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Items: 9

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CYP24A1
(R466*)
Single nucleotide variant
(nonsense +1 more)
not provided
+1 more
GPathogenic
CYP24A1
(V457I)
Single nucleotide variant
(missense variant +1 more)
Hypercalcemia, infantile, 1
+1 more
GUncertain significance
CYP24A1
(L409S)
Single nucleotide variant
(missense variant)
not provided
+1 more
GPathogenic/Likely pathogenic
CYP24A1
(R396W)
Single nucleotide variant
(missense variant)
Muscle spasm
+2 more
GPathogenic/Likely pathogenic
CYP24A1
(K229*)
Single nucleotide variant
(nonsense)
Hypercalcemia, infantile, 1
GLikely pathogenic
CYP24A1
(R157W)
Single nucleotide variant
(missense variant)
Hypercalcemia, infantile, 1
+2 more
GConflicting classifications of pathogenicity
CYP24A1
(E143del)
Microsatellite
(inframe_deletion)
not provided
+1 more
GPathogenic
CYP24A1
(K142R)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
CYP24A1
(E122D)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
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