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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC130059554, MLYCD
(M1L)
Single nucleotide variant
(missense variant +1 more)
Deficiency of malonyl-CoA decarboxylase
GPathogenic/Likely pathogenic
MLYCD
(G149D)
Single nucleotide variant
(missense variant)
Deficiency of malonyl-CoA decarboxylase
+2 more
GUncertain significance
LOC126862422, MLYCD
(T284A)
Single nucleotide variant
(missense variant)
not specified
+2 more
GBenign/Likely benign
LOC126862422, MLYCD
(R310P)
Single nucleotide variant
(missense variant)
Deficiency of malonyl-CoA decarboxylase
+1 more
GUncertain significance
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