ClinVar Miner

List of variants studied for Spermatogenic Failure

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Total variants: 11
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HGVS dbSNP gnomAD frequency
NM_176822.4(NLRP14):c.322A>T (p.Lys108Ter) rs76274604 0.00480
NM_001101677.2(SOHLH1):c.346-1G>A rs140132974 0.00173
NM_031955.5(SPATA16):c.-159C>A rs528313469 0.00088
NM_031955.6(SPATA16):c.-141C>T rs886058188 0.00004
NM_176822.4(NLRP14):c.257A>T (p.Asp86Val) rs199735773 0.00001
NM_001015878.2(AURKC):c.-80dup rs140452971
NM_001015878.2(AURKC):c.-99dup rs74179426
NM_001031748.4(REDIC1):c.233_234insTT (p.Met78fs)
NM_001177949.2(SYCP3):c.*239CT[1] rs370467855
NM_001177949.2(SYCP3):c.454-13_454-9del rs145003954
NM_031955.6(SPATA16):c.848+15del rs143941722

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