Protein level identifier (NP_006740):
p.Ser434Trp
cDNA level identifier (NM_006749):
c.1301C>G
Gene level identifier:
g.102341C>G
Archive identifier/Other designation:
p.S434W
Reference, alternative allele:
G, C
Genomic location hg(19)
8:42294729 (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).