Mutation details:

Protein level identifier (n.a.):

p.Ala639Thr

cDNA level identifier (n.a.):

c.1915G>A

Gene level identifier:

g.76455G>A

Reference, alternative allele:

C, T

Genomic location hg(0)

22:38511653 (not available on ExAC)

Gene name:

PLA2G6

Consequence:

missense

Pathogenicity scoring:

Probably pathogenic

CADD score:

29

Phosphorylation activity:

Positive functional evidence:

not available

Number of all included cases:

1 compound heterozygous (1 in total).