ClinVar Miner

List of variants in gene SELENON reported as likely benign by GeneDx

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 60
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HGVS dbSNP gnomAD frequency
NM_020451.3(SELENON):c.301+114G>T rs7514866 0.01568
NM_020451.3(SELENON):c.538-156C>T rs114688353 0.01527
NM_020451.3(SELENON):c.1011-181T>C rs148884185 0.01492
NM_020451.3(SELENON):c.1282-89_1282-83del rs1361442950 0.01438
NM_020451.3(SELENON):c.748-40G>A rs115488291 0.01415
NM_020451.3(SELENON):c.537+205C>T rs145442409 0.01217
NC_000001.11:g.25800001G>A rs116470826 0.01167
NM_020451.3(SELENON):c.404-115C>T rs115441796 0.01063
NM_020451.3(SELENON):c.*228C>T rs115473437 0.00976
NC_000001.11:g.25800107A>C rs115775394 0.00879
NM_020451.3(SELENON):c.747+39C>T rs114458946 0.00808
NM_020451.3(SELENON):c.183+141G>T rs114881403 0.00807
NM_020451.3(SELENON):c.1282-225T>C rs377063951 0.00632
NM_020451.3(SELENON):c.183+176G>A rs192817585 0.00608
NC_000001.11:g.25800132T>G rs548911393 0.00458
NM_020451.3(SELENON):c.*938C>T rs116835124 0.00453
NM_020451.3(SELENON):c.873-168C>T rs76061061 0.00287
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.846C>T (p.Ser282=) rs34177164 0.00175
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.1602+14C>T rs41284307 0.00120
NM_020451.3(SELENON):c.1596C>T (p.Gly532=) rs149623434 0.00085
NM_020451.3(SELENON):c.1623C>T (p.Asn541=) rs199911454 0.00070
NM_020451.3(SELENON):c.-35T>C rs886038656 0.00066
NM_020451.3(SELENON):c.1500+7G>A rs200724231 0.00044
NM_020451.3(SELENON):c.1654G>A (p.Glu552Lys) rs200128474 0.00036
NM_020451.3(SELENON):c.1092+16G>C rs199937216 0.00028
NM_020451.3(SELENON):c.1638C>T (p.Ile546=) rs201066183 0.00017
NM_020451.3(SELENON):c.301+18C>T rs373189692 0.00009
NM_020451.3(SELENON):c.717C>T (p.Arg239=) rs377562721 0.00006
NM_020451.3(SELENON):c.-1C>T rs1023302860 0.00004
NM_020451.3(SELENON):c.1455C>T (p.Ser485=) rs575407217 0.00004
NM_020451.3(SELENON):c.1704G>A (p.Pro568=) rs754350384 0.00003
NM_020451.3(SELENON):c.183+11G>A rs1015099314 0.00003
NM_020451.3(SELENON):c.9G>C (p.Arg3=) rs1057521978 0.00003
NM_020451.3(SELENON):c.1644C>T (p.Ser548=) rs368507434 0.00002
NM_020451.3(SELENON):c.1602+12C>T rs903798730 0.00001
NM_020451.3(SELENON):c.537+16C>T rs774621017 0.00001
NM_020451.3(SELENON):c.693C>T (p.Phe231=) rs903926749 0.00001
NM_020451.3(SELENON):c.748-9C>T rs752180175 0.00001
NC_000001.11:g.25800121dup rs1245396370
NC_000001.11:g.25800126_25800130del rs1437300656
NM_020451.2(SELENON):c.-58_-47dup rs1553198442
NM_020451.3(SELENON):c.*267C>G rs184807941
NM_020451.3(SELENON):c.-22_-13dup rs1553198459
NM_020451.3(SELENON):c.1010+20C>T rs1553120231
NM_020451.3(SELENON):c.1011-128G>T rs74753273
NM_020451.3(SELENON):c.1282-122AC[26] rs59333545
NM_020451.3(SELENON):c.1282-123_1282-110del rs1424842411
NM_020451.3(SELENON):c.1282-123_1282-112del rs1195650090
NM_020451.3(SELENON):c.1282-123_1282-118del rs879841213
NM_020451.3(SELENON):c.1282-123_1282-122del rs751498637
NM_020451.3(SELENON):c.1635C>T (p.Asp545=) rs1398526314
NM_020451.3(SELENON):c.1710G>A (p.Thr570=) rs371398538
NM_020451.3(SELENON):c.171G>A (p.Ala57=) rs1057523110
NM_020451.3(SELENON):c.301+6A>T rs1553198615
NM_020451.3(SELENON):c.404-329G>A rs139733429
NM_020451.3(SELENON):c.948C>T (p.His316=) rs1553120209

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