Primary Site >> Esophagus Cancer
Gene >> DNAH9
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262442 |
| Start | 11704369:11704369(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759673753 |
| CDS Mutation | c.5318G>A |
| AA Mutation | p.Arg1773Gln(p.R1773Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262442 |
| Start | 11933943:11933943(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.12361G>A |
| AA Mutation | p.Asp4121Asn(p.D4121N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262442 |
| Start | 11807761:11807761(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.8450C>A |
| AA Mutation | p.Pro2817Gln(p.P2817Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262442 |
| Start | 11854102:11854102(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.9607C>T |
| AA Mutation | p.Pro3203Ser(p.P3203S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262442 |
| Start | 11608241:11608241(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.530T>A |
| AA Mutation | p.Leu177His(p.L177H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262442 |
| Start | 11689873:11689873(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4051A>G |
| AA Mutation | p.Arg1351Gly(p.R1351G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262442 |
| Start | 11807793:11807793(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.8482G>T |
| AA Mutation | p.Gly2828Trp(p.G2828W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262442 |
| Start | 11756643:11756643(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6814C>G |
| AA Mutation | p.Arg2272Gly(p.R2272G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262442 |
| Start | 11690048:11690048(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4226T>C |
| AA Mutation | p.Leu1409Pro(p.L1409P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262442 |
| Start | 11757667:11757667(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6970A>C |
| AA Mutation | p.Thr2324Pro(p.T2324P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262442 |
| Start | 11669727:11669727(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3286C>A |
| AA Mutation | p.Leu1096Met(p.L1096M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262442 |
| Start | 11937514:11937514(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.12652G>A |
| AA Mutation | p.Glu4218Lys(p.E4218K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262442 |
| Start | 11744886:11744886(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6201C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262442 |
| Start | 11894442:11894442(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.11352G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000262442 |
| Start | 11880190:11880190(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200261738 |
| CDS Mutation | c.10591A>T |
| AA Mutation | p.Lys3531Ter(p.K3531*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |