Protein level identifier (NP_000152):
p.Ser76*
cDNA level identifier (NM_000161):
c.227C>A
Gene level identifier:
g.416C>A
Reference, alternative allele:
G, T
Genomic location hg(0)
14:55369155 (not available on ExAC)
Gene name:
Consequence:
nonsense
Pathogenicity scoring:
Probably pathogenic
CADD score:
36
Positive functional evidence:
not available
Number of all included cases:
1 heterozygous (1 in total).