Protein level identifier (n.a.):
p.Pro87Leu
cDNA level identifier (n.a.):
c.260C>T
Gene level identifier:
g.6815C>T
Reference, alternative allele:
C, T
Genomic location hg(0)
11:112103902 (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:
2 homozygous, 2 compound heterozygous (4 in total).