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Items: 42

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NFATC4
(P25A +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
NFATC4
(L26R +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
NFATC4
(L26P +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
NFATC4
(A28G +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
NFATC4
(R45L +2 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
NFATC4
(R45H +2 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
NFATC4
(P46T +2 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
NFATC4
(P145S +3 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
NFATC4
(A153S +3 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
NFATC4
(L111F +3 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
NFATC4
(E175Q +3 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
NFATC4
(P125L +3 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
NFATC4
(P115T +3 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
NFATC4
(D203Y +3 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
NFATC4
(G102C +3 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
NFATC4
(G169R +3 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
NFATC4
(P260L +3 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
NFATC4
(P190Q +3 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
NFATC4
(P298S +3 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
NFATC4
(P252L +3 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
NFATC4
(R453W +3 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
NFATC4
(I379V +3 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
NFATC4
(I351M +3 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
NFATC4
(R360Q +3 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
NFATC4
(V439I +3 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
NFATC4
(T463A +3 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
NFATC4
(T557M +3 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
NFATC4
(T529M +3 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
NFATC4
(L606M +3 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
NFATC4
(N540K +3 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
NFATC4
(I608T +3 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
NFATC4
(A731V +3 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
NFATC4
(Y673S +3 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
NFATC4
(R693Q +3 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
NFATC4
(P766H +3 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
NFATC4
(P774A +3 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
NFATC4
(F787L +3 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
NFATC4
(S852R +3 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
NFATC4
(P807L +3 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
NFATC4
(L885F +3 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
NFATC4
(G776V +3 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
NFATC4
(R779Q +6 more)
Single nucleotide variant
(3 prime UTR variant +1 more)
Inborn genetic diseases
GUncertain significance
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