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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TENM4
(A1442T)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
TENM4
(T1367N)
Single nucleotide variant
(missense variant)
Tremor, hereditary essential, 5
GPathogenic
TENM4
(V1138M)
Single nucleotide variant
(missense variant)
Tremor, hereditary essential, 5
+1 more
GUncertain significance
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