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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DOK7
(L245fs +2 more)
Microsatellite
(3 prime UTR variant +1 more)
Congenital myasthenic syndrome 10
GLikely pathogenic
DOK7
(S112fs +2 more)
Deletion
(3 prime UTR variant +1 more)
not provided
+3 more
GPathogenic/Likely pathogenic
DOK7
(A130T +2 more)
Single nucleotide variant
(3 prime UTR variant +1 more)
Congenital myasthenic syndrome 10
+3 more
GConflicting classifications of pathogenicity
DOK7
(P133S +2 more)
Single nucleotide variant
(3 prime UTR variant +1 more)
Congenital myasthenic syndrome 10
+2 more
GConflicting classifications of pathogenicity
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