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Items: 70

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
STOX1
(R38C)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
STOX1
(A45G)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
STOX1
(N50T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
STOX1
(A54T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
STOX1
(R55G)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
STOX1
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
STOX1
(W65C)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
STOX1
(R68P)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
STOX1
(G69R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
STOX1
(V70A)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
STOX1
(P76T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
STOX1
(V82A)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
STOX1
Single nucleotide variant
(intron variant)
not provided
GLikely benign
STOX1
(H152Y)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
STOX1
(Y153H)
Single nucleotide variant
(missense variant)
Preeclampsia/eclampsia 4
Grisk factor
STOX1
(P154S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
STOX1
(P154L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
STOX1
(S160L)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
STOX1
(T170M)
Single nucleotide variant
(missense variant +1 more)
not specified
GLikely benign
STOX1
(H179P)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
STOX1
(T188N)
Single nucleotide variant
(missense variant +1 more)
not provided
GBenign
STOX1
(P189S)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
STOX1
(E201G)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
STOX1
(K203R)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
STOX1
(M224V)
Single nucleotide variant
(missense variant +1 more)
not specified
GLikely benign
STOX1
(R248W)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
STOX1
(M250L)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
STOX1
(M250V)
Single nucleotide variant
(missense variant +1 more)
not specified
GLikely benign
STOX1
Single nucleotide variant
(synonymous variant +1 more)
STOX1-related disorder
GLikely benign
STOX1
(K267Q)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
STOX1
(H269P)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
STOX1
(S277C)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
STOX1
(H291R)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
STOX1
(T302A)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
STOX1
(G308A)
Single nucleotide variant
(missense variant +1 more)
STOX1-related disorder
GLikely benign
STOX1
(E324K)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
STOX1
(R345Q)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
STOX1
(R355Q)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
STOX1
(I361T)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
STOX1
(M381I)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
STOX1
(G403R)
Single nucleotide variant
(missense variant +1 more)
not specified
GLikely benign
STOX1
(Q423E)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
STOX1
(L519P)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
STOX1
(L582F)
Single nucleotide variant
(missense variant +1 more)
not provided
GBenign
STOX1
(Q588H)
Single nucleotide variant
(missense variant +1 more)
not specified
GLikely benign
STOX1
(Q592H)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
STOX1
(E608D)
Single nucleotide variant
(missense variant +1 more)
not specified
+1 more
GBenign
STOX1
(P618S)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
STOX1
(F628C)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
STOX1
(E633K)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
STOX1
(E633D)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
STOX1
Single nucleotide variant
(synonymous variant +1 more)
not provided
GLikely benign
STOX1
(L671V)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
STOX1
(V678M)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
STOX1
(R686S)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
STOX1
(G698E)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
STOX1
(N710S)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
STOX1
Single nucleotide variant
(synonymous variant +1 more)
STOX1-related disorder
GBenign
STOX1
(R749H)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
STOX1
(S756G)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
STOX1
Single nucleotide variant
(synonymous variant +1 more)
STOX1-related disorder
GLikely benign
STOX1
Single nucleotide variant
(synonymous variant +1 more)
not provided
GLikely benign
STOX1
(M786V)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
STOX1
(C799S)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
STOX1
Single nucleotide variant
(synonymous variant +1 more)
not provided
GBenign
STOX1
(F855L)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
STOX1
(S935N)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
STOX1
(W167G +1 more)
Single nucleotide variant
(3 prime UTR variant +1 more)
not specified
GUncertain significance
STOX1
(S971N)
Single nucleotide variant
(3 prime UTR variant +1 more)
not specified
GLikely benign
STOX1
(P982L)
Single nucleotide variant
(3 prime UTR variant +1 more)
not specified
GUncertain significance
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