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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DLAT
(P89T +1 more)
Single nucleotide variant
(missense variant +3 more)
Pyruvate dehydrogenase E2 deficiency
GUncertain significance
DLAT
(I146M +6 more)
Single nucleotide variant
(missense variant +1 more)
Pyruvate dehydrogenase E2 deficiency
GUncertain significance
DLAT, PIH1D2
(I377V +12 more)
Single nucleotide variant
(missense variant +1 more)
Pyruvate dehydrogenase E2 deficiency
GUncertain significance
DLAT, PIH1D2
(F576L +12 more)
Single nucleotide variant
(missense variant +1 more)
Pyruvate dehydrogenase E2 deficiency
GLikely pathogenic
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