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

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: 43

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HGVS	dbSNP	gnomAD frequency
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.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.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.846C>T (p.Ser282=)	rs34177164	0.00175
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.1623C>T (p.Asn541=)	rs199911454	0.00070
NM_020451.3(SELENON):c.-35T>C	rs886038656	0.00066
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.81C>T (p.Arg27=)	rs886038660	0.00014
NM_020451.3(SELENON):c.1093-45T>C	rs549130801	0.00009
NM_020451.3(SELENON):c.301+18C>T	rs373189692	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.-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.1281+15G>T	rs886038657	0.00001
NM_020451.3(SELENON):c.1602+12C>T	rs903798730	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.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
NM_020451.2(SELENON):c.-58_-47dup	rs1553198442
NM_020451.3(SELENON):c.-22_-13dup	rs1553198459
NM_020451.3(SELENON):c.1010+20C>T	rs1553120231
NM_020451.3(SELENON):c.1092+6C>G	rs148071754
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.948C>T (p.His316=)	rs1553120209

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