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Items: 15

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
F5
(W2004R)
Single nucleotide variant
(missense variant)
Factor V deficiency
GUncertain significance
F5
(L1865R)
Single nucleotide variant
(missense variant)
Factor V deficiency
GUncertain significance
F5
(M1764V)
Single nucleotide variant
(missense variant)
not specified
+3 more
GConflicting classifications of pathogenicity
F5
(L1675fs)
Deletion
(frameshift variant)
Factor V deficiency
GUncertain significance
F5
(L1433F)
Single nucleotide variant
(missense variant)
Factor V deficiency
GUncertain significance
F5
(L1332P)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
F5
(A1225D)
Single nucleotide variant
(missense variant)
Factor V deficiency
GLikely benign
F5
Deletion
(nonsense)
Factor V deficiency
GLikely pathogenic
F5
(R946I)
Single nucleotide variant
(missense variant)
Factor V deficiency
GUncertain significance
F5
(R872fs)
Deletion
(frameshift variant)
Factor V deficiency
GPathogenic
F5
(N745S)
Single nucleotide variant
(missense variant)
Factor V deficiency
GUncertain significance
F5
(L744F)
Single nucleotide variant
(missense variant)
Factor V deficiency
GUncertain significance
F5
(R534Q)
Single nucleotide variant
(missense variant)
hormonal contraceptives for systemic use response - Toxicity
Gdrug response
F5
(R441C)
Single nucleotide variant
(missense variant)
Factor V deficiency
+2 more
GConflicting classifications of pathogenicity
F5
(A38T)
Single nucleotide variant
(missense variant)
Thrombophilia due to activated protein C resistance
GUncertain significance
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