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Links from Gene

Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
COX11, TOM1L1
(I386T +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
COX11
(Q223R)
Single nucleotide variant
(missense variant +2 more)
Mitochondrial complex IV deficiency, nuclear type 23
GUncertain significance
COX11
(F262L)
Single nucleotide variant
(missense variant +2 more)
Mitochondrial complex IV deficiency, nuclear type 23
GUncertain significance
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