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Items: 17

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KCNH5
(S883C)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
KCNH5
(E850G)
Single nucleotide variant
(missense variant +1 more)
Early infantile epileptic encephalopathy with suppression bursts
+1 more
GUncertain significance
KCNH5
(A626T)
Single nucleotide variant
(missense variant +1 more)
not provided
+1 more
GUncertain significance
KCNH5
(V612I)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
KCNH5
(V590G)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
KCNH5
(Q567P)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
KCNH5
(M506I)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
KCNH5
(R504Q)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
KCNH5
(I438fs)
Deletion
(frameshift variant)
Early infantile epileptic encephalopathy with suppression bursts
+1 more
GUncertain significance
KCNH5
(C354Y)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
KCNH5
(R327H)
Single nucleotide variant
(missense variant)
not provided
+3 more
GPathogenic
KCNH5
(D255N)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
KCNH5
(S252I)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
KCNH5
Single nucleotide variant
(intron variant)
Early infantile epileptic encephalopathy with suppression bursts
+1 more
GBenign
KCNH5
(L181P)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
KCNH5
(H54R)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
KCNH5
(G465E)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
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