Mutation details:

Protein level identifier (NP_006507):

p.Arg223Trp

cDNA level identifier (NM_006516):

c.667C>T

Gene level identifier:

g.28975C>T

Reference, alternative allele:

G, A

Genomic location hg(19)

1:43395556 (not available on ExAC)

Gene name:

SLC2A1

Consequence:

missense

Pathogenicity scoring:

Probably pathogenic

CADD score:

34

Phosphorylation activity:

Positive functional evidence:

25564316;

Number of all included cases:

1 heterozygous (1 in total).

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