| Primary Identifier | MGI:1857780 | Allele Type | Radiation induced |
| Gene | Nsdhl | Inheritance Mode | Dominant |
| Strain of Origin | C3H/HeH | Is Recombinase | false |
| Is Wild Type | false |
| molecularNote | A point mutation alters coding nucleotide 293 from a C to a T (c.293C>T). This changes the corresponding amino acid 98 from a proline to a leucine in the encoded protein (p.P98L). |
