ClinVar Miner

List of variants in gene MNX1 reported as uncertain significance for Currarino triad

Included ClinVar conditions (1):
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Total variants: 58
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HGVS dbSNP gnomAD frequency
NM_005515.4(MNX1):c.1136C>T (p.Ala379Val) rs780826565 0.00003
NM_005515.4(MNX1):c.274C>T (p.Pro92Ser) rs1311353245 0.00003
NM_005515.4(MNX1):c.676A>G (p.Met226Val) rs889871814 0.00002
NM_005515.4(MNX1):c.1048G>A (p.Asp350Asn) rs1292330977 0.00001
NM_005515.4(MNX1):c.1168C>G (p.Pro390Ala) rs760934530 0.00001
NM_005515.4(MNX1):c.124G>C (p.Gly42Arg) rs1249063712 0.00001
NM_005515.4(MNX1):c.145G>A (p.Gly49Arg) rs1472400448 0.00001
NM_005515.4(MNX1):c.689A>G (p.Asn230Ser) rs765767987 0.00001
NM_005515.4(MNX1):c.870G>A (p.Gln290=) rs774179857 0.00001
NM_005515.4(MNX1):c.956G>A (p.Gly319Asp) rs758672581 0.00001
NM_005515.4(MNX1):c.102CGC[5] (p.Ala38_Ser39insAla)
NM_005515.4(MNX1):c.1055G>C (p.Arg352Thr) rs988657656
NM_005515.4(MNX1):c.1074GGACGA[2] (p.358ED[2]) rs763608839
NM_005515.4(MNX1):c.1081GACGAGGAC[1] (p.361DED[1]) rs762400153
NM_005515.4(MNX1):c.1105C>A (p.Pro369Thr)
NM_005515.4(MNX1):c.1124G>C (p.Ser375Thr)
NM_005515.4(MNX1):c.1166C>T (p.Ser389Leu) rs200578176
NM_005515.4(MNX1):c.1171C>A (p.Pro391Thr) rs767605620
NM_005515.4(MNX1):c.1175C>A (p.Pro392Gln)
NM_005515.4(MNX1):c.1175C>T (p.Pro392Leu)
NM_005515.4(MNX1):c.1177C>G (p.Arg393Gly)
NM_005515.4(MNX1):c.1198C>T (p.Pro400Ser)
NM_005515.4(MNX1):c.132CGG[6] (p.Gly49_Ala50insGly) rs781217883
NM_005515.4(MNX1):c.132CGG[7] (p.Gly49_Ala50insGlyGly) rs781217883
NM_005515.4(MNX1):c.132CGG[8] (p.Gly47_Gly49dup) rs781217883
NM_005515.4(MNX1):c.14A>G (p.Lys5Arg)
NM_005515.4(MNX1):c.155G>A (p.Gly52Asp)
NM_005515.4(MNX1):c.158G>A (p.Gly53Glu) rs1805688499
NM_005515.4(MNX1):c.196C>T (p.Pro66Ser)
NM_005515.4(MNX1):c.205C>T (p.Pro69Ser)
NM_005515.4(MNX1):c.224C>T (p.Ala75Val) rs1338839358
NM_005515.4(MNX1):c.269T>C (p.Leu90Pro)
NM_005515.4(MNX1):c.298GGC[7] (p.Gly105dup) rs757330807
NM_005515.4(MNX1):c.305G>C (p.Gly102Ala)
NM_005515.4(MNX1):c.331G>C (p.Gly111Arg)
NM_005515.4(MNX1):c.355C>A (p.Pro119Thr) rs1456554355
NM_005515.4(MNX1):c.359G>T (p.Gly120Val)
NM_005515.4(MNX1):c.377_378insTGCCGCCGCCGCCGC (p.Ala134_Gly135insAlaAlaAlaAlaAla)
NM_005515.4(MNX1):c.44T>C (p.Val15Ala)
NM_005515.4(MNX1):c.528G>T (p.Ala176=)
NM_005515.4(MNX1):c.529G>T (p.Gly177Cys) rs778434757
NM_005515.4(MNX1):c.574G>A (p.Ala192Thr)
NM_005515.4(MNX1):c.580C>T (p.Pro194Ser)
NM_005515.4(MNX1):c.619A>G (p.Thr207Ala)
NM_005515.4(MNX1):c.655G>A (p.Ala219Thr)
NM_005515.4(MNX1):c.656C>G (p.Ala219Gly)
NM_005515.4(MNX1):c.662T>A (p.Met221Lys)
NM_005515.4(MNX1):c.675G>C (p.Lys225Asn)
NM_005515.4(MNX1):c.721T>G (p.Cys241Gly)
NM_005515.4(MNX1):c.728G>A (p.Arg243Gln)
NM_005515.4(MNX1):c.76G>C (p.Ala26Pro)
NM_005515.4(MNX1):c.808A>C (p.Lys270Gln) rs1191651587
NM_005515.4(MNX1):c.820G>A (p.Val274Met)
NM_005515.4(MNX1):c.852G>A (p.Gln284=) rs2537773764
NM_005515.4(MNX1):c.904G>C (p.Ala302Pro)
NM_005515.4(MNX1):c.973G>T (p.Ala325Ser)
NM_005515.4(MNX1):c.980A>G (p.Glu327Gly)
NM_005515.4(MNX1):c.983C>G (p.Pro328Arg)

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