| Primary Identifier | MGI:6477935 | Allele Type | Spontaneous |
| Gene | Fmr1nb | Is Recombinase | false |
| Is Wild Type | false |
| molecularNote | This allele represents two point mutations that are found in the PWD and PWK strains: chrX:g.68762025C>G (minor variant of SNP rs29049709; changes codon 31 from threonine to arginine (p.T31R)) and 68769064T>A (minor variant of SNP rs29049158; changes codon 162 from isoleucine to lysine (p.I162K)) (GRCm38 coordinates). |
