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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TENT4A
(G290C)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
TENT4A
(E307A)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
TENT4A
(A527T)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
TENT4A
(R774K +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
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