List of variants in gene CCIN reported as pathogenic for Spermatogenic failure 91

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_005893.3(CCIN):c.853G>A (p.Gly285Ser)	rs750854950	0.00004
NM_005893.3(CCIN):c.125A>T (p.His42Leu)
NM_005893.3(CCIN):c.1294C>T (p.Arg432Trp)
NM_005893.3(CCIN):c.1341C>A (p.Cys447Ter)
NM_005893.3(CCIN):c.230T>C (p.Leu77Pro)

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