ClinVar Miner

List of variants in gene SELENOO studied for not specified

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Gene type:
ClinVar version:
Total variants: 115
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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.958C>T (p.Arg320Trp) rs543629121 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.1579G>A (p.Ala527Thr)
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.1726G>A (p.Ala576Thr)
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.1946A>G (p.Gln649Arg)
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.499A>G (p.Thr167Ala) rs2519091521
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.868T>A (p.Ser290Thr)
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)

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