ClinVar Miner

List of variants reported as benign for male infertility with teratozoospermia due to single gene mutation

Included ClinVar conditions (6):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 10
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HGVS dbSNP gnomAD frequency
NM_001015878.2(AURKC):c.-145G>C rs11084490 0.86511
NM_001015878.2(AURKC):c.-128C>T rs58264281 0.75512
NM_031955.6(SPATA16):c.397A>G (p.Met133Val) rs1515442 0.39106
NM_031955.6(SPATA16):c.675C>T (p.Ser225=) rs508508 0.17696
NM_031955.6(SPATA16):c.232G>A (p.Glu78Lys) rs1515441 0.11912
NM_031955.6(SPATA16):c.440G>A (p.Gly147Glu) rs16846616 0.09632
NM_031955.6(SPATA16):c.720G>A (p.Arg240=) rs55724801 0.02430
NM_031955.6(SPATA16):c.130T>A (p.Ser44Thr) rs146572379 0.02122
NM_001015878.2(AURKC):c.235A>G (p.Ile79Val) rs61736320 0.00180
NM_001015878.2(AURKC):c.*38G>A rs35582299

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