Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
1 | g.25809101G>A | CA339113933 | SELENON | c.652G>A (p.Val218Met) c.721G>A (p.Val241Met) c.823G>A (p.Val275Met) | |
1 | g.25809101G>C | CA339113932 | SELENON | c.652G>C (p.Val218Leu) c.721G>C (p.Val241Leu) c.823G>C (p.Val275Leu) | |
1 | g.25809101G>T | CA339113935 | SELENON | c.652G>T (p.Val218Leu) c.721G>T (p.Val241Leu) c.823G>T (p.Val275Leu) | |
1 | g.25809102T>A | CA339113938 | SELENON | c.653T>A (p.Val218Glu) c.722T>A (p.Val241Glu) c.824T>A (p.Val275Glu) | |
1 | g.25809102T>C | CA339113941 | SELENON | c.653T>C (p.Val218Ala) c.722T>C (p.Val241Ala) c.824T>C (p.Val275Ala) | |
1 | g.25809102T>G | CA339113944 | SELENON | c.653T>G (p.Val218Gly) c.722T>G (p.Val241Gly) c.824T>G (p.Val275Gly) | |
1 | g.25809103G>A | CA416759089 | SELENON | c.654G>A (p.Val218=) c.723G>A (p.Val241=) c.825G>A (p.Val275=) | |
1 | g.25809103G>C | CA416759090 | SELENON | c.654G>C (p.Val218=) c.723G>C (p.Val241=) c.825G>C (p.Val275=) | |
1 | g.25809103G>T | CA416759091 | SELENON | c.654G>T (p.Val218=) c.723G>T (p.Val241=) c.825G>T (p.Val275=) | |
1 | g.25809104dup | CA2843107339 | SELENON | c.655dup (p.Ala219GlyfsTer25) c.724dup (p.Ala242GlyfsTer25) c.826dup (p.Ala276GlyfsTer25) | |
1 | g.25809104G>A | CA339113947 | SELENON | c.655G>A (p.Ala219Thr) c.724G>A (p.Ala242Thr) c.826G>A (p.Ala276Thr) | |
1 | g.25809104G>C | CA339113949 | SELENON | c.655G>C (p.Ala219Pro) c.724G>C (p.Ala242Pro) c.826G>C (p.Ala276Pro) | |
1 | g.25809104G= | CA1159806153 | SELENON | c.655G= (p.Ala219=) c.724G= (p.Ala242=) c.826G= (p.Ala276=) | |
1 | g.25809104G>T | CA339113951 | SELENON | c.655G>T (p.Ala219Ser) c.724G>T (p.Ala242Ser) c.826G>T (p.Ala276Ser) | gnomAD v4 |
1 | g.25809105C>A | CA339113958 | SELENON | c.656C>A (p.Ala219Asp) c.725C>A (p.Ala242Asp) c.827C>A (p.Ala276Asp) | |
1 | g.25809105C= | CA1159806154 | SELENON | c.656C= (p.Ala219=) c.725C= (p.Ala242=) c.827C= (p.Ala276=) | |
1 | g.25809105C>G | CA339113960 | SELENON | c.656C>G (p.Ala219Gly) c.725C>G (p.Ala242Gly) c.827C>G (p.Ala276Gly) | gnomAD v4 |
1 | g.25809105C>T | CA19698405 | SELENON | c.656C>T (p.Ala219Val) c.725C>T (p.Ala242Val) c.827C>T (p.Ala276Val) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.25809105_25809107dup | CA276995 | SELENON | c.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 |
1 | g.25809106C>A | CA416759092 | SELENON | c.657C>A (p.Ala219=) c.726C>A (p.Ala242=) c.828C>A (p.Ala276=) | |
1 | g.25809106C= | CA1159806155 | SELENON | c.657C= (p.Ala219=) c.726C= (p.Ala242=) c.828C= (p.Ala276=) | |
1 | g.25809106C>G | CA416759093 | SELENON | c.657C>G (p.Ala219=) c.726C>G (p.Ala242=) c.828C>G (p.Ala276=) | |
1 | g.25809106C>T | CA416759094 | SELENON | c.657C>T (p.Ala219=) c.726C>T (p.Ala242=) c.828C>T (p.Ala276=) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
1 | g.25809107T>A | CA339113965 | SELENON | c.658T>A (p.Cys220Ser) c.727T>A (p.Cys243Ser) c.829T>A (p.Cys277Ser) | |
1 | g.25809107T>C | CA339113968 | SELENON | c.658T>C (p.Cys220Arg) c.727T>C (p.Cys243Arg) c.829T>C (p.Cys277Arg) | |
1 | g.25809107T>G | CA19698407 | SELENON | c.658T>G (p.Cys220Gly) c.727T>G (p.Cys243Gly) c.829T>G (p.Cys277Gly) | dbSNP gnomAD v4 |
1 | g.25809107T= | CA1159806156 | SELENON | c.658T= (p.Cys220=) c.727T= (p.Cys243=) c.829T= (p.Cys277=) | |
1 | g.25809108G>A | CA339113974 | SELENON | c.659G>A (p.Cys220Tyr) c.728G>A (p.Cys243Tyr) c.830G>A (p.Cys277Tyr) | gnomAD v4 |
1 | g.25809108G>C | CA339113984 | SELENON | c.659G>C (p.Cys220Ser) c.728G>C (p.Cys243Ser) c.830G>C (p.Cys277Ser) | |
1 | g.25809108G>T | CA339113976 | SELENON | c.659G>T (p.Cys220Phe) c.728G>T (p.Cys243Phe) c.830G>T (p.Cys277Phe) | |
1 | g.25809109C>A | CA339113987 | SELENON | c.660C>A (p.Cys220Ter) c.729C>A (p.Cys243Ter) c.831C>A (p.Cys277Ter) | |
1 | g.25809109C>G | CA339113995 | SELENON | c.660C>G (p.Cys220Trp) c.729C>G (p.Cys243Trp) c.831C>G (p.Cys277Trp) | |
1 | g.25809109C>T | CA416759095 | SELENON | c.660C>T (p.Cys220=) c.729C>T (p.Cys243=) c.831C>T (p.Cys277=) | |
1 | g.25809110C>A | CA339114001 | SELENON | c.661C>A (p.Leu221Met) c.730C>A (p.Leu244Met) c.832C>A (p.Leu278Met) | |
1 | g.25809110C>G | CA339114007 | SELENON | c.661C>G (p.Leu221Val) c.730C>G (p.Leu244Val) c.832C>G (p.Leu278Val) | |
1 | g.25809110C>T | CA416759096 | SELENON | c.661C>T (p.Leu221=) c.730C>T (p.Leu244=) c.832C>T (p.Leu278=) | |
1 | g.25809111T>A | CA339114009 | SELENON | c.662T>A (p.Leu221Gln) c.731T>A (p.Leu244Gln) c.833T>A (p.Leu278Gln) | |
1 | g.25809111T>C | CA339114013 | SELENON | c.662T>C (p.Leu221Pro) c.731T>C (p.Leu244Pro) c.833T>C (p.Leu278Pro) | dbSNP gnomAD v4 |
1 | g.25809111T>G | CA339114016 | SELENON | c.662T>G (p.Leu221Arg) c.731T>G (p.Leu244Arg) c.833T>G (p.Leu278Arg) | |
1 | g.25809111T= | CA1159806157 | SELENON | c.662T= (p.Leu221=) c.731T= (p.Leu244=) c.833T= (p.Leu278=) | |
1 | g.25809112G>A | CA416759097 | SELENON | c.663G>A (p.Leu221=) c.732G>A (p.Leu244=) c.834G>A (p.Leu278=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.25809112G>C | CA416759098 | SELENON | c.663G>C (p.Leu221=) c.732G>C (p.Leu244=) c.834G>C (p.Leu278=) | |
1 | g.25809112G= | CA1159806158 | SELENON | c.663G= (p.Leu221=) c.732G= (p.Leu244=) c.834G= (p.Leu278=) | |
1 | g.25809112G>T | CA416759099 | SELENON | c.663G>T (p.Leu221=) c.732G>T (p.Leu244=) c.834G>T (p.Leu278=) | gnomAD v4 |
1 | g.25809113A>C | CA339114034 | SELENON | c.664A>C (p.Thr222Pro) c.733A>C (p.Thr245Pro) c.835A>C (p.Thr279Pro) | |
1 | g.25809113A>G | CA339114035 | SELENON | c.664A>G (p.Thr222Ala) c.733A>G (p.Thr245Ala) c.835A>G (p.Thr279Ala) | COSMIC |
1 | g.25809113A>T | CA339114039 | SELENON | c.664A>T (p.Thr222Ser) c.733A>T (p.Thr245Ser) c.835A>T (p.Thr279Ser) | |
1 | g.25809114C>A | CA339114049 | SELENON | c.665C>A (p.Thr222Asn) c.734C>A (p.Thr245Asn) c.836C>A (p.Thr279Asn) | |
1 | g.25809114C= | CA1159806159 | SELENON | c.665C= (p.Thr222=) c.734C= (p.Thr245=) c.836C= (p.Thr279=) | |
1 | g.25809114C>G | CA339114046 | SELENON | c.665C>G (p.Thr222Ser) c.734C>G (p.Thr245Ser) c.836C>G (p.Thr279Ser) | |
1 | g.25809114C>T | CA339114043 | SELENON | c.665C>T (p.Thr222Ile) c.734C>T (p.Thr245Ile) c.836C>T (p.Thr279Ile) | dbSNP gnomAD v2 gnomAD v4 |
1 | g.25809115T>A | CA416759100 | SELENON | c.666T>A (p.Thr222=) c.735T>A (p.Thr245=) c.837T>A (p.Thr279=) | |
1 | g.25809115T>C | CA416759101 | SELENON | c.666T>C (p.Thr222=) c.735T>C (p.Thr245=) c.837T>C (p.Thr279=) | gnomAD v4 |
1 | g.25809115T>G | CA416759102 | SELENON | c.666T>G (p.Thr222=) c.735T>G (p.Thr245=) c.837T>G (p.Thr279=) | |
1 | g.25809116G>A | CA339114051 | SELENON | c.667G>A (p.Ala223Thr) c.736G>A (p.Ala246Thr) c.838G>A (p.Ala280Thr) | |
1 | g.25809116G>C | CA339114055 | SELENON | c.667G>C (p.Ala223Pro) c.736G>C (p.Ala246Pro) c.838G>C (p.Ala280Pro) | |
1 | g.25809116G>T | CA339114059 | SELENON | c.667G>T (p.Ala223Ser) c.736G>T (p.Ala246Ser) c.838G>T (p.Ala280Ser) | |
1 | g.25809117C>A | CA339114063 | SELENON | c.668C>A (p.Ala223Asp) c.737C>A (p.Ala246Asp) c.839C>A (p.Ala280Asp) | COSMIC |
1 | g.25809117C>G | CA339114067 | SELENON | c.668C>G (p.Ala223Gly) c.737C>G (p.Ala246Gly) c.839C>G (p.Ala280Gly) | |
1 | g.25809117C>T | CA339114069 | SELENON | c.668C>T (p.Ala223Val) c.737C>T (p.Ala246Val) c.839C>T (p.Ala280Val) | COSMIC |
1 | g.25809118C>A | CA416759104 | SELENON | c.669C>A (p.Ala223=) c.738C>A (p.Ala246=) c.840C>A (p.Ala280=) | gnomAD v4 |
1 | g.25809118C>G | CA416759105 | SELENON | c.669C>G (p.Ala223=) c.738C>G (p.Ala246=) c.840C>G (p.Ala280=) | |
1 | g.25809118C>T | CA416759103 | SELENON | c.669C>T (p.Ala223=) c.738C>T (p.Ala246=) c.840C>T (p.Ala280=) | gnomAD v4 |
1 | g.25809119A>C | CA339114072 | SELENON | c.670A>C (p.Ile224Leu) c.739A>C (p.Ile247Leu) c.841A>C (p.Ile281Leu) | |
1 | g.25809119A>G | CA339114073 | SELENON | c.670A>G (p.Ile224Val) c.739A>G (p.Ile247Val) c.841A>G (p.Ile281Val) | gnomAD v4 |
1 | g.25809119A>T | CA339114074 | SELENON | c.670A>T (p.Ile224Phe) c.739A>T (p.Ile247Phe) c.841A>T (p.Ile281Phe) | |
1 | g.25809120T>A | CA339114077 | SELENON | c.671T>A (p.Ile224Asn) c.740T>A (p.Ile247Asn) c.842T>A (p.Ile281Asn) | |
1 | g.25809120T>C | CA339114080 | SELENON | c.671T>C (p.Ile224Thr) c.740T>C (p.Ile247Thr) c.842T>C (p.Ile281Thr) | |
1 | g.25809120T>G | CA339114082 | SELENON | c.671T>G (p.Ile224Ser) c.740T>G (p.Ile247Ser) c.842T>G (p.Ile281Ser) | |
1 | g.25809121C>A | CA416759106 | SELENON | c.672C>A (p.Ile224=) c.741C>A (p.Ile247=) c.843C>A (p.Ile281=) | |
1 | g.25809121C>G | CA339114084 | SELENON | c.672C>G (p.Ile224Met) c.741C>G (p.Ile247Met) c.843C>G (p.Ile281Met) | ClinVar gnomAD v4 |
1 | g.25809121C>T | CA416759107 | SELENON | c.672C>T (p.Ile224=) c.741C>T (p.Ile247=) c.843C>T (p.Ile281=) | |
1 | g.25809122A>C | CA339114095 | SELENON | c.673A>C (p.Ser225Arg) c.742A>C (p.Ser248Arg) c.844A>C (p.Ser282Arg) | |
1 | g.25809122A>G | CA339114089 | SELENON | c.673A>G (p.Ser225Gly) c.742A>G (p.Ser248Gly) c.844A>G (p.Ser282Gly) | gnomAD v4 |
1 | g.25809122A>T | CA339114092 | SELENON | c.673A>T (p.Ser225Cys) c.742A>T (p.Ser248Cys) c.844A>T (p.Ser282Cys) | |
1 | g.25809123G>A | CA339114102 | SELENON | c.674G>A (p.Ser225Asn) c.743G>A (p.Ser248Asn) c.845G>A (p.Ser282Asn) | |
1 | g.25809123G>C | CA339114105 | SELENON | c.674G>C (p.Ser225Thr) c.743G>C (p.Ser248Thr) c.845G>C (p.Ser282Thr) | |
1 | g.25809123G>T | CA339114108 | SELENON | c.674G>T (p.Ser225Ile) c.743G>T (p.Ser248Ile) c.845G>T (p.Ser282Ile) | |
1 | g.25809124C>A | CA339114110 | SELENON | c.675C>A (p.Ser225Arg) c.744C>A (p.Ser248Arg) c.846C>A (p.Ser282Arg) | |
1 | g.25809124C= | CA1140506082 | SELENON | c.675C= (p.Ser225=) c.744C= (p.Ser248=) c.846C= (p.Ser282=) | |
1 | g.25809124C>G | CA339114113 | SELENON | c.675C>G (p.Ser225Arg) c.744C>G (p.Ser248Arg) c.846C>G (p.Ser282Arg) | dbSNP gnomAD v3 gnomAD v4 |
1 | g.25809124C>T | CA203325 | SELENON | c.675C>T (p.Ser225=) c.744C>T (p.Ser248=) c.846C>T (p.Ser282=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.25809125G>A | CA696651 | SELENON | c.676G>A (p.Asp226Asn) c.745G>A (p.Asp249Asn) c.847G>A (p.Asp283Asn) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.25809125G>C | CA339114132 | SELENON | c.676G>C (p.Asp226His) c.745G>C (p.Asp249His) c.847G>C (p.Asp283His) | |
1 | g.25809125G= | CA1159806160 | SELENON | c.676G= (p.Asp226=) c.745G= (p.Asp249=) c.847G= (p.Asp283=) | |
1 | g.25809125G>T | CA339114136 | SELENON | c.676G>T (p.Asp226Tyr) c.745G>T (p.Asp249Tyr) c.847G>T (p.Asp283Tyr) | dbSNP gnomAD v4 |
1 | g.25809126A>C | CA339114145 | SELENON | c.677A>C (p.Asp226Ala) c.746A>C (p.Asp249Ala) c.848A>C (p.Asp283Ala) | |
1 | g.25809126A>G | CA339114147 | SELENON | c.677A>G (p.Asp226Gly) c.746A>G (p.Asp249Gly) c.848A>G (p.Asp283Gly) | |
1 | g.25809126A>T | CA339114150 | SELENON | c.677A>T (p.Asp226Val) c.746A>T (p.Asp249Val) c.848A>T (p.Asp283Val) | |
1 | g.25809127C>A | CA339114155 | SELENON | c.678C>A (p.Asp226Glu) c.747C>A (p.Asp249Glu) c.849C>A (p.Asp283Glu) | |
1 | g.25809127C>G | CA339114154 | SELENON | c.678C>G (p.Asp226Glu) c.747C>G (p.Asp249Glu) c.849C>G (p.Asp283Glu) | |
1 | g.25809127C>T | CA416759108 | SELENON | c.678C>T (p.Asp226=) c.747C>T (p.Asp249=) c.849C>T (p.Asp283=) | |
1 | g.25809128T>A | CA339114159 | SELENON | c.679T>A (p.Phe227Ile) c.748T>A (p.Phe250Ile) c.850T>A (p.Phe284Ile) | |
1 | g.25809128T>C | CA339114166 | SELENON | c.679T>C (p.Phe227Leu) c.748T>C (p.Phe250Leu) c.850T>C (p.Phe284Leu) | |
1 | g.25809128T>G | CA339114162 | SELENON | c.679T>G (p.Phe227Val) c.748T>G (p.Phe250Val) c.850T>G (p.Phe284Val) | |
1 | g.25809128_25809129del | CA2644199765 | SELENON | c.679_680del (p.Phe227LeufsTer16) c.748_749del (p.Phe250LeufsTer16) c.850_851del (p.Phe284LeufsTer16) | gnomAD v4 |
1 | g.25809129T>A | CA339114170 | SELENON | c.680T>A (p.Phe227Tyr) c.749T>A (p.Phe250Tyr) c.851T>A (p.Phe284Tyr) | |
1 | g.25809129T>C | CA339114171 | SELENON | c.680T>C (p.Phe227Ser) c.749T>C (p.Phe250Ser) c.851T>C (p.Phe284Ser) | |
1 | g.25809129T>G | CA339114172 | SELENON | c.680T>G (p.Phe227Cys) c.749T>G (p.Phe250Cys) c.851T>G (p.Phe284Cys) | gnomAD v4 |
1 | g.25809130del | CA2644199766 | SELENON | c.681del (p.Tyr228ThrfsTer4) c.750del (p.Tyr251ThrfsTer4) c.852del (p.Tyr285ThrfsTer4) | gnomAD v4 |
1 | g.25809130C>A | CA339114174 | SELENON | c.681C>A (p.Phe227Leu) c.750C>A (p.Phe250Leu) c.852C>A (p.Phe284Leu) | |
1 | g.25809130C= | CA1142954282 | SELENON | c.681C= (p.Phe227=) c.750C= (p.Phe250=) c.852C= (p.Phe284=) | |
1 | g.25809130C>G | CA339114177 | SELENON | c.681C>G (p.Phe227Leu) c.750C>G (p.Phe250Leu) c.852C>G (p.Phe284Leu) | |
1 | g.25809130C>T | CA696652 | SELENON | c.681C>T (p.Phe227=) c.750C>T (p.Phe250=) c.852C>T (p.Phe284=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.25809134_25809136del | CA2644199767 | SELENON | c.685_687del (p.Tyr229del) c.754_756del (p.Tyr252del) c.856_858del (p.Tyr286del) | gnomAD v4 |
1 | g.25809131T>A | CA339114183 | SELENON | c.682T>A (p.Tyr228Asn) c.751T>A (p.Tyr251Asn) c.853T>A (p.Tyr285Asn) | |
1 | g.25809131T>C | CA339114187 | SELENON | c.682T>C (p.Tyr228His) c.751T>C (p.Tyr251His) c.853T>C (p.Tyr285His) | |
1 | g.25809131T>G | CA339114190 | SELENON | c.682T>G (p.Tyr228Asp) c.751T>G (p.Tyr251Asp) c.853T>G (p.Tyr285Asp) | |
1 | g.25809132A>C | CA339114193 | SELENON | c.683A>C (p.Tyr228Ser) c.752A>C (p.Tyr251Ser) c.854A>C (p.Tyr285Ser) | |
1 | g.25809132A>G | CA339114198 | SELENON | c.683A>G (p.Tyr228Cys) c.752A>G (p.Tyr251Cys) c.854A>G (p.Tyr285Cys) | |
1 | g.25809132A>T | CA339114202 | SELENON | c.683A>T (p.Tyr228Phe) c.752A>T (p.Tyr251Phe) c.854A>T (p.Tyr285Phe) | |
1 | g.25809133C>A | CA339114206 | SELENON | c.684C>A (p.Tyr228Ter) c.753C>A (p.Tyr251Ter) c.855C>A (p.Tyr285Ter) | |
1 | g.25809133C= | CA1159806161 | SELENON | c.684C= (p.Tyr228=) c.753C= (p.Tyr251=) c.855C= (p.Tyr285=) | |
1 | g.25809133C>G | CA339114209 | SELENON | c.684C>G (p.Tyr228Ter) c.753C>G (p.Tyr251Ter) c.855C>G (p.Tyr285Ter) | ClinVar dbSNP |
1 | g.25809133C>T | CA416759109 | SELENON | c.684C>T (p.Tyr228=) c.753C>T (p.Tyr251=) c.855C>T (p.Tyr285=) | gnomAD v4 |
1 | g.25809134T>A | CA339114213 | SELENON | c.685T>A (p.Tyr229Asn) c.754T>A (p.Tyr252Asn) c.856T>A (p.Tyr286Asn) | |
1 | g.25809134T>C | CA339114215 | SELENON | c.685T>C (p.Tyr229His) c.754T>C (p.Tyr252His) c.856T>C (p.Tyr286His) | |
1 | g.25809134T>G | CA339114220 | SELENON | c.685T>G (p.Tyr229Asp) c.754T>G (p.Tyr252Asp) c.856T>G (p.Tyr286Asp) | |
1 | g.25809135A= | CA1159806162 | SELENON | c.686A= (p.Tyr229=) c.755A= (p.Tyr252=) c.857A= (p.Tyr286=) | |
1 | g.25809135A>C | CA339114222 | SELENON | c.686A>C (p.Tyr229Ser) c.755A>C (p.Tyr252Ser) c.857A>C (p.Tyr286Ser) | |
1 | g.25809135A>G | CA696653 | SELENON | c.686A>G (p.Tyr229Cys) c.755A>G (p.Tyr252Cys) c.857A>G (p.Tyr286Cys) | dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.25809135A>T | CA339114228 | SELENON | c.686A>T (p.Tyr229Phe) c.755A>T (p.Tyr252Phe) c.857A>T (p.Tyr286Phe) | |
1 | g.25809136C>A | CA339114231 | SELENON | c.687C>A (p.Tyr229Ter) c.756C>A (p.Tyr252Ter) c.858C>A (p.Tyr286Ter) | |
1 | g.25809136C= | CA1159806163 | SELENON | c.687C= (p.Tyr229=) c.756C= (p.Tyr252=) c.858C= (p.Tyr286=) | |
1 | g.25809136C>G | CA696654 | SELENON | c.687C>G (p.Tyr229Ter) c.756C>G (p.Tyr252Ter) c.858C>G (p.Tyr286Ter) | dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.25809136C>T | CA19698416 | SELENON | c.687C>T (p.Tyr229=) c.756C>T (p.Tyr252=) c.858C>T (p.Tyr286=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.25809137A= | CA1159806164 | SELENON | c.688A= (p.Thr230=) c.757A= (p.Thr253=) c.859A= (p.Thr287=) | |
1 | g.25809137A>C | CA339114237 | SELENON | c.688A>C (p.Thr230Pro) c.757A>C (p.Thr253Pro) c.859A>C (p.Thr287Pro) | gnomAD v4 |
1 | g.25809137A>G | CA696655 | SELENON | c.688A>G (p.Thr230Ala) c.757A>G (p.Thr253Ala) c.859A>G (p.Thr287Ala) | dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.25809137A>T | CA339114241 | SELENON | c.688A>T (p.Thr230Ser) c.757A>T (p.Thr253Ser) c.859A>T (p.Thr287Ser) | |
1 | g.25809138C>A | CA339114246 | SELENON | c.689C>A (p.Thr230Asn) c.758C>A (p.Thr253Asn) c.860C>A (p.Thr287Asn) | |
1 | g.25809138C= | CA1159806166 | SELENON | c.689C= (p.Thr230=) c.758C= (p.Thr253=) c.860C= (p.Thr287=) | |
1 | g.25809138C>G | CA339114248 | SELENON | c.689C>G (p.Thr230Ser) c.758C>G (p.Thr253Ser) c.860C>G (p.Thr287Ser) | |
1 | g.25809138C>T | CA339114244 | SELENON | c.689C>T (p.Thr230Ile) c.758C>T (p.Thr253Ile) c.860C>T (p.Thr287Ile) | dbSNP gnomAD v3 gnomAD v4 |
1 | g.25809138_25809140delinsCTG | CA1159806165 | SELENON | c.689_691delinsCTG (p.Thr230=) c.758_760delinsCTG (p.Thr253=) c.860_862delinsCTG (p.Thr287=) | |
1 | g.25809139_25809149del | CA2586966306 | SELENON | c.690_700del (p.Val231AspfsTer9) c.759_769del (p.Val254AspfsTer9) c.861_871del (p.Val288AspfsTer9) | |
1 | g.25809139T>A | CA696656 | SELENON | c.690T>A (p.Thr230=) c.759T>A (p.Thr253=) c.861T>A (p.Thr287=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.25809139T>C | CA416759111 | SELENON | c.690T>C (p.Thr230=) c.759T>C (p.Thr253=) c.861T>C (p.Thr287=) | gnomAD v4 |
1 | g.25809139T>G | CA416759110 | SELENON | c.690T>G (p.Thr230=) c.759T>G (p.Thr253=) c.861T>G (p.Thr287=) | |
1 | g.25809139T= | CA1159806167 | SELENON | c.690T= (p.Thr230=) c.759T= (p.Thr253=) c.861T= (p.Thr287=) | |
1 | g.25809141_25809142del | CA734440819 | SELENON | c.692_693del (p.Val231AspfsTer12) c.761_762del (p.Val254AspfsTer12) c.863_864del (p.Val288AspfsTer12) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
1 | g.25809140G>A | CA339114251 | SELENON | c.691G>A (p.Val231Met) c.760G>A (p.Val254Met) c.862G>A (p.Val288Met) | dbSNP gnomAD v3 gnomAD v4 |
1 | g.25809140G>C | CA339114252 | SELENON | c.691G>C (p.Val231Leu) c.760G>C (p.Val254Leu) c.862G>C (p.Val288Leu) | gnomAD v4 |
1 | g.25809140G= | CA1159806168 | SELENON | c.691G= (p.Val231=) c.760G= (p.Val254=) c.862G= (p.Val288=) | |
1 | g.25809140G>T | CA339114255 | SELENON | c.691G>T (p.Val231Leu) c.760G>T (p.Val254Leu) c.862G>T (p.Val288Leu) | |
1 | g.25809141T>A | CA339114257 | SELENON | c.692T>A (p.Val231Glu) c.761T>A (p.Val254Glu) c.863T>A (p.Val288Glu) | |
1 | g.25809141T>C | CA339114259 | SELENON | c.692T>C (p.Val231Ala) c.761T>C (p.Val254Ala) c.863T>C (p.Val288Ala) | |
1 | g.25809141T>G | CA339114260 | SELENON | c.692T>G (p.Val231Gly) c.761T>G (p.Val254Gly) c.863T>G (p.Val288Gly) | |
1 | g.25809142G>A | CA416759115 | SELENON | c.693G>A (p.Val231=) c.762G>A (p.Val254=) c.864G>A (p.Val288=) | |
1 | g.25809142G>C | CA416759116 | SELENON | c.693G>C (p.Val231=) c.762G>C (p.Val254=) c.864G>C (p.Val288=) | |
1 | g.25809142G>T | CA416759117 | SELENON | c.693G>T (p.Val231=) c.762G>T (p.Val254=) c.864G>T (p.Val288=) | |
1 | g.25809143A= | CA1159806169 | SELENON | c.694A= (p.Met232=) c.763A= (p.Met255=) c.865A= (p.Met289=) | |
1 | g.25809143A>C | CA339114262 | SELENON | c.694A>C (p.Met232Leu) c.763A>C (p.Met255Leu) c.865A>C (p.Met289Leu) | |
1 | g.25809143A>G | CA19698421 | SELENON | c.694A>G (p.Met232Val) c.763A>G (p.Met255Val) c.865A>G (p.Met289Val) | dbSNP |
1 | g.25809143A>T | CA339114265 | SELENON | c.694A>T (p.Met232Leu) c.763A>T (p.Met255Leu) c.865A>T (p.Met289Leu) | |
1 | g.25809144T>A | CA339114267 | SELENON | c.695T>A (p.Met232Lys) c.764T>A (p.Met255Lys) c.866T>A (p.Met289Lys) | |
1 | g.25809144T>C | CA339114270 | SELENON | c.695T>C (p.Met232Thr) c.764T>C (p.Met255Thr) c.866T>C (p.Met289Thr) | gnomAD v4 |
1 | g.25809144T>G | CA339114272 | SELENON | c.695T>G (p.Met232Arg) c.764T>G (p.Met255Arg) c.866T>G (p.Met289Arg) | |
1 | g.25809145G>A | CA339114281 | SELENON | c.696G>A (p.Met232Ile) c.765G>A (p.Met255Ile) c.867G>A (p.Met289Ile) | dbSNP |
1 | g.25809145G>C | CA339114277 | SELENON | c.696G>C (p.Met232Ile) c.765G>C (p.Met255Ile) c.867G>C (p.Met289Ile) | |
1 | g.25809145G= | CA1159806170 | SELENON | c.696G= (p.Met232=) c.765G= (p.Met255=) c.867G= (p.Met289=) | |
1 | g.25809145G>T | CA339114275 | SELENON | c.696G>T (p.Met232Ile) c.765G>T (p.Met255Ile) c.867G>T (p.Met289Ile) | |
1 | g.25809146T>A | CA339114284 | SELENON | c.697T>A (p.Phe233Ile) c.766T>A (p.Phe256Ile) c.868T>A (p.Phe290Ile) | |
1 | g.25809146T>C | CA339114286 | SELENON | c.697T>C (p.Phe233Leu) c.766T>C (p.Phe256Leu) c.868T>C (p.Phe290Leu) | |
1 | g.25809146T>G | CA339114288 | SELENON | c.697T>G (p.Phe233Val) c.766T>G (p.Phe256Val) c.868T>G (p.Phe290Val) | |
1 | g.25809147T>A | CA696657 | SELENON | c.698T>A (p.Phe233Tyr) c.767T>A (p.Phe256Tyr) c.869T>A (p.Phe290Tyr) | dbSNP ExAC gnomAD v4 |
1 | g.25809147T>C | CA339114293 | SELENON | c.698T>C (p.Phe233Ser) c.767T>C (p.Phe256Ser) c.869T>C (p.Phe290Ser) | |
1 | g.25809147T>G | CA339114295 | SELENON | c.698T>G (p.Phe233Cys) c.767T>G (p.Phe256Cys) c.869T>G (p.Phe290Cys) | |
1 | g.25809147T= | CA1159806172 | SELENON | c.698T= (p.Phe233=) c.767T= (p.Phe256=) c.869T= (p.Phe290=) | |
1 | g.25809147_25809148del | CA2573051548 | SELENON | c.698_699del (p.Phe233SerfsTer10) c.767_768del (p.Phe256SerfsTer10) c.869_870del (p.Phe290SerfsTer10) | ClinVar dbSNP |
1 | g.25809147_25809148delinsTC | CA1159806171 | SELENON | c.698_699delinsTC (p.Phe233=) c.767_768delinsTC (p.Phe256=) c.869_870delinsTC (p.Phe290=) | |
1 | g.25809148C>A | CA339114298 | SELENON | c.699C>A (p.Phe233Leu) c.768C>A (p.Phe256Leu) c.870C>A (p.Phe290Leu) | |
1 | g.25809148C>G | CA339114300 | SELENON | c.699C>G (p.Phe233Leu) c.768C>G (p.Phe256Leu) c.870C>G (p.Phe290Leu) | gnomAD v4 |
1 | g.25809148C>T | CA416759125 | SELENON | c.699C>T (p.Phe233=) c.768C>T (p.Phe256=) c.870C>T (p.Phe290=) | |
1 | g.25809149del | CA696658 | SELENON | c.700del (p.Arg234GlyfsTer?) c.769del (p.Arg257GlyfsTer?) c.871del (p.Arg291GlyfsTer?) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.25809149C>A | CA416759126 | SELENON | c.700C>A (p.Arg234=) c.769C>A (p.Arg257=) c.871C>A (p.Arg291=) | gnomAD v4 |
1 | g.25809149C= | CA1159806173 | SELENON | c.700C= (p.Arg234=) c.769C= (p.Arg257=) c.871C= (p.Arg291=) | |
1 | g.25809149C>G | CA339114304 | SELENON | c.700C>G (p.Arg234Gly) c.769C>G (p.Arg257Gly) c.871C>G (p.Arg291Gly) | gnomAD v4 |
1 | g.25809149C>T | CA696659 | SELENON | c.700C>T (p.Arg234Trp) c.769C>T (p.Arg257Trp) c.871C>T (p.Arg291Trp) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.25809150G>A | CA696660 | SELENON | c.701G>A (p.Arg234Gln) c.770G>A (p.Arg257Gln) c.872G>A (p.Arg291Gln) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.25809150G>C | CA339114309 | SELENON | c.701G>C (p.Arg234Pro) c.770G>C (p.Arg257Pro) c.872G>C (p.Arg291Pro) | |
1 | g.25809150G= | CA1143359861 | SELENON | c.701G= (p.Arg234=) c.770G= (p.Arg257=) c.872G= (p.Arg291=) | |
1 | g.25809150G>T | CA339114312 | SELENON | c.701G>T (p.Arg234Leu) c.770G>T (p.Arg257Leu) c.872G>T (p.Arg291Leu) | |
1 | g.25809151G>A | CA339114319 | SELENON | c.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 |
1 | g.25809151G>C | CA339114317 | SELENON | c.701+1G>C (n.701+1G>C) c.770+1G>C (n.770+1G>C) c.872+1G>C (n.872+1G>C) | |
1 | g.25809151G= | CA1159806174 | SELENON | c.701+1G= (n.701+1G=) c.770+1G= (n.770+1G=) c.872+1G= (n.872+1G=) | |
1 | g.25809151G>T | CA339114314 | SELENON | c.701+1G>T (n.701+1G>T) c.770+1G>T (n.770+1G>T) c.872+1G>T (n.872+1G>T) | COSMIC |
1 | g.25809152T>A | CA339114321 | SELENON | c.701+2T>A (n.701+2T>A) c.770+2T>A (n.770+2T>A) c.872+2T>A (n.872+2T>A) | |
1 | g.25809152T>C | CA275352 | SELENON | c.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 |
1 | g.25809152T>G | CA339114323 | SELENON | c.701+2T>G (n.701+2T>G) c.770+2T>G (n.770+2T>G) c.872+2T>G (n.872+2T>G) | |
1 | g.25809152T= | CA1159806175 | SELENON | c.701+2T= (n.701+2T=) c.770+2T= (n.770+2T=) c.872+2T= (n.872+2T=) | |
1 | g.25809153G>A | CA2644199768 | SELENON | c.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 |
1 | g.25809154A>T | CA2644199769 | SELENON | c.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 |
1 | g.25809157G>A | CA696661 | SELENON | c.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 |
1 | g.25809157G= | CA1159806176 | SELENON | c.701+7G= (n.701+7G=) c.770+7G= (n.770+7G=) c.872+7G= (n.872+7G=) | |
1 | g.25809157G>T | CA2843107340 | SELENON | c.701+7G>T (n.701+7G>T) c.770+7G>T (n.770+7G>T) c.872+7G>T (n.872+7G>T) | |
1 | g.25809158G>A | CA1159806178 | SELENON | c.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 |
1 | g.25809158G= | CA1159806177 | SELENON | c.701+8G= (n.701+8G=) c.770+8G= (n.770+8G=) c.872+8G= (n.872+8G=) | |
1 | g.25809159G>A | CA1159806180 | SELENON | c.701+9G>A (n.701+9G>A) c.770+9G>A (n.770+9G>A) c.872+9G>A (n.872+9G>A) | dbSNP |
1 | g.25809159G= | CA1159806179 | SELENON | c.701+9G= (n.701+9G=) c.770+9G= (n.770+9G=) c.872+9G= (n.872+9G=) | |
1 | g.25809160C>A | CA2839032284 | SELENON | c.701+10C>A (n.701+10C>A) c.770+10C>A (n.770+10C>A) c.872+10C>A (n.872+10C>A) | |
1 | g.25809161C>A | CA521738355 | SELENON | c.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 |
1 | g.25809161C= | CA1159806181 | SELENON | c.701+11C= (n.701+11C=) c.770+11C= (n.770+11C=) c.872+11C= (n.872+11C=) | |
1 | g.25809161C>T | CA2644199771 | SELENON | c.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 |
1 | g.25809164_25809165del | CA2644199770 | SELENON | c.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 |
1 | g.25809163C>T | CA2580062608 | SELENON | c.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 |
1 | g.25809164dup | CA2839032282 | SELENON | c.701+14dup (n.701+14dup) c.770+14dup (n.770+14dup) c.872+14dup (n.872+14dup) | |
1 | g.25809165C>A | CA2580062609 | SELENON | c.701+15C>A (n.701+15C>A) c.770+15C>A (n.770+15C>A) c.872+15C>A (n.872+15C>A) | ClinVar |
1 | g.25809167G>A | CA696662 | SELENON | c.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 |
1 | g.25809167G= | CA1159806182 | SELENON | c.701+17G= (n.701+17G=) c.770+17G= (n.770+17G=) c.872+17G= (n.872+17G=) | |
1 | g.25809167G>T | CA2573132211 | SELENON | c.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 |
1 | g.25809168del | CA2843107341 | SELENON | c.701+18del (n.701+18del) c.770+18del (n.770+18del) c.872+18del (n.872+18del) | |
1 | g.25809168G>T | CA2644199772 | SELENON | c.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 |
1 | g.25809169C>T | CA2574271270 | SELENON | c.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 |
1 | g.25809170T>C | CA2843107342 | SELENON | c.701+20T>C (n.701+20T>C) c.770+20T>C (n.770+20T>C) c.872+20T>C (n.872+20T>C) | |
1 | g.25809173C>A | CA2843107343 | SELENON | c.701+23C>A (n.701+23C>A) c.770+23C>A (n.770+23C>A) c.872+23C>A (n.872+23C>A) | |
1 | g.25809173C= | CA1159806183 | SELENON | c.701+23C= (n.701+23C=) c.770+23C= (n.770+23C=) c.872+23C= (n.872+23C=) | |
1 | g.25809173C>T | CA521738358 | SELENON | c.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 |
1 | g.25809173_25809174insG | CA2644199773 | SELENON | c.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 |
1 | g.25809174C>A | CA2838205026 | SELENON | c.701+24C>A (n.701+24C>A) c.770+24C>A (n.770+24C>A) c.872+24C>A (n.872+24C>A) | |
1 | g.25809175T>C | CA1159806185 | SELENON | c.701+25T>C (n.701+25T>C) c.770+25T>C (n.770+25T>C) c.872+25T>C (n.872+25T>C) | dbSNP |
1 | g.25809175T>G | CA2644199774 | SELENON | c.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 |
1 | g.25809175T= | CA1159806184 | SELENON | c.701+25T= (n.701+25T=) c.770+25T= (n.770+25T=) c.872+25T= (n.872+25T=) | |
1 | g.25809176G>A | CA2843107345 | SELENON | c.701+26G>A (n.701+26G>A) c.770+26G>A (n.770+26G>A) c.872+26G>A (n.872+26G>A) | |
1 | g.25809176G>T | CA2644199775 | SELENON | c.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 |
1 | g.25809177del | CA2843107344 | SELENON | c.701+27del (n.701+27del) c.770+27del (n.770+27del) c.872+27del (n.872+27del) | |
1 | g.25809178del | CA2838198978 | SELENON | c.701+28del (n.701+28del) c.770+28del (n.770+28del) c.872+28del (n.872+28del) | |
1 | g.25809178A>G | CA2644199776 | SELENON | c.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 |
1 | g.25809179G>A | CA2644199777 | SELENON | c.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 |
1 | g.25809180C= | CA1159806186 | SELENON | c.701+30C= (n.701+30C=) c.770+30C= (n.770+30C=) c.872+30C= (n.872+30C=) | |
1 | g.25809180C>T | CA19698430 | SELENON | c.701+30C>T (n.701+30C>T) c.770+30C>T (n.770+30C>T) c.872+30C>T (n.872+30C>T) | dbSNP |
1 | g.25809182C>A | CA2644199778 | SELENON | c.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 |
1 | g.25809183C= | CA1143790738 | SELENON | c.701+33C= (n.701+33C=) c.770+33C= (n.770+33C=) c.872+33C= (n.872+33C=) | |
1 | g.25809183C>G | CA521738362 | SELENON | c.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 |
1 | g.25809183C>T | CA696663 | SELENON | c.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 |
1 | g.25809184G>A | CA696664 | SELENON | c.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 |
1 | g.25809184G= | CA1144147391 | SELENON | c.701+34G= (n.701+34G=) c.770+34G= (n.770+34G=) c.872+34G= (n.872+34G=) | |
1 | g.25809184G>T | CA2839032278 | SELENON | c.701+34G>T (n.701+34G>T) c.770+34G>T (n.770+34G>T) c.872+34G>T (n.872+34G>T) | |
1 | g.25809185G>A | CA2644199779 | SELENON | c.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 |
1 | g.25809185G>C | CA696665 | SELENON | c.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 |
1 | g.25809185G= | CA1159806187 | SELENON | c.701+35G= (n.701+35G=) c.770+35G= (n.770+35G=) c.872+35G= (n.872+35G=) | |
1 | g.25809185G>T | CA1159806188 | SELENON | c.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 |
1 | g.25809186G>T | CA2843107346 | SELENON | c.701+36G>T (n.701+36G>T) c.770+36G>T (n.770+36G>T) c.872+36G>T (n.872+36G>T) | |
1 | g.25809187G>A | CA2644199780 | SELENON | c.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 |
1 | g.25809188A= | CA1159806190 | SELENON | c.701+38A= (n.701+38A=) c.770+38A= (n.770+38A=) c.872+38A= (n.872+38A=) | |
1 | g.25809188A>G | CA1159806189 | SELENON | c.701+38A>G (n.701+38A>G) c.770+38A>G (n.770+38A>G) c.872+38A>G (n.872+38A>G) | dbSNP |
1 | g.25809190G>A | CA521738371 | SELENON | c.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 |
1 | g.25809190G= | CA1159806191 | SELENON | c.701+40G= (n.701+40G=) c.770+40G= (n.770+40G=) c.872+40G= (n.872+40G=) | |
1 | g.25809191C= | CA1159806192 | SELENON | c.701+41C= (n.701+41C=) c.770+41C= (n.770+41C=) c.872+41C= (n.872+41C=) | |
1 | g.25809191C>T | CA1159806193 | SELENON | c.701+41C>T (n.701+41C>T) c.770+41C>T (n.770+41C>T) c.872+41C>T (n.872+41C>T) | dbSNP |
1 | g.25809192A= | CA1159806194 | SELENON | c.701+42A= (n.701+42A=) c.770+42A= (n.770+42A=) c.872+42A= (n.872+42A=) | |
1 | g.25809192A>G | CA1159806195 | SELENON | c.701+42A>G (n.701+42A>G) c.770+42A>G (n.770+42A>G) c.872+42A>G (n.872+42A>G) | dbSNP |
1 | g.25809193T>C | CA1159806197 | SELENON | c.701+43T>C (n.701+43T>C) c.770+43T>C (n.770+43T>C) c.872+43T>C (n.872+43T>C) | dbSNP |
1 | g.25809193T= | CA1159806196 | SELENON | c.701+43T= (n.701+43T=) c.770+43T= (n.770+43T=) c.872+43T= (n.872+43T=) | |
1 | g.25809196C= | CA1143684974 | SELENON | c.701+46C= (n.701+46C=) c.770+46C= (n.770+46C=) c.872+46C= (n.872+46C=) | |
1 | g.25809196C>G | CA696666 | SELENON | c.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 |
1 | g.25809196C>T | CA19698433 | SELENON | c.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 |
1 | g.25809197G>A | CA696667 | SELENON | c.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 |
1 | g.25809197G= | CA1143202153 | SELENON | c.701+47G= (n.701+47G=) c.770+47G= (n.770+47G=) c.872+47G= (n.872+47G=) | |
1 | g.25809197G>T | CA2843107347 | SELENON | c.701+47G>T (n.701+47G>T) c.770+47G>T (n.770+47G>T) c.872+47G>T (n.872+47G>T) | |
1 | g.25809198G>T | CA2839032275 | SELENON | c.701+48G>T (n.701+48G>T) c.770+48G>T (n.770+48G>T) c.872+48G>T (n.872+48G>T) | |
1 | g.25809199T>C | CA2644199782 | SELENON | c.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 |
1 | g.25809199T>G | CA1159806199 | SELENON | c.701+49T>G (n.701+49T>G) c.770+49T>G (n.770+49T>G) c.872+49T>G (n.872+49T>G) | dbSNP |
1 | g.25809199T= | CA1159806198 | SELENON | c.701+49T= (n.701+49T=) c.770+49T= (n.770+49T=) c.872+49T= (n.872+49T=) | |
1 | g.25809199_25809200delinsTA | CA1159806200 | SELENON | c.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) | |
1 | g.25809200del | CA521738373 | SELENON | c.701+50del (n.701+50del) c.770+50del (n.770+50del) c.872+50del (n.872+50del) | dbSNP gnomAD v2 gnomAD v4 |
1 | g.25809201C>A | CA2839696482 | SELENON | c.701+51C>A (n.701+51C>A) c.770+51C>A (n.770+51C>A) c.872+51C>A (n.872+51C>A) | |
1 | g.25809201C>T | CA2644199783 | SELENON | c.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 |