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Links from MedGen

Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ENTREP2, NSMCE3
(I193V)
Single nucleotide variant
(missense variant +1 more)
Lung disease, immunodeficiency, and chromosome breakage syndrome;
+1 more
GUncertain significance
ENTREP2, NSMCE3
(Q14P)
Indel
(missense variant +1 more)
Lung disease, immunodeficiency, and chromosome breakage syndrome;
+1 more
GUncertain significance
ENTREP2, NSMCE3
(T196A)
Single nucleotide variant
(missense variant +1 more)
Lung disease, immunodeficiency, and chromosome breakage syndrome;
+1 more
GUncertain significance
NSMCE3, ENTREP2
(P209L)
Single nucleotide variant
(missense variant +1 more)
Lung damage, immunodeficiency and chromosome breakage syndrome
GPathogenic
ENTREP2, NSMCE3
(L264F)
Single nucleotide variant
(missense variant +1 more)
Lung damage, immunodeficiency and chromosome breakage syndrome
+2 more
GPathogenic
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