Protein level identifier (n.a.):
p.Gln161*
cDNA level identifier (n.a.):
c.481C>T
Gene level identifier:
g.37271C>T
Reference, alternative allele:
G, A
Genomic location hg(19)
Gene name:
Consequence:
nonsense
Pathogenicity scoring:
Probably pathogenic
CADD score:
not available
Positive functional evidence:
not available
Number of all included cases:
1 heterozygous (1 in total).