Mutation details:

Protein level identifier (NP_006507):

p.Arg212Cys

cDNA level identifier (NM_006516):

c.634C>T

Gene level identifier:

g.28942C>T

Reference, alternative allele:

G, A

Genomic location hg(19)

1:43395589 (not available on ExAC)

Gene name:

SLC2A1

Consequence:

missense

Pathogenicity scoring:

Probably pathogenic

CADD score:

34

Phosphorylation activity:

Positive functional evidence:

22622956; 26982753;

Number of all included cases:

14 heterozygous (14 in total).

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