List of variants in gene AURKC reported as likely benign for spermatogenic failure

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_001015878.2(AURKC):c.396G>A (p.Leu132=)	rs55710619	0.00991
NM_001015878.2(AURKC):c.621G>A (p.Pro207=)	rs148940837	0.00593
NM_001015878.2(AURKC):c.-80dup	rs140452971
NM_001015878.2(AURKC):c.-99dup	rs74179426

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