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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DDIT3
(R180Q +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
DDIT3
(K130E +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
DDIT3
(E149Q +1 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
DDIT3
(Q148E +1 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
DDIT3
(P11R)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
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