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Items: 6

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SERAC1
Single nucleotide variant
(intron variant)
3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome
GUncertain significance
SERAC1
(V588fs)
Deletion
(frameshift variant)
3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome
+1 more
GConflicting classifications of pathogenicity
SERAC1
(P312L)
Single nucleotide variant
(missense variant +1 more)
3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome
GUncertain significance
SERAC1
(R148*)
Single nucleotide variant
(nonsense +1 more)
3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome
+1 more
GPathogenic
SERAC1
(T147fs)
Deletion
(frameshift variant +1 more)
3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome
GPathogenic
SERAC1
(C7W)
Single nucleotide variant
(missense variant +1 more)
3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome
+2 more
GConflicting classifications of pathogenicity
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