Mutation details:

Protein level identifier (n.a.):

p.Ala499Thr

cDNA level identifier (n.a.):

c.1495G>A

Gene level identifier:

g.68910G>A

Reference, alternative allele:

C, T

Genomic location hg(0)

22:38519198 (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:

2 homozygous (2 in total).