Mutation details:

Protein level identifier:

p.Leu9Arg

cDNA level identifier:

c.26T>G

Genome level identifier:

g.814T>G

Reference, alternative allele:

A, C

Genetic location (hg19):

chr22:39639943 (not available on ExAC)

Gene name:

PDGFB

Consequence:

missense

Pathogenicity scoring:

probably pathogenic

CADD score:

23

Positive functional evidence:

26599395

Diseases reported for this mutation:

PFBC-PDGFB

Number of all included cases:

4 heterozygous (4 in total).

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