Primary Site >> Stomach Cancer
Gene >> CHRM1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306960 |
| Start | 62910286:62910286(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.815A>C |
| AA Mutation | p.Tyr272Ser(p.Y272S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306960 |
| Start | 62910392:62910392(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.709A>G |
| AA Mutation | p.Ser237Gly(p.S237G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306960 |
| Start | 62910143:62910143(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749521197 |
| CDS Mutation | c.958C>T |
| AA Mutation | p.Arg320Trp(p.R320W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306960 |
| Start | 62910142:62910142(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs773788891 |
| CDS Mutation | c.959G>A |
| AA Mutation | p.Arg320Gln(p.R320Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000306960 |
| Start | 62910312:62910312(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.789C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000306960 |
| Start | 62909961:62909961(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373622413 |
| CDS Mutation | c.1140G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | inframe_deletion |
| Transcription ID | ENST00000306960 |
| Start | 62910035:62910037(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1064_1066delTCT |
| AA Mutation | p.Phe355del(p.F355del) |
| Mutation Classification | In_Frame_Del |
| Feature Type | Transcript |