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Items: 6

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NTNG2
(C81Y)
Single nucleotide variant
(missense variant)
Neurodevelopmental disorder with behavioral abnormalities, absent speech, and hypotonia
+1 more
GPathogenic/Likely pathogenic
NTNG2
(W107G)
Single nucleotide variant
(missense variant)
Neurodevelopmental disorder with behavioral abnormalities, absent speech, and hypotonia
+1 more
GPathogenic/Likely pathogenic
NTNG2
(S126fs)
Duplication
(frameshift variant)
Neurodevelopmental disorder with behavioral abnormalities, absent speech, and hypotonia
+4 more
GPathogenic
NTNG2
(M149T)
Single nucleotide variant
(missense variant)
Neurodevelopmental disorder with hypotonia, seizures, and absent language
GUncertain significance
NTNG2
(C355W)
Single nucleotide variant
(missense variant)
Neurodevelopmental disorder with behavioral abnormalities, absent speech, and hypotonia
+1 more
GPathogenic/Likely pathogenic
NTNG2
(C456Y)
Single nucleotide variant
(missense variant)
Neurodevelopmental disorder with behavioral abnormalities, absent speech, and hypotonia
+1 more
GPathogenic/Likely pathogenic
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