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Items: 9

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
OXCT1
(R438C +4 more)
Single nucleotide variant
(missense variant +1 more)
not provided
+1 more
GLikely pathogenic
OXCT1
(T455R +4 more)
Single nucleotide variant
(missense variant +1 more)
Succinyl-CoA acetoacetate transferase deficiency
+1 more
GUncertain significance
OXCT1
(G102A +3 more)
Single nucleotide variant
(missense variant +1 more)
Succinyl-CoA acetoacetate transferase deficiency
+1 more
GUncertain significance
OXCT1
Single nucleotide variant
(intron variant)
Succinyl-CoA acetoacetate transferase deficiency
GUncertain significance
OXCT1
(N175D +1 more)
Single nucleotide variant
(missense variant +1 more)
Succinyl-CoA acetoacetate transferase deficiency
GUncertain significance
OXCT1
(G151fs +1 more)
Duplication
(frameshift variant +1 more)
Succinyl-CoA acetoacetate transferase deficiency
GLikely pathogenic
OXCT1
(R124* +1 more)
Single nucleotide variant
(nonsense +1 more)
Succinyl-CoA acetoacetate transferase deficiency
GLikely pathogenic
OXCT1
Single nucleotide variant
(splice donor variant)
Succinyl-CoA acetoacetate transferase deficiency
GLikely pathogenic
OXCT1
(G84E +1 more)
Single nucleotide variant
(missense variant +1 more)
Succinyl-CoA acetoacetate transferase deficiency
GUncertain significance
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