List of variants in gene SELENOO reported as uncertain significance 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: 109

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_031454.2(SELENOO):c.319G>A (p.Gly107Ser)	rs184575812	0.00119
NM_031454.2(SELENOO):c.1919C>T (p.Thr640Met)	rs372550959	0.00040
NM_031454.2(SELENOO):c.352G>T (p.Ala118Ser)	rs750577534	0.00033
NM_031454.2(SELENOO):c.685G>A (p.Asp229Asn)	rs377092978	0.00033
NM_031454.2(SELENOO):c.806G>A (p.Arg269His)	rs200468030	0.00022
NM_031454.2(SELENOO):c.971A>G (p.Glu324Gly)	rs201643496	0.00017
NM_031454.2(SELENOO):c.959G>A (p.Arg320Gln)	rs367633071	0.00013
NM_031454.2(SELENOO):c.1853G>A (p.Arg618Gln)	rs780780228	0.00012
NM_031454.2(SELENOO):c.1754G>A (p.Arg585His)	rs376531221	0.00011
NM_031454.2(SELENOO):c.688G>A (p.Val230Met)	rs200964762	0.00011
NM_031454.2(SELENOO):c.1285G>A (p.Val429Met)	rs200939056	0.00010
NM_031454.2(SELENOO):c.300G>T (p.Glu100Asp)	rs1372124250	0.00010
NM_031454.2(SELENOO):c.1171G>A (p.Glu391Lys)	rs370874005	0.00007
NM_031454.2(SELENOO):c.1553C>T (p.Ala518Val)	rs547589952	0.00007
NM_031454.2(SELENOO):c.1595G>A (p.Arg532His)	rs554842345	0.00007
NM_031454.2(SELENOO):c.263C>T (p.Thr88Ile)	rs1211155589	0.00007
NM_031454.2(SELENOO):c.592C>T (p.Arg198Trp)	rs201752848	0.00007
NM_031454.2(SELENOO):c.935G>A (p.Arg312Gln)	rs780144198	0.00007
NM_031454.2(SELENOO):c.1704G>C (p.Lys568Asn)	rs34658004	0.00006
NM_031454.2(SELENOO):c.1756G>A (p.Val586Met)	rs200868550	0.00006
NM_031454.2(SELENOO):c.1834G>C (p.Asp612His)	rs776118713	0.00006
NM_031454.2(SELENOO):c.1694G>A (p.Arg565Gln)	rs760826494	0.00005
NM_031454.2(SELENOO):c.345G>T (p.Glu115Asp)	rs897355754	0.00005
NM_031454.2(SELENOO):c.1607A>G (p.Gln536Arg)	rs778705234	0.00004
NM_031454.2(SELENOO):c.1753C>T (p.Arg585Cys)	rs548507703	0.00004
NM_031454.2(SELENOO):c.1954T>C (p.Tyr652His)	rs760622131	0.00004
NM_031454.2(SELENOO):c.1012G>A (p.Asp338Asn)	rs780133528	0.00003
NM_031454.2(SELENOO):c.1111G>A (p.Gly371Ser)	rs749302718	0.00003
NM_031454.2(SELENOO):c.1717G>A (p.Ala573Thr)	rs570141203	0.00003
NM_031454.2(SELENOO):c.1765G>A (p.Ala589Thr)	rs570812157	0.00003
NM_031454.2(SELENOO):c.1828C>T (p.Arg610Cys)	rs772001158	0.00003
NM_031454.2(SELENOO):c.1990T>C (p.Cys664Arg)	rs778019495	0.00003
NM_031454.2(SELENOO):c.581G>A (p.Arg194Gln)	rs769253863	0.00003
NM_031454.2(SELENOO):c.670T>G (p.Ser224Ala)	rs763880889	0.00003
NM_031454.2(SELENOO):c.503G>A (p.Gly168Asp)	rs1277308583	0.00002
NM_031454.2(SELENOO):c.1000G>A (p.Val334Met)	rs763930780	0.00001
NM_031454.2(SELENOO):c.1018A>G (p.Met340Val)	rs749879227	0.00001
NM_031454.2(SELENOO):c.1081G>A (p.Asp361Asn)	rs775166076	0.00001
NM_031454.2(SELENOO):c.1114C>T (p.Arg372Cys)	rs187774731	0.00001
NM_031454.2(SELENOO):c.1445A>G (p.Glu482Gly)	rs921069886	0.00001
NM_031454.2(SELENOO):c.1631C>T (p.Ala544Val)	rs537037852	0.00001
NM_031454.2(SELENOO):c.1636G>C (p.Glu546Gln)	rs371055203	0.00001
NM_031454.2(SELENOO):c.1768A>G (p.Asn590Asp)	rs758808541	0.00001
NM_031454.2(SELENOO):c.305C>T (p.Ala102Val)	rs753992805	0.00001
NM_031454.2(SELENOO):c.361G>T (p.Ala121Ser)	rs1385096181	0.00001
NM_031454.2(SELENOO):c.730G>C (p.Val244Leu)	rs765180742	0.00001
NM_031454.2(SELENOO):c.799A>G (p.Thr267Ala)	rs765693822	0.00001
NM_031454.2(SELENOO):c.970G>A (p.Glu324Lys)	rs747525320	0.00001
NM_031454.2(SELENOO):c.1042G>A (p.Asp348Asn)
NM_031454.2(SELENOO):c.1087G>C (p.Val363Leu)
NM_031454.2(SELENOO):c.1102G>A (p.Asp368Asn)	rs373024917
NM_031454.2(SELENOO):c.1115G>A (p.Arg372His)
NM_031454.2(SELENOO):c.1121C>T (p.Ala374Val)
NM_031454.2(SELENOO):c.1138G>A (p.Glu380Lys)	rs750808619
NM_031454.2(SELENOO):c.1168G>C (p.Ala390Pro)
NM_031454.2(SELENOO):c.1169C>G (p.Ala390Gly)
NM_031454.2(SELENOO):c.1200G>C (p.Glu400Asp)
NM_031454.2(SELENOO):c.1234G>C (p.Ala412Pro)	rs200138432
NM_031454.2(SELENOO):c.1285G>T (p.Val429Leu)	rs200939056
NM_031454.2(SELENOO):c.1298T>G (p.Leu433Arg)
NM_031454.2(SELENOO):c.1357G>A (p.Asp453Asn)
NM_031454.2(SELENOO):c.1421C>T (p.Ala474Val)
NM_031454.2(SELENOO):c.1433C>T (p.Ala478Val)
NM_031454.2(SELENOO):c.1483C>T (p.Arg495Trp)
NM_031454.2(SELENOO):c.1484G>A (p.Arg495Gln)
NM_031454.2(SELENOO):c.1543C>G (p.Gln515Glu)
NM_031454.2(SELENOO):c.1552G>A (p.Ala518Thr)
NM_031454.2(SELENOO):c.1561G>A (p.Gly521Ser)
NM_031454.2(SELENOO):c.1661A>G (p.His554Arg)
NM_031454.2(SELENOO):c.1667C>G (p.Ala556Gly)
NM_031454.2(SELENOO):c.1682C>T (p.Ala561Val)	rs768111760
NM_031454.2(SELENOO):c.1693C>T (p.Arg565Trp)
NM_031454.2(SELENOO):c.1706A>C (p.Asp569Ala)
NM_031454.2(SELENOO):c.1720G>T (p.Gly574Trp)
NM_031454.2(SELENOO):c.1732G>A (p.Ala578Thr)	rs369750052
NM_031454.2(SELENOO):c.1747C>G (p.His583Asp)	rs776868831
NM_031454.2(SELENOO):c.1750G>A (p.Val584Met)
NM_031454.2(SELENOO):c.1813A>T (p.Ile605Phe)	rs751973996
NM_031454.2(SELENOO):c.1846G>A (p.Val616Met)	rs2519116134
NM_031454.2(SELENOO):c.1849C>T (p.Arg617Trp)
NM_031454.2(SELENOO):c.1882C>A (p.His628Asn)
NM_031454.2(SELENOO):c.1884C>G (p.His628Gln)	rs374856550
NM_031454.2(SELENOO):c.1904C>T (p.Thr635Ile)
NM_031454.2(SELENOO):c.1938C>A (p.Asp646Glu)
NM_031454.2(SELENOO):c.1949G>A (p.Arg650His)
NM_031454.2(SELENOO):c.1952C>T (p.Ser651Phe)
NM_031454.2(SELENOO):c.1986A>T (p.Glu662Asp)
NM_031454.2(SELENOO):c.2000G>C
NM_031454.2(SELENOO):c.2001A>G
NM_031454.2(SELENOO):c.2001A>T
NM_031454.2(SELENOO):c.260C>G (p.Pro87Arg)
NM_031454.2(SELENOO):c.280C>A (p.Arg94Ser)
NM_031454.2(SELENOO):c.281G>A (p.Arg94His)	rs2519090529
NM_031454.2(SELENOO):c.341G>A (p.Arg114His)	rs2519090779
NM_031454.2(SELENOO):c.349G>C (p.Glu117Gln)
NM_031454.2(SELENOO):c.550T>C (p.Ser184Pro)	rs1193254499
NM_031454.2(SELENOO):c.559G>T (p.Ala187Ser)
NM_031454.2(SELENOO):c.568C>T (p.Arg190Cys)
NM_031454.2(SELENOO):c.622C>T (p.His208Tyr)
NM_031454.2(SELENOO):c.646G>T (p.Ala216Ser)
NM_031454.2(SELENOO):c.671C>T (p.Ser224Phe)	rs1362834633
NM_031454.2(SELENOO):c.719A>C (p.Gln240Pro)	rs1453602249
NM_031454.2(SELENOO):c.869C>A (p.Ser290Tyr)
NM_031454.2(SELENOO):c.910G>A (p.Val304Met)	rs375249006
NM_031454.2(SELENOO):c.923C>T (p.Ala308Val)
NM_031454.2(SELENOO):c.946C>G (p.Arg316Gly)	rs375363660
NM_031454.2(SELENOO):c.947G>A (p.Arg316Gln)
NM_031454.2(SELENOO):c.950G>A (p.Arg317His)
NM_031454.2(SELENOO):c.988T>C (p.Phe330Leu)

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.