Protein level identifier (NP_055542):
p.Ala1632Val
cDNA level identifier (NM_014727):
c.4895C>T
Gene level identifier:
g.11255C>T
Reference, alternative allele:
C, T
Genomic location hg(0)
19:36220175 (not available on ExAC)
Gene name:
Consequence:
missense
Pathogenicity scoring:
Probably pathogenic
CADD score:
32
Positive functional evidence:
not available
Number of all included cases:
1 heterozygous (1 in total).