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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC101928525, MRPS2
(R110C)
Single nucleotide variant
(non-coding transcript variant +1 more)
Combined oxidative phosphorylation deficiency 36
GPathogenic
LOC101928525, MRPS2
(D114N)
Single nucleotide variant
(missense variant +1 more)
Combined oxidative phosphorylation deficiency 36
+1 more
GConflicting classifications of pathogenicity
LOC101928525, MRPS2
(R138H)
Single nucleotide variant
(non-coding transcript variant +1 more)
Combined oxidative phosphorylation deficiency 36
GConflicting classifications of pathogenicity
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