Primary Site >> Stomach Cancer
Gene >> ACTN1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000193403 |
| Start | 68925641:68925641(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs387907348 |
| CDS Mutation | c.137G>A |
| AA Mutation | p.Arg46Gln(p.R46Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000193403 |
| Start | 68874953:68874953(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199901015 |
| CDS Mutation | c.2585C>T |
| AA Mutation | p.Ala862Val(p.A862V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000193403 |
| Start | 68882574:68882574(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1837C>T |
| AA Mutation | p.Arg613Trp(p.R613W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000193403 |
| Start | 68880872:68880872(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763573834 |
| CDS Mutation | c.2071G>A |
| AA Mutation | p.Asp691Asn(p.D691N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000193403 |
| Start | 68880850:68880850(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2093C>T |
| AA Mutation | p.Ala698Val(p.A698V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000193403 |
| Start | 68892166:68892166(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.973C>T |
| AA Mutation | p.Pro325Ser(p.P325S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000193403 |
| Start | 68902557:68902557(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs151249499 |
| CDS Mutation | c.682G>A |
| AA Mutation | p.Val228Ile(p.V228I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000193403 |
| Start | 68978961:68978961(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.96G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000193403 |
| Start | 68925592:68925592(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.186C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000193403 |
| Start | 68921064:68921064(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs137965016 |
| CDS Mutation | c.282C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000193403 |
| Start | 68892254:68892254(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs139710798 |
| CDS Mutation | c.885G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000193403 |
| Start | 68880843:68880843(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs577992605 |
| CDS Mutation | c.2100C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000193403 |
| Start | 68892191:68892191(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.948C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000193403 |
| Start | 68902516:68902516(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs149168564 |
| CDS Mutation | c.723C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000193403 |
| Start | 68892164:68892164(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774117795 |
| CDS Mutation | c.975G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |