Primary Site >> Stomach Cancer
Gene >> PAX7
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000420770 |
| Start | 18735753:18735753(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs371958619 |
| CDS Mutation | c.1277G>A |
| AA Mutation | p.Arg426Gln(p.R426Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000420770 |
| Start | 18735758:18735758(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs568673882 |
| CDS Mutation | c.1282G>A |
| AA Mutation | p.Asp428Asn(p.D428N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000420770 |
| Start | 18700672:18700672(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs371475871 |
| CDS Mutation | c.806G>A |
| AA Mutation | p.Arg269His(p.R269H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000420770 |
| Start | 18735669:18735669(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs149436157 |
| CDS Mutation | c.1193C>T |
| AA Mutation | p.Pro398Leu(p.P398L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000420770 |
| Start | 18735864:18735864(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758921663 |
| CDS Mutation | c.1388G>T |
| AA Mutation | p.Gly463Val(p.G463V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000420770 |
| Start | 18700674:18700674(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs745583358 |
| CDS Mutation | c.808G>A |
| AA Mutation | p.Ala270Thr(p.A270T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000420770 |
| Start | 18735725:18735725(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1249A>G |
| AA Mutation | p.Thr417Ala(p.T417A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000420770 |
| Start | 18635190:18635190(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.401G>T |
| AA Mutation | p.Arg134Leu(p.R134L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000420770 |
| Start | 18735863:18735863(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs140323790 |
| CDS Mutation | c.1387G>A |
| AA Mutation | p.Gly463Ser(p.G463S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000420770 |
| Start | 18691901:18691901(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.734A>G |
| AA Mutation | p.Tyr245Cys(p.Y245C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000420770 |
| Start | 18703282:18703282(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1141G>T |
| AA Mutation | p.Gly381Cys(p.G381C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000420770 |
| Start | 18735850:18735850(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760844061 |
| CDS Mutation | c.1374C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000420770 |
| Start | 18735871:18735871(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143552197 |
| CDS Mutation | c.1395C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000420770 |
| Start | 18703152:18703152(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1011C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000420770 |
| Start | 18700676:18700676(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758316511 |
| CDS Mutation | c.810C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000420770 |
| Start | 18735661:18735661(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs138918372 |
| CDS Mutation | c.1185G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000420770 |
| Start | 18631663:18631663(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.64delC |
| AA Mutation | p.Arg22AlafsTer38(p.R22Afs*38) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |