Unknown
Yes
| Variant Name | Allele Count | Allele Frequency | Associated Disease | Associated Gene |
|---|---|---|---|---|
| NM_007294.4:c.131G>T | ||||
| NM_000059.4:c.1151C>T | ||||
| NM_032444.4:c.421G>T | ||||
| NM_000455.5:c.1211C>T | ||||
| NM_024675.4:c.2993G>A | ||||
| NM_001287435.1:c.122T>C | ||||
| NM_004260.3:c.3314G>A | ||||
| NM_030621.4:c.5276A>G |