Mutation details:

Protein level identifier (n.a.):

p.Arg635Gln

cDNA level identifier (n.a.):

c.1904G>A

Gene level identifier:

g.76444G>A

Reference, alternative allele:

C, T

Genomic location hg(0)

22:38511664 (not available on ExAC)

Gene name:

PLA2G6

Consequence:

missense

Pathogenicity scoring:

Probably pathogenic

CADD score:

32

Phosphorylation activity:

Positive functional evidence:

not available

Number of all included cases:

3 compound heterozygous (3 in total).