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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NEFL
(R399*)
Single nucleotide variant
(nonsense)
not provided
+1 more
GPathogenic/Likely pathogenic
NEFL
(N98S)
Single nucleotide variant
(missense variant)
not provided
+6 more
GPathogenic/Likely pathogenic
NEFL
(Y6*)
Single nucleotide variant
(nonsense)
Charcot-Marie-Tooth disease type 1F
GPathogenic
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