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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KCNT1
(M516V +1 more)
Single nucleotide variant
(missense variant)
Developmental and epileptic encephalopathy, 14
+3 more
GPathogenic/Likely pathogenic
KCNT1
(R600Q +1 more)
Single nucleotide variant
(missense variant)
Developmental and epileptic encephalopathy, 14
+2 more
GConflicting classifications of pathogenicity
KCNT1
(K947E +1 more)
Single nucleotide variant
(missense variant)
Malignant migrating partial seizures of infancy
GLikely pathogenic
KCNT1
(R961H +1 more)
Single nucleotide variant
(missense variant)
not provided
+4 more
GConflicting classifications of pathogenicity
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