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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CFAP58
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
CFAP58
Single nucleotide variant
(intron variant)
not provided
GUncertain significance
CFAP58
(R678C +1 more)
Single nucleotide variant
(missense variant)
not provided
GLikely benign
CFAP58
(R749H +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
CFAP58
(T850N +1 more)
Single nucleotide variant
(missense variant)
not provided
GBenign
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