ClinVar Miner

List of variants in gene MIB1 reported as benign for not specified

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Gene type:
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Total variants: 21
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HGVS dbSNP gnomAD frequency
NM_020774.4(MIB1):c.2393+10A>G rs11877131 0.09299
NM_020774.4(MIB1):c.1962+17A>G rs139079482 0.00792
NM_020774.4(MIB1):c.1479+18A>G rs12605999 0.00637
NM_020774.4(MIB1):c.843A>T (p.Thr281=) rs137957940 0.00231
NM_020774.4(MIB1):c.1963-6G>A rs186680702 0.00108
NM_020774.4(MIB1):c.603T>G (p.Ala201=) rs35738763 0.00094
NM_020774.4(MIB1):c.2586+17A>G rs370642266 0.00048
NM_020774.4(MIB1):c.2337C>T (p.Leu779=) rs146430244 0.00037
NM_020774.4(MIB1):c.736T>C (p.Leu246=) rs188600853 0.00036
NM_020774.4(MIB1):c.2676C>T (p.Asn892=) rs77329509 0.00027
NM_020774.4(MIB1):c.1830-18T>C rs201761957 0.00026
NM_020774.4(MIB1):c.2445C>G (p.Thr815=) rs150116970 0.00025
NM_020774.4(MIB1):c.1470C>T (p.Val490=) rs141701856 0.00023
NM_020774.4(MIB1):c.1092+3A>G rs372212766 0.00016
NM_020774.4(MIB1):c.636+7A>C rs765948951 0.00010
NM_020774.4(MIB1):c.1238-11A>T rs757539398 0.00004
NM_020774.4(MIB1):c.138G>A (p.Glu46=) rs376396687 0.00004
NM_020774.4(MIB1):c.2325G>A (p.Ser775=) rs781491471 0.00004
NM_020774.4(MIB1):c.1372-12T>A rs772089721 0.00001
NM_020774.4(MIB1):c.2580G>A (p.Arg860=) rs762343314 0.00001
NM_020774.4(MIB1):c.230-13C>T rs374307694

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