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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MMUT
(L736F)
Single nucleotide variant
(missense variant)
not provided
+2 more
GConflicting classifications of pathogenicity
MMUT
(V645fs)
Deletion
(frameshift variant)
Methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency
GPathogenic
MMUT
(Y146*)
Single nucleotide variant
(nonsense)
Methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency
GPathogenic
MMUT
(R93H)
Single nucleotide variant
(missense variant)
Methylmalonic acidemia
+2 more
GPathogenic
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