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Items: 20

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SLU7
(R560Q +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SLU7
(N530D +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SLU7
(A538V +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SLU7
(R509Q +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SLU7
(K501T +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SLU7
(K499R +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SLU7
(L494P +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LOC129389407, SLU7
(M487I +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LOC129389407, SLU7
(G476R +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SLU7
(G448E +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SLU7
(I425N +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SLU7
(I440V +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SLU7
(V414A +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SLU7
(K390M +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SLU7
(L329S +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SLU7
(D247Y +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SLU7
(E223V +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SLU7
(H218Q +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SLU7
(R149Q +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SLU7
(R126H +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
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