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Items: 19

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FKBP10
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GConflicting classifications of pathogenicity
FKBP10
Single nucleotide variant
(synonymous variant)
not provided
GConflicting classifications of pathogenicity
FKBP10
Single nucleotide variant
(intron variant)
FKBP10-related condition
+4 more
GConflicting classifications of pathogenicity
FKBP10
Single nucleotide variant
(synonymous variant)
not provided
GConflicting classifications of pathogenicity
FKBP10
(Y141C)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
FKBP10
(D143E)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
FKBP10
(V158A)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+2 more
GUncertain significance
FKBP10
Single nucleotide variant
(synonymous variant)
not specified
+2 more
GBenign/Likely benign
FKBP10
Single nucleotide variant
(synonymous variant)
not provided
GConflicting classifications of pathogenicity
FKBP10
Single nucleotide variant
(intron variant)
not provided
GUncertain significance
FKBP10
(R387Q)
Single nucleotide variant
(missense variant)
not specified
+1 more
GUncertain significance
FKBP10
(R403Q)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
FKBP10
Single nucleotide variant
(synonymous variant)
not provided
GConflicting classifications of pathogenicity
FKBP10
(I436T)
Single nucleotide variant
(missense variant)
FKBP10-related condition
+4 more
GBenign/Likely benign
FKBP10
(E464K)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
FKBP10
Single nucleotide variant
(splice donor variant)
not provided
GPathogenic
FKBP10
Single nucleotide variant
(intron variant)
not provided
GConflicting classifications of pathogenicity
FKBP10
(V517D)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
FKBP10
(R556H)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+3 more
GUncertain significance
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