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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CCDC65
(M1K)
Single nucleotide variant
(5 prime UTR variant +2 more)
Primary ciliary dyskinesia 27
GUncertain significance
CCDC65
(A109V)
Single nucleotide variant
(5 prime UTR variant +1 more)
Primary ciliary dyskinesia 27
+1 more
GUncertain significance
CCDC65
Single nucleotide variant
(synonymous variant)
Primary ciliary dyskinesia 27
GLikely benign
CCDC65
(D341Y +1 more)
Single nucleotide variant
(missense variant)
Primary ciliary dyskinesia 27
+1 more
GBenign/Likely benign
CCDC65
Single nucleotide variant
(synonymous variant)
Primary ciliary dyskinesia 27
GBenign/Likely benign
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