ClinVar Miner

List of variants in gene SPATA16 studied for spermatogenic failure

Included ClinVar conditions (116):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 52
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HGVS dbSNP gnomAD frequency
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_031955.6(SPATA16):c.1577T>C (p.Met526Thr) rs62622782 0.01931
NM_031955.6(SPATA16):c.1526C>T (p.Ala509Val) rs115095786 0.01910
NM_031955.6(SPATA16):c.149A>G (p.Asn50Ser) rs16846624 0.01264
NM_031955.6(SPATA16):c.1143A>G (p.Gln381=) rs73041295 0.00685
NM_031955.6(SPATA16):c.-121G>A rs189972919 0.00657
NM_031955.6(SPATA16):c.53A>G (p.His18Arg) rs115897458 0.00450
NM_031955.6(SPATA16):c.736C>T (p.Leu246Phe) rs116466451 0.00183
NM_031955.6(SPATA16):c.430A>C (p.Met144Leu) rs140920981 0.00099
NM_031955.5(SPATA16):c.-159C>A rs528313469 0.00088
NM_031955.6(SPATA16):c.328A>C (p.Met110Leu) rs147011314 0.00046
NM_031955.6(SPATA16):c.848G>A (p.Arg283Gln) rs137853118 0.00032
NM_031955.6(SPATA16):c.117C>T (p.Asn39=) rs372937515 0.00022
NM_031955.6(SPATA16):c.996G>A (p.Ala332=) rs138951243 0.00021
NM_031955.6(SPATA16):c.105G>A (p.Ala35=) rs141312480 0.00019
NM_031955.6(SPATA16):c.1401G>T (p.Gln467His) rs143774140 0.00019
NM_031955.6(SPATA16):c.104C>T (p.Ala35Val) rs200483368 0.00010
NM_031955.6(SPATA16):c.576C>T (p.Tyr192=) rs146363552 0.00010
NM_031955.6(SPATA16):c.*92A>G rs892103462 0.00009
NM_031955.6(SPATA16):c.-142G>A rs566046620 0.00009
NM_031955.6(SPATA16):c.25T>C (p.Leu9=) rs150041488 0.00008
NM_031955.6(SPATA16):c.-141C>T rs886058188 0.00004
NM_031955.6(SPATA16):c.91A>T (p.Met31Leu) rs200087565 0.00004
NM_031955.6(SPATA16):c.1513C>T (p.Leu505=) rs758141708 0.00003
NM_031955.6(SPATA16):c.995C>T (p.Ala332Val) rs544088248 0.00003
NM_031955.6(SPATA16):c.251G>A (p.Arg84Gln) rs143065627 0.00002
NM_031955.6(SPATA16):c.613-13A>G rs749048781 0.00002
NM_031955.6(SPATA16):c.750T>C (p.His250=) rs758393334 0.00002
NM_031955.6(SPATA16):c.873G>A (p.Met291Ile) rs368670834 0.00002
NM_031955.6(SPATA16):c.*157C>T rs540340589 0.00001
NM_031955.6(SPATA16):c.1361G>A (p.Gly454Asp) rs774830755 0.00001
NM_031955.6(SPATA16):c.1365G>T (p.Val455=) rs199707743 0.00001
NM_031955.6(SPATA16):c.1503+15T>C rs776183936 0.00001
NM_031955.6(SPATA16):c.1588-2A>G rs757711631 0.00001
NM_031955.6(SPATA16):c.205A>G (p.Ile69Val) rs558144498 0.00001
NM_031955.6(SPATA16):c.406C>T (p.Arg136Cys) rs144595913 0.00001
NM_031955.6(SPATA16):c.490C>T (p.His164Tyr) rs780372927 0.00001
NM_031955.6(SPATA16):c.546T>C (p.Asp182=) rs886058187 0.00001
NM_031955.6(SPATA16):c.719G>A (p.Arg240Gln) rs200456888 0.00001
NM_031955.6(SPATA16):c.828G>A (p.Glu276=) rs776236874 0.00001
NM_031955.6(SPATA16):c.*138C>A rs903704544
NM_031955.6(SPATA16):c.-2C>T rs1737947552
NM_031955.6(SPATA16):c.1117G>A (p.Asp373Asn) rs763912965
NM_031955.6(SPATA16):c.1324A>G (p.Ser442Gly) rs886058186
NM_031955.6(SPATA16):c.1389C>A (p.Ser463Arg) rs1732489716
NM_031955.6(SPATA16):c.430A>G (p.Met144Val) rs140920981
NM_031955.6(SPATA16):c.848+15del rs143941722

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