(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1496C>T |
| AA Mutation | p.Ala499Val(p.A499V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000255380 |
| Start | 239909031:239909031(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1580A>C |
| AA Mutation | p.Asn527Thr(p.N527T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000255380 |
| Start | 239908040:239908040(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.589T>C |
| AA Mutation | p.Phe197Leu(p.F197L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000255380 |
| Start | 239908317:239908317(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.866G>A |
| AA Mutation | p.Ser289Asn(p.S289N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000255380 |
| Start | 239908371:239908371(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.920A>C |
| AA Mutation | p.Lys307Thr(p.K307T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000255380 |
| Start | 239907974:239907974(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.523A>G |
| AA Mutation | p.Thr175Ala(p.T175A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000255380 |
| Start | 239907866:239907866(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.415T>A |
| AA Mutation | p.Leu139Met(p.L139M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000255380 |
| Start | 239909045:239909045(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1594C>A |
| AA Mutation | p.Leu532Met(p.L532M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000255380 |
| Start | 239907582:239907582(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201425358 |
| CDS Mutation | c.131G>A |
| AA Mutation | p.Arg44Gln(p.R44Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000255380 |
| Start | 239907544:239907544(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771480057 |
| CDS Mutation | c.93G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000255380 |
| Start | 239909203:239909203(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201601302 |
| CDS Mutation | c.1752C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000255380 |
| Start | 239908498:239908498(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200197901 |
| CDS Mutation | c.1047C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000255380 |
| Start | 239908804:239908804(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs367860952 |
| CDS Mutation | c.1353G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000255380 |
| Start | 239908598:239908598(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1147T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000255380 |
| Start | 239909144:239909145(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1699_1700delAA |
| AA Mutation | p.Lys567GlufsTer26(p.K567Efs*26) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000255380 |
| Start | 239909144:239909144(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs754500041 |
| CDS Mutation | c.1700delA |
| AA Mutation | p.Lys567ArgfsTer31(p.K567Rfs*31) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000255380 |
| Start | 239907848:239907848(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.397C>T |
| AA Mutation | p.Arg133Ter(p.R133*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000255380 |
| Start | 239909143:239909144(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs751548647 |
| CDS Mutation | c.1700dupA |
| AA Mutation | p.Arg568GlufsTer26(p.R568Efs*26) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |