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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NMNAT1
(G52V)
Single nucleotide variant
(missense variant)
Leber congenital amaurosis 9
GUncertain significance
NMNAT1
(S162Y)
Single nucleotide variant
(missense variant)
Leber congenital amaurosis
GLikely pathogenic
NMNAT1
(I221fs)
Duplication
(frameshift variant)
Leber congenital amaurosis
GLikely pathogenic
NMNAT1
(E246Q)
Single nucleotide variant
(missense variant)
Leber congenital amaurosis
GLikely pathogenic
NMNAT1
(E257K)
Single nucleotide variant
(missense variant)
not provided
+4 more
GPathogenic
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