ClinVar Miner

List of variants in gene SELENON reported as benign for not provided

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Gene type:
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Total variants: 60
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HGVS dbSNP gnomAD frequency
NM_020451.2(SELENON):c.-42T>C rs12121707 0.99972
NM_020451.3(SELENON):c.302-200C>T rs10902683 0.85751
NM_020451.3(SELENON):c.873-261T>C rs7542128 0.82217
NM_020451.3(SELENON):c.183+298T>G rs6676342 0.81433
NM_020451.3(SELENON):c.183+299T>C rs6676343 0.81411
NM_020451.3(SELENON):c.183+116G>A rs13373825 0.81358
NM_020451.3(SELENON):c.*1722T>C rs4659383 0.80506
NM_020451.3(SELENON):c.425G>A (p.Cys142Tyr) rs7349185 0.78899
NM_020451.3(SELENON):c.1010+141A>C rs6686366 0.75913
NM_020451.3(SELENON):c.1387+109A>G rs3738451 0.73993
NM_020451.3(SELENON):c.1281+81A>G rs11247744 0.73944
NM_020451.3(SELENON):c.1173T>C (p.Pro391=) rs760597 0.73933
NM_020451.3(SELENON):c.*1612T>C rs3203750 0.70822
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.1387+161G>A rs10751726 0.63143
NM_020451.3(SELENON):c.184-109G>A rs6659086 0.63022
NM_020451.2(SELENON):c.-347A>G rs7524771 0.57373
NM_020451.3(SELENON):c.404-174G>A rs11247735 0.50004
NM_020451.3(SELENON):c.872+100C>G rs2280997 0.19814
NM_020451.3(SELENON):c.*2465G>A rs6872 0.16329
NM_020451.3(SELENON):c.1501-31C>T rs72877469 0.03988
NM_020451.3(SELENON):c.872+215T>C rs72877458 0.03505
NM_020451.3(SELENON):c.1281+291A>G rs114228052 0.03025
NM_020451.3(SELENON):c.538-170G>A rs78829313 0.02990
NM_020451.3(SELENON):c.1282-247A>G rs78518541 0.02826
NM_020451.3(SELENON):c.981C>T (p.Arg327=) rs147587542 0.02788
NM_020451.3(SELENON):c.1603-65G>C rs58399004 0.02697
NM_020451.3(SELENON):c.*144C>G rs58895091 0.02379
NM_020451.3(SELENON):c.1745G>A (p.Arg582Gln) rs74060854 0.02376
NM_020451.3(SELENON):c.1011-103T>A rs58522269 0.02311
NM_020451.3(SELENON):c.42C>T (p.Pro14=) rs187960531 0.02295
NM_020451.3(SELENON):c.1010+72A>G rs184840644 0.02081
NM_020451.3(SELENON):c.1010+76G>A rs190134128 0.02067
NM_020451.3(SELENON):c.1602+125A>G rs72877471 0.01909
NM_020451.3(SELENON):c.1387+11C>T rs59653066 0.01839
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.1645G>A (p.Val549Met) rs147131452 0.00268
NM_020451.3(SELENON):c.729G>A (p.Pro243=) rs139020143 0.00131
NM_020451.3(SELENON):c.1162A>G (p.Ser388Gly) rs562843129 0.00001
NM_020451.3(SELENON):c.1092+6C>G rs148071754
NM_020451.3(SELENON):c.1282-122AC[17] rs59333545
NM_020451.3(SELENON):c.1282-122AC[22] rs59333545
NM_020451.3(SELENON):c.1282-122AC[23] rs59333545
NM_020451.3(SELENON):c.1282-122AC[24] rs59333545
NM_020451.3(SELENON):c.1282-122AC[25] rs59333545
NM_020451.3(SELENON):c.1282-123_1282-102del rs1470720382
NM_020451.3(SELENON):c.1282-123_1282-108del rs1432868639
NM_020451.3(SELENON):c.1282-123_1282-114del rs746421369
NM_020451.3(SELENON):c.1282-206_1282-205insCATA rs57085889
NM_020451.3(SELENON):c.1282-224AC[4] rs201582677
NM_020451.3(SELENON):c.1603-236G>T rs12121793
NM_020451.3(SELENON):c.302-8del rs746918551
NM_020451.3(SELENON):c.302-8dup rs746918551
NM_020451.3(SELENON):c.427GAG[5] (p.Glu146dup) rs141295085
NM_020451.3(SELENON):c.538-145C>G rs4659382
NM_020451.3(SELENON):c.538-253_538-209del rs55828916
NM_020451.3(SELENON):c.538-282GCCTGGGTGGGCTGT[3] rs55828916

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