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Items: 21

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
XPO7
(P77R)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
XPO7
(T102A)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
XPO7
(A133V)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
XPO7
(E188G +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
XPO7
(V308A +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
XPO7
(N329K +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
XPO7
(Q418H +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
XPO7
(R546H +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
XPO7
(I571V +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
XPO7
(I587V +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
XPO7
(N641K +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
XPO7
(R652H +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
XPO7
(F709L +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
XPO7
(S716R +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
XPO7
(I736V +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
XPO7
(K782T +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
XPO7
(S837C +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
XPO7
(L917V +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
XPO7
(V1089M +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
XPO7
(S1082N +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
XPO7
(N1083D +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
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