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Items: 7

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MLYCD
Single nucleotide variant
(synonymous variant)
not specified
+1 more
GBenign
LOC130059555, MLYCD
Single nucleotide variant
(intron variant)
not specified
+1 more
GBenign
MLYCD
Single nucleotide variant
(intron variant)
not specified
+2 more
GBenign
MLYCD
Single nucleotide variant
(intron variant)
not specified
+1 more
GBenign
MLYCD
Duplication
(inframe_insertion)
not provided
GPathogenic
MLYCD
(G259A)
Single nucleotide variant
(missense variant)
not specified
+1 more
GBenign/Likely benign
MLYCD
(I474V)
Single nucleotide variant
(missense variant)
Deficiency of malonyl-CoA decarboxylase
+1 more
GConflicting classifications of pathogenicity
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