Mutation details:

Protein level identifier (NP_001073136):

p.Tyr387*

cDNA level identifier (NM_001079668):

c.1161C>G

Gene level identifier:

g.3827C>G

Reference, alternative allele:

G, C

Genomic location hg(19)

14:36986528 (not available on ExAC)

Gene name:

NKX2-1

Consequence:

nonsense

Pathogenicity scoring:

Probably pathogenic

CADD score:

36

Phosphorylation activity:

Positive functional evidence:

not available

Number of all included cases:

1 heterozygous (1 in total).

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