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Links from Gene

Items: 11

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
H2BC12, H4C9
(V88I)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
H2BC12, H4C9
(H19Q)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
H2BC12, H4C9
(G14R)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
H2BC12, H4C9
(G103C)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
H2BC12, H4C9
(G8A)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
H2BC12, H4C9
(G8S)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
H2BC12, H4C9
(K45R)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
H2BC12, H4C9
(L91F)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
H2BC12, H4C9
(H76R)
Single nucleotide variant
(missense variant +1 more)
Tessadori-Van Haaften neurodevelopmental syndrome 4
GPathogenic
H2BC12, H4C9
(R41L)
Single nucleotide variant
(missense variant +1 more)
Tessadori-Van Haaften neurodevelopmental syndrome 4
GPathogenic
H2BC12, H4C9
Single nucleotide variant
(synonymous variant +1 more)
not provided
GBenign
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