List of variants in gene AURKC reported as uncertain significance 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: 20

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HGVS	dbSNP	gnomAD frequency
NM_001015878.2(AURKC):c.436-4A>G	rs148623255	0.00299
NM_001015878.2(AURKC):c.760-12T>C	rs148264225	0.00279
NM_001015878.2(AURKC):c.12C>G (p.Pro4=)	rs73633650	0.00225
NM_001015878.2(AURKC):c.435+11G>A	rs193015358	0.00130
NM_001015878.2(AURKC):c.*6G>C	rs138125119	0.00114
NM_001015878.2(AURKC):c.-139C>T	rs138814299	0.00022
NM_001015878.2(AURKC):c.762A>G (p.Val254=)	rs55898757	0.00014
NM_001015878.2(AURKC):c.675T>C (p.Ile225=)	rs145271279	0.00006
NM_001015878.2(AURKC):c.-38G>T	rs770401705	0.00001
NM_001015878.2(AURKC):c.184C>T (p.Leu62Phe)	rs886054645	0.00001
NM_001015878.2(AURKC):c.689A>G (p.Tyr230Cys)	rs761881153	0.00001
NM_001015878.2(AURKC):c.779T>C (p.Leu260Pro)	rs763668016	0.00001
NM_001015878.2(AURKC):c.-53A>C	rs2087484333
NM_001015878.2(AURKC):c.-84C>T	rs552823754
NM_001015878.2(AURKC):c.-99dup	rs74179426
NM_001015878.2(AURKC):c.209C>G (p.Ala70Gly)	rs2087499420
NM_001015878.2(AURKC):c.351C>T (p.Tyr117=)	rs886054646
NM_001015878.2(AURKC):c.656A>C (p.Lys219Thr)	rs2087531534
NM_001015878.2(AURKC):c.780A>G (p.Leu260=)	rs189830354
NM_001015878.2(AURKC):c.94_101dup (p.Met35fs)	rs749123022

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