Mutation details:

Protein level identifier (n.a.):

p.Arg632Trp

cDNA level identifier (n.a.):

c.1894C>T

Gene level identifier:

g.76434C>T

Reference, alternative allele:

G, A

Genomic location hg(0)

22:38511674 (not available on ExAC)

Gene name:

PLA2G6

Consequence:

missense

Pathogenicity scoring:

Probably pathogenic

CADD score:

25

Phosphorylation activity:

Positive functional evidence:

not available

Number of all included cases:

3 homozygous (3 in total).