Mutation details:

Protein level identifier (NP_001135811):

p.Ile222Ile

cDNA level identifier (NM_001142339):

c.666C>T

Gene level identifier:

g.178258C>T

Reference, alternative allele:

C, T

Genomic location hg(19)

18:11867212 (not available on ExAC)

Gene name:

GNAL

Consequence:

silent

Pathogenicity scoring:

Possibly pathogenic

CADD score:

17

Positive functional evidence:

not available

Number of all included cases:

1 heterozygous (1 in total).

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