Chr Mutation (hg38) CAid Gene Transcript Linkouts
4g.67740682C>ACA357048322GNRHRc.785G>T (p.Arg262Leu)
c.657G>T (p.Thr219=)
4g.67740682C=CA1465409209GNRHRc.785G= (p.Arg262=)
c.657G= (p.Thr219=)
4g.67740682C>GCA357048329GNRHRc.785G>C (p.Arg262Pro)
c.657G>C (p.Thr219=)
4g.67740682C>TCA130198GNRHRc.785G>A (p.Arg262Gln)
c.657G>A (p.Thr219=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.67740683G>ACA2938854GNRHRc.784C>T (p.Arg262Trp)
c.656C>T (p.Thr219Met)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
4g.67740683G>CCA357048331GNRHRc.784C>G (p.Arg262Gly)
c.656C>G (p.Thr219Arg)
4g.67740683G=CA1465409214GNRHRc.784C= (p.Arg262=)
c.656C= (p.Thr219=)
4g.67740683G>TCA357048334GNRHRc.784C>A (p.Arg262=)
c.656C>A (p.Thr219Lys)
 gnomAD v4
4g.67740684T>ACA357048337GNRHRc.783A>T (p.Ala261=)
c.655A>T (p.Thr219Ser)
 dbSNP gnomAD v2 gnomAD v4
4g.67740684T>CCA357048339GNRHRc.783A>G (p.Ala261=)
c.655A>G (p.Thr219Ala)
 ClinVar dbSNP
4g.67740684T>GCA357048344GNRHRc.783A>C (p.Ala261=)
c.655A>C (p.Thr219Pro)
 gnomAD v4
4g.67740684T=CA1465409218GNRHRc.783A= (p.Ala261=)
c.655A= (p.Thr219=)
4g.67740685G>ACA357048348GNRHRc.782C>T (p.Ala261Val)
c.654C>T (p.Ser218=)
 gnomAD v4
4g.67740685G>CCA357048356GNRHRc.782C>G (p.Ala261Gly)
c.654C>G (p.Ser218Arg)
 dbSNP
4g.67740685G=CA1465409226GNRHRc.782C= (p.Ala261=)
c.654C= (p.Ser218=)
4g.67740685G>TCA357048349GNRHRc.782C>A (p.Ala261Glu)
c.654C>A (p.Ser218Arg)
4g.67740686delCA2670819809GNRHRc.781del (p.Ala261HisfsTer3)
c.653del (p.Ser218ThrfsTer?)
 gnomAD v4
4g.67740686C>ACA357048361GNRHRc.781G>T (p.Ala261Ser)
c.653G>T (p.Ser218Ile)
4g.67740686C>GCA357048363GNRHRc.781G>C (p.Ala261Pro)
c.653G>C (p.Ser218Thr)
4g.67740686C>TCA357048366GNRHRc.781G>A (p.Ala261Thr)
c.653G>A (p.Ser218Asn)
4g.67740687T>ACA357048368GNRHRc.780A>T (p.Arg260Ser)
c.652A>T (p.Ser218Cys)
4g.67740687T>CCA357048371GNRHRc.780A>G (p.Arg260=)
c.652A>G (p.Ser218Gly)
4g.67740687T>GCA357048375GNRHRc.780A>C (p.Arg260Ser)
c.652A>C (p.Ser218Arg)
4g.67740688C>ACA357048383GNRHRc.779G>T (p.Arg260Ile)
c.651G>T (p.Lys217Asn)
4g.67740688C=CA1465409229GNRHRc.779G= (p.Arg260=)
c.651G= (p.Lys217=)
4g.67740688C>GCA357048386GNRHRc.779G>C (p.Arg260Thr)
c.651G>C (p.Lys217Asn)
4g.67740688C>TCA357048388GNRHRc.779G>A (p.Arg260Lys)
c.651G>A (p.Lys217=)
 dbSNP gnomAD v4
4g.67740689T>ACA357048391GNRHRc.778A>T (p.Arg260Ter)
c.650A>T (p.Lys217Met)
4g.67740689T>CCA357048397GNRHRc.778A>G (p.Arg260Gly)
c.650A>G (p.Lys217Arg)
4g.67740689T>GCA357048398GNRHRc.778A>C (p.Arg260=)
c.650A>C (p.Lys217Thr)
4g.67740690T>ACA2938855GNRHRc.777A>T (p.Pro259=)
c.649A>T (p.Lys217Ter)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.67740690T>CCA357048400GNRHRc.777A>G (p.Pro259=)
c.649A>G (p.Lys217Glu)
 dbSNP
4g.67740690T>GCA357048403GNRHRc.777A>C (p.Pro259=)
c.649A>C (p.Lys217Gln)
4g.67740690T=CA1465409233GNRHRc.777A= (p.Pro259=)
c.649A= (p.Lys217=)
4g.67740691G>ACA357048406GNRHRc.776C>T (p.Pro259Leu)
c.648C>T (p.Thr216=)
4g.67740691G>CCA357048407GNRHRc.776C>G (p.Pro259Arg)
c.648C>G (p.Thr216=)
4g.67740691G>TCA357048408GNRHRc.776C>A (p.Pro259Gln)
c.648C>A (p.Thr216=)
4g.67740692G>ACA357048409GNRHRc.775C>T (p.Pro259Ser)
c.647C>T (p.Thr216Ile)
4g.67740692G>CCA357048412GNRHRc.775C>G (p.Pro259Ala)
c.647C>G (p.Thr216Ser)
4g.67740692G>TCA357048415GNRHRc.775C>A (p.Pro259Thr)
c.647C>A (p.Thr216Asn)
 gnomAD v4
4g.67740693T>ACA357048418GNRHRc.774A>T (p.Ile258=)
c.646A>T (p.Thr216Ser)
4g.67740693T>CCA357048419GNRHRc.774A>G (p.Ile258Met)
c.646A>G (p.Thr216Ala)
4g.67740693T>GCA357048420GNRHRc.774A>C (p.Ile258=)
c.646A>C (p.Thr216Pro)
4g.67740696_67740697delCA2670819810GNRHRc.773_774del (p.Ile258ThrfsTer?)
c.645_646del (p.Thr216GlnfsTer5)
 gnomAD v4
4g.67740693_67740698delCA2522396109GNRHRc.769_774del (p.Asn257_Ile258del)
c.641_646del (p.Gln214_Thr216delinsPro)
4g.67740694A=CA1465409241GNRHRc.773T= (p.Ile258=)
c.645T= (p.Tyr215=)
4g.67740694A>CCA357048421GNRHRc.773T>G (p.Ile258Arg)
c.645T>G (p.Tyr215Ter)
4g.67740694A>GCA10621558GNRHRc.773T>C (p.Ile258Thr)
c.645T>C (p.Tyr215=)
 ClinVar dbSNP gnomAD v4
4g.67740694A>TCA357048423GNRHRc.773T>A (p.Ile258Lys)
c.645T>A (p.Tyr215Ter)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.67740695T>ACA357048426GNRHRc.772A>T (p.Ile258Leu)
c.644A>T (p.Tyr215Phe)
4g.67740695T>CCA357048429GNRHRc.772A>G (p.Ile258Val)
c.644A>G (p.Tyr215Cys)
4g.67740695T>GCA357048424GNRHRc.772A>C (p.Ile258Leu)
c.644A>C (p.Tyr215Ser)
4g.67740696A>CCA357048434GNRHRc.771T>G (p.Asn257Lys)
c.643T>G (p.Tyr215Asp)
4g.67740696A>GCA357048430GNRHRc.771T>C (p.Asn257=)
c.643T>C (p.Tyr215His)
4g.67740696A>TCA357048435GNRHRc.771T>A (p.Asn257Lys)
c.643T>A (p.Tyr215Asn)
4g.67740697T>ACA357048436GNRHRc.770A>T (p.Asn257Ile)
c.642A>T (p.Gln214His)
4g.67740697T>CCA357048437GNRHRc.770A>G (p.Asn257Ser)
c.642A>G (p.Gln214=)
4g.67740697T>GCA357048438GNRHRc.770A>C (p.Asn257Thr)
c.642A>C (p.Gln214His)
4g.67740698T>ACA357048441GNRHRc.769A>T (p.Asn257Tyr)
c.641A>T (p.Gln214Leu)
4g.67740698T>CCA357048445GNRHRc.769A>G (p.Asn257Asp)
c.641A>G (p.Gln214Arg)
4g.67740698T>GCA357048446GNRHRc.769A>C (p.Asn257His)
c.641A>C (p.Gln214Pro)
 dbSNP gnomAD v3 gnomAD v4
4g.67740698T=CA1465409248GNRHRc.769A= (p.Asn257=)
c.641A= (p.Gln214=)
4g.67740699G>ACA98667586GNRHRc.768C>T (p.Asn256=)
c.640C>T (p.Gln214Ter)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.67740699G>CCA357048449GNRHRc.768C>G (p.Asn256Lys)
c.640C>G (p.Gln214Glu)
4g.67740699G=CA1465409251GNRHRc.768C= (p.Asn256=)
c.640C= (p.Gln214=)
4g.67740699G>TCA357048451GNRHRc.768C>A (p.Asn256Lys)
c.640C>A (p.Gln214Lys)
 gnomAD v4
4g.67740700T>ACA357048453GNRHRc.767A>T (p.Asn256Ile)
c.639A>T (p.Glu213Asp)
4g.67740700T>CCA357048455GNRHRc.767A>G (p.Asn256Ser)
c.639A>G (p.Glu213=)
 dbSNP gnomAD v4
4g.67740700T>GCA357048457GNRHRc.767A>C (p.Asn256Thr)
c.639A>C (p.Glu213Asp)
4g.67740700T=CA1465409255GNRHRc.767A= (p.Asn256=)
c.639A= (p.Glu213=)
4g.67740701T>ACA357048465GNRHRc.766A>T (p.Asn256Tyr)
c.638A>T (p.Glu213Val)
4g.67740701T>CCA357048463GNRHRc.766A>G (p.Asn256Asp)
c.638A>G (p.Glu213Gly)
4g.67740701T>GCA357048461GNRHRc.766A>C (p.Asn256His)
c.638A>C (p.Glu213Ala)
4g.67740702C>ACA357048466GNRHRc.765G>T (p.Lys255Asn)
c.637G>T (p.Glu213Ter)
4g.67740702C=CA1465409257GNRHRc.765G= (p.Lys255=)
c.637G= (p.Glu213=)
4g.67740702C>GCA357048469GNRHRc.765G>C (p.Lys255Asn)
c.637G>C (p.Glu213Gln)
4g.67740702C>TCA2938856GNRHRc.765G>A (p.Lys255=)
c.637G>A (p.Glu213Lys)
 dbSNP ExAC gnomAD v2 gnomAD v4
4g.67740703T>ACA357048472GNRHRc.764A>T (p.Lys255Met)
c.636A>T (p.Gln212His)
4g.67740703T>CCA357048473GNRHRc.764A>G (p.Lys255Arg)
c.636A>G (p.Gln212=)
4g.67740703T>GCA357048475GNRHRc.764A>C (p.Lys255Thr)
c.636A>C (p.Gln212His)
4g.67740704T>ACA357048476GNRHRc.763A>T (p.Lys255Ter)
c.635A>T (p.Gln212Leu)
4g.67740704T>CCA357048478GNRHRc.763A>G (p.Lys255Glu)
c.635A>G (p.Gln212Arg)
4g.67740704T>GCA357048480GNRHRc.763A>C (p.Lys255Gln)
c.635A>C (p.Gln212Pro)
4g.67740705G>ACA357048482GNRHRc.762C>T (p.Ser254=)
c.634C>T (p.Gln212Ter)
4g.67740705G>CCA357048490GNRHRc.762C>G (p.Ser254=)
c.634C>G (p.Gln212Glu)
4g.67740705G>TCA357048491GNRHRc.762C>A (p.Ser254=)
c.634C>A (p.Gln212Lys)
 gnomAD v4
4g.67740706G>ACA357048496GNRHRc.761C>T (p.Ser254Phe)
c.633C>T (p.Val211=)
4g.67740706G>CCA357048495GNRHRc.761C>G (p.Ser254Cys)
c.633C>G (p.Val211=)
4g.67740706G>TCA357048493GNRHRc.761C>A (p.Ser254Tyr)
c.633C>A (p.Val211=)
 gnomAD v4
4g.67740707A>CCA357048497GNRHRc.760T>G (p.Ser254Ala)
c.632T>G (p.Val211Gly)
4g.67740707A>GCA357048499GNRHRc.760T>C (p.Ser254Pro)
c.632T>C (p.Val211Ala)
4g.67740707A>TCA357048500GNRHRc.760T>A (p.Ser254Thr)
c.632T>A (p.Val211Asp)
4g.67740708C>ACA357048502GNRHRc.759G>T (p.Gln253His)
c.631G>T (p.Val211Phe)
4g.67740708C=CA1465409261GNRHRc.759G= (p.Gln253=)
c.631G= (p.Val211=)
4g.67740708C>GCA357048503GNRHRc.759G>C (p.Gln253His)
c.631G>C (p.Val211Leu)
4g.67740708C>TCA357048505GNRHRc.759G>A (p.Gln253=)
c.631G>A (p.Val211Ile)
 dbSNP
4g.67740709T>ACA357048508GNRHRc.758A>T (p.Gln253Leu)
c.630A>T (p.Ser210=)
4g.67740709T>CCA357048507GNRHRc.758A>G (p.Gln253Arg)
c.630A>G (p.Ser210=)
4g.67740709T>GCA357048506GNRHRc.758A>C (p.Gln253Pro)
c.630A>C (p.Ser210=)
4g.67740710G>ACA357048509GNRHRc.757C>T (p.Gln253Ter)
c.629C>T (p.Ser210Leu)
 dbSNP gnomAD v4
4g.67740710G>CCA357048510GNRHRc.757C>G (p.Gln253Glu)
c.629C>G (p.Ser210Ter)
4g.67740710G=CA1465409269GNRHRc.757C= (p.Gln253=)
c.629C= (p.Ser210=)
4g.67740710G>TCA357048511GNRHRc.757C>A (p.Gln253Lys)
c.629C>A (p.Ser210Ter)
4g.67740711A=CA1465409272GNRHRc.756T= (p.Asn252=)
c.628T= (p.Ser210=)
4g.67740711A>CCA357048513GNRHRc.756T>G (p.Asn252Lys)
c.628T>G (p.Ser210Ala)
4g.67740711A>GCA357048514GNRHRc.756T>C (p.Asn252=)
c.628T>C (p.Ser210Pro)
4g.67740711A>TCA357048516GNRHRc.756T>A (p.Asn252Lys)
c.628T>A (p.Ser210Thr)
4g.67740711_67740712insAATGTTAAACAGGCA1465409275GNRHRc.755_756insCCTGTTTAACATT (p.Gln253LeufsTer?)
c.627_628insCCTGTTTAACATT (p.Ser210ProfsTer3)
 dbSNP
4g.67740712T>ACA357048518GNRHRc.755A>T (p.Asn252Ile)
c.627A>T (p.Glu209Asp)
4g.67740712T>CCA357048521GNRHRc.755A>G (p.Asn252Ser)
c.627A>G (p.Glu209=)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.67740712T>GCA357048520GNRHRc.755A>C (p.Asn252Thr)
c.627A>C (p.Glu209Asp)
4g.67740712T=CA1465409277GNRHRc.755A= (p.Asn252=)
c.627A= (p.Glu209=)
4g.67740713T>ACA357048523GNRHRc.754A>T (p.Asn252Tyr)
c.626A>T (p.Glu209Val)
 gnomAD v4
4g.67740713T>CCA357048524GNRHRc.754A>G (p.Asn252Asp)
c.626A>G (p.Glu209Gly)
4g.67740713T>GCA357048526GNRHRc.754A>C (p.Asn252His)
c.626A>C (p.Glu209Ala)
4g.67740714C>ACA357048528GNRHRc.753G>T (p.Leu251=)
c.625G>T (p.Glu209Ter)
4g.67740714C>GCA357048529GNRHRc.753G>C (p.Leu251=)
c.625G>C (p.Glu209Gln)
 gnomAD v4
4g.67740714C>TCA357048530GNRHRc.753G>A (p.Leu251=)
c.625G>A (p.Glu209Lys)
4g.67740715A=CA1465409280GNRHRc.752T= (p.Leu251=)
c.624T= (p.Thr208=)
4g.67740715A>CCA2938857GNRHRc.752T>G (p.Leu251Arg)
c.624T>G (p.Thr208=)
 dbSNP ExAC gnomAD v2 gnomAD v4
4g.67740715A>GCA357048532GNRHRc.752T>C (p.Leu251Pro)
c.624T>C (p.Thr208=)
4g.67740715A>TCA357048534GNRHRc.752T>A (p.Leu251Gln)
c.624T>A (p.Thr208=)
4g.67740716G>ACA357048535GNRHRc.751C>T (p.Leu251=)
c.623C>T (p.Thr208Ile)
4g.67740716G>CCA98667587GNRHRc.751C>G (p.Leu251Val)
c.623C>G (p.Thr208Ser)
 dbSNP gnomAD v4
4g.67740716G=CA1465409286GNRHRc.751C= (p.Leu251=)
c.623C= (p.Thr208=)
4g.67740716G>TCA357048540GNRHRc.751C>A (p.Leu251Met)
c.623C>A (p.Thr208Asn)
 gnomAD v4
4g.67740717T>ACA357048543GNRHRc.750A>T (p.Gln250His)
c.622A>T (p.Thr208Ser)
4g.67740717T>CCA357048544GNRHRc.750A>G (p.Gln250=)
c.622A>G (p.Thr208Ala)
 gnomAD v4
4g.67740717T>GCA357048542GNRHRc.750A>C (p.Gln250His)
c.622A>C (p.Thr208Pro)
4g.67740718T>ACA357048546GNRHRc.749A>T (p.Gln250Leu)
c.621A>T (p.Thr207=)
4g.67740718T>CCA357048545GNRHRc.749A>G (p.Gln250Arg)
c.621A>G (p.Thr207=)
4g.67740718T>GCA2938858GNRHRc.749A>C (p.Gln250Pro)
c.621A>C (p.Thr207=)
 dbSNP ExAC gnomAD v2
4g.67740718T=CA1465409290GNRHRc.749A= (p.Gln250=)
c.621A= (p.Thr207=)
4g.67740719G>ACA357048550GNRHRc.748C>T (p.Gln250Ter)
c.620C>T (p.Thr207Ile)
 gnomAD v4
4g.67740719G>CCA357048555GNRHRc.748C>G (p.Gln250Glu)
c.620C>G (p.Thr207Arg)
4g.67740719G>TCA357048552GNRHRc.748C>A (p.Gln250Lys)
c.620C>A (p.Thr207Lys)
4g.67740720T>ACA357048557GNRHRc.747A>T (p.Leu249=)
c.619A>T (p.Thr207Ser)
4g.67740720T>CCA2938859GNRHRc.747A>G (p.Leu249=)
c.619A>G (p.Thr207Ala)
 dbSNP ExAC gnomAD v2 gnomAD v4
4g.67740720T>GCA357048561GNRHRc.747A>C (p.Leu249=)
c.619A>C (p.Thr207Pro)
4g.67740720T=CA1465409293GNRHRc.747A= (p.Leu249=)
c.619A= (p.Thr207=)
4g.67740721A=CA1465409297GNRHRc.746T= (p.Leu249=)
c.618T= (p.Thr206=)
4g.67740721A>CCA2938860GNRHRc.746T>G (p.Leu249Arg)
c.618T>G (p.Thr206=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.67740721A>GCA357048564GNRHRc.746T>C (p.Leu249Pro)
c.618T>C (p.Thr206=)
 dbSNP gnomAD v4
4g.67740721A>TCA357048566GNRHRc.746T>A (p.Leu249Gln)
c.618T>A (p.Thr206=)
 dbSNP gnomAD v3 gnomAD v4
4g.67740722G>ACA357048569GNRHRc.745C>T (p.Leu249=)
c.617C>T (p.Thr206Ile)
4g.67740722G>CCA357048570GNRHRc.745C>G (p.Leu249Val)
c.617C>G (p.Thr206Ser)
4g.67740722G>TCA357048572GNRHRc.745C>A (p.Leu249Ile)
c.617C>A (p.Thr206Asn)
4g.67740723T>ACA357048575GNRHRc.744A>T (p.Glu248Asp)
c.616A>T (p.Thr206Ser)
4g.67740723T>CCA357048577GNRHRc.744A>G (p.Glu248=)
c.616A>G (p.Thr206Ala)
4g.67740723T>GCA357048579GNRHRc.744A>C (p.Glu248Asp)
c.616A>C (p.Thr206Pro)
4g.67740724T>ACA357048587GNRHRc.743A>T (p.Glu248Val)
c.615A>T (p.Arg205=)
 gnomAD v4
4g.67740724T>CCA357048582GNRHRc.743A>G (p.Glu248Gly)
c.615A>G (p.Arg205=)
4g.67740724T>GCA357048585GNRHRc.743A>C (p.Glu248Ala)
c.615A>C (p.Arg205=)
4g.67740725C>ACA357048591GNRHRc.743-1G>T (n.743-1G>T)
c.615-1G>T (n.615-1G>T)
4g.67740725C>GCA357048594GNRHRc.743-1G>C (n.743-1G>C)
c.615-1G>C (n.615-1G>C)
4g.67740725C>TCA357048597GNRHRc.743-1G>A (n.743-1G>A)
c.615-1G>A (n.615-1G>A)
4g.67740726T>ACA357048603GNRHRc.743-2A>T (n.743-2A>T)
c.615-2A>T (n.615-2A>T)
4g.67740726T>CCA357048609GNRHRc.743-2A>G (n.743-2A>G)
c.615-2A>G (n.615-2A>G)
4g.67740726T>GCA357048614GNRHRc.743-2A>C (n.743-2A>C)
c.615-2A>C (n.615-2A>C)
4g.67740727G=CA1465409303GNRHRc.743-3C= (n.743-3C=)
c.615-3C= (n.615-3C=)
4g.67740727G>TCA797693901GNRHRc.743-3C>A (n.743-3C>A)
c.615-3C>A (n.615-3C>A)
 dbSNP gnomAD v4
4g.67740730G>TCA2670819811GNRHRc.743-6C>A (n.743-6C>A)
c.615-6C>A (n.615-6C>A)
 gnomAD v4
4g.67740731G>TCA2670819812GNRHRc.743-7C>A (n.743-7C>A)
c.615-7C>A (n.615-7C>A)
 gnomAD v4
4g.67740732A>CCA2706125270GNRHRc.743-8T>G (n.743-8T>G)
c.615-8T>G (n.615-8T>G)
 dbSNP
4g.67740732A>TCA2670819813GNRHRc.743-8T>A (n.743-8T>A)
c.615-8T>A (n.615-8T>A)
 gnomAD v4
4g.67740733T>CCA10621583GNRHRc.743-9A>G (n.743-9A>G)
c.615-9A>G (n.615-9A>G)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.67740733T=CA1465409306GNRHRc.743-9A= (n.743-9A=)
c.615-9A= (n.615-9A=)
4g.67740734A>GCA2670819814GNRHRc.743-10T>C (n.743-10T>C)
c.615-10T>C (n.615-10T>C)
 gnomAD v4
4g.67740734_67740735insTTTTTCTCTCA2559420397GNRHRc.743-11_743-10insAGAGAAAAA (n.743-11_743-10insAGAGAAAAA)
c.615-11_615-10insAGAGAAAAA (n.615-11_615-10insAGAGAAAAA)
4g.67740735G=CA1465409309GNRHRc.743-11C= (n.743-11C=)
c.615-11C= (n.615-11C=)
4g.67740735G>TCA2670819815GNRHRc.743-11C>A (n.743-11C>A)
c.615-11C>A (n.615-11C>A)
 gnomAD v4
4g.67740736_67740737insCTACACA552611465GNRHRc.743-12_743-11insGTAGT (n.743-12_743-11insGTAGT)
c.615-12_615-11insGTAGT (n.615-12_615-11insGTAGT)
 dbSNP gnomAD v2
4g.67740737G>CCA552611466GNRHRc.743-13C>G (n.743-13C>G)
c.615-13C>G (n.615-13C>G)
 dbSNP gnomAD v2
4g.67740737G=CA1465409312GNRHRc.743-13C= (n.743-13C=)
c.615-13C= (n.615-13C=)
4g.67740741delCA2670819816GNRHRc.743-14del (n.743-14del)
c.615-14del (n.615-14del)
 gnomAD v4
4g.67740739A>GCA2670819817GNRHRc.743-15T>C (n.743-15T>C)
c.615-15T>C (n.615-15T>C)
 gnomAD v4
4g.67740741A=CA1465409314GNRHRc.743-17T= (n.743-17T=)
c.615-17T= (n.615-17T=)
4g.67740741A>GCA98667598GNRHRc.743-17T>C (n.743-17T>C)
c.615-17T>C (n.615-17T>C)
 dbSNP gnomAD v4
4g.67740742G>ACA2670819818GNRHRc.743-18C>T (n.743-18C>T)
c.615-18C>T (n.615-18C>T)
 gnomAD v4
4g.67740742G>CCA1063693004GNRHRc.743-18C>G (n.743-18C>G)
c.615-18C>G (n.615-18C>G)
 dbSNP gnomAD v3 gnomAD v4
4g.67740742G=CA1465409317GNRHRc.743-18C= (n.743-18C=)
c.615-18C= (n.615-18C=)
4g.67740743A=CA1465409319GNRHRc.743-19T= (n.743-19T=)
c.615-19T= (n.615-19T=)
4g.67740743A>GCA552611467GNRHRc.743-19T>C (n.743-19T>C)
c.615-19T>C (n.615-19T>C)
 dbSNP gnomAD v2 gnomAD v4
4g.67740743A>TCA1465409321GNRHRc.743-19T>A (n.743-19T>A)
c.615-19T>A (n.615-19T>A)
 dbSNP
4g.67740744G>ACA2670819819GNRHRc.743-20C>T (n.743-20C>T)
c.615-20C>T (n.615-20C>T)
 gnomAD v4
4g.67740744G>TCA2670819820GNRHRc.743-20C>A (n.743-20C>A)
c.615-20C>A (n.615-20C>A)
 gnomAD v4
4g.67740745_67740748delCA2762037083GNRHRc.743-23_743-20del (n.743-23_743-20del)
c.615-23_615-20del (n.615-23_615-20del)
4g.67740745C>TCA2670819821GNRHRc.743-21G>A (n.743-21G>A)
c.615-21G>A (n.615-21G>A)
 gnomAD v4
4g.67740746A=CA1465409323GNRHRc.743-22T= (n.743-22T=)
c.615-22T= (n.615-22T=)
4g.67740746A>CCA2938861GNRHRc.743-22T>G (n.743-22T>G)
c.615-22T>G (n.615-22T>G)
 dbSNP ExAC
4g.67740746A>GCA797693913GNRHRc.743-22T>C (n.743-22T>C)
c.615-22T>C (n.615-22T>C)
 dbSNP
4g.67740748G>ACA2938862GNRHRc.743-24C>T (n.743-24C>T)
c.615-24C>T (n.615-24C>T)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.67740748G>CCA2670819822GNRHRc.743-24C>G (n.743-24C>G)
c.615-24C>G (n.615-24C>G)
 gnomAD v4
4g.67740748G=CA1465409327GNRHRc.743-24C= (n.743-24C=)
c.615-24C= (n.615-24C=)
4g.67740748G>TCA2670819823GNRHRc.743-24C>A (n.743-24C>A)
c.615-24C>A (n.615-24C>A)
 gnomAD v4
4g.67740749T>CCA98667607GNRHRc.743-25A>G (n.743-25A>G)
c.615-25A>G (n.615-25A>G)
 dbSNP gnomAD v4
4g.67740749T=CA1465409329GNRHRc.743-25A= (n.743-25A=)
c.615-25A= (n.615-25A=)
4g.67740750G>ACA2670819824GNRHRc.743-26C>T (n.743-26C>T)
c.615-26C>T (n.615-26C>T)
 gnomAD v4
4g.67740750G>TCA2670819825GNRHRc.743-26C>A (n.743-26C>A)
c.615-26C>A (n.615-26C>A)
 gnomAD v4
4g.67740751T>CCA2670819826GNRHRc.743-27A>G (n.743-27A>G)
c.615-27A>G (n.615-27A>G)
 gnomAD v4
4g.67740754A=CA1465409333GNRHRc.743-30T= (n.743-30T=)
c.615-30T= (n.615-30T=)
4g.67740754A>CCA98667610GNRHRc.743-30T>G (n.743-30T>G)
c.615-30T>G (n.615-30T>G)
 dbSNP gnomAD v3 gnomAD v4
4g.67740754A>GCA2670819828GNRHRc.743-30T>C (n.743-30T>C)
c.615-30T>C (n.615-30T>C)
 gnomAD v4
4g.67740754A>TCA2670819827GNRHRc.743-30T>A (n.743-30T>A)
c.615-30T>A (n.615-30T>A)
 gnomAD v4
4g.67740755A>GCA2670819829GNRHRc.743-31T>C (n.743-31T>C)
c.615-31T>C (n.615-31T>C)
 gnomAD v4
4g.67740756A=CA1465409335GNRHRc.743-32T= (n.743-32T=)
c.615-32T= (n.615-32T=)
4g.67740756A>CCA2938863GNRHRc.743-32T>G (n.743-32T>G)
c.615-32T>G (n.615-32T>G)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.67740757G>TCA2670819830GNRHRc.743-33C>A (n.743-33C>A)
c.615-33C>A (n.615-33C>A)
 gnomAD v4
4g.67740758A=CA1465409339GNRHRc.743-34T= (n.743-34T=)
c.615-34T= (n.615-34T=)
4g.67740758A>GCA1465409340GNRHRc.743-34T>C (n.743-34T>C)
c.615-34T>C (n.615-34T>C)
 dbSNP
4g.67740760C>ACA2670819831GNRHRc.743-36G>T (n.743-36G>T)
c.615-36G>T (n.615-36G>T)
 gnomAD v4
4g.67740760C>GCA2670819832GNRHRc.743-36G>C (n.743-36G>C)
c.615-36G>C (n.615-36G>C)
 gnomAD v4
4g.67740761A>GCA2670819833GNRHRc.743-37T>C (n.743-37T>C)
c.615-37T>C (n.615-37T>C)
 gnomAD v4
4g.67740762G>CCA2670819834GNRHRc.743-38C>G (n.743-38C>G)
c.615-38C>G (n.615-38C>G)
 gnomAD v4
4g.67740762G>TCA2670819835GNRHRc.743-38C>A (n.743-38C>A)
c.615-38C>A (n.615-38C>A)
 gnomAD v4
4g.67740763T=CA1465409342GNRHRc.743-39A= (n.743-39A=)
c.615-39A= (n.615-39A=)
4g.67740763_67740764insAAACA552611469GNRHRc.743-40_743-39insTTT (n.743-40_743-39insTTT)
c.615-40_615-39insTTT (n.615-40_615-39insTTT)
 gnomAD v2
4g.67740763_67740764insAAATCACCA552611468GNRHRc.743-40_743-39insGTGATTT (n.743-40_743-39insGTGATTT)
c.615-40_615-39insGTGATTT (n.615-40_615-39insGTGATTT)
 gnomAD v2
4g.67740763_67740764insAAATCACTTCTTCCA1465409348GNRHRc.743-40_743-39insGAAGAAGTGATTT (n.743-40_743-39insGAAGAAGTGATTT)
c.615-40_615-39insGAAGAAGTGATTT (n.615-40_615-39insGAAGAAGTGATTT)
 dbSNP
4g.67740764T>CCA2670819836GNRHRc.743-40A>G (n.743-40A>G)
c.615-40A>G (n.615-40A>G)
 gnomAD v4
4g.67740764T=CA1465409347GNRHRc.743-40A= (n.743-40A=)
c.615-40A= (n.615-40A=)
4g.67740764_67740765insCACTTCCA552611470GNRHRc.743-41_743-40insGAAGTG (n.743-41_743-40insGAAGTG)
c.615-41_615-40insGAAGTG (n.615-41_615-40insGAAGTG)
 dbSNP gnomAD v2
4g.67740766T>CCA2670819837GNRHRc.743-42A>G (n.743-42A>G)
c.615-42A>G (n.615-42A>G)
 gnomAD v4
4g.67740767C>ACA2670819838GNRHRc.743-43G>T (n.743-43G>T)
c.615-43G>T (n.615-43G>T)
 gnomAD v4
4g.67740767C=CA1465409352GNRHRc.743-43G= (n.743-43G=)
c.615-43G= (n.615-43G=)
4g.67740767C>GCA552611471GNRHRc.743-43G>C (n.743-43G>C)
c.615-43G>C (n.615-43G>C)
 dbSNP gnomAD v2 gnomAD v4
4g.67740767C>TCA2670819839GNRHRc.743-43G>A (n.743-43G>A)
c.615-43G>A (n.615-43G>A)
 gnomAD v4
4g.67740768T>CCA1465409356GNRHRc.743-44A>G (n.743-44A>G)
c.615-44A>G (n.615-44A>G)
 dbSNP
4g.67740768T>GCA1063693016GNRHRc.743-44A>C (n.743-44A>C)
c.615-44A>C (n.615-44A>C)
 dbSNP gnomAD v3 gnomAD v4
4g.67740768T=CA1465409355GNRHRc.743-44A= (n.743-44A=)
c.615-44A= (n.615-44A=)
4g.67740769T>CCA2578100641GNRHRc.743-45A>G (n.743-45A>G)
c.615-45A>G (n.615-45A>G)
 gnomAD v4
4g.67740769T>GCA2938864GNRHRc.743-45A>C (n.743-45A>C)
c.615-45A>C (n.615-45A>C)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.67740769T=CA1465409359GNRHRc.743-45A= (n.743-45A=)
c.615-45A= (n.615-45A=)
4g.67740771C=CA1465409362GNRHRc.743-47G= (n.743-47G=)
c.615-47G= (n.615-47G=)
4g.67740771C>GCA552611472GNRHRc.743-47G>C (n.743-47G>C)
c.615-47G>C (n.615-47G>C)
 dbSNP gnomAD v2 gnomAD v4
4g.67740771C>TCA2670819840GNRHRc.743-47G>A (n.743-47G>A)
c.615-47G>A (n.615-47G>A)
 gnomAD v4
4g.67740772A>GCA2670819841GNRHRc.743-48T>C (n.743-48T>C)
c.615-48T>C (n.615-48T>C)
 gnomAD v4
4g.67740774A>GCA2670819842GNRHRc.743-50T>C (n.743-50T>C)
c.615-50T>C (n.615-50T>C)
 gnomAD v4
4g.67740775A>GCA2670819843GNRHRc.743-51T>C (n.743-51T>C)
c.615-51T>C (n.615-51T>C)
 gnomAD v4
4g.67740776C=CA1465409365GNRHRc.743-52G= (n.743-52G=)
c.615-52G= (n.615-52G=)
4g.67740776C>GCA797693939GNRHRc.743-52G>C (n.743-52G>C)
c.615-52G>C (n.615-52G>C)
 dbSNP gnomAD v4
4g.67740776_67740777delCA2670819844GNRHRc.743-53_743-52del (n.743-53_743-52del)
c.615-53_615-52del (n.615-53_615-52del)
 gnomAD v4
4g.67740777C>ACA2670819845GNRHRc.743-53G>T (n.743-53G>T)
c.615-53G>T (n.615-53G>T)
 gnomAD v4
4g.67740778A=CA1465409367GNRHRc.743-54T= (n.743-54T=)
c.615-54T= (n.615-54T=)
4g.67740778A>CCA2762037084GNRHRc.743-54T>G (n.743-54T>G)
c.615-54T>G (n.615-54T>G)
4g.67740778A>GCA1465409369GNRHRc.743-54T>C (n.743-54T>C)
c.615-54T>C (n.615-54T>C)
 dbSNP
4g.67740780delCA2670819846GNRHRc.743-54del (n.743-54del)
c.615-54del (n.615-54del)
 gnomAD v4
4g.67740778_67740779insCCCAAACACACCCAACACCA2762037085GNRHRc.743-55_743-54insGTGTTGGGTGTGTTTGGG (n.743-55_743-54insGTGTTGGGTGTGTTTGGG)
c.615-55_615-54insGTGTTGGGTGTGTTTGGG (n.615-55_615-54insGTGTTGGGTGTGTTTGGG)
4g.67740779A>CCA2670819847GNRHRc.743-55T>G (n.743-55T>G)
c.615-55T>G (n.615-55T>G)
 gnomAD v4
4g.67740779_67740780insCCAAACACACCCAACACCA2762037086GNRHRc.743-56_743-55insGTGTTGGGTGTGTTTGG (n.743-56_743-55insGTGTTGGGTGTGTTTGG)
c.615-56_615-55insGTGTTGGGTGTGTTTGG (n.615-56_615-55insGTGTTGGGTGTGTTTGG)
4g.67740780A>GCA2670819848GNRHRc.743-56T>C (n.743-56T>C)
c.615-56T>C (n.615-56T>C)
 gnomAD v4
4g.67740781G>ACA2670819850GNRHRc.743-57C>T (n.743-57C>T)
c.615-57C>T (n.615-57C>T)
 gnomAD v4
4g.67740781G>TCA2578100642GNRHRc.743-57C>A (n.743-57C>A)
c.615-57C>A (n.615-57C>A)
 gnomAD v4
4g.67740781_67740784delCA2670819849GNRHRc.743-60_743-57del (n.743-60_743-57del)
c.615-60_615-57del (n.615-60_615-57del)
 gnomAD v4
4g.67740782T>ACA2670819851GNRHRc.743-58A>T (n.743-58A>T)
c.615-58A>T (n.615-58A>T)
 gnomAD v4
4g.67740782T>CCA552611473GNRHRc.743-58A>G (n.743-58A>G)
c.615-58A>G (n.615-58A>G)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.67740782T=CA1465409370GNRHRc.743-58A= (n.743-58A=)
c.615-58A= (n.615-58A=)

Number of alleles fetched