Primary Site >> Stomach Cancer
Gene >> ACHE
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000241069 |
| Start | 100894006:100894006(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200961647 |
| CDS Mutation | c.227G>A |
| AA Mutation | p.Arg76His(p.R76H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000241069 |
| Start | 100892406:100892406(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374462106 |
| CDS Mutation | c.1481G>A |
| AA Mutation | p.Arg494Gln(p.R494Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000241069 |
| Start | 100893427:100893427(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775312669 |
| CDS Mutation | c.806C>T |
| AA Mutation | p.Thr269Met(p.T269M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000241069 |
| Start | 100893197:100893197(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1036C>A |
| AA Mutation | p.Leu346Ile(p.L346I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000241069 |
| Start | 100891238:100891238(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1654C>T |
| AA Mutation | p.Arg552Trp(p.R552W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000241069 |
| Start | 100892443:100892443(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1444A>G |
| AA Mutation | p.Ile482Val(p.I482V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000241069 |
| Start | 100893677:100893677(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.556G>A |
| AA Mutation | p.Ala186Thr(p.A186T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000241069 |
| Start | 100893469:100893469(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.764G>T |
| AA Mutation | p.Arg255Met(p.R255M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000241069 |
| Start | 100893858:100893858(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.375G>T |
| AA Mutation | p.Glu125Asp(p.E125D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000241069 |
| Start | 100893581:100893581(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.652G>A |
| AA Mutation | p.Val218Met(p.V218M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000241069 |
| Start | 100892496:100892496(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780056308 |
| CDS Mutation | c.1391G>A |
| AA Mutation | p.Arg464His(p.R464H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000241069 |
| Start | 100893956:100893956(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.277G>A |
| AA Mutation | p.Ala93Thr(p.A93T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000241069 |
| Start | 100891335:100891335(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1557T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000241069 |
| Start | 100893954:100893954(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.279T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000241069 |
| Start | 100893927:100893927(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.306A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000241069 |
| Start | 100893939:100893939(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.294T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000241069 |
| Start | 100892378:100892378(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1509C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | splice_donor_variant |
| Transcription ID | ENST00000241069 |
| Start | 100892333:100892333(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1553+1G>A |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | inframe_deletion |
| Transcription ID | ENST00000241069 |
| Start | 100893585:100893587(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs761701642 |
| CDS Mutation | c.646_648delGAG |
| AA Mutation | p.Glu216del(p.E216del) |
| Mutation Classification | In_Frame_Del |
| Feature Type | Transcript |