Primary Site >> Pancreatic Cancer
Gene >> DNAH8
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359357 |
| Start | 38734581:38734581(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.67C>A |
| AA Mutation | p.Arg23Ser(p.R23S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359357 |
| Start | 38775883:38775883(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1243C>A |
| AA Mutation | p.Leu415Met(p.L415M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359357 |
| Start | 38822852:38822852(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201917454 |
| CDS Mutation | c.2887G>A |
| AA Mutation | p.Ala963Thr(p.A963T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359357 |
| Start | 38866604:38866604(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5861C>T |
| AA Mutation | p.Ala1954Val(p.A1954V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000359357 |
| Start | 38923185:38923185(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.10139G>T |
| AA Mutation | p.Arg3380Ile(p.R3380I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359357 |
| Start | 38783029:38783029(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1634C>A |
| AA Mutation | p.Pro545Gln(p.P545Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000359357 |
| Start | 38872712:38872712(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6516C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | splice_acceptor_variant |
| Transcription ID | ENST00000359357 |
| Start | 38723335:38723335(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.-176-2A>G |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |