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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NBEA
(S206G)
Single nucleotide variant
(missense variant)
Neurodevelopmental disorder with or without early-onset generalized epilepsy
GUncertain significance
NBEA
(L886*)
Single nucleotide variant
(nonsense)
Neurodevelopmental disorder with or without early-onset generalized epilepsy
GPathogenic
NBEA
(T1016N)
Single nucleotide variant
(missense variant)
Neurodevelopmental disorder with or without early-onset generalized epilepsy
GUncertain significance
NBEA
(K1157E)
Single nucleotide variant
(missense variant)
Neurodevelopmental disorder with or without early-onset generalized epilepsy
GUncertain significance
NBEA
(D1304fs)
Duplication
(frameshift variant)
Neurodevelopmental disorder with or without early-onset generalized epilepsy
GPathogenic
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