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Items: 15

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PROP1
Single nucleotide variant
(synonymous variant)
not provided
GConflicting classifications of pathogenicity
PROP1
Single nucleotide variant
(synonymous variant)
not specified
+1 more
GConflicting classifications of pathogenicity
PROP1
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GConflicting classifications of pathogenicity
PROP1
(A184P)
Single nucleotide variant
(missense variant)
not specified
+1 more
GUncertain significance
PROP1
Single nucleotide variant
(synonymous variant)
not specified
+3 more
GConflicting classifications of pathogenicity
PROP1
Single nucleotide variant
(synonymous variant)
PROP1-related condition
+1 more
GConflicting classifications of pathogenicity
PROP1
(A142V)
Single nucleotide variant
(missense variant)
not specified
+2 more
GConflicting classifications of pathogenicity
PROP1
(A142T)
Single nucleotide variant
(missense variant)
not specified
+2 more
GBenign
PROP1
Single nucleotide variant
(synonymous variant)
not provided
GConflicting classifications of pathogenicity
PROP1
(I113M)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
PROP1
(L102fs)
Microsatellite
(frameshift variant)
Pituitary hormone deficiency, combined, 2
+3 more
GPathogenic/Likely pathogenic
PROP1
(R65C)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
PROP1
(G51A)
Single nucleotide variant
(missense variant)
not provided
+2 more
GBenign
PROP1
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GConflicting classifications of pathogenicity
PROP1
(G18S)
Single nucleotide variant
(missense variant)
Pituitary hormone deficiency, combined, 2
+1 more
GConflicting classifications of pathogenicity
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