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Items: 9

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
HERC1
(V3803I)
Single nucleotide variant
(missense variant)
Macrocephaly, dysmorphic facies, and psychomotor retardation
+1 more
GConflicting classifications of pathogenicity
HERC1
(N3300K)
Single nucleotide variant
(missense variant)
Macrocephaly, dysmorphic facies, and psychomotor retardation
GUncertain significance
HERC1
Single nucleotide variant
(splice donor variant)
Macrocephaly, dysmorphic facies, and psychomotor retardation
GLikely pathogenic
HERC1
(A2539T)
Single nucleotide variant
(missense variant)
Macrocephaly, dysmorphic facies, and psychomotor retardation
+3 more
GUncertain significance
HERC1
(S2363L)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
HERC1
(L2317I)
Single nucleotide variant
(missense variant)
Macrocephaly, dysmorphic facies, and psychomotor retardation
GUncertain significance
HERC1
(N2047S)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+1 more
GUncertain significance
HERC1
(Y115F)
Single nucleotide variant
(missense variant)
Macrocephaly, dysmorphic facies, and psychomotor retardation
GUncertain significance
HERC1
(L10V)
Single nucleotide variant
(missense variant)
Macrocephaly, dysmorphic facies, and psychomotor retardation
GUncertain significance
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