Chr Mutation (hg38) CAid Gene Transcript Linkouts
1g.25809104G>ACA339113947SELENONc.655G>A (p.Ala219Thr)
c.724G>A (p.Ala242Thr)
c.826G>A (p.Ala276Thr)
1g.25809104G>CCA339113949SELENONc.655G>C (p.Ala219Pro)
c.724G>C (p.Ala242Pro)
c.826G>C (p.Ala276Pro)
1g.25809104G=CA1159806153SELENONc.655G= (p.Ala219=)
c.724G= (p.Ala242=)
c.826G= (p.Ala276=)
1g.25809104G>TCA339113951SELENONc.655G>T (p.Ala219Ser)
c.724G>T (p.Ala242Ser)
c.826G>T (p.Ala276Ser)
 gnomAD v4
1g.25809105C>ACA339113958SELENONc.656C>A (p.Ala219Asp)
c.725C>A (p.Ala242Asp)
c.827C>A (p.Ala276Asp)
1g.25809105C=CA1159806154SELENONc.656C= (p.Ala219=)
c.725C= (p.Ala242=)
c.827C= (p.Ala276=)
1g.25809105C>GCA339113960SELENONc.656C>G (p.Ala219Gly)
c.725C>G (p.Ala242Gly)
c.827C>G (p.Ala276Gly)
 gnomAD v4
1g.25809105C>TCA19698405SELENONc.656C>T (p.Ala219Val)
c.725C>T (p.Ala242Val)
c.827C>T (p.Ala276Val)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
1g.25809105_25809107dupCA276995SELENONc.656_658dup (p.Ala219_Cys220insSer)
c.725_727dup (p.Ala242_Cys243insSer)
c.827_829dup (p.Ala276_Cys277insSer)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
1g.25809106C>ACA416759092SELENONc.657C>A (p.Ala219=)
c.726C>A (p.Ala242=)
c.828C>A (p.Ala276=)
1g.25809106C=CA1159806155SELENONc.657C= (p.Ala219=)
c.726C= (p.Ala242=)
c.828C= (p.Ala276=)
1g.25809106C>GCA416759093SELENONc.657C>G (p.Ala219=)
c.726C>G (p.Ala242=)
c.828C>G (p.Ala276=)
1g.25809106C>TCA416759094SELENONc.657C>T (p.Ala219=)
c.726C>T (p.Ala242=)
c.828C>T (p.Ala276=)
 ClinVar dbSNP gnomAD v2 gnomAD v4
1g.25809107T>ACA339113965SELENONc.658T>A (p.Cys220Ser)
c.727T>A (p.Cys243Ser)
c.829T>A (p.Cys277Ser)
1g.25809107T>CCA339113968SELENONc.658T>C (p.Cys220Arg)
c.727T>C (p.Cys243Arg)
c.829T>C (p.Cys277Arg)
1g.25809107T>GCA19698407SELENONc.658T>G (p.Cys220Gly)
c.727T>G (p.Cys243Gly)
c.829T>G (p.Cys277Gly)
 dbSNP gnomAD v4
1g.25809107T=CA1159806156SELENONc.658T= (p.Cys220=)
c.727T= (p.Cys243=)
c.829T= (p.Cys277=)
1g.25809108G>ACA339113974SELENONc.659G>A (p.Cys220Tyr)
c.728G>A (p.Cys243Tyr)
c.830G>A (p.Cys277Tyr)
 gnomAD v4
1g.25809108G>CCA339113984SELENONc.659G>C (p.Cys220Ser)
c.728G>C (p.Cys243Ser)
c.830G>C (p.Cys277Ser)
1g.25809108G>TCA339113976SELENONc.659G>T (p.Cys220Phe)
c.728G>T (p.Cys243Phe)
c.830G>T (p.Cys277Phe)
1g.25809109C>ACA339113987SELENONc.660C>A (p.Cys220Ter)
c.729C>A (p.Cys243Ter)
c.831C>A (p.Cys277Ter)
1g.25809109C>GCA339113995SELENONc.660C>G (p.Cys220Trp)
c.729C>G (p.Cys243Trp)
c.831C>G (p.Cys277Trp)
1g.25809109C>TCA416759095SELENONc.660C>T (p.Cys220=)
c.729C>T (p.Cys243=)
c.831C>T (p.Cys277=)
1g.25809110C>ACA339114001SELENONc.661C>A (p.Leu221Met)
c.730C>A (p.Leu244Met)
c.832C>A (p.Leu278Met)
1g.25809110C>GCA339114007SELENONc.661C>G (p.Leu221Val)
c.730C>G (p.Leu244Val)
c.832C>G (p.Leu278Val)
1g.25809110C>TCA416759096SELENONc.661C>T (p.Leu221=)
c.730C>T (p.Leu244=)
c.832C>T (p.Leu278=)
1g.25809111T>ACA339114009SELENONc.662T>A (p.Leu221Gln)
c.731T>A (p.Leu244Gln)
c.833T>A (p.Leu278Gln)
1g.25809111T>CCA339114013SELENONc.662T>C (p.Leu221Pro)
c.731T>C (p.Leu244Pro)
c.833T>C (p.Leu278Pro)
 dbSNP gnomAD v4
1g.25809111T>GCA339114016SELENONc.662T>G (p.Leu221Arg)
c.731T>G (p.Leu244Arg)
c.833T>G (p.Leu278Arg)
1g.25809111T=CA1159806157SELENONc.662T= (p.Leu221=)
c.731T= (p.Leu244=)
c.833T= (p.Leu278=)
1g.25809112G>ACA416759097SELENONc.663G>A (p.Leu221=)
c.732G>A (p.Leu244=)
c.834G>A (p.Leu278=)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
1g.25809112G>CCA416759098SELENONc.663G>C (p.Leu221=)
c.732G>C (p.Leu244=)
c.834G>C (p.Leu278=)
1g.25809112G=CA1159806158SELENONc.663G= (p.Leu221=)
c.732G= (p.Leu244=)
c.834G= (p.Leu278=)
1g.25809112G>TCA416759099SELENONc.663G>T (p.Leu221=)
c.732G>T (p.Leu244=)
c.834G>T (p.Leu278=)
 gnomAD v4
1g.25809113A>CCA339114034SELENONc.664A>C (p.Thr222Pro)
c.733A>C (p.Thr245Pro)
c.835A>C (p.Thr279Pro)
1g.25809113A>GCA339114035SELENONc.664A>G (p.Thr222Ala)
c.733A>G (p.Thr245Ala)
c.835A>G (p.Thr279Ala)
 COSMIC
1g.25809113A>TCA339114039SELENONc.664A>T (p.Thr222Ser)
c.733A>T (p.Thr245Ser)
c.835A>T (p.Thr279Ser)
1g.25809114C>ACA339114049SELENONc.665C>A (p.Thr222Asn)
c.734C>A (p.Thr245Asn)
c.836C>A (p.Thr279Asn)
1g.25809114C=CA1159806159SELENONc.665C= (p.Thr222=)
c.734C= (p.Thr245=)
c.836C= (p.Thr279=)
1g.25809114C>GCA339114046SELENONc.665C>G (p.Thr222Ser)
c.734C>G (p.Thr245Ser)
c.836C>G (p.Thr279Ser)
1g.25809114C>TCA339114043SELENONc.665C>T (p.Thr222Ile)
c.734C>T (p.Thr245Ile)
c.836C>T (p.Thr279Ile)
 dbSNP gnomAD v2 gnomAD v4
1g.25809115T>ACA416759100SELENONc.666T>A (p.Thr222=)
c.735T>A (p.Thr245=)
c.837T>A (p.Thr279=)
1g.25809115T>CCA416759101SELENONc.666T>C (p.Thr222=)
c.735T>C (p.Thr245=)
c.837T>C (p.Thr279=)
 gnomAD v4
1g.25809115T>GCA416759102SELENONc.666T>G (p.Thr222=)
c.735T>G (p.Thr245=)
c.837T>G (p.Thr279=)
1g.25809116G>ACA339114051SELENONc.667G>A (p.Ala223Thr)
c.736G>A (p.Ala246Thr)
c.838G>A (p.Ala280Thr)
1g.25809116G>CCA339114055SELENONc.667G>C (p.Ala223Pro)
c.736G>C (p.Ala246Pro)
c.838G>C (p.Ala280Pro)
1g.25809116G>TCA339114059SELENONc.667G>T (p.Ala223Ser)
c.736G>T (p.Ala246Ser)
c.838G>T (p.Ala280Ser)
1g.25809117C>ACA339114063SELENONc.668C>A (p.Ala223Asp)
c.737C>A (p.Ala246Asp)
c.839C>A (p.Ala280Asp)
 COSMIC
1g.25809117C>GCA339114067SELENONc.668C>G (p.Ala223Gly)
c.737C>G (p.Ala246Gly)
c.839C>G (p.Ala280Gly)
1g.25809117C>TCA339114069SELENONc.668C>T (p.Ala223Val)
c.737C>T (p.Ala246Val)
c.839C>T (p.Ala280Val)
 COSMIC
1g.25809118C>ACA416759104SELENONc.669C>A (p.Ala223=)
c.738C>A (p.Ala246=)
c.840C>A (p.Ala280=)
 gnomAD v4
1g.25809118C>GCA416759105SELENONc.669C>G (p.Ala223=)
c.738C>G (p.Ala246=)
c.840C>G (p.Ala280=)
1g.25809118C>TCA416759103SELENONc.669C>T (p.Ala223=)
c.738C>T (p.Ala246=)
c.840C>T (p.Ala280=)
 gnomAD v4
1g.25809119A>CCA339114072SELENONc.670A>C (p.Ile224Leu)
c.739A>C (p.Ile247Leu)
c.841A>C (p.Ile281Leu)
1g.25809119A>GCA339114073SELENONc.670A>G (p.Ile224Val)
c.739A>G (p.Ile247Val)
c.841A>G (p.Ile281Val)
 gnomAD v4
1g.25809119A>TCA339114074SELENONc.670A>T (p.Ile224Phe)
c.739A>T (p.Ile247Phe)
c.841A>T (p.Ile281Phe)
1g.25809120T>ACA339114077SELENONc.671T>A (p.Ile224Asn)
c.740T>A (p.Ile247Asn)
c.842T>A (p.Ile281Asn)
1g.25809120T>CCA339114080SELENONc.671T>C (p.Ile224Thr)
c.740T>C (p.Ile247Thr)
c.842T>C (p.Ile281Thr)
1g.25809120T>GCA339114082SELENONc.671T>G (p.Ile224Ser)
c.740T>G (p.Ile247Ser)
c.842T>G (p.Ile281Ser)
1g.25809121C>ACA416759106SELENONc.672C>A (p.Ile224=)
c.741C>A (p.Ile247=)
c.843C>A (p.Ile281=)
1g.25809121C>GCA339114084SELENONc.672C>G (p.Ile224Met)
c.741C>G (p.Ile247Met)
c.843C>G (p.Ile281Met)
 ClinVar gnomAD v4
1g.25809121C>TCA416759107SELENONc.672C>T (p.Ile224=)
c.741C>T (p.Ile247=)
c.843C>T (p.Ile281=)
1g.25809122A>CCA339114095SELENONc.673A>C (p.Ser225Arg)
c.742A>C (p.Ser248Arg)
c.844A>C (p.Ser282Arg)
1g.25809122A>GCA339114089SELENONc.673A>G (p.Ser225Gly)
c.742A>G (p.Ser248Gly)
c.844A>G (p.Ser282Gly)
 gnomAD v4
1g.25809122A>TCA339114092SELENONc.673A>T (p.Ser225Cys)
c.742A>T (p.Ser248Cys)
c.844A>T (p.Ser282Cys)
1g.25809123G>ACA339114102SELENONc.674G>A (p.Ser225Asn)
c.743G>A (p.Ser248Asn)
c.845G>A (p.Ser282Asn)
1g.25809123G>CCA339114105SELENONc.674G>C (p.Ser225Thr)
c.743G>C (p.Ser248Thr)
c.845G>C (p.Ser282Thr)
1g.25809123G>TCA339114108SELENONc.674G>T (p.Ser225Ile)
c.743G>T (p.Ser248Ile)
c.845G>T (p.Ser282Ile)
1g.25809124C>ACA339114110SELENONc.675C>A (p.Ser225Arg)
c.744C>A (p.Ser248Arg)
c.846C>A (p.Ser282Arg)
1g.25809124C=CA1140506082SELENONc.675C= (p.Ser225=)
c.744C= (p.Ser248=)
c.846C= (p.Ser282=)
1g.25809124C>GCA339114113SELENONc.675C>G (p.Ser225Arg)
c.744C>G (p.Ser248Arg)
c.846C>G (p.Ser282Arg)
 dbSNP gnomAD v3 gnomAD v4
1g.25809124C>TCA203325SELENONc.675C>T (p.Ser225=)
c.744C>T (p.Ser248=)
c.846C>T (p.Ser282=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
1g.25809125G>ACA696651SELENONc.676G>A (p.Asp226Asn)
c.745G>A (p.Asp249Asn)
c.847G>A (p.Asp283Asn)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
1g.25809125G>CCA339114132SELENONc.676G>C (p.Asp226His)
c.745G>C (p.Asp249His)
c.847G>C (p.Asp283His)
1g.25809125G=CA1159806160SELENONc.676G= (p.Asp226=)
c.745G= (p.Asp249=)
c.847G= (p.Asp283=)
1g.25809125G>TCA339114136SELENONc.676G>T (p.Asp226Tyr)
c.745G>T (p.Asp249Tyr)
c.847G>T (p.Asp283Tyr)
 dbSNP gnomAD v4
1g.25809126A>CCA339114145SELENONc.677A>C (p.Asp226Ala)
c.746A>C (p.Asp249Ala)
c.848A>C (p.Asp283Ala)
1g.25809126A>GCA339114147SELENONc.677A>G (p.Asp226Gly)
c.746A>G (p.Asp249Gly)
c.848A>G (p.Asp283Gly)
1g.25809126A>TCA339114150SELENONc.677A>T (p.Asp226Val)
c.746A>T (p.Asp249Val)
c.848A>T (p.Asp283Val)
1g.25809127C>ACA339114155SELENONc.678C>A (p.Asp226Glu)
c.747C>A (p.Asp249Glu)
c.849C>A (p.Asp283Glu)
1g.25809127C>GCA339114154SELENONc.678C>G (p.Asp226Glu)
c.747C>G (p.Asp249Glu)
c.849C>G (p.Asp283Glu)
1g.25809127C>TCA416759108SELENONc.678C>T (p.Asp226=)
c.747C>T (p.Asp249=)
c.849C>T (p.Asp283=)
1g.25809128T>ACA339114159SELENONc.679T>A (p.Phe227Ile)
c.748T>A (p.Phe250Ile)
c.850T>A (p.Phe284Ile)
1g.25809128T>CCA339114166SELENONc.679T>C (p.Phe227Leu)
c.748T>C (p.Phe250Leu)
c.850T>C (p.Phe284Leu)
1g.25809128T>GCA339114162SELENONc.679T>G (p.Phe227Val)
c.748T>G (p.Phe250Val)
c.850T>G (p.Phe284Val)
1g.25809128_25809129delCA2644199765SELENONc.679_680del (p.Phe227LeufsTer16)
c.748_749del (p.Phe250LeufsTer16)
c.850_851del (p.Phe284LeufsTer16)
 gnomAD v4
1g.25809129T>ACA339114170SELENONc.680T>A (p.Phe227Tyr)
c.749T>A (p.Phe250Tyr)
c.851T>A (p.Phe284Tyr)
1g.25809129T>CCA339114171SELENONc.680T>C (p.Phe227Ser)
c.749T>C (p.Phe250Ser)
c.851T>C (p.Phe284Ser)
1g.25809129T>GCA339114172SELENONc.680T>G (p.Phe227Cys)
c.749T>G (p.Phe250Cys)
c.851T>G (p.Phe284Cys)
 gnomAD v4
1g.25809130delCA2644199766SELENONc.681del (p.Tyr228ThrfsTer4)
c.750del (p.Tyr251ThrfsTer4)
c.852del (p.Tyr285ThrfsTer4)
 gnomAD v4
1g.25809130C>ACA339114174SELENONc.681C>A (p.Phe227Leu)
c.750C>A (p.Phe250Leu)
c.852C>A (p.Phe284Leu)
1g.25809130C=CA1142954282SELENONc.681C= (p.Phe227=)
c.750C= (p.Phe250=)
c.852C= (p.Phe284=)
1g.25809130C>GCA339114177SELENONc.681C>G (p.Phe227Leu)
c.750C>G (p.Phe250Leu)
c.852C>G (p.Phe284Leu)
1g.25809130C>TCA696652SELENONc.681C>T (p.Phe227=)
c.750C>T (p.Phe250=)
c.852C>T (p.Phe284=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
1g.25809134_25809136delCA2644199767SELENONc.685_687del (p.Tyr229del)
c.754_756del (p.Tyr252del)
c.856_858del (p.Tyr286del)
 gnomAD v4
1g.25809131T>ACA339114183SELENONc.682T>A (p.Tyr228Asn)
c.751T>A (p.Tyr251Asn)
c.853T>A (p.Tyr285Asn)
1g.25809131T>CCA339114187SELENONc.682T>C (p.Tyr228His)
c.751T>C (p.Tyr251His)
c.853T>C (p.Tyr285His)
1g.25809131T>GCA339114190SELENONc.682T>G (p.Tyr228Asp)
c.751T>G (p.Tyr251Asp)
c.853T>G (p.Tyr285Asp)
1g.25809132A>CCA339114193SELENONc.683A>C (p.Tyr228Ser)
c.752A>C (p.Tyr251Ser)
c.854A>C (p.Tyr285Ser)
1g.25809132A>GCA339114198SELENONc.683A>G (p.Tyr228Cys)
c.752A>G (p.Tyr251Cys)
c.854A>G (p.Tyr285Cys)
1g.25809132A>TCA339114202SELENONc.683A>T (p.Tyr228Phe)
c.752A>T (p.Tyr251Phe)
c.854A>T (p.Tyr285Phe)
1g.25809133C>ACA339114206SELENONc.684C>A (p.Tyr228Ter)
c.753C>A (p.Tyr251Ter)
c.855C>A (p.Tyr285Ter)
1g.25809133C=CA1159806161SELENONc.684C= (p.Tyr228=)
c.753C= (p.Tyr251=)
c.855C= (p.Tyr285=)
1g.25809133C>GCA339114209SELENONc.684C>G (p.Tyr228Ter)
c.753C>G (p.Tyr251Ter)
c.855C>G (p.Tyr285Ter)
 ClinVar dbSNP
1g.25809133C>TCA416759109SELENONc.684C>T (p.Tyr228=)
c.753C>T (p.Tyr251=)
c.855C>T (p.Tyr285=)
 gnomAD v4
1g.25809134T>ACA339114213SELENONc.685T>A (p.Tyr229Asn)
c.754T>A (p.Tyr252Asn)
c.856T>A (p.Tyr286Asn)
1g.25809134T>CCA339114215SELENONc.685T>C (p.Tyr229His)
c.754T>C (p.Tyr252His)
c.856T>C (p.Tyr286His)
1g.25809134T>GCA339114220SELENONc.685T>G (p.Tyr229Asp)
c.754T>G (p.Tyr252Asp)
c.856T>G (p.Tyr286Asp)
1g.25809135A=CA1159806162SELENONc.686A= (p.Tyr229=)
c.755A= (p.Tyr252=)
c.857A= (p.Tyr286=)
1g.25809135A>CCA339114222SELENONc.686A>C (p.Tyr229Ser)
c.755A>C (p.Tyr252Ser)
c.857A>C (p.Tyr286Ser)
1g.25809135A>GCA696653SELENONc.686A>G (p.Tyr229Cys)
c.755A>G (p.Tyr252Cys)
c.857A>G (p.Tyr286Cys)
 dbSNP ExAC gnomAD v2 gnomAD v4
1g.25809135A>TCA339114228SELENONc.686A>T (p.Tyr229Phe)
c.755A>T (p.Tyr252Phe)
c.857A>T (p.Tyr286Phe)
1g.25809136C>ACA339114231SELENONc.687C>A (p.Tyr229Ter)
c.756C>A (p.Tyr252Ter)
c.858C>A (p.Tyr286Ter)
1g.25809136C=CA1159806163SELENONc.687C= (p.Tyr229=)
c.756C= (p.Tyr252=)
c.858C= (p.Tyr286=)
1g.25809136C>GCA696654SELENONc.687C>G (p.Tyr229Ter)
c.756C>G (p.Tyr252Ter)
c.858C>G (p.Tyr286Ter)
 dbSNP ExAC gnomAD v2 gnomAD v4
1g.25809136C>TCA19698416SELENONc.687C>T (p.Tyr229=)
c.756C>T (p.Tyr252=)
c.858C>T (p.Tyr286=)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
1g.25809137A=CA1159806164SELENONc.688A= (p.Thr230=)
c.757A= (p.Thr253=)
c.859A= (p.Thr287=)
1g.25809137A>CCA339114237SELENONc.688A>C (p.Thr230Pro)
c.757A>C (p.Thr253Pro)
c.859A>C (p.Thr287Pro)
 gnomAD v4
1g.25809137A>GCA696655SELENONc.688A>G (p.Thr230Ala)
c.757A>G (p.Thr253Ala)
c.859A>G (p.Thr287Ala)
 dbSNP ExAC gnomAD v2 gnomAD v4
1g.25809137A>TCA339114241SELENONc.688A>T (p.Thr230Ser)
c.757A>T (p.Thr253Ser)
c.859A>T (p.Thr287Ser)
1g.25809138C>ACA339114246SELENONc.689C>A (p.Thr230Asn)
c.758C>A (p.Thr253Asn)
c.860C>A (p.Thr287Asn)
1g.25809138C=CA1159806166SELENONc.689C= (p.Thr230=)
c.758C= (p.Thr253=)
c.860C= (p.Thr287=)
1g.25809138C>GCA339114248SELENONc.689C>G (p.Thr230Ser)
c.758C>G (p.Thr253Ser)
c.860C>G (p.Thr287Ser)
1g.25809138C>TCA339114244SELENONc.689C>T (p.Thr230Ile)
c.758C>T (p.Thr253Ile)
c.860C>T (p.Thr287Ile)
 dbSNP gnomAD v3 gnomAD v4
1g.25809138_25809140delinsCTGCA1159806165SELENONc.689_691delinsCTG (p.Thr230=)
c.758_760delinsCTG (p.Thr253=)
c.860_862delinsCTG (p.Thr287=)
1g.25809139_25809149delCA2586966306SELENONc.690_700del (p.Val231AspfsTer9)
c.759_769del (p.Val254AspfsTer9)
c.861_871del (p.Val288AspfsTer9)
1g.25809139T>ACA696656SELENONc.690T>A (p.Thr230=)
c.759T>A (p.Thr253=)
c.861T>A (p.Thr287=)
 dbSNP ExAC gnomAD v2 gnomAD v4
1g.25809139T>CCA416759111SELENONc.690T>C (p.Thr230=)
c.759T>C (p.Thr253=)
c.861T>C (p.Thr287=)
 gnomAD v4
1g.25809139T>GCA416759110SELENONc.690T>G (p.Thr230=)
c.759T>G (p.Thr253=)
c.861T>G (p.Thr287=)
1g.25809139T=CA1159806167SELENONc.690T= (p.Thr230=)
c.759T= (p.Thr253=)
c.861T= (p.Thr287=)
1g.25809141_25809142delCA734440819SELENONc.692_693del (p.Val231AspfsTer12)
c.761_762del (p.Val254AspfsTer12)
c.863_864del (p.Val288AspfsTer12)
 ClinVar dbSNP gnomAD v3 gnomAD v4
1g.25809140G>ACA339114251SELENONc.691G>A (p.Val231Met)
c.760G>A (p.Val254Met)
c.862G>A (p.Val288Met)
 dbSNP gnomAD v3 gnomAD v4
1g.25809140G>CCA339114252SELENONc.691G>C (p.Val231Leu)
c.760G>C (p.Val254Leu)
c.862G>C (p.Val288Leu)
 gnomAD v4
1g.25809140G=CA1159806168SELENONc.691G= (p.Val231=)
c.760G= (p.Val254=)
c.862G= (p.Val288=)
1g.25809140G>TCA339114255SELENONc.691G>T (p.Val231Leu)
c.760G>T (p.Val254Leu)
c.862G>T (p.Val288Leu)
1g.25809141T>ACA339114257SELENONc.692T>A (p.Val231Glu)
c.761T>A (p.Val254Glu)
c.863T>A (p.Val288Glu)
1g.25809141T>CCA339114259SELENONc.692T>C (p.Val231Ala)
c.761T>C (p.Val254Ala)
c.863T>C (p.Val288Ala)
1g.25809141T>GCA339114260SELENONc.692T>G (p.Val231Gly)
c.761T>G (p.Val254Gly)
c.863T>G (p.Val288Gly)
1g.25809142G>ACA416759115SELENONc.693G>A (p.Val231=)
c.762G>A (p.Val254=)
c.864G>A (p.Val288=)
1g.25809142G>CCA416759116SELENONc.693G>C (p.Val231=)
c.762G>C (p.Val254=)
c.864G>C (p.Val288=)
1g.25809142G>TCA416759117SELENONc.693G>T (p.Val231=)
c.762G>T (p.Val254=)
c.864G>T (p.Val288=)
1g.25809143A=CA1159806169SELENONc.694A= (p.Met232=)
c.763A= (p.Met255=)
c.865A= (p.Met289=)
1g.25809143A>CCA339114262SELENONc.694A>C (p.Met232Leu)
c.763A>C (p.Met255Leu)
c.865A>C (p.Met289Leu)
1g.25809143A>GCA19698421SELENONc.694A>G (p.Met232Val)
c.763A>G (p.Met255Val)
c.865A>G (p.Met289Val)
 dbSNP
1g.25809143A>TCA339114265SELENONc.694A>T (p.Met232Leu)
c.763A>T (p.Met255Leu)
c.865A>T (p.Met289Leu)
1g.25809144T>ACA339114267SELENONc.695T>A (p.Met232Lys)
c.764T>A (p.Met255Lys)
c.866T>A (p.Met289Lys)
1g.25809144T>CCA339114270SELENONc.695T>C (p.Met232Thr)
c.764T>C (p.Met255Thr)
c.866T>C (p.Met289Thr)
 gnomAD v4
1g.25809144T>GCA339114272SELENONc.695T>G (p.Met232Arg)
c.764T>G (p.Met255Arg)
c.866T>G (p.Met289Arg)
1g.25809145G>ACA339114281SELENONc.696G>A (p.Met232Ile)
c.765G>A (p.Met255Ile)
c.867G>A (p.Met289Ile)
 dbSNP
1g.25809145G>CCA339114277SELENONc.696G>C (p.Met232Ile)
c.765G>C (p.Met255Ile)
c.867G>C (p.Met289Ile)
1g.25809145G=CA1159806170SELENONc.696G= (p.Met232=)
c.765G= (p.Met255=)
c.867G= (p.Met289=)
1g.25809145G>TCA339114275SELENONc.696G>T (p.Met232Ile)
c.765G>T (p.Met255Ile)
c.867G>T (p.Met289Ile)
1g.25809146T>ACA339114284SELENONc.697T>A (p.Phe233Ile)
c.766T>A (p.Phe256Ile)
c.868T>A (p.Phe290Ile)
1g.25809146T>CCA339114286SELENONc.697T>C (p.Phe233Leu)
c.766T>C (p.Phe256Leu)
c.868T>C (p.Phe290Leu)
1g.25809146T>GCA339114288SELENONc.697T>G (p.Phe233Val)
c.766T>G (p.Phe256Val)
c.868T>G (p.Phe290Val)
1g.25809147T>ACA696657SELENONc.698T>A (p.Phe233Tyr)
c.767T>A (p.Phe256Tyr)
c.869T>A (p.Phe290Tyr)
 dbSNP ExAC gnomAD v4
1g.25809147T>CCA339114293SELENONc.698T>C (p.Phe233Ser)
c.767T>C (p.Phe256Ser)
c.869T>C (p.Phe290Ser)
1g.25809147T>GCA339114295SELENONc.698T>G (p.Phe233Cys)
c.767T>G (p.Phe256Cys)
c.869T>G (p.Phe290Cys)
1g.25809147T=CA1159806172SELENONc.698T= (p.Phe233=)
c.767T= (p.Phe256=)
c.869T= (p.Phe290=)
1g.25809147_25809148delCA2573051548SELENONc.698_699del (p.Phe233SerfsTer10)
c.767_768del (p.Phe256SerfsTer10)
c.869_870del (p.Phe290SerfsTer10)
 ClinVar dbSNP
1g.25809147_25809148delinsTCCA1159806171SELENONc.698_699delinsTC (p.Phe233=)
c.767_768delinsTC (p.Phe256=)
c.869_870delinsTC (p.Phe290=)
1g.25809148C>ACA339114298SELENONc.699C>A (p.Phe233Leu)
c.768C>A (p.Phe256Leu)
c.870C>A (p.Phe290Leu)
1g.25809148C>GCA339114300SELENONc.699C>G (p.Phe233Leu)
c.768C>G (p.Phe256Leu)
c.870C>G (p.Phe290Leu)
 gnomAD v4
1g.25809148C>TCA416759125SELENONc.699C>T (p.Phe233=)
c.768C>T (p.Phe256=)
c.870C>T (p.Phe290=)
1g.25809149delCA696658SELENONc.700del (p.Arg234GlyfsTer?)
c.769del (p.Arg257GlyfsTer?)
c.871del (p.Arg291GlyfsTer?)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
1g.25809149C>ACA416759126SELENONc.700C>A (p.Arg234=)
c.769C>A (p.Arg257=)
c.871C>A (p.Arg291=)
 gnomAD v4
1g.25809149C=CA1159806173SELENONc.700C= (p.Arg234=)
c.769C= (p.Arg257=)
c.871C= (p.Arg291=)
1g.25809149C>GCA339114304SELENONc.700C>G (p.Arg234Gly)
c.769C>G (p.Arg257Gly)
c.871C>G (p.Arg291Gly)
 gnomAD v4
1g.25809149C>TCA696659SELENONc.700C>T (p.Arg234Trp)
c.769C>T (p.Arg257Trp)
c.871C>T (p.Arg291Trp)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
1g.25809150G>ACA696660SELENONc.701G>A (p.Arg234Gln)
c.770G>A (p.Arg257Gln)
c.872G>A (p.Arg291Gln)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
1g.25809150G>CCA339114309SELENONc.701G>C (p.Arg234Pro)
c.770G>C (p.Arg257Pro)
c.872G>C (p.Arg291Pro)
1g.25809150G=CA1143359861SELENONc.701G= (p.Arg234=)
c.770G= (p.Arg257=)
c.872G= (p.Arg291=)
1g.25809150G>TCA339114312SELENONc.701G>T (p.Arg234Leu)
c.770G>T (p.Arg257Leu)
c.872G>T (p.Arg291Leu)
1g.25809151G>ACA339114319SELENONc.701+1G>A (n.701+1G>A)
c.770+1G>A (n.770+1G>A)
c.872+1G>A (n.872+1G>A)
 ClinVar dbSNP gnomAD v4
1g.25809151G>CCA339114317SELENONc.701+1G>C (n.701+1G>C)
c.770+1G>C (n.770+1G>C)
c.872+1G>C (n.872+1G>C)
1g.25809151G=CA1159806174SELENONc.701+1G= (n.701+1G=)
c.770+1G= (n.770+1G=)
c.872+1G= (n.872+1G=)
1g.25809151G>TCA339114314SELENONc.701+1G>T (n.701+1G>T)
c.770+1G>T (n.770+1G>T)
c.872+1G>T (n.872+1G>T)
 COSMIC
1g.25809152T>ACA339114321SELENONc.701+2T>A (n.701+2T>A)
c.770+2T>A (n.770+2T>A)
c.872+2T>A (n.872+2T>A)
1g.25809152T>CCA275352SELENONc.701+2T>C (n.701+2T>C)
c.770+2T>C (n.770+2T>C)
c.872+2T>C (n.872+2T>C)
 ClinVar dbSNP gnomAD v2 gnomAD v4
1g.25809152T>GCA339114323SELENONc.701+2T>G (n.701+2T>G)
c.770+2T>G (n.770+2T>G)
c.872+2T>G (n.872+2T>G)
1g.25809152T=CA1159806175SELENONc.701+2T= (n.701+2T=)
c.770+2T= (n.770+2T=)
c.872+2T= (n.872+2T=)
1g.25809153G>ACA2644199768SELENONc.701+3G>A (n.701+3G>A)
c.770+3G>A (n.770+3G>A)
c.872+3G>A (n.872+3G>A)
 gnomAD v4
1g.25809154A>TCA2644199769SELENONc.701+4A>T (n.701+4A>T)
c.770+4A>T (n.770+4A>T)
c.872+4A>T (n.872+4A>T)
 gnomAD v4
1g.25809157G>ACA696661SELENONc.701+7G>A (n.701+7G>A)
c.770+7G>A (n.770+7G>A)
c.872+7G>A (n.872+7G>A)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
1g.25809157G=CA1159806176SELENONc.701+7G= (n.701+7G=)
c.770+7G= (n.770+7G=)
c.872+7G= (n.872+7G=)
1g.25809158G>ACA1159806178SELENONc.701+8G>A (n.701+8G>A)
c.770+8G>A (n.770+8G>A)
c.872+8G>A (n.872+8G>A)
 dbSNP gnomAD v4
1g.25809158G=CA1159806177SELENONc.701+8G= (n.701+8G=)
c.770+8G= (n.770+8G=)
c.872+8G= (n.872+8G=)
1g.25809159G>ACA1159806180SELENONc.701+9G>A (n.701+9G>A)
c.770+9G>A (n.770+9G>A)
c.872+9G>A (n.872+9G>A)
 dbSNP
1g.25809159G=CA1159806179SELENONc.701+9G= (n.701+9G=)
c.770+9G= (n.770+9G=)
c.872+9G= (n.872+9G=)
1g.25809161C>ACA521738355SELENONc.701+11C>A (n.701+11C>A)
c.770+11C>A (n.770+11C>A)
c.872+11C>A (n.872+11C>A)
 dbSNP gnomAD v2 gnomAD v4
1g.25809161C=CA1159806181SELENONc.701+11C= (n.701+11C=)
c.770+11C= (n.770+11C=)
c.872+11C= (n.872+11C=)
1g.25809161C>TCA2644199771SELENONc.701+11C>T (n.701+11C>T)
c.770+11C>T (n.770+11C>T)
c.872+11C>T (n.872+11C>T)
 gnomAD v4
1g.25809164_25809165delCA2644199770SELENONc.701+14_701+15del (n.701+14_701+15del)
c.770+14_770+15del (n.770+14_770+15del)
c.872+14_872+15del (n.872+14_872+15del)
 gnomAD v4
1g.25809163C>TCA2580062608SELENONc.701+13C>T (n.701+13C>T)
c.770+13C>T (n.770+13C>T)
c.872+13C>T (n.872+13C>T)
 ClinVar gnomAD v4
1g.25809165C>ACA2580062609SELENONc.701+15C>A (n.701+15C>A)
c.770+15C>A (n.770+15C>A)
c.872+15C>A (n.872+15C>A)
 ClinVar
1g.25809167G>ACA696662SELENONc.701+17G>A (n.701+17G>A)
c.770+17G>A (n.770+17G>A)
c.872+17G>A (n.872+17G>A)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
1g.25809167G=CA1159806182SELENONc.701+17G= (n.701+17G=)
c.770+17G= (n.770+17G=)
c.872+17G= (n.872+17G=)
1g.25809167G>TCA2573132211SELENONc.701+17G>T (n.701+17G>T)
c.770+17G>T (n.770+17G>T)
c.872+17G>T (n.872+17G>T)
 ClinVar dbSNP gnomAD v4
1g.25809168G>TCA2644199772SELENONc.701+18G>T (n.701+18G>T)
c.770+18G>T (n.770+18G>T)
c.872+18G>T (n.872+18G>T)
 gnomAD v4
1g.25809169C>TCA2574271270SELENONc.701+19C>T (n.701+19C>T)
c.770+19C>T (n.770+19C>T)
c.872+19C>T (n.872+19C>T)
 gnomAD v4
1g.25809173C=CA1159806183SELENONc.701+23C= (n.701+23C=)
c.770+23C= (n.770+23C=)
c.872+23C= (n.872+23C=)
1g.25809173C>TCA521738358SELENONc.701+23C>T (n.701+23C>T)
c.770+23C>T (n.770+23C>T)
c.872+23C>T (n.872+23C>T)
 dbSNP gnomAD v2 gnomAD v4
1g.25809173_25809174insGCA2644199773SELENONc.701+23_701+24insG (n.701+23_701+24insG)
c.770+23_770+24insG (n.770+23_770+24insG)
c.872+23_872+24insG (n.872+23_872+24insG)
 gnomAD v4
1g.25809175T>CCA1159806185SELENONc.701+25T>C (n.701+25T>C)
c.770+25T>C (n.770+25T>C)
c.872+25T>C (n.872+25T>C)
 dbSNP
1g.25809175T>GCA2644199774SELENONc.701+25T>G (n.701+25T>G)
c.770+25T>G (n.770+25T>G)
c.872+25T>G (n.872+25T>G)
 gnomAD v4
1g.25809175T=CA1159806184SELENONc.701+25T= (n.701+25T=)
c.770+25T= (n.770+25T=)
c.872+25T= (n.872+25T=)
1g.25809176G>TCA2644199775SELENONc.701+26G>T (n.701+26G>T)
c.770+26G>T (n.770+26G>T)
c.872+26G>T (n.872+26G>T)
 gnomAD v4
1g.25809178A>GCA2644199776SELENONc.701+28A>G (n.701+28A>G)
c.770+28A>G (n.770+28A>G)
c.872+28A>G (n.872+28A>G)
 gnomAD v4
1g.25809179G>ACA2644199777SELENONc.701+29G>A (n.701+29G>A)
c.770+29G>A (n.770+29G>A)
c.872+29G>A (n.872+29G>A)
 gnomAD v4
1g.25809180C=CA1159806186SELENONc.701+30C= (n.701+30C=)
c.770+30C= (n.770+30C=)
c.872+30C= (n.872+30C=)
1g.25809180C>TCA19698430SELENONc.701+30C>T (n.701+30C>T)
c.770+30C>T (n.770+30C>T)
c.872+30C>T (n.872+30C>T)
 dbSNP
1g.25809182C>ACA2644199778SELENONc.701+32C>A (n.701+32C>A)
c.770+32C>A (n.770+32C>A)
c.872+32C>A (n.872+32C>A)
 gnomAD v4
1g.25809183C=CA1143790738SELENONc.701+33C= (n.701+33C=)
c.770+33C= (n.770+33C=)
c.872+33C= (n.872+33C=)
1g.25809183C>GCA521738362SELENONc.701+33C>G (n.701+33C>G)
c.770+33C>G (n.770+33C>G)
c.872+33C>G (n.872+33C>G)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
1g.25809183C>TCA696663SELENONc.701+33C>T (n.701+33C>T)
c.770+33C>T (n.770+33C>T)
c.872+33C>T (n.872+33C>T)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
1g.25809184G>ACA696664SELENONc.701+34G>A (n.701+34G>A)
c.770+34G>A (n.770+34G>A)
c.872+34G>A (n.872+34G>A)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
1g.25809184G=CA1144147391SELENONc.701+34G= (n.701+34G=)
c.770+34G= (n.770+34G=)
c.872+34G= (n.872+34G=)
1g.25809185G>ACA2644199779SELENONc.701+35G>A (n.701+35G>A)
c.770+35G>A (n.770+35G>A)
c.872+35G>A (n.872+35G>A)
 gnomAD v4
1g.25809185G>CCA696665SELENONc.701+35G>C (n.701+35G>C)
c.770+35G>C (n.770+35G>C)
c.872+35G>C (n.872+35G>C)
 dbSNP ExAC gnomAD v2
1g.25809185G=CA1159806187SELENONc.701+35G= (n.701+35G=)
c.770+35G= (n.770+35G=)
c.872+35G= (n.872+35G=)
1g.25809185G>TCA1159806188SELENONc.701+35G>T (n.701+35G>T)
c.770+35G>T (n.770+35G>T)
c.872+35G>T (n.872+35G>T)
 dbSNP gnomAD v4
1g.25809187G>ACA2644199780SELENONc.701+37G>A (n.701+37G>A)
c.770+37G>A (n.770+37G>A)
c.872+37G>A (n.872+37G>A)
 gnomAD v4
1g.25809188A=CA1159806190SELENONc.701+38A= (n.701+38A=)
c.770+38A= (n.770+38A=)
c.872+38A= (n.872+38A=)
1g.25809188A>GCA1159806189SELENONc.701+38A>G (n.701+38A>G)
c.770+38A>G (n.770+38A>G)
c.872+38A>G (n.872+38A>G)
 dbSNP
1g.25809190G>ACA521738371SELENONc.701+40G>A (n.701+40G>A)
c.770+40G>A (n.770+40G>A)
c.872+40G>A (n.872+40G>A)
 dbSNP gnomAD v2
1g.25809190G=CA1159806191SELENONc.701+40G= (n.701+40G=)
c.770+40G= (n.770+40G=)
c.872+40G= (n.872+40G=)
1g.25809191C=CA1159806192SELENONc.701+41C= (n.701+41C=)
c.770+41C= (n.770+41C=)
c.872+41C= (n.872+41C=)
1g.25809191C>TCA1159806193SELENONc.701+41C>T (n.701+41C>T)
c.770+41C>T (n.770+41C>T)
c.872+41C>T (n.872+41C>T)
 dbSNP
1g.25809192A=CA1159806194SELENONc.701+42A= (n.701+42A=)
c.770+42A= (n.770+42A=)
c.872+42A= (n.872+42A=)
1g.25809192A>GCA1159806195SELENONc.701+42A>G (n.701+42A>G)
c.770+42A>G (n.770+42A>G)
c.872+42A>G (n.872+42A>G)
 dbSNP
1g.25809193T>CCA1159806197SELENONc.701+43T>C (n.701+43T>C)
c.770+43T>C (n.770+43T>C)
c.872+43T>C (n.872+43T>C)
 dbSNP
1g.25809193T=CA1159806196SELENONc.701+43T= (n.701+43T=)
c.770+43T= (n.770+43T=)
c.872+43T= (n.872+43T=)
1g.25809196C=CA1143684974SELENONc.701+46C= (n.701+46C=)
c.770+46C= (n.770+46C=)
c.872+46C= (n.872+46C=)
1g.25809196C>GCA696666SELENONc.701+46C>G (n.701+46C>G)
c.770+46C>G (n.770+46C>G)
c.872+46C>G (n.872+46C>G)
 dbSNP ExAC gnomAD v2 gnomAD v4
1g.25809196C>TCA19698433SELENONc.701+46C>T (n.701+46C>T)
c.770+46C>T (n.770+46C>T)
c.872+46C>T (n.872+46C>T)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
1g.25809197G>ACA696667SELENONc.701+47G>A (n.701+47G>A)
c.770+47G>A (n.770+47G>A)
c.872+47G>A (n.872+47G>A)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
1g.25809197G=CA1143202153SELENONc.701+47G= (n.701+47G=)
c.770+47G= (n.770+47G=)
c.872+47G= (n.872+47G=)
1g.25809199T>CCA2644199782SELENONc.701+49T>C (n.701+49T>C)
c.770+49T>C (n.770+49T>C)
c.872+49T>C (n.872+49T>C)
 gnomAD v4
1g.25809199T>GCA1159806199SELENONc.701+49T>G (n.701+49T>G)
c.770+49T>G (n.770+49T>G)
c.872+49T>G (n.872+49T>G)
 dbSNP
1g.25809199T=CA1159806198SELENONc.701+49T= (n.701+49T=)
c.770+49T= (n.770+49T=)
c.872+49T= (n.872+49T=)
1g.25809199_25809200delinsTACA1159806200SELENONc.701+49_701+50delinsTA (n.701+49_701+50delinsTA)
c.770+49_770+50delinsTA (n.770+49_770+50delinsTA)
c.872+49_872+50delinsTA (n.872+49_872+50delinsTA)
1g.25809200delCA521738373SELENONc.701+50del (n.701+50del)
c.770+50del (n.770+50del)
c.872+50del (n.872+50del)
 dbSNP gnomAD v2 gnomAD v4
1g.25809201C>TCA2644199783SELENONc.701+51C>T (n.701+51C>T)
c.770+51C>T (n.770+51C>T)
c.872+51C>T (n.872+51C>T)
 gnomAD v4
1g.25809202A=CA1159806201SELENONc.701+52A= (n.701+52A=)
c.770+52A= (n.770+52A=)
c.872+52A= (n.872+52A=)
1g.25809202A>GCA1159806202SELENONc.701+52A>G (n.701+52A>G)
c.770+52A>G (n.770+52A>G)
c.872+52A>G (n.872+52A>G)
 dbSNP
1g.25809204C=CA1159806203SELENONc.701+54C= (n.701+54C=)
c.770+54C= (n.770+54C=)
c.872+54C= (n.872+54C=)
1g.25809204C>GCA734440886SELENONc.701+54C>G (n.701+54C>G)
c.770+54C>G (n.770+54C>G)
c.872+54C>G (n.872+54C>G)
 dbSNP gnomAD v4
1g.25809204C>TCA734440882SELENONc.701+54C>T (n.701+54C>T)
c.770+54C>T (n.770+54C>T)
c.872+54C>T (n.872+54C>T)
 dbSNP gnomAD v3 gnomAD v4

Number of alleles fetched