ClinVar Miner

List of variants in gene SELENON reported by PreventionGenetics, part of Exact Sciences

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Gene type:
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Total variants: 41
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HGVS dbSNP gnomAD frequency
NM_020451.2(SELENON):c.-42T>C rs12121707 0.99972
NM_020451.3(SELENON):c.425G>A (p.Cys142Tyr) rs7349185 0.78899
NM_020451.3(SELENON):c.1173T>C (p.Pro391=) rs760597 0.73933
NM_020451.3(SELENON):c.1093-46C>A rs760598 0.68499
NM_020451.3(SELENON):c.1282-41C>T rs10902685 0.64052
NM_020451.3(SELENON):c.1506C>A (p.Asn502Lys) rs2294228 0.64022
NM_020451.3(SELENON):c.1501-31C>T rs72877469 0.03988
NM_020451.3(SELENON):c.981C>T (p.Arg327=) rs147587542 0.02788
NM_020451.3(SELENON):c.1745G>A (p.Arg582Gln) rs74060854 0.02376
NM_020451.3(SELENON):c.42C>T (p.Pro14=) rs187960531 0.02295
NM_020451.3(SELENON):c.1387+11C>T rs59653066 0.01839
NM_020451.3(SELENON):c.748-40G>A rs115488291 0.01415
NM_020451.3(SELENON):c.409A>G (p.Thr137Ala) rs35019869 0.01231
NM_020451.3(SELENON):c.583G>A (p.Ala195Thr) rs115852080 0.01060
NM_020451.3(SELENON):c.747+39C>T rs114458946 0.00808
NM_020451.3(SELENON):c.-14C>A rs867555591 0.00642
NM_020451.3(SELENON):c.1281+42G>A rs201047535 0.00286
NM_020451.3(SELENON):c.1645G>A (p.Val549Met) rs147131452 0.00268
NM_020451.3(SELENON):c.*44G>T rs116931343 0.00258
NM_020451.3(SELENON):c.550G>C (p.Ala184Pro) rs199742668 0.00240
NM_020451.3(SELENON):c.852C>T (p.Phe284=) rs187880136 0.00141
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.1602+14C>T rs41284307 0.00120
NM_020451.3(SELENON):c.1596C>T (p.Gly532=) rs149623434 0.00085
NM_020451.3(SELENON):c.-35T>C rs886038656 0.00066
NM_020451.3(SELENON):c.1282-10G>A rs556910756 0.00060
NM_020451.3(SELENON):c.81C>T (p.Arg27=) rs886038660 0.00014
NM_020451.3(SELENON):c.1093-45T>C rs549130801 0.00009
NM_020451.3(SELENON):c.465G>A (p.Thr155=) rs753774853 0.00006
NM_020451.3(SELENON):c.732G>A (p.Pro244=) rs200765195 0.00006
NM_020451.3(SELENON):c.1455C>T (p.Ser485=) rs575407217 0.00004
NM_020451.3(SELENON):c.1162A>G (p.Ser388Gly) rs562843129 0.00001
NM_020451.3(SELENON):c.1281+15G>T rs886038657 0.00001
NM_020451.3(SELENON):c.403+47T>A rs886038658 0.00001
NM_020451.3(SELENON):c.404-23dup rs560595923 0.00001
NM_020451.3(SELENON):c.1092+6C>G rs148071754
NM_020451.3(SELENON):c.1118C>T (p.Ser373Phe)
NM_020451.3(SELENON):c.1123C>A (p.Pro375Thr) rs1379278116
NM_020451.3(SELENON):c.1710G>A (p.Thr570=) rs371398538
NM_020451.3(SELENON):c.427GAG[5] (p.Glu146dup) rs141295085

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