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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
COX14
Single nucleotide variant
(intron variant)
Mitochondrial complex 4 deficiency, nuclear type 10
+1 more
GLikely benign
COX14
(Y25C)
Single nucleotide variant
(missense variant)
Mitochondrial complex 4 deficiency, nuclear type 10
+1 more
GUncertain significance
COX14
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GLikely benign
COX14
(S54P)
Single nucleotide variant
(missense variant)
Mitochondrial complex 4 deficiency, nuclear type 10
+1 more
GUncertain significance
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