Primary Site >> Stomach Cancer
Gene >> ACTB
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000331789 |
| Start | 5528026:5528026(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.962C>T |
| AA Mutation | p.Ala321Val(p.A321V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000331789 |
| Start | 5528497:5528497(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs281875333 |
| CDS Mutation | c.586C>T |
| AA Mutation | p.Arg196Cys(p.R196C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000331789 |
| Start | 5529387:5529387(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.137G>T |
| AA Mutation | p.Gly46Val(p.G46V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000331789 |
| Start | 5529339:5529339(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.185G>C |
| AA Mutation | p.Arg62Thr(p.R62T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000331789 |
| Start | 5528107:5528107(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.881A>G |
| AA Mutation | p.Tyr294Cys(p.Y294C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000331789 |
| Start | 5527861:5527861(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1015G>A |
| AA Mutation | p.Val339Met(p.V339M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000331789 |
| Start | 5528351:5528351(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs552269338 |
| CDS Mutation | c.732C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000331789 |
| Start | 5528414:5528414(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369943480 |
| CDS Mutation | c.669C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000331789 |
| Start | 5528124:5528124(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766044090 |
| CDS Mutation | c.864C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000331789 |
| Start | 5527810:5527811(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.1065_1066insGATGTTTTGGTGTATAGAAA |
| AA Mutation | p.Trp356AspfsTer33(p.W356Dfs*33) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | inframe_deletion |
| Transcription ID | ENST00000331789 |
| Start | 5528504:5528506(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.577_579delCTC |
| AA Mutation | p.Leu193del(p.L193del) |
| Mutation Classification | In_Frame_Del |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | inframe_deletion |
| Transcription ID | ENST00000331789 |
| Start | 5529276:5529284(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.240_248delCGACATGGA |
| AA Mutation | p.Asp80_Met82del(p.D80_M82del) |
| Mutation Classification | In_Frame_Del |
| Feature Type | Transcript |