Mutation details:

Protein level identifier (NP_899200):

p.Ala726Thr

cDNA level identifier (NM_183357):

c.2176G>A

Gene level identifier:

g.130005G>A

Archive identifier/Other designation:

p.A726T

Reference, alternative allele:

C, T

Genomic location hg(19)

3:123038601 (not available on ExAC)

Gene name:

ADCY5

Consequence:

missense

Pathogenicity scoring:

Definitely pathogenic

CADD score:

not available

Positive functional evidence:

not available

Number of all included cases:

15 heterozygous (15 in total).

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