Mutation details:

Protein level identifier (NP_113606):

p.Val463Met

cDNA level identifier (NM_031418):

c.1387G>A

Gene level identifier:

g.370438G>A

Reference, alternative allele:

G, A

Genomic location hg(19)

11:26581266 (not available on ExAC)

Gene name:

ANO3

Consequence:

missense

Pathogenicity scoring:

Possibly pathogenic

CADD score:

24

Phosphorylation activity:

Positive functional evidence:

not available

Number of all included cases:

1 heterozygous (1 in total).