Mutation details:

Protein level identifier (NP_115785):

p.Ala217Asp

cDNA level identifier (NM_032409):

c.650C>A

Gene level identifier:

g.4650C>A

Reference, alternative allele:

C, A

Genomic location hg(19)

1:20964597 (not available on ExAC)

Gene name:

PINK1

Consequence:

missense

Pathogenicity scoring:

Probably pathogenic

CADD score:

33

Phosphorylation activity:

Positive functional evidence:

22645651;

Number of all included cases:

6 homozygous (6 in total).

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