ClinVar Miner

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

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Total variants: 21
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HGVS dbSNP gnomAD frequency
NM_020774.4(MIB1):c.843A>T (p.Thr281=) rs137957940 0.00231
NM_020774.4(MIB1):c.2779+8G>A rs148003129 0.00034
NM_020774.4(MIB1):c.2445C>G (p.Thr815=) rs150116970 0.00025
NM_020774.4(MIB1):c.2050-15A>C rs373738054 0.00016
NM_020774.4(MIB1):c.636+7A>C rs765948951 0.00010
NM_020774.4(MIB1):c.1093-9T>C rs762889843 0.00009
NM_020774.4(MIB1):c.376C>T (p.Arg126Ter) rs190657514 0.00006
NM_020774.4(MIB1):c.597T>C (p.Asn199=) rs1323108897 0.00006
NM_020774.4(MIB1):c.1548A>G (p.Leu516=) rs745431396 0.00004
NM_020774.4(MIB1):c.908+11T>C rs747807993 0.00003
NM_020774.4(MIB1):c.1245C>G (p.Leu415=) rs768457898 0.00001
NM_020774.4(MIB1):c.1848A>G (p.Leu616=) rs745924072 0.00001
NM_020774.4(MIB1):c.2037C>T (p.Thr679=) rs1232246381 0.00001
NM_020774.4(MIB1):c.933C>T (p.Leu311=) rs888626600 0.00001
NM_020774.4(MIB1):c.1450T>C (p.Leu484=) rs1555692874
NM_020774.4(MIB1):c.1678-10A>T rs1555694067
NM_020774.4(MIB1):c.1678-18A>T rs1555694061
NM_020774.4(MIB1):c.2244G>A (p.Glu748=) rs1555696198
NM_020774.4(MIB1):c.230-6T>C rs1555689079
NM_020774.4(MIB1):c.2802A>G (p.Leu934=) rs754841638
NM_020774.4(MIB1):c.696T>G (p.Pro232=) rs1555690373

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