ClinVar Miner

List of variants in gene MIB1 reported as uncertain significance by GeneDx

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Total variants: 57
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HGVS dbSNP gnomAD frequency
NM_020774.4(MIB1):c.2411G>A (p.Arg804Gln) rs200809199 0.00026
NM_020774.4(MIB1):c.2746G>A (p.Gly916Arg) rs147206277 0.00016
NM_020774.4(MIB1):c.1295A>G (p.Asn432Ser) rs759225220 0.00014
NM_020774.4(MIB1):c.2827G>T (p.Val943Phe) rs200035428 0.00013
NM_020774.4(MIB1):c.1771A>T (p.Ile591Phe) rs149201924 0.00012
NM_020774.4(MIB1):c.1111C>T (p.Arg371Ter) rs141236852 0.00010
NM_020774.4(MIB1):c.2026C>T (p.Arg676Ter) rs200545301 0.00009
NM_020774.4(MIB1):c.2716C>T (p.Arg906Ter) rs201146927 0.00009
NM_020774.4(MIB1):c.1588C>T (p.Arg530Ter) rs201850378 0.00007
NM_020774.4(MIB1):c.952C>T (p.Arg318Ter) rs142475589 0.00006
NM_020774.4(MIB1):c.1039C>T (p.Arg347Ter) rs376597435 0.00004
NM_020774.4(MIB1):c.1355A>C (p.Lys452Thr) rs752947479 0.00004
NM_020774.4(MIB1):c.442G>T (p.Ala148Ser) rs369261422 0.00004
NM_020774.4(MIB1):c.2305C>T (p.Arg769Ter) rs752243957 0.00003
NM_020774.4(MIB1):c.2650_2651del (p.Met884fs) rs765387378 0.00003
NM_020774.4(MIB1):c.388C>T (p.Pro130Ser) rs998773897 0.00003
NM_020774.4(MIB1):c.2458A>G (p.Met820Val) rs574146329 0.00002
NM_020774.4(MIB1):c.1417C>T (p.Gln473Ter) rs1386314249 0.00001
NM_020774.4(MIB1):c.1786G>T (p.Gly596Ter) rs1555694075 0.00001
NM_020774.4(MIB1):c.2653T>G (p.Cys885Gly) rs1286211902 0.00001
NM_020774.4(MIB1):c.434A>G (p.Lys145Arg) rs1243877213 0.00001
NM_020774.4(MIB1):c.1066G>A (p.Gly356Arg)
NM_020774.4(MIB1):c.1108G>A (p.Gly370Ser) rs1057520754
NM_020774.4(MIB1):c.1226A>G (p.Asn409Ser)
NM_020774.4(MIB1):c.1235G>A (p.Gly412Asp)
NM_020774.4(MIB1):c.1322A>G (p.Asn441Ser) rs730880135
NM_020774.4(MIB1):c.1372-10A>G
NM_020774.4(MIB1):c.1589G>A (p.Arg530Gln)
NM_020774.4(MIB1):c.1593_1596del (p.Gln531fs) rs2146474858
NM_020774.4(MIB1):c.1709C>T (p.Ala570Val)
NM_020774.4(MIB1):c.1952T>A (p.Leu651Ter) rs201349172
NM_020774.4(MIB1):c.1967A>C (p.Asn656Thr) rs369313882
NM_020774.4(MIB1):c.1982T>G (p.Ile661Ser) rs2146505212
NM_020774.4(MIB1):c.2140C>T (p.Gln714Ter) rs1555696015
NM_020774.4(MIB1):c.2234del (p.Gln745fs) rs1463825087
NM_020774.4(MIB1):c.2235G>T (p.Gln745His) rs1057518310
NM_020774.4(MIB1):c.229+3A>T
NM_020774.4(MIB1):c.2309A>G (p.Asn770Ser)
NM_020774.4(MIB1):c.2318del (p.Gly773fs) rs1555696210
NM_020774.4(MIB1):c.2322del (p.Gln774fs) rs2146508957
NM_020774.4(MIB1):c.2416C>T (p.Pro806Ser)
NM_020774.4(MIB1):c.2587-12_2587-11del
NM_020774.4(MIB1):c.2635C>T (p.Gln879Ter) rs1555696617
NM_020774.4(MIB1):c.2665+4A>G rs2042196777
NM_020774.4(MIB1):c.2666-11_2666-10delinsAG
NM_020774.4(MIB1):c.2749A>T (p.Lys917Ter) rs1019483000
NM_020774.4(MIB1):c.2881-1_2883del rs1555697356
NM_020774.4(MIB1):c.2888_2889delinsTT (p.Cys963Phe)
NM_020774.4(MIB1):c.2905C>T (p.Arg969Cys) rs749620047
NM_020774.4(MIB1):c.2963G>T (p.Arg988Leu) rs775477290
NM_020774.4(MIB1):c.2986dup (p.Arg996fs) rs2146527210
NM_020774.4(MIB1):c.407del (p.Leu136fs) rs770988700
NM_020774.4(MIB1):c.448G>T (p.Gly150Ter) rs1555689348
NM_020774.4(MIB1):c.705T>C (p.Gly235=) rs755288537
NM_020774.4(MIB1):c.856T>C (p.Cys286Arg)
NM_020774.4(MIB1):c.912del (p.Arg303_Trp304insTer)
NM_020774.4(MIB1):c.939dup (p.Ala314fs) rs1555691689

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