Protein level identifier (n.a.):
p.Thr156Ile
cDNA level identifier (n.a.):
c.467C>T
Gene level identifier:
g.59076C>T
Reference, alternative allele:
C, T
Genomic location hg(0)
not available
Gene name:
Consequence:
missense
Pathogenicity scoring:
Probably pathogenic
CADD score:
26
Positive functional evidence:
not available
Number of all included cases:
6 heterozygous (6 in total).