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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC129996027, H4C5
(K32T)
Single nucleotide variant
(missense variant)
Tessadori-Van Haaften neurodevelopmental syndrome 3
GPathogenic
H4C5, LOC129996027
(P33R)
Single nucleotide variant
(missense variant)
Tessadori-Van Haaften neurodevelopmental syndrome 3
GPathogenic
H4C5, LOC129996027
(R36W)
Single nucleotide variant
(missense variant)
Tessadori-Van Haaften neurodevelopmental syndrome 3
GPathogenic
H4C5, LOC129996027
(R46C)
Single nucleotide variant
(missense variant)
not provided
+2 more
GConflicting classifications of pathogenicity
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