Protein level identifier (NP_060575):
p.Met143Val
cDNA level identifier (NM_018105):
c.427A>G
Gene level identifier:
g.5149A>G
Reference, alternative allele:
T, C
Genomic location hg(19)
Gene name:
Consequence:
missense
Pathogenicity scoring:
Possibly pathogenic
CADD score:
1
Positive functional evidence:
not available
Number of all included cases:
3 heterozygous (3 in total).