Mutation details:

Protein level identifier (NP_061183):

p.His336Tyr

cDNA level identifier (NM_018713):

c.1006C>T

Gene level identifier:

g.42747C>T

Reference, alternative allele:

G, A

Genomic location hg(19)

1:220089243

Gene name:

SLC30A10

Consequence:

missense

Pathogenicity scoring:

Probably pathogenic

CADD score:

not available

Phosphorylation activity:

Positive functional evidence:

not available

Number of all included cases:

3 homozygous (3 in total).

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