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Items: 8

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
STAT1
(P695L +11 more)
Single nucleotide variant
(missense variant +1 more)
Autoimmune enteropathy and endocrinopathy - susceptibility to chronic infections syndrome
GUncertain significance
STAT1
(G527S +9 more)
Single nucleotide variant
(missense variant)
Autoimmune enteropathy and endocrinopathy - susceptibility to chronic infections syndrome
GUncertain significance
STAT1
Single nucleotide variant
(intron variant)
Mendelian susceptibility to mycobacterial diseases due to partial STAT1 deficiency
+2 more
GConflicting classifications of pathogenicity
STAT1
(T385M +9 more)
Single nucleotide variant
(missense variant)
Inherited Immunodeficiency Diseases
+17 more
GPathogenic
STAT1
(A267V +4 more)
Single nucleotide variant
(missense variant +1 more)
Autoimmune enteropathy and endocrinopathy - susceptibility to chronic infections syndrome
+4 more
GPathogenic
STAT1
Single nucleotide variant
(intron variant)
Mendelian susceptibility to mycobacterial diseases due to partial STAT1 deficiency
+3 more
GConflicting classifications of pathogenicity
STAT1
(I160L +4 more)
Single nucleotide variant
(missense variant)
Mendelian susceptibility to mycobacterial diseases due to partial STAT1 deficiency
+3 more
GUncertain significance
STAT1
(R68H +2 more)
Single nucleotide variant
(missense variant)
Mendelian susceptibility to mycobacterial diseases due to partial STAT1 deficiency
GUncertain significance
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