Mutation details:

cDNA level identifier (n.a.):

c.619-1G>A

Gene level identifier:

g.754354G>A

Archive identifier/Other designation:

IVS5-1G>A

Reference, alternative allele:

C, T

Genomic location hg(19)

6:162394450 (not available on ExAC)

Gene name:

Parkin

Consequence:

splice site 1 3bp

Pathogenicity scoring:

Probably pathogenic

CADD score:

not available

Phosphorylation activity:

Positive functional evidence:

not available

Number of all included cases:

1 compound heterozygous (1 in total).