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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PLCB1
(A10S)
Single nucleotide variant
(missense variant)
not provided
+3 more
GConflicting classifications of pathogenicity
PLCB1
(R297H)
Single nucleotide variant
(missense variant)
Developmental and epileptic encephalopathy, 12
GUncertain significance
PLCB1
(S679fs)
Deletion
(frameshift variant)
Developmental and epileptic encephalopathy, 12
GLikely pathogenic
PLCB1
(L1184F)
Single nucleotide variant
(missense variant +1 more)
not provided
+4 more
GConflicting classifications of pathogenicity
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