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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GAGE12J
(Y9S)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
GAGE12J
(E22G)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
GAGE12J
(P26L)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
GAGE12J
(R28W)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
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