Primary Site >> Stomach Cancer
Gene >> MYO18A
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000527372 |
| Start | 29166030:29166030(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751612877 |
| CDS Mutation | c.911G>A |
| AA Mutation | p.Arg304Gln(p.R304Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000527372 |
| Start | 29089980:29089980(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200336680 |
| CDS Mutation | c.5507C>T |
| AA Mutation | p.Thr1836Met(p.T1836M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000527372 |
| Start | 29097830:29097830(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201591312 |
| CDS Mutation | c.4060C>T |
| AA Mutation | p.Arg1354Trp(p.R1354W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000527372 |
| Start | 29121636:29121636(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1282C>T |
| AA Mutation | p.Arg428Cys(p.R428C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000527372 |
| Start | 29166127:29166127(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.814C>A |
| AA Mutation | p.Pro272Thr(p.P272T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000527372 |
| Start | 29110555:29110555(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2968G>A |
| AA Mutation | p.Gly990Ser(p.G990S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000527372 |
| Start | 29092950:29092950(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754320950 |
| CDS Mutation | c.4978C>T |
| AA Mutation | p.Arg1660Cys(p.R1660C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000527372 |
| Start | 29090073:29090073(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5414A>G |
| AA Mutation | p.Glu1805Gly(p.E1805G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000527372 |
| Start | 29121641:29121641(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs371862120 |
| CDS Mutation | c.1277G>A |
| AA Mutation | p.Arg426His(p.R426H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000527372 |
| Start | 29115091:29115091(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2327A>T |
| AA Mutation | p.Lys776Met(p.K776M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000527372 |
| Start | 29093366:29093366(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4883A>C |
| AA Mutation | p.Glu1628Ala(p.E1628A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000527372 |
| Start | 29110014:29110014(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200969774 |
| CDS Mutation | c.3175C>T |
| AA Mutation | p.Arg1059Cys(p.R1059C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000527372 |
| Start | 29094823:29094823(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4537A>G |
| AA Mutation | p.Thr1513Ala(p.T1513A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000527372 |
| Start | 29098872:29098872(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3734C>T |
| AA Mutation | p.Pro1245Leu(p.P1245L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000527372 |
| Start | 29111732:29111732(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2730T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000527372 |
| Start | 29119360:29119360(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1804C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000527372 |
| Start | 29166479:29166479(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.462G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000527372 |
| Start | 29119403:29119403(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1761G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000527372 |
| Start | 29121143:29121143(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772969442 |
| CDS Mutation | c.1440C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |