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Items: 13

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PKLR
(W494* +1 more)
Single nucleotide variant
(nonsense)
Pyruvate kinase deficiency of red cells
GUncertain significance
PKLR
(R486W +1 more)
Single nucleotide variant
(missense variant)
not provided
+3 more
GConflicting classifications of pathogenicity
PKLR
(G375E +1 more)
Single nucleotide variant
(missense variant)
Pyruvate kinase deficiency of red cells
GUncertain significance
PKLR
(N362S +1 more)
Single nucleotide variant
(missense variant)
not provided
+2 more
GPathogenic/Likely pathogenic
PKLR
(K323R +1 more)
Single nucleotide variant
(missense variant)
Pyruvate kinase deficiency of red cells
GUncertain significance
PKLR
(E312D +1 more)
Single nucleotide variant
(missense variant)
Pyruvate kinase hyperactivity
GUncertain significance
PKLR
(D308fs +1 more)
Deletion
(frameshift variant)
Pyruvate kinase deficiency of red cells
GPathogenic
PKLR
(D339N +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GConflicting classifications of pathogenicity
PKLR
(E284D +1 more)
Single nucleotide variant
(missense variant)
Pyruvate kinase deficiency of red cells
GUncertain significance
PKLR
(R239* +1 more)
Single nucleotide variant
(nonsense)
not provided
+1 more
GPathogenic
PKLR
Single nucleotide variant
(intron variant)
Pyruvate kinase deficiency of red cells
GUncertain significance
PKLR
(V120M +1 more)
Single nucleotide variant
(missense variant)
Pyruvate kinase deficiency of red cells
GUncertain significance
PKLR
(L45P +1 more)
Single nucleotide variant
(missense variant)
Pyruvate kinase deficiency of red cells
GUncertain significance
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