Primary Site >> Stomach Cancer
Gene >> ARID4A
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355431 |
| Start | 58323537:58323537(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770373766 |
| CDS Mutation | c.502C>T |
| AA Mutation | p.Arg168Cys(p.R168C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355431 |
| Start | 58366188:58366188(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3481C>G |
| AA Mutation | p.Pro1161Ala(p.P1161A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355431 |
| Start | 58366990:58366990(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3631G>A |
| AA Mutation | p.Asp1211Asn(p.D1211N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355431 |
| Start | 58344750:58344750(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.962A>C |
| AA Mutation | p.Lys321Thr(p.K321T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355431 |
| Start | 58353756:58353756(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774285006 |
| CDS Mutation | c.1754G>A |
| AA Mutation | p.Arg585Gln(p.R585Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000355431 |
| Start | 58347827:58347827(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774332476 |
| CDS Mutation | c.1353C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000355431 |
| Start | 58364254:58364254(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2171delA |
| AA Mutation | p.Asn724MetfsTer4(p.N724Mfs*4) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000355431 |
| Start | 58347733:58347733(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs776520069 |
| CDS Mutation | c.1266delA |
| AA Mutation | p.Asp423ThrfsTer2(p.D423Tfs*2) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000355431 |
| Start | 58330149:58330149(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.890delA |
| AA Mutation | p.Lys297ArgfsTer81(p.K297Rfs*81) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000355431 |
| Start | 58351231:58351231(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1568delA |
| AA Mutation | p.Asn523IlefsTer52(p.N523Ifs*52) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000355431 |
| Start | 58364401:58364401(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.2316delT |
| AA Mutation | p.Phe772LeufsTer33(p.F772Lfs*33) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000355431 |
| Start | 58365138:58365138(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3049C>T |
| AA Mutation | p.Arg1017Ter(p.R1017*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000355431 |
| Start | 58328294:58328294(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375498932 |
| CDS Mutation | c.640C>T |
| AA Mutation | p.Arg214Ter(p.R214*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |