FAM114A1
family with sequence similarity 114 member A1
Summary
The protein encoded by this gene belongs to the FAM114 family and may play a role in neuronal cell development. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2017]
Known Variants32 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2529752856 | 4:38,879,706 | G/A | — | uncertain significance |
| rs775380738 | 4:38,879,727 | G/A | — | uncertain significance |
| rs202009975 | 4:38,879,793 | G/C | — | uncertain significance |
| rs529130872 | 4:38,879,821 | A/G | — | uncertain significance |
| rs139197115 | 4:38,879,895 | A/G | — | uncertain significance |
| rs200233551 | 4:38,879,896 | T/C | — | likely benign |
| rs149201693 | 4:38,880,018 | G/A | — | uncertain significance |
| rs545106237 | 4:38,893,409 | T/G | — | uncertain significance |
| rs988761378 | 4:38,893,433 | T/A | — | uncertain significance |
| rs202220961 | 4:38,907,155 | C/T | — | uncertain significance |
| rs139238894 | 4:38,907,405 | G/A | — | uncertain significance |
| rs139789863 | 4:38,907,441 | C/T | — | uncertain significance |
| rs778231131 | 4:38,907,442 | G/A | — | uncertain significance |
| rs2529868656 | 4:38,907,474 | C/G | — | uncertain significance |
| rs1718238797 | 4:38,910,214 | G/A | — | uncertain significance |
| rs763900636 | 4:38,910,258 | G/C | — | uncertain significance |
| rs386352300 | 4:38,910,259 | G/C | — | uncertain significance |
| rs756588177 | 4:38,910,295 | C/T | — | uncertain significance |
| rs766612147 | 4:38,916,543 | T/C | — | uncertain significance |
| rs770599161 | 4:38,916,594 | C/T | — | uncertain significance |
| rs772948767 | 4:38,916,612 | A/G | — | uncertain significance |
| rs748129330 | 4:38,924,406 | G/T | — | uncertain significance |
| rs2529946040 | 4:38,924,481 | G/A | — | uncertain significance |
| rs759121456 | 4:38,933,132 | G/A | — | uncertain significance |
| rs532922655 | 4:38,933,882 | T/G | — | uncertain significance |
| rs745801701 | 4:38,933,887 | C/G | — | uncertain significance |
| rs140042546 | 4:38,937,384 | G/A | — | likely benign |
| rs369797523 | 4:38,937,400 | A/G | — | uncertain significance |
| rs1553479 | 4:38,939,257 | T/C | regulatory region variant | — |
| rs144610116 | 4:38,942,848 | T/C | intron variant | — |
| rs773272688 | 4:38,945,135 | A/G | — | uncertain significance |
| rs763838400 | 4:38,945,157 | T/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.