Primary Site >> Esophagus Cancer
Gene >> DOCK2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256935 |
| Start | 169759766:169759766(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2438A>C |
| AA Mutation | p.Lys813Thr(p.K813T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256935 |
| Start | 170057626:170057626(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs561287880 |
| CDS Mutation | c.4427C>T |
| AA Mutation | p.Pro1476Leu(p.P1476L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256935 |
| Start | 169840762:169840762(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2709C>A |
| AA Mutation | p.Phe903Leu(p.F903L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256935 |
| Start | 170079002:170079002(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5022G>C |
| AA Mutation | p.Lys1674Asn(p.K1674N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256935 |
| Start | 170080270:170080270(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5274G>A |
| AA Mutation | p.Met1758Ile(p.M1758I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256935 |
| Start | 169670547:169670547(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.174T>G |
| AA Mutation | p.Ile58Met(p.I58M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256935 |
| Start | 169670552:169670552(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.179C>G |
| AA Mutation | p.Pro60Arg(p.P60R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256935 |
| Start | 170081956:170081956(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143896166 |
| CDS Mutation | c.5402A>G |
| AA Mutation | p.Lys1801Arg(p.K1801R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256935 |
| Start | 169684272:169684272(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.683G>A |
| AA Mutation | p.Arg228Lys(p.R228K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256935 |
| Start | 170079067:170079067(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs371229305 |
| CDS Mutation | c.5087G>A |
| AA Mutation | p.Arg1696Gln(p.R1696Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000256935 |
| Start | 170008597:170008597(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3173A>C |
| AA Mutation | p.Lys1058Thr(p.K1058T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256935 |
| Start | 169996109:169996109(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763218061 |
| CDS Mutation | c.3017A>C |
| AA Mutation | p.Lys1006Thr(p.K1006T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000256935 |
| Start | 170079029:170079029(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5049G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000256935 |
| Start | 169681820:169681820(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.547T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | splice_donor_variant |
| Transcription ID | ENST00000256935 |
| Start | 169996166:169996166(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3072+2T>C |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |