Entrez Gene ID | 221061 |
---|---|
Official Gene Symbol | FAM171A1 (GeneCards) |
Full name | family with sequence similarity 171 member A1 |
Location | 10p13 |
Other ids | Vega : OTTHUMG00000017732 HGNC : HGNC:23522 Ensembl : ENSG00000148468 |
Other names | C10orf38 |
Summary | None |
Found 9 variants in this database.
Variant ID | Entrez Gene ID | Gene | Chromsome | Start | End | Disease | Method |
---|---|---|---|---|---|---|---|
14174 | 221061 | FAM171A1 | 10 | 15311757 | 15311757 | Asymptomatic | HiSeq X Ten |
14342 | 221061 | FAM171A1 | 10 | 15485708 | 15485708 | Asymptomatic | HiSeq X Ten |
14481 | 221061 | FAM171A1 | 10 | 15275649 | 15275649 | Asymptomatic | HiSeq X Ten |
14482 | 221061 | FAM171A1 | 10 | 15488665 | 15488665 | Asymptomatic | HiSeq X Ten |
14774 | 221061 | FAM171A1 | 10 | 15469089 | 15469089 | Cockayne syndrome | HiSeq X Ten |
14847 | 221061 | FAM171A1 | 10 | 15390122 | 15390122 | Xeroderma Pigmentosum | HiSeq X Ten |
14848 | 221061 | FAM171A1 | 10 | 15399653 | 15399653 | Xeroderma Pigmentosum | HiSeq X Ten |
23543 | 221061 | FAM171A1 | 10 | 15351179 | 15351179 | Asymptomatic | HiSeq X Ten Single cell Sequencing Cell cloning |
27140 | 221061 | FAM171A1 | 10 | 15319029 | 15319029 | Asymptomatic | HiSeq X Ten Single cell Sequencing Cell cloning |