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Items: 11

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ALKBH6
(R149G +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ALKBH6
(N131T +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ALKBH6
(R167C +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ALKBH6
(P148H +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ALKBH6
(D146N +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ALKBH6
(R73W +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ALKBH6
(D136N +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ALKBH6
(E115K +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ALKBH6
(L95P +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ALKBH6
(F92S +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ALKBH6
(G18D)
Single nucleotide variant
(5 prime UTR variant +1 more)
not specified
GUncertain significance
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