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

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 49

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HGVS	dbSNP	gnomAD frequency
NM_020451.3(SELENON):c.981C>T (p.Arg327=)	rs147587542	0.02788
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.409A>G (p.Thr137Ala)	rs35019869	0.01231
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.583G>A (p.Ala195Thr)	rs115852080	0.01060
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.852C>T (p.Phe284=)	rs187880136	0.00141
NM_020451.3(SELENON):c.1596C>T (p.Gly532=)	rs149623434	0.00085
NM_020451.3(SELENON):c.1282-10G>A	rs556910756	0.00060
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.717C>T (p.Arg239=)	rs377562721	0.00006
NM_020451.3(SELENON):c.1344C>T (p.His448=)	rs752098351	0.00005
NM_020451.3(SELENON):c.1162A>G (p.Ser388Gly)	rs562843129	0.00001
NM_020451.3(SELENON):c.1239G>A (p.Glu413=)	rs770918460	0.00001
NM_020451.3(SELENON):c.414C>T (p.Pro138=)	rs374681184	0.00001
NM_020451.3(SELENON):c.748-7C>T	rs760108862	0.00001
NC_000001.11:g.25800121dup	rs1245396370
NC_000001.11:g.25800126_25800130del	rs1437300656
NM_020451.3(SELENON):c.*267C>G	rs184807941
NM_020451.3(SELENON):c.-14_-5dup
NM_020451.3(SELENON):c.1011-128G>T	rs74753273
NM_020451.3(SELENON):c.1017G>A (p.Leu339=)	rs1572234725
NM_020451.3(SELENON):c.1092+6C>G	rs148071754
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.1314C>T (p.Asp438=)	rs1572236004
NM_020451.3(SELENON):c.1710G>A (p.Thr570=)	rs371398538
NM_020451.3(SELENON):c.404-329G>A	rs139733429
NM_020451.3(SELENON):c.747+8C>T	rs1265307063

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