ClinVar Miner

List of variants in gene SELENON reported as uncertain significance for not provided

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Gene type:
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Total variants: 54
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HGVS dbSNP gnomAD frequency
NM_020451.3(SELENON):c.-14C>A rs867555591 0.00642
NM_020451.3(SELENON):c.729G>A (p.Pro243=) rs139020143 0.00131
NM_020451.3(SELENON):c.1715C>A (p.Thr572Asn) rs183272965 0.00124
NM_020451.3(SELENON):c.1596C>T (p.Gly532=) rs149623434 0.00085
NM_020451.3(SELENON):c.415G>A (p.Ala139Thr) rs201692549 0.00054
NM_020451.3(SELENON):c.427G>A (p.Glu143Lys) rs200958015 0.00054
NM_020451.3(SELENON):c.1654G>A (p.Glu552Lys) rs200128474 0.00036
NM_020451.3(SELENON):c.1428G>A (p.Ser476=) rs41284305 0.00029
NM_020451.3(SELENON):c.716G>A (p.Arg239His) rs199709671 0.00029
NM_020451.3(SELENON):c.4G>T (p.Gly2Cys) rs982364753 0.00028
NM_020451.3(SELENON):c.1603-14G>A rs370300935 0.00022
NM_020451.3(SELENON):c.103G>C (p.Gly35Arg) rs398124359 0.00020
NM_020451.3(SELENON):c.1638C>T (p.Ile546=) rs201066183 0.00017
NM_020451.3(SELENON):c.7C>A (p.Arg3=) rs866566089 0.00016
NM_020451.3(SELENON):c.1744C>T (p.Arg582Trp) rs373530866 0.00015
NM_020451.3(SELENON):c.81C>T (p.Arg27=) rs886038660 0.00014
NM_020451.3(SELENON):c.1517C>T (p.Ser506Leu) rs766798515 0.00009
NM_020451.3(SELENON):c.402G>A (p.Leu134=) rs759256016 0.00008
NM_020451.3(SELENON):c.457G>A (p.Glu153Lys) rs374512346 0.00008
NM_020451.3(SELENON):c.253A>G (p.Met85Val) rs761605974 0.00007
NM_020451.3(SELENON):c.1191G>T (p.Gln397His) rs1311923186 0.00006
NM_020451.3(SELENON):c.1636A>G (p.Ile546Val) rs749237378 0.00006
NM_020451.3(SELENON):c.465G>A (p.Thr155=) rs753774853 0.00006
NM_020451.3(SELENON):c.183+14C>G rs794726949 0.00004
NM_020451.3(SELENON):c.1249C>T (p.Arg417Cys) rs769840172 0.00003
NM_020451.3(SELENON):c.1535C>T (p.Ala512Val) rs202167521 0.00003
NM_020451.3(SELENON):c.545G>A (p.Arg182His) rs200224030 0.00003
NM_020451.3(SELENON):c.1427C>T (p.Ser476Leu) rs368377980 0.00002
NM_020451.3(SELENON):c.500C>T (p.Pro167Leu) rs747408056 0.00002
NM_020451.3(SELENON):c.883G>A (p.Glu295Lys) rs978886878 0.00002
NM_020451.3(SELENON):c.988C>T (p.Arg330Trp) rs1489695877 0.00002
NM_020451.3(SELENON):c.-19G>C rs794726948 0.00001
NM_020451.3(SELENON):c.1112G>T (p.Gly371Val) rs745886248 0.00001
NM_020451.3(SELENON):c.1246C>T (p.Arg416Trp) rs369207232 0.00001
NM_020451.3(SELENON):c.1318G>A (p.Ala440Thr) rs779899932 0.00001
NM_020451.3(SELENON):c.581C>T (p.Ala194Val) rs727504148 0.00001
NM_020451.3(SELENON):c.610C>T (p.Arg204Cys) rs754161311 0.00001
NM_020451.3(SELENON):c.976G>A (p.Val326Ile) rs764032922 0.00001
NM_020451.3(SELENON):c.-12C>T rs866547663
NM_020451.3(SELENON):c.1049G>C (p.Ser350Thr) rs777864718
NM_020451.3(SELENON):c.1112G>A (p.Gly371Asp) rs745886248
NM_020451.3(SELENON):c.1148GCA[1] (p.Ser384del) rs770747626
NM_020451.3(SELENON):c.1351C>G (p.Leu451Val) rs200431320
NM_020451.3(SELENON):c.1450G>A (p.Glu484Lys) rs727504149
NM_020451.3(SELENON):c.14G>A (p.Arg5Gln) rs794726947
NM_020451.3(SELENON):c.1549G>A (p.Glu517Lys)
NM_020451.3(SELENON):c.20G>A (p.Gly7Asp) rs886043768
NM_020451.3(SELENON):c.427GAG[5] (p.Glu146dup) rs141295085
NM_020451.3(SELENON):c.538G>T (p.Val180Phe) rs751053087
NM_020451.3(SELENON):c.580G>A (p.Ala194Thr) rs560203077
NM_020451.3(SELENON):c.680A>G (p.Glu227Gly) rs1085307758
NM_020451.3(SELENON):c.711C>A (p.Asn237Lys)
NM_020451.3(SELENON):c.760C>T (p.Arg254Trp) rs374195814
NM_020451.3(SELENON):c.992T>C (p.Leu331Pro) rs1572233653

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