Protein level identifier (n.a.):
p.Ser136Phe
cDNA level identifier (n.a.):
c.407C>T
Gene level identifier:
g.1057C>T
Reference, alternative allele:
C, T
Genomic location hg(0)
2:73115545 (not available on ExAC)
Gene name:
Consequence:
missense
Pathogenicity scoring:
Probably pathogenic
CADD score:
not available
Positive functional evidence:
not available
Number of all included cases:
1 compound heterozygous (1 in total).