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Items: 22

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
IFT52
(R33W)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
IFT52
(E48D)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
IFT52
(E63G)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
IFT52
(T66A)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
IFT52
(A68P)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
IFT52
(V116I)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
IFT52
(G134E)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
IFT52
(I152T)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
IFT52
(L164F)
Single nucleotide variant
(missense variant +1 more)
not provided
+1 more
GUncertain significance
IFT52
(F15L +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
IFT52
(D17V +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
IFT52
(T24M +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
IFT52
(E275G +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
IFT52
(E103Q +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
IFT52
(I119V +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
IFT52
(E308D +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
IFT52
(T157A +2 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
IFT52
(F381L +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
IFT52
(V392A +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
IFT52
(P180S +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
+1 more
GUncertain significance
IFT52
(I189T +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
IFT52
(V415M +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
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