Protein level identifier (NP_899200):
p.Glu908Lys
cDNA level identifier (NM_183357):
c.2722G>A
Gene level identifier:
g.146702G>A
Archive identifier/Other designation:
p.E908K
Reference, alternative allele:
C, T
Genomic location hg(19)
3:123021904 (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 heterozygous (1 in total).