Chr Mutation (hg38) CAid Gene Transcript Linkouts
4g.67740553T>ACA357047433GNRHRc.914A>T (p.Asn305Ile)
c.786A>T (n.786A>T)
c.*36A>T (n.*36A>T)
4g.67740553T>CCA357047435GNRHRc.914A>G (p.Asn305Ser)
c.786A>G (n.786A>G)
c.*36A>G (n.*36A>G)
4g.67740553T>GCA357047437GNRHRc.914A>C (p.Asn305Thr)
c.786A>C (n.786A>C)
c.*36A>C (n.*36A>C)
4g.67740554T>ACA2938840GNRHRc.913A>T (p.Asn305Tyr)
c.785A>T (n.785A>T)
c.*35A>T (n.*35A>T)
 dbSNP ExAC gnomAD v2 gnomAD v4
4g.67740554T>CCA357047439GNRHRc.913A>G (p.Asn305Asp)
c.785A>G (n.785A>G)
c.*35A>G (n.*35A>G)
 dbSNP gnomAD v3 gnomAD v4
4g.67740554T>GCA357047441GNRHRc.913A>C (p.Asn305His)
c.785A>C (n.785A>C)
c.*35A>C (n.*35A>C)
4g.67740554T=CA1465409059GNRHRc.913A= (p.Asn305=)
c.785A= (n.785A=)
c.*35A= (n.*35A=)
4g.67740555T>ACA439924248GNRHRc.912A>T (p.Val304=)
c.784A>T (n.784A>T)
c.*34A>T (n.*34A>T)
4g.67740555T>CCA439924251GNRHRc.912A>G (p.Val304=)
c.784A>G (n.784A>G)
c.*34A>G (n.*34A>G)
4g.67740555T>GCA439924258GNRHRc.912A>C (p.Val304=)
c.784A>C (n.784A>C)
c.*34A>C (n.*34A>C)
4g.67740556A>CCA357047445GNRHRc.911T>G (p.Val304Gly)
c.783T>G (n.783T>G)
c.*33T>G (n.*33T>G)
4g.67740556A>GCA357047446GNRHRc.911T>C (p.Val304Ala)
c.783T>C (n.783T>C)
c.*33T>C (n.*33T>C)
 gnomAD v4
4g.67740556A>TCA357047449GNRHRc.911T>A (p.Val304Glu)
c.783T>A (n.783T>A)
c.*33T>A (n.*33T>A)
4g.67740557C>ACA357047450GNRHRc.910G>T (p.Val304Leu)
c.782G>T (n.782G>T)
c.*32G>T (n.*32G>T)
4g.67740557C>GCA357047456GNRHRc.910G>C (p.Val304Leu)
c.782G>C (n.782G>C)
c.*32G>C (n.*32G>C)
 ClinVar
4g.67740557C>TCA357047457GNRHRc.910G>A (p.Val304Ile)
c.782G>A (n.782G>A)
c.*32G>A (n.*32G>A)
 gnomAD v4
4g.67740558T>ACA439924270GNRHRc.909A>T (p.Pro303=)
c.781A>T (n.781A>T)
c.*31A>T (n.*31A>T)
 dbSNP
4g.67740558T>CCA439924271GNRHRc.909A>G (p.Pro303=)
c.781A>G (n.781A>G)
c.*31A>G (n.*31A>G)
4g.67740558T>GCA439924272GNRHRc.909A>C (p.Pro303=)
c.781A>C (n.781A>C)
c.*31A>C (n.*31A>C)
 dbSNP gnomAD v2 gnomAD v4
4g.67740558T=CA1465409060GNRHRc.909A= (p.Pro303=)
c.781A= (n.781A=)
c.*31A= (n.*31A=)
4g.67740559G>ACA357047469GNRHRc.908C>T (p.Pro303Leu)
c.780C>T (n.780C>T)
c.*30C>T (n.*30C>T)
 gnomAD v4
4g.67740559G>CCA357047461GNRHRc.908C>G (p.Pro303Arg)
c.780C>G (n.780C>G)
c.*30C>G (n.*30C>G)
4g.67740559G=CA1465409061GNRHRc.908C= (p.Pro303=)
c.780C= (n.780C=)
c.*30C= (n.*30C=)
4g.67740559G>TCA357047463GNRHRc.908C>A (p.Pro303Gln)
c.780C>A (n.780C>A)
c.*30C>A (n.*30C>A)
 dbSNP gnomAD v2
4g.67740560G>ACA357047472GNRHRc.907C>T (p.Pro303Ser)
c.779C>T (n.779C>T)
c.*29C>T (n.*29C>T)
 gnomAD v4
4g.67740560G>CCA357047473GNRHRc.907C>G (p.Pro303Ala)
c.779C>G (n.779C>G)
c.*29C>G (n.*29C>G)
4g.67740560G>TCA357047475GNRHRc.907C>A (p.Pro303Thr)
c.779C>A (n.779C>A)
c.*29C>A (n.*29C>A)
4g.67740561G>ACA439924279GNRHRc.906C>T (p.Asp302=)
c.778C>T (n.778C>T)
c.*28C>T (n.*28C>T)
4g.67740561G>CCA357047477GNRHRc.906C>G (p.Asp302Glu)
c.778C>G (n.778C>G)
c.*28C>G (n.*28C>G)
4g.67740561G>TCA357047479GNRHRc.906C>A (p.Asp302Glu)
c.778C>A (n.778C>A)
c.*28C>A (n.*28C>A)
 gnomAD v4
4g.67740562T>ACA357047480GNRHRc.905A>T (p.Asp302Val)
c.777A>T (n.777A>T)
c.*27A>T (n.*27A>T)
4g.67740562T>CCA357047483GNRHRc.905A>G (p.Asp302Gly)
c.777A>G (n.777A>G)
c.*27A>G (n.*27A>G)
4g.67740562T>GCA357047485GNRHRc.905A>C (p.Asp302Ala)
c.777A>C (n.777A>C)
c.*27A>C (n.*27A>C)
 dbSNP gnomAD v3 gnomAD v4
4g.67740562T=CA1465409063GNRHRc.905A= (p.Asp302=)
c.777A= (n.777A=)
c.*27A= (n.*27A=)
4g.67740563C>ACA357047487GNRHRc.904G>T (p.Asp302Tyr)
c.776G>T (n.776G>T)
c.*26G>T (n.*26G>T)
4g.67740563C>GCA357047490GNRHRc.904G>C (p.Asp302His)
c.776G>C (n.776G>C)
c.*26G>C (n.*26G>C)
4g.67740563C>TCA357047491GNRHRc.904G>A (p.Asp302Asn)
c.776G>A (n.776G>A)
c.*26G>A (n.*26G>A)
4g.67740564T>ACA439924290GNRHRc.903A>T (p.Ser301=)
c.775A>T (n.775A>T)
c.*25A>T (n.*25A>T)
4g.67740564T>CCA2938841GNRHRc.903A>G (p.Ser301=)
c.775A>G (n.775A>G)
c.*25A>G (n.*25A>G)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.67740564T>GCA439924293GNRHRc.903A>C (p.Ser301=)
c.775A>C (n.775A>C)
c.*25A>C (n.*25A>C)
4g.67740564T=CA1465409064GNRHRc.903A= (p.Ser301=)
c.775A= (n.775A=)
c.*25A= (n.*25A=)
4g.67740565G>ACA357047496GNRHRc.902C>T (p.Ser301Leu)
c.774C>T (n.774C>T)
c.*24C>T (n.*24C>T)
4g.67740565G>CCA357047497GNRHRc.902C>G (p.Ser301Ter)
c.774C>G (n.774C>G)
c.*24C>G (n.*24C>G)
4g.67740565G>TCA357047495GNRHRc.902C>A (p.Ser301Ter)
c.774C>A (n.774C>A)
c.*24C>A (n.*24C>A)
4g.67740566A>CCA357047498GNRHRc.901T>G (p.Ser301Ala)
c.773T>G (n.773T>G)
c.*23T>G (n.*23T>G)
4g.67740566A>GCA357047500GNRHRc.901T>C (p.Ser301Pro)
c.773T>C (n.773T>C)
c.*23T>C (n.*23T>C)
4g.67740566A>TCA357047499GNRHRc.901T>A (p.Ser301Thr)
c.773T>A (n.773T>A)
c.*23T>A (n.*23T>A)
4g.67740567C>ACA357047501GNRHRc.900G>T (p.Leu300Phe)
c.772G>T (n.772G>T)
c.*22G>T (n.*22G>T)
4g.67740567C>GCA357047505GNRHRc.900G>C (p.Leu300Phe)
c.772G>C (n.772G>C)
c.*22G>C (n.*22G>C)
4g.67740567C>TCA439924302GNRHRc.900G>A (p.Leu300=)
c.772G>A (n.772G>A)
c.*22G>A (n.*22G>A)
 gnomAD v4
4g.67740568A>CCA357047507GNRHRc.899T>G (p.Leu300Trp)
c.771T>G (n.771T>G)
c.*21T>G (n.*21T>G)
4g.67740568A>GCA357047508GNRHRc.899T>C (p.Leu300Ser)
c.771T>C (n.771T>C)
c.*21T>C (n.*21T>C)
4g.67740568A>TCA357047510GNRHRc.899T>A (p.Leu300Ter)
c.771T>A (n.771T>A)
c.*21T>A (n.*21T>A)
4g.67740569A=CA1465409066GNRHRc.898T= (p.Leu300=)
c.770T= (n.770T=)
c.*20T= (n.*20T=)
4g.67740569A>CCA357047512GNRHRc.898T>G (p.Leu300Val)
c.770T>G (n.770T>G)
c.*20T>G (n.*20T>G)
 dbSNP
4g.67740569A>GCA2938842GNRHRc.898T>C (p.Leu300=)
c.770T>C (n.770T>C)
c.*20T>C (n.*20T>C)
 dbSNP ExAC gnomAD v2 gnomAD v4
4g.67740569A>TCA357047513GNRHRc.898T>A (p.Leu300Met)
c.770T>A (n.770T>A)
c.*20T>A (n.*20T>A)
 gnomAD v4
4g.67740570C>ACA357047514GNRHRc.897G>T (p.Arg299Ser)
c.769G>T (n.769G>T)
c.*19G>T (n.*19G>T)
4g.67740570C>GCA357047515GNRHRc.897G>C (p.Arg299Ser)
c.769G>C (n.769G>C)
c.*19G>C (n.*19G>C)
4g.67740570C>TCA439924309GNRHRc.897G>A (p.Arg299=)
c.769G>A (n.769G>A)
c.*19G>A (n.*19G>A)
 gnomAD v4
4g.67740571C>ACA357047522GNRHRc.896G>T (p.Arg299Met)
c.768G>T (n.768G>T)
c.*18G>T (n.*18G>T)
4g.67740571C>GCA357047519GNRHRc.896G>C (p.Arg299Thr)
c.768G>C (n.768G>C)
c.*18G>C (n.*18G>C)
 gnomAD v4
4g.67740571C>TCA357047517GNRHRc.896G>A (p.Arg299Lys)
c.768G>A (n.768G>A)
c.*18G>A (n.*18G>A)
4g.67740572T>ACA357047524GNRHRc.895A>T (p.Arg299Trp)
c.767A>T (n.767A>T)
c.*17A>T (n.*17A>T)
4g.67740572T>CCA357047526GNRHRc.895A>G (p.Arg299Gly)
c.767A>G (n.767A>G)
c.*17A>G (n.*17A>G)
4g.67740572T>GCA439924314GNRHRc.895A>C (p.Arg299=)
c.767A>C (n.767A>C)
c.*17A>C (n.*17A>C)
4g.67740573G>ACA98667532GNRHRc.894C>T (p.Asn298=)
c.766C>T (n.766C>T)
c.*16C>T (n.*16C>T)
 dbSNP gnomAD v3 gnomAD v4 COSMIC
4g.67740573G>CCA357047529GNRHRc.894C>G (p.Asn298Lys)
c.766C>G (n.766C>G)
c.*16C>G (n.*16C>G)
4g.67740573G=CA1465409068GNRHRc.894C= (p.Asn298=)
c.766C= (n.766C=)
c.*16C= (n.*16C=)
4g.67740573G>TCA357047531GNRHRc.894C>A (p.Asn298Lys)
c.766C>A (n.766C>A)
c.*16C>A (n.*16C>A)
4g.67740574T>ACA357047533GNRHRc.893A>T (p.Asn298Ile)
c.765A>T (n.765A>T)
c.*15A>T (n.*15A>T)
4g.67740574T>CCA357047534GNRHRc.893A>G (p.Asn298Ser)
c.765A>G (n.765A>G)
c.*15A>G (n.*15A>G)
4g.67740574T>GCA357047536GNRHRc.893A>C (p.Asn298Thr)
c.765A>C (n.765A>C)
c.*15A>C (n.*15A>C)
4g.67740576dupCA2938843GNRHRc.893dup (p.Asn298LysfsTer22)
c.765dup (n.765dup)
c.*15dup (n.*15dup)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.67740575T>ACA357047538GNRHRc.892A>T (p.Asn298Tyr)
c.764A>T (n.764A>T)
c.*14A>T (n.*14A>T)
4g.67740575T>CCA357047539GNRHRc.892A>G (p.Asn298Asp)
c.764A>G (n.764A>G)
c.*14A>G (n.*14A>G)
4g.67740575T>GCA357047540GNRHRc.892A>C (p.Asn298His)
c.764A>C (n.764A>C)
c.*14A>C (n.*14A>C)
4g.67740576T>ACA357047542GNRHRc.891A>T (p.Leu297Phe)
c.763A>T (n.763A>T)
c.*13A>T (n.*13A>T)
4g.67740576T>CCA439924324GNRHRc.891A>G (p.Leu297=)
c.763A>G (n.763A>G)
c.*13A>G (n.*13A>G)
4g.67740576T>GCA357047541GNRHRc.891A>C (p.Leu297Phe)
c.763A>C (n.763A>C)
c.*13A>C (n.*13A>C)
4g.67740577A>CCA357047544GNRHRc.890T>G (p.Leu297Ter)
c.762T>G (n.762T>G)
c.*12T>G (n.*12T>G)
4g.67740577A>GCA357047546GNRHRc.890T>C (p.Leu297Ser)
c.762T>C (n.762T>C)
c.*12T>C (n.*12T>C)
4g.67740577A>TCA357047547GNRHRc.890T>A (p.Leu297Ter)
c.762T>A (n.762T>A)
c.*12T>A (n.*12T>A)
4g.67740578A=CA1465409072GNRHRc.889T= (p.Leu297=)
c.761T= (n.761T=)
c.*11T= (n.*11T=)
4g.67740578A>CCA357047552GNRHRc.889T>G (p.Leu297Val)
c.761T>G (n.761T>G)
c.*11T>G (n.*11T>G)
4g.67740578A>GCA439924331GNRHRc.889T>C (p.Leu297=)
c.761T>C (n.761T>C)
c.*11T>C (n.*11T>C)
 dbSNP gnomAD v4
4g.67740578A>TCA357047553GNRHRc.889T>A (p.Leu297Ile)
c.761T>A (n.761T>A)
c.*11T>A (n.*11T>A)
4g.67740579C>ACA357047554GNRHRc.888G>T (p.Met296Ile)
c.760G>T (n.760G>T)
c.*10G>T (n.*10G>T)
4g.67740579C=CA1465409074GNRHRc.888G= (p.Met296=)
c.760G= (n.760G=)
c.*10G= (n.*10G=)
4g.67740579C>GCA357047555GNRHRc.888G>C (p.Met296Ile)
c.760G>C (n.760G>C)
c.*10G>C (n.*10G>C)
 ClinVar dbSNP gnomAD v4
4g.67740579C>TCA2938844GNRHRc.888G>A (p.Met296Ile)
c.760G>A (n.760G>A)
c.*10G>A (n.*10G>A)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.67740580A=CA1465409077GNRHRc.887T= (p.Met296=)
c.759T= (n.759T=)
c.*9T= (n.*9T=)
4g.67740580A>CCA357047556GNRHRc.887T>G (p.Met296Arg)
c.759T>G (n.759T>G)
c.*9T>G (n.*9T>G)
4g.67740580A>GCA357047557GNRHRc.887T>C (p.Met296Thr)
c.759T>C (n.759T>C)
c.*9T>C (n.*9T>C)
 gnomAD v4
4g.67740580A>TCA357047558GNRHRc.887T>A (p.Met296Lys)
c.759T>A (n.759T>A)
c.*9T>A (n.*9T>A)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.67740581T>ACA357047559GNRHRc.886A>T (p.Met296Leu)
c.758A>T (n.758A>T)
c.*8A>T (n.*8A>T)
4g.67740581T>CCA357047560GNRHRc.886A>G (p.Met296Val)
c.758A>G (n.758A>G)
c.*8A>G (n.*8A>G)
4g.67740581T>GCA357047561GNRHRc.886A>C (p.Met296Leu)
c.758A>C (n.758A>C)
c.*8A>C (n.*8A>C)
4g.67740582T>ACA357047562GNRHRc.885A>T (p.Glu295Asp)
c.757A>T (n.757A>T)
c.*7A>T (n.*7A>T)
4g.67740582T>CCA439924346GNRHRc.885A>G (p.Glu295=)
c.757A>G (n.757A>G)
c.*7A>G (n.*7A>G)
4g.67740582T>GCA357047563GNRHRc.885A>C (p.Glu295Asp)
c.757A>C (n.757A>C)
c.*7A>C (n.*7A>C)
4g.67740583T>ACA357047564GNRHRc.884A>T (p.Glu295Val)
c.756A>T (n.756A>T)
c.*6A>T (n.*6A>T)
4g.67740583T>CCA357047565GNRHRc.884A>G (p.Glu295Gly)
c.756A>G (n.756A>G)
c.*6A>G (n.*6A>G)
4g.67740583T>GCA357047566GNRHRc.884A>C (p.Glu295Ala)
c.756A>C (n.756A>C)
c.*6A>C (n.*6A>C)
4g.67740584C>ACA357047567GNRHRc.883G>T (p.Glu295Ter)
c.755G>T (n.755G>T)
c.*5G>T (n.*5G>T)
 COSMIC
4g.67740584C>GCA357047568GNRHRc.883G>C (p.Glu295Gln)
c.755G>C (n.755G>C)
c.*5G>C (n.*5G>C)
4g.67740584C>TCA357047569GNRHRc.883G>A (p.Glu295Lys)
c.755G>A (n.755G>A)
c.*5G>A (n.*5G>A)
4g.67740585A>CCA439924352GNRHRc.882T>G (p.Pro294=)
c.754T>G (n.754T>G)
c.*4T>G (n.*4T>G)
4g.67740585A>GCA439924353GNRHRc.882T>C (p.Pro294=)
c.754T>C (n.754T>C)
c.*4T>C (n.*4T>C)
 gnomAD v4
4g.67740585A>TCA439924355GNRHRc.882T>A (p.Pro294=)
c.754T>A (n.754T>A)
c.*4T>A (n.*4T>A)
4g.67740586G>ACA357047570GNRHRc.881C>T (p.Pro294Leu)
c.753C>T (n.753C>T)
c.*3C>T (n.*3C>T)
4g.67740586G>CCA357047571GNRHRc.881C>G (p.Pro294Arg)
c.753C>G (n.753C>G)
c.*3C>G (n.*3C>G)
4g.67740586G>TCA357047572GNRHRc.881C>A (p.Pro294His)
c.753C>A (n.753C>A)
c.*3C>A (n.*3C>A)
 gnomAD v4
4g.67740587G>ACA357047574GNRHRc.880C>T (p.Pro294Ser)
c.752C>T (n.752C>T)
c.*2C>T (n.*2C>T)
4g.67740587G>CCA357047578GNRHRc.880C>G (p.Pro294Ala)
c.752C>G (n.752C>G)
c.*2C>G (n.*2C>G)
4g.67740587G>TCA357047580GNRHRc.880C>A (p.Pro294Thr)
c.752C>A (n.752C>A)
c.*2C>A (n.*2C>A)
4g.67740588A=CA1465409080GNRHRc.879T= (p.Asp293=)
c.751T= (n.751T=)
c.*1T= (n.*1T=)
4g.67740588A>CCA357047582GNRHRc.879T>G (p.Asp293Glu)
c.751T>G (n.751T>G)
c.*1T>G (n.*1T>G)
4g.67740588A>GCA439924361GNRHRc.879T>C (p.Asp293=)
c.751T>C (n.751T>C)
c.*1T>C (n.*1T>C)
4g.67740588A>TCA357047584GNRHRc.879T>A (p.Asp293Glu)
c.751T>A (n.751T>A)
c.*1T>A (n.*1T>A)
 dbSNP gnomAD v2 gnomAD v4
4g.67740589T>ACA357047586GNRHRc.878A>T (p.Asp293Val)
c.750A>T (p.Ter250Cys)
4g.67740589T>CCA357047589GNRHRc.878A>G (p.Asp293Gly)
c.750A>G (p.Ter250Trp)
 gnomAD v4
4g.67740589T>GCA357047588GNRHRc.878A>C (p.Asp293Ala)
c.750A>C (p.Ter250Cys)
4g.67740590C>ACA357047594GNRHRc.877G>T (p.Asp293Tyr)
c.749G>T (p.Ter250Leu)
4g.67740590C>GCA357047597GNRHRc.877G>C (p.Asp293His)
c.749G>C (p.Ter250Ser)
4g.67740590C>TCA357047599GNRHRc.877G>A (p.Asp293Asn)
c.749G>A (p.Ter250=)
4g.67740591A>CCA357047601GNRHRc.876T>G (p.Phe292Leu)
c.748T>G (p.Ter250Gly)
4g.67740591A>GCA357047603GNRHRc.876T>C (p.Phe292=)
c.748T>C (p.Ter250Arg)
4g.67740591A>TCA357047605GNRHRc.876T>A (p.Phe292Leu)
c.748T>A (p.Ter250Arg)
4g.67740592A>CCA357047614GNRHRc.875T>G (p.Phe292Cys)
c.747T>G (p.Val249=)
4g.67740592A>GCA357047612GNRHRc.875T>C (p.Phe292Ser)
c.747T>C (p.Val249=)
4g.67740592A>TCA357047608GNRHRc.875T>A (p.Phe292Tyr)
c.747T>A (p.Val249=)
4g.67740593A>CCA357047618GNRHRc.874T>G (p.Phe292Val)
c.746T>G (p.Val249Gly)
4g.67740593A>GCA357047619GNRHRc.874T>C (p.Phe292Leu)
c.746T>C (p.Val249Ala)
4g.67740593A>TCA357047621GNRHRc.874T>A (p.Phe292Ile)
c.746T>A (p.Val249Asp)
4g.67740594C>ACA357047625GNRHRc.873G>T (p.Trp291Cys)
c.745G>T (p.Val249Phe)
4g.67740594C>GCA357047627GNRHRc.873G>C (p.Trp291Cys)
c.745G>C (p.Val249Leu)
4g.67740594C>TCA357047628GNRHRc.873G>A (p.Trp291Ter)
c.745G>A (p.Val249Ile)
4g.67740595C>ACA357047629GNRHRc.872G>T (p.Trp291Leu)
c.744G>T (p.Leu248Phe)
 dbSNP gnomAD v2 gnomAD v4
4g.67740595C=CA1465409084GNRHRc.872G= (p.Trp291=)
c.744G= (p.Leu248=)
4g.67740595C>GCA2938845GNRHRc.872G>C (p.Trp291Ser)
c.744G>C (p.Leu248Phe)
 dbSNP ExAC gnomAD v2 gnomAD v4
4g.67740595C>TCA357047631GNRHRc.872G>A (p.Trp291Ter)
c.744G>A (p.Leu248=)
 COSMIC
4g.67740596A>CCA357047634GNRHRc.871T>G (p.Trp291Gly)
c.743T>G (p.Leu248Trp)
4g.67740596A>GCA357047635GNRHRc.871T>C (p.Trp291Arg)
c.743T>C (p.Leu248Ser)
4g.67740596A>TCA357047636GNRHRc.871T>A (p.Trp291Arg)
c.743T>A (p.Leu248Ter)
4g.67740597A=CA1465409086GNRHRc.870T= (p.Tyr290=)
c.742T= (p.Leu248=)
4g.67740597A>CCA357047638GNRHRc.870T>G (p.Tyr290Ter)
c.742T>G (p.Leu248Val)
4g.67740597A>GCA439924385GNRHRc.870T>C (p.Tyr290=)
c.742T>C (p.Leu248=)
 dbSNP gnomAD v4
4g.67740597A>TCA357047640GNRHRc.870T>A (p.Tyr290Ter)
c.742T>A (p.Leu248Met)
4g.67740598T>ACA357047642GNRHRc.869A>T (p.Tyr290Phe)
c.741A>T (p.Val247=)
4g.67740598T>CCA357047643GNRHRc.869A>G (p.Tyr290Cys)
c.741A>G (p.Val247=)
4g.67740598T>GCA357047645GNRHRc.869A>C (p.Tyr290Ser)
c.741A>C (p.Val247=)
4g.67740599A=CA1465409088GNRHRc.868T= (p.Tyr290=)
c.740T= (p.Val247=)
4g.67740599A>CCA357047647GNRHRc.868T>G (p.Tyr290Asp)
c.740T>G (p.Val247Gly)
4g.67740599A>GCA357047648GNRHRc.868T>C (p.Tyr290His)
c.740T>C (p.Val247Ala)
 ClinVar dbSNP gnomAD v4
4g.67740599A>TCA357047650GNRHRc.868T>A (p.Tyr290Asn)
c.740T>A (p.Val247Glu)
4g.67740600C>ACA357047652GNRHRc.867G>T (p.Trp289Cys)
c.739G>T (p.Val247Leu)
4g.67740600C>GCA357047655GNRHRc.867G>C (p.Trp289Cys)
c.739G>C (p.Val247Leu)
4g.67740600C>TCA357047654GNRHRc.867G>A (p.Trp289Ter)
c.739G>A (p.Val247Ile)
 gnomAD v4 COSMIC
4g.67740601C>ACA357047657GNRHRc.866G>T (p.Trp289Leu)
c.738G>T (p.Leu246Phe)
4g.67740601C>GCA357047659GNRHRc.866G>C (p.Trp289Ser)
c.738G>C (p.Leu246Phe)
4g.67740601C>TCA357047660GNRHRc.866G>A (p.Trp289Ter)
c.738G>A (p.Leu246=)
 COSMIC
4g.67740602A>CCA357047662GNRHRc.865T>G (p.Trp289Gly)
c.737T>G (p.Leu246Trp)
4g.67740602A>GCA357047664GNRHRc.865T>C (p.Trp289Arg)
c.737T>C (p.Leu246Ser)
4g.67740602A>TCA357047665GNRHRc.865T>A (p.Trp289Arg)
c.737T>A (p.Leu246Ter)
4g.67740603A>CCA357047667GNRHRc.864T>G (p.Ile288Met)
c.736T>G (p.Leu246Val)
4g.67740603A>GCA439924400GNRHRc.864T>C (p.Ile288=)
c.736T>C (p.Leu246=)
4g.67740603A>TCA357047669GNRHRc.864T>A (p.Ile288=)
c.736T>A (p.Leu246Met)
4g.67740604A=CA1465409089GNRHRc.863T= (p.Ile288=)
c.735T= (p.Asn245=)
4g.67740604A>CCA357047671GNRHRc.863T>G (p.Ile288Ser)
c.735T>G (p.Asn245Lys)
4g.67740604A>GCA357047672GNRHRc.863T>C (p.Ile288Thr)
c.735T>C (p.Asn245=)
4g.67740604A>TCA357047674GNRHRc.863T>A (p.Ile288Asn)
c.735T>A (p.Asn245Lys)
 dbSNP gnomAD v2 gnomAD v4
4g.67740605T>ACA357047681GNRHRc.862A>T (p.Ile288Phe)
c.734A>T (p.Asn245Ile)
4g.67740605T>CCA357047679GNRHRc.862A>G (p.Ile288Val)
c.734A>G (p.Asn245Ser)
4g.67740605T>GCA357047676GNRHRc.862A>C (p.Ile288Leu)
c.734A>C (p.Asn245Thr)
4g.67740606T>ACA357047684GNRHRc.861A>T (p.Gly287=)
c.733A>T (p.Asn245Tyr)
4g.67740606T>CCA357047685GNRHRc.861A>G (p.Gly287=)
c.733A>G (p.Asn245Asp)
4g.67740606T>GCA357047688GNRHRc.861A>C (p.Gly287=)
c.733A>C (p.Asn245His)
 gnomAD v4
4g.67740607C>ACA357047691GNRHRc.860G>T (p.Gly287Val)
c.732G>T (p.Arg244Ser)
4g.67740607C=CA1465409091GNRHRc.860G= (p.Gly287=)
c.732G= (p.Arg244=)
4g.67740607C>GCA357047694GNRHRc.860G>C (p.Gly287Ala)
c.732G>C (p.Arg244Ser)
4g.67740607C>TCA2938846GNRHRc.860G>A (p.Gly287Glu)
c.732G>A (p.Arg244=)
 dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
4g.67740608C>ACA357047700GNRHRc.859G>T (p.Gly287Ter)
c.731G>T (p.Arg244Met)
4g.67740608C>GCA357047702GNRHRc.859G>C (p.Gly287Arg)
c.731G>C (p.Arg244Thr)
4g.67740608C>TCA357047704GNRHRc.859G>A (p.Gly287Arg)
c.731G>A (p.Arg244Lys)
4g.67740609T>ACA357047707GNRHRc.858A>T (p.Leu286=)
c.730A>T (p.Arg244Trp)
4g.67740609T>CCA357047708GNRHRc.858A>G (p.Leu286=)
c.730A>G (p.Arg244Gly)
4g.67740609T>GCA439924415GNRHRc.858A>C (p.Leu286=)
c.730A>C (p.Arg244=)
 dbSNP gnomAD v4
4g.67740609T=CA1465409094GNRHRc.858A= (p.Leu286=)
c.730A= (p.Arg244=)
4g.67740610A=CA1465409099GNRHRc.857T= (p.Leu286=)
c.729T= (p.Pro243=)
4g.67740610A>CCA357047716GNRHRc.857T>G (p.Leu286Arg)
c.729T>G (p.Pro243=)
4g.67740610A>GCA98667545GNRHRc.857T>C (p.Leu286Pro)
c.729T>C (p.Pro243=)
 dbSNP gnomAD v4
4g.67740610A>TCA357047712GNRHRc.857T>A (p.Leu286Gln)
c.729T>A (p.Pro243=)
4g.67740611G>ACA357047727GNRHRc.856C>T (p.Leu286=)
c.728C>T (p.Pro243Leu)
4g.67740611G>CCA357047730GNRHRc.856C>G (p.Leu286Val)
c.728C>G (p.Pro243Arg)
4g.67740611G>TCA357047728GNRHRc.856C>A (p.Leu286Ile)
c.728C>A (p.Pro243His)
4g.67740612G>ACA357047732GNRHRc.855C>T (p.Val285=)
c.727C>T (p.Pro243Ser)
 gnomAD v4 COSMIC
4g.67740612G>CCA357047735GNRHRc.855C>G (p.Val285=)
c.727C>G (p.Pro243Ala)
 dbSNP gnomAD v4
4g.67740612G=CA1465409102GNRHRc.855C= (p.Val285=)
c.727C= (p.Pro243=)
4g.67740612G>TCA357047737GNRHRc.855C>A (p.Val285=)
c.727C>A (p.Pro243Thr)
4g.67740613A>CCA357047739GNRHRc.854T>G (p.Val285Gly)
c.726T>G (p.Cys242Trp)
4g.67740613A>GCA357047741GNRHRc.854T>C (p.Val285Ala)
c.726T>C (p.Cys242=)
 gnomAD v4
4g.67740613A>TCA357047743GNRHRc.854T>A (p.Val285Asp)
c.726T>A (p.Cys242Ter)
4g.67740614C>ACA357047747GNRHRc.853G>T (p.Val285Phe)
c.725G>T (p.Cys242Phe)
4g.67740614C>GCA357047749GNRHRc.853G>C (p.Val285Leu)
c.725G>C (p.Cys242Ser)
4g.67740614C>TCA357047752GNRHRc.853G>A (p.Val285Ile)
c.725G>A (p.Cys242Tyr)
4g.67740615A>CCA357047754GNRHRc.852T>G (p.Tyr284Ter)
c.724T>G (p.Cys242Gly)
4g.67740615A>GCA357047756GNRHRc.852T>C (p.Tyr284=)
c.724T>C (p.Cys242Arg)
 dbSNP gnomAD v4
4g.67740615A>TCA357047758GNRHRc.852T>A (p.Tyr284Ter)
c.724T>A (p.Cys242Ser)
4g.67740616T>ACA357047766GNRHRc.851A>T (p.Tyr284Phe)
c.723A>T (p.Leu241=)
4g.67740616T>CCA130201GNRHRc.851A>G (p.Tyr284Cys)
c.723A>G (p.Leu241=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.67740616T>GCA357047764GNRHRc.851A>C (p.Tyr284Ser)
c.723A>C (p.Leu241=)
4g.67740616T=CA1465409107GNRHRc.851A= (p.Tyr284=)
c.723A= (p.Leu241=)
4g.67740617A>CCA357047769GNRHRc.850T>G (p.Tyr284Asp)
c.722T>G (p.Leu241Arg)
4g.67740617A>GCA357047772GNRHRc.850T>C (p.Tyr284His)
c.722T>C (p.Leu241Pro)
4g.67740617A>TCA357047774GNRHRc.850T>A (p.Tyr284Asn)
c.722T>A (p.Leu241Gln)
4g.67740618G>ACA439924438GNRHRc.849C>T (p.Tyr283=)
c.721C>T (p.Leu241=)
4g.67740618G>CCA2938847GNRHRc.849C>G (p.Tyr283Ter)
c.721C>G (p.Leu241Val)
 dbSNP ExAC gnomAD v2 gnomAD v4
4g.67740618G=CA1465409111GNRHRc.849C= (p.Tyr283=)
c.721C= (p.Leu241=)
4g.67740618G>TCA357047777GNRHRc.849C>A (p.Tyr283Ter)
c.721C>A (p.Leu241Ile)
4g.67740619T>ACA357047781GNRHRc.848A>T (p.Tyr283Phe)
c.720A>T (p.Leu240=)
4g.67740619T>CCA357047784GNRHRc.848A>G (p.Tyr283Cys)
c.720A>G (p.Leu240=)
4g.67740619T>GCA357047786GNRHRc.848A>C (p.Tyr283Ser)
c.720A>C (p.Leu240=)
 ClinVar
4g.67740620A=CA1465409113GNRHRc.847T= (p.Tyr283=)
c.719T= (p.Leu240=)
4g.67740620A>CCA357047790GNRHRc.847T>G (p.Tyr283Asp)
c.719T>G (p.Leu240Arg)
4g.67740620A>GCA357047792GNRHRc.847T>C (p.Tyr283His)
c.719T>C (p.Leu240Pro)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.67740620A>TCA357047794GNRHRc.847T>A (p.Tyr283Asn)
c.719T>A (p.Leu240Gln)
4g.67740621G>ACA439924446GNRHRc.846C>T (p.Pro282=)
c.718C>T (p.Leu240=)
 gnomAD v4
4g.67740621G>CCA357047797GNRHRc.846C>G (p.Pro282=)
c.718C>G (p.Leu240Val)
4g.67740621G>TCA357047795GNRHRc.846C>A (p.Pro282=)
c.718C>A (p.Leu240Ile)
4g.67740622G>ACA357047799GNRHRc.845C>T (p.Pro282Leu)
c.717C>T (p.Ser239=)
 ClinVar dbSNP gnomAD v2 gnomAD v4
4g.67740622G>CCA357047800GNRHRc.845C>G (p.Pro282Arg)
c.717C>G (p.Ser239=)
4g.67740622G=CA1465409114GNRHRc.845C= (p.Pro282=)
c.717C= (p.Ser239=)
4g.67740622G>TCA357047803GNRHRc.845C>A (p.Pro282His)
c.717C>A (p.Ser239=)
4g.67740623G>ACA357047806GNRHRc.844C>T (p.Pro282Ser)
c.716C>T (p.Ser239Phe)
4g.67740623G>CCA357047808GNRHRc.844C>G (p.Pro282Ala)
c.716C>G (p.Ser239Cys)
 gnomAD v4
4g.67740623G>TCA357047811GNRHRc.844C>A (p.Pro282Thr)
c.716C>A (p.Ser239Tyr)
4g.67740624A>CCA357047813GNRHRc.843T>G (p.Thr281=)
c.715T>G (p.Ser239Ala)
4g.67740624A>GCA357047815GNRHRc.843T>C (p.Thr281=)
c.715T>C (p.Ser239Pro)
4g.67740624A>TCA357047818GNRHRc.843T>A (p.Thr281=)
c.715T>A (p.Ser239Thr)
4g.67740625G>ACA269458GNRHRc.842C>T (p.Thr281Ile)
c.714C>T (p.Asp238=)
 ClinVar dbSNP
4g.67740625G>CCA357047823GNRHRc.842C>G (p.Thr281Ser)
c.714C>G (p.Asp238Glu)
4g.67740625G=CA1465409118GNRHRc.842C= (p.Thr281=)
c.714C= (p.Asp238=)
4g.67740625G>TCA357047825GNRHRc.842C>A (p.Thr281Asn)
c.714C>A (p.Asp238Glu)
4g.67740626T>ACA357047831GNRHRc.841A>T (p.Thr281Ser)
c.713A>T (p.Asp238Val)
4g.67740626T>CCA357047833GNRHRc.841A>G (p.Thr281Ala)
c.713A>G (p.Asp238Gly)
4g.67740626T>GCA357047828GNRHRc.841A>C (p.Thr281Pro)
c.713A>C (p.Asp238Ala)
4g.67740627C>ACA357047836GNRHRc.840G>T (p.Trp280Cys)
c.712G>T (p.Asp238Tyr)
 dbSNP
4g.67740627C=CA1465409126GNRHRc.840G= (p.Trp280=)
c.712G= (p.Asp238=)
4g.67740627C>GCA357047839GNRHRc.840G>C (p.Trp280Cys)
c.712G>C (p.Asp238His)
 ClinVar
4g.67740627C>TCA357047842GNRHRc.840G>A (p.Trp280Ter)
c.712G>A (p.Asp238Asn)
4g.67740628C>ACA357047846GNRHRc.839G>T (p.Trp280Leu)
c.711G>T (p.Leu237=)
4g.67740628C>GCA357047849GNRHRc.839G>C (p.Trp280Ser)
c.711G>C (p.Leu237=)
4g.67740628C>TCA357047853GNRHRc.839G>A (p.Trp280Ter)
c.711G>A (p.Leu237=)
4g.67740629A>CCA357047856GNRHRc.838T>G (p.Trp280Gly)
c.710T>G (p.Leu237Arg)
4g.67740629A>GCA357047860GNRHRc.838T>C (p.Trp280Arg)
c.710T>C (p.Leu237Pro)
 gnomAD v4
4g.67740629A>TCA357047859GNRHRc.838T>A (p.Trp280Arg)
c.710T>A (p.Leu237Gln)
4g.67740630G>ACA439924469GNRHRc.837C>T (p.Cys279=)
c.709C>T (p.Leu237=)
 COSMIC
4g.67740630G>CCA357047864GNRHRc.837C>G (p.Cys279Trp)
c.709C>G (p.Leu237Val)
4g.67740630G>TCA357047866GNRHRc.837C>A (p.Cys279Ter)
c.709C>A (p.Leu237Met)
4g.67740631C>ACA357047869GNRHRc.836G>T (p.Cys279Phe)
c.708G>T (p.Leu236=)
 dbSNP gnomAD v3 gnomAD v4
4g.67740631C=CA1465409128GNRHRc.836G= (p.Cys279=)
c.708G= (p.Leu236=)
4g.67740631C>GCA357047872GNRHRc.836G>C (p.Cys279Ser)
c.708G>C (p.Leu236=)
4g.67740631C>TCA2938848GNRHRc.836G>A (p.Cys279Tyr)
c.708G>A (p.Leu236=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.67740632A=CA1465409130GNRHRc.835T= (p.Cys279=)
c.707T= (p.Leu236=)
4g.67740632A>CCA357047879GNRHRc.835T>G (p.Cys279Gly)
c.707T>G (p.Leu236Arg)
4g.67740632A>GCA357047881GNRHRc.835T>C (p.Cys279Arg)
c.707T>C (p.Leu236Pro)
 dbSNP gnomAD v2 gnomAD v4
4g.67740632A>TCA357047876GNRHRc.835T>A (p.Cys279Ser)
c.707T>A (p.Leu236Gln)
4g.67740633G>ACA439924480GNRHRc.834C>T (p.Val278=)
c.706C>T (p.Leu236=)
 gnomAD v4
4g.67740633G>CCA357047885GNRHRc.834C>G (p.Val278=)
c.706C>G (p.Leu236Val)
4g.67740633G>TCA357047883GNRHRc.834C>A (p.Val278=)
c.706C>A (p.Leu236Met)
 gnomAD v4
4g.67740634A=CA1465409132GNRHRc.833T= (p.Val278=)
c.705T= (p.Cys235=)
4g.67740634A>CCA357047890GNRHRc.833T>G (p.Val278Gly)
c.705T>G (p.Cys235Trp)
4g.67740634A>GCA357047888GNRHRc.833T>C (p.Val278Ala)
c.705T>C (p.Cys235=)
 dbSNP
4g.67740634A>TCA357047892GNRHRc.833T>A (p.Val278Asp)
c.705T>A (p.Cys235Ter)
4g.67740635C>ACA357047896GNRHRc.832G>T (p.Val278Phe)
c.704G>T (p.Cys235Phe)
4g.67740635C=CA1465409135GNRHRc.832G= (p.Val278=)
c.704G= (p.Cys235=)
4g.67740635C>GCA357047899GNRHRc.832G>C (p.Val278Leu)
c.704G>C (p.Cys235Ser)
4g.67740635C>TCA357047902GNRHRc.832G>A (p.Val278Ile)
c.704G>A (p.Cys235Tyr)
 dbSNP gnomAD v3 gnomAD v4
4g.67740636A>CCA357047906GNRHRc.831T>G (p.Thr277=)
c.703T>G (p.Cys235Gly)
4g.67740636A>GCA357047910GNRHRc.831T>C (p.Thr277=)
c.703T>C (p.Cys235Arg)
4g.67740636A>TCA357047911GNRHRc.831T>A (p.Thr277=)
c.703T>A (p.Cys235Ser)
4g.67740637G>ACA357047913GNRHRc.830C>T (p.Thr277Ile)
c.702C>T (p.Tyr234=)
4g.67740637G>CCA357047915GNRHRc.830C>G (p.Thr277Ser)
c.702C>G (p.Tyr234Ter)
4g.67740637G>TCA357047918GNRHRc.830C>A (p.Thr277Asn)
c.702C>A (p.Tyr234Ter)
4g.67740638T>ACA357047928GNRHRc.829A>T (p.Thr277Ser)
c.701A>T (p.Tyr234Phe)
4g.67740638T>CCA357047931GNRHRc.829A>G (p.Thr277Ala)
c.701A>G (p.Tyr234Cys)
 gnomAD v4
4g.67740638T>GCA357047933GNRHRc.829A>C (p.Thr277Pro)
c.701A>C (p.Tyr234Ser)
4g.67740639A>CCA357047936GNRHRc.828T>G (p.Phe276Leu)
c.700T>G (p.Tyr234Asp)
4g.67740639A>GCA357047941GNRHRc.828T>C (p.Phe276=)
c.700T>C (p.Tyr234His)
4g.67740639A>TCA357047939GNRHRc.828T>A (p.Phe276Leu)
c.700T>A (p.Tyr234Asn)
4g.67740640A>CCA357047945GNRHRc.827T>G (p.Phe276Cys)
c.699T>G (p.Ile233Met)
 gnomAD v4
4g.67740640A>GCA357047947GNRHRc.827T>C (p.Phe276Ser)
c.699T>C (p.Ile233=)
 gnomAD v4
4g.67740640A>TCA357047950GNRHRc.827T>A (p.Phe276Tyr)
c.699T>A (p.Ile233=)
4g.67740641A>CCA357047952GNRHRc.826T>G (p.Phe276Val)
c.698T>G (p.Ile233Ser)
4g.67740641A>GCA357047955GNRHRc.826T>C (p.Phe276Leu)
c.698T>C (p.Ile233Thr)
4g.67740641A>TCA357047957GNRHRc.826T>A (p.Phe276Ile)
c.698T>A (p.Ile233Asn)
4g.67740642T>ACA357047960GNRHRc.825A>T (p.Ser275=)
c.697A>T (p.Ile233Phe)
4g.67740642T>CCA357047963GNRHRc.825A>G (p.Ser275=)
c.697A>G (p.Ile233Val)
 gnomAD v4
4g.67740642T>GCA357047965GNRHRc.825A>C (p.Ser275=)
c.697A>C (p.Ile233Leu)
4g.67740643G>ACA357047972GNRHRc.824C>T (p.Ser275Leu)
c.696C>T (p.Phe232=)
 gnomAD v4
4g.67740643G>CCA357047974GNRHRc.824C>G (p.Ser275Ter)
c.696C>G (p.Phe232Leu)
4g.67740643G>TCA357047970GNRHRc.824C>A (p.Ser275Ter)
c.696C>A (p.Phe232Leu)
4g.67740644A>CCA357047976GNRHRc.823T>G (p.Ser275Ala)
c.695T>G (p.Phe232Cys)
4g.67740644A>GCA357047978GNRHRc.823T>C (p.Ser275Pro)
c.695T>C (p.Phe232Ser)
4g.67740644A>TCA357047981GNRHRc.823T>A (p.Ser275Thr)
c.695T>A (p.Phe232Tyr)
4g.67740644_67740645insGCA98667552GNRHRc.822_823insC (p.Ser275LeufsTer19)
c.694_695insC (p.Phe232SerfsTer13)
4g.67740645A=CA1465409138GNRHRc.822T= (p.Thr274=)
c.694T= (p.Phe232=)
4g.67740645A>CCA357047990GNRHRc.822T>G (p.Thr274=)
c.694T>G (p.Phe232Val)
4g.67740645A>GCA357047987GNRHRc.822T>C (p.Thr274=)
c.694T>C (p.Phe232Leu)
4g.67740645A>TCA357047984GNRHRc.822T>A (p.Thr274=)
c.694T>A (p.Phe232Ile)
4g.67740646G>ACA357047993GNRHRc.821C>T (p.Thr274Ile)
c.693C>T (p.His231=)
4g.67740646G>CCA357047995GNRHRc.821C>G (p.Thr274Ser)
c.693C>G (p.His231Gln)
4g.67740646G>TCA357047998GNRHRc.821C>A (p.Thr274Asn)
c.693C>A (p.His231Gln)
 gnomAD v4
4g.67740646dupCA797693718GNRHRc.821dup (p.Ser275PhefsTer19)
c.693dup (p.Phe232LeufsTer13)
 dbSNP
4g.67740647T>ACA357048002GNRHRc.820A>T (p.Thr274Ser)
c.692A>T (p.His231Leu)
4g.67740647T>CCA357048005GNRHRc.820A>G (p.Thr274Ala)
c.692A>G (p.His231Arg)
 ClinVar dbSNP gnomAD v4
4g.67740647T>GCA357048007GNRHRc.820A>C (p.Thr274Pro)
c.692A>C (p.His231Pro)
4g.67740647T=CA1465409143GNRHRc.820A= (p.Thr274=)
c.692A= (p.His231=)
4g.67740648G>ACA357048010GNRHRc.819C>T (p.Ala273=)
c.691C>T (p.His231Tyr)
4g.67740648G>CCA357048016GNRHRc.819C>G (p.Ala273=)
c.691C>G (p.His231Asp)
4g.67740648G>TCA357048015GNRHRc.819C>A (p.Ala273=)
c.691C>A (p.His231Asn)
4g.67740649G>ACA357048018GNRHRc.818C>T (p.Ala273Val)
c.690C>T (p.Cys230=)
 gnomAD v4
4g.67740649G>CCA357048020GNRHRc.818C>G (p.Ala273Gly)
c.690C>G (p.Cys230Trp)
4g.67740649G>TCA357048024GNRHRc.818C>A (p.Ala273Asp)
c.690C>A (p.Cys230Ter)
 gnomAD v4
4g.67740650C>ACA357048027GNRHRc.817G>T (p.Ala273Ser)
c.689G>T (p.Cys230Phe)
 gnomAD v4
4g.67740650C>GCA357048028GNRHRc.817G>C (p.Ala273Pro)
c.689G>C (p.Cys230Ser)
4g.67740650C>TCA357048031GNRHRc.817G>A (p.Ala273Thr)
c.689G>A (p.Cys230Tyr)
4g.67740651A>CCA357048034GNRHRc.816T>G (p.Phe272Leu)
c.688T>G (p.Cys230Gly)
4g.67740651A>GCA357048037GNRHRc.816T>C (p.Phe272=)
c.688T>C (p.Cys230Arg)
4g.67740651A>TCA357048039GNRHRc.816T>A (p.Phe272Leu)
c.688T>A (p.Cys230Ser)
 gnomAD v4
4g.67740652A>CCA357048042GNRHRc.815T>G (p.Phe272Cys)
c.687T>G (p.Ile229Met)
4g.67740652A>GCA357048045GNRHRc.815T>C (p.Phe272Ser)
c.687T>C (p.Ile229=)
4g.67740652A>TCA357048055GNRHRc.815T>A (p.Phe272Tyr)
c.687T>A (p.Ile229=)
4g.67740653A>CCA357048063GNRHRc.814T>G (p.Phe272Val)
c.686T>G (p.Ile229Ser)
4g.67740653A>GCA357048066GNRHRc.814T>C (p.Phe272Leu)
c.686T>C (p.Ile229Thr)
4g.67740653A>TCA357048062GNRHRc.814T>A (p.Phe272Ile)
c.686T>A (p.Ile229Asn)

Number of alleles fetched