Chr Mutation (hg38) CAid Gene Transcript Linkouts
4g.67753762_67753765delCA1465420366GNRHRc.522+52_522+55del (n.522+52_522+55del)
dbSNP gnomAD v4
4g.67753764A=CA1465420374GNRHRc.522+50T= (n.522+50T=)
4g.67753764A>GCA2938919GNRHRc.522+50T>C (n.522+50T>C)
dbSNP ExAC gnomAD v2 gnomAD v4
4g.67753764A>TCA2670820587GNRHRc.522+50T>A (n.522+50T>A)
gnomAD v4
4g.67753765G>TCA2670820588GNRHRc.522+49C>A (n.522+49C>A)
gnomAD v4
4g.67753766G>ACA2578100693GNRHRc.522+48C>T (n.522+48C>T)
gnomAD v4
4g.67753766G>TCA2670820589GNRHRc.522+48C>A (n.522+48C>A)
gnomAD v4
4g.67753766_67753767insTAGACA2521968773GNRHRc.522+47_522+48insTCTA (n.522+47_522+48insTCTA)
4g.67753767A>GCA2670820590GNRHRc.522+47T>C (n.522+47T>C)
gnomAD v4
4g.67753768A=CA1465420377GNRHRc.522+46T= (n.522+46T=)
4g.67753768A>TCA1465420379GNRHRc.522+46T>A (n.522+46T>A)
dbSNP
4g.67753770T>CCA2578100694GNRHRc.522+44A>G (n.522+44A>G)
4g.67753771C>ACA2558421149GNRHRc.522+43G>T (n.522+43G>T)
4g.67753773A=CA1465420382GNRHRc.522+41T= (n.522+41T=)
4g.67753773A>CCA2938920GNRHRc.522+41T>G (n.522+41T>G)
dbSNP ExAC gnomAD v2 gnomAD v4
4g.67753773A>GCA552611508GNRHRc.522+41T>C (n.522+41T>C)
dbSNP gnomAD v2 gnomAD v4
4g.67753773A>TCA2670820591GNRHRc.522+41T>A (n.522+41T>A)
gnomAD v4
4g.67753774T>CCA2670820592GNRHRc.522+40A>G (n.522+40A>G)
gnomAD v4
4g.67753775G>ACA2938921GNRHRc.522+39C>T (n.522+39C>T)
dbSNP ExAC gnomAD v2 gnomAD v4
4g.67753775G=CA1465420386GNRHRc.522+39C= (n.522+39C=)
4g.67753775G>TCA1465420388GNRHRc.522+39C>A (n.522+39C>A)
dbSNP gnomAD v4
4g.67753776A=CA1465420390GNRHRc.522+38T= (n.522+38T=)
4g.67753776A>TCA1063695174GNRHRc.522+38T>A (n.522+38T>A)
dbSNP gnomAD v3 gnomAD v4
4g.67753777T>CCA552611509GNRHRc.522+37A>G (n.522+37A>G)
dbSNP gnomAD v2 gnomAD v4
4g.67753777T=CA1465420391GNRHRc.522+37A= (n.522+37A=)
4g.67753778C>TCA2670820593GNRHRc.522+36G>A (n.522+36G>A)
gnomAD v4
4g.67753779A>GCA2578100695GNRHRc.522+35T>C (n.522+35T>C)
4g.67753780C>TCA2670820594GNRHRc.522+34G>A (n.522+34G>A)
gnomAD v4
4g.67753781C>TCA2578100696GNRHRc.522+33G>A (n.522+33G>A)
gnomAD v4
4g.67753782A=CA1465420394GNRHRc.522+32T= (n.522+32T=)
4g.67753782A>GCA797701433GNRHRc.522+32T>C (n.522+32T>C)
dbSNP gnomAD v3 gnomAD v4
4g.67753783T>CCA2762037551GNRHRc.522+31A>G (n.522+31A>G)
4g.67753784A=CA1465420397GNRHRc.522+30T= (n.522+30T=)
4g.67753784A>GCA2938922GNRHRc.522+30T>C (n.522+30T>C)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.67753786C>TCA2670820595GNRHRc.522+28G>A (n.522+28G>A)
gnomAD v4
4g.67753787C>ACA2670820596GNRHRc.522+27G>T (n.522+27G>T)
gnomAD v4
4g.67753788A>GCA2762037552GNRHRc.522+26T>C (n.522+26T>C)
4g.67753788A>TCA2670820598GNRHRc.522+26T>A (n.522+26T>A)
gnomAD v4
4g.67753790delCA2670820597GNRHRc.522+26del (n.522+26del)
gnomAD v4
4g.67753789A>CCA2670820599GNRHRc.522+25T>G (n.522+25T>G)
gnomAD v4
4g.67753793A=CA1465420399GNRHRc.522+21T= (n.522+21T=)
4g.67753793A>GCA1063695185GNRHRc.522+21T>C (n.522+21T>C)
dbSNP
4g.67753794G>ACA2578100697GNRHRc.522+20C>T (n.522+20C>T)
gnomAD v4
4g.67753794G>TCA2670820600GNRHRc.522+20C>A (n.522+20C>A)
gnomAD v4
4g.67753798G>ACA2670820601GNRHRc.522+16C>T (n.522+16C>T)
gnomAD v4
4g.67753798G>TCA2670820602GNRHRc.522+16C>A (n.522+16C>A)
gnomAD v4
4g.67753799T>CCA2938923GNRHRc.522+15A>G (n.522+15A>G)
dbSNP ExAC gnomAD v2 gnomAD v4
4g.67753799T=CA1465420402GNRHRc.522+15A= (n.522+15A=)
4g.67753800G>ACA797701438GNRHRc.522+14C>T (n.522+14C>T)
dbSNP gnomAD v4
4g.67753800G=CA1465420406GNRHRc.522+14C= (n.522+14C=)
4g.67753800G>TCA2670820603GNRHRc.522+14C>A (n.522+14C>A)
gnomAD v4
4g.67753801T>ACA2938924GNRHRc.522+13A>T (n.522+13A>T)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.67753801T=CA1465420408GNRHRc.522+13A= (n.522+13A=)
4g.67753802A=CA1465420415GNRHRc.522+12T= (n.522+12T=)
4g.67753802A>GCA552611510GNRHRc.522+12T>C (n.522+12T>C)
dbSNP gnomAD v2 gnomAD v4
4g.67753802A>TCA552611511GNRHRc.522+12T>A (n.522+12T>A)
dbSNP gnomAD v2
4g.67753804A>GCA645518040GNRHRc.522+10T>C (n.522+10T>C)
gnomAD v4 COSMIC
4g.67753805delCA2578100698GNRHRc.522+10del (n.522+10del)
4g.67753805A=CA1465420419GNRHRc.522+9T= (n.522+9T=)
4g.67753805A>GCA552611512GNRHRc.522+9T>C (n.522+9T>C)
dbSNP gnomAD v2 gnomAD v4
4g.67753806T>CCA552611513GNRHRc.522+8A>G (n.522+8A>G)
dbSNP gnomAD v2 gnomAD v4
4g.67753806T=CA1465420422GNRHRc.522+8A= (n.522+8A=)
4g.67753806_67753807delinsTGCA1465420421GNRHRc.522+7_522+8delinsCA (n.522+7_522+8delinsCA)
4g.67753807G>TCA2670820604GNRHRc.522+7C>A (n.522+7C>A)
gnomAD v4
4g.67753808delCA552611514GNRHRc.522+7del (n.522+7del)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.67753808G>ACA552611515GNRHRc.522+6C>T (n.522+6C>T)
dbSNP gnomAD v2 gnomAD v4
4g.67753808G>CCA2670820605GNRHRc.522+6C>G (n.522+6C>G)
gnomAD v4
4g.67753808G=CA1465420428GNRHRc.522+6C= (n.522+6C=)
4g.67753808G>TCA2670820606GNRHRc.522+6C>A (n.522+6C>A)
gnomAD v4
4g.67753812A>CCA357054270GNRHRc.522+2T>G (n.522+2T>G)
4g.67753812A>GCA357054268GNRHRc.522+2T>C (n.522+2T>C)
4g.67753812A>TCA357054269GNRHRc.522+2T>A (n.522+2T>A)
4g.67753813C>ACA357054271GNRHRc.522+1G>T (n.522+1G>T)
4g.67753813C>GCA357054272GNRHRc.522+1G>C (n.522+1G>C)
4g.67753813C>TCA357054273GNRHRc.522+1G>A (n.522+1G>A)
4g.67753814C>ACA357054274GNRHRc.522G>T (p.Gln174His)
gnomAD v4
4g.67753814C=CA1465420430GNRHRc.522G= (p.Gln174=)
4g.67753814C>GCA357054275GNRHRc.522G>C (p.Gln174His)
dbSNP gnomAD v2 gnomAD v4
4g.67753814C>TCA2938925GNRHRc.522G>A (p.Gln174=)
dbSNP ExAC gnomAD v2 gnomAD v4
4g.67753815T>ACA2938926GNRHRc.521A>T (p.Gln174Leu)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.67753815T>CCA357054276GNRHRc.521A>G (p.Gln174Arg)
ClinVar dbSNP gnomAD v2 gnomAD v4
4g.67753815T>GCA357054277GNRHRc.521A>C (p.Gln174Pro)
4g.67753815T=CA1465420435GNRHRc.521A= (p.Gln174=)
4g.67753816G>ACA357054278GNRHRc.520C>T (p.Gln174Ter)
4g.67753816G>CCA357054279GNRHRc.520C>G (p.Gln174Glu)
4g.67753816G>TCA357054280GNRHRc.520C>A (p.Gln174Lys)
gnomAD v4
4g.67753817T>ACA439928696GNRHRc.519A>T (p.Pro173=)
4g.67753817T>CCA439928700GNRHRc.519A>G (p.Pro173=)
4g.67753817T>GCA439928702GNRHRc.519A>C (p.Pro173=)
4g.67753818G>ACA357054283GNRHRc.518C>T (p.Pro173Leu)
4g.67753818G>CCA357054282GNRHRc.518C>G (p.Pro173Arg)
4g.67753818G>TCA357054281GNRHRc.518C>A (p.Pro173Gln)
4g.67753819G>ACA357054284GNRHRc.517C>T (p.Pro173Ser)
4g.67753819G>CCA357054286GNRHRc.517C>G (p.Pro173Ala)
4g.67753819G>TCA357054285GNRHRc.517C>A (p.Pro173Thr)
4g.67753820T>ACA439928751GNRHRc.516A>T (p.Gly172=)
4g.67753820T>CCA439928756GNRHRc.516A>G (p.Gly172=)
4g.67753820T>GCA439928760GNRHRc.516A>C (p.Gly172=)
4g.67753821C>ACA357054287GNRHRc.515G>T (p.Gly172Val)
COSMIC
4g.67753821C=CA1465420438GNRHRc.515G= (p.Gly172=)
4g.67753821C>GCA357054289GNRHRc.515G>C (p.Gly172Ala)
gnomAD v4
4g.67753821C>TCA357054288GNRHRc.515G>A (p.Gly172Glu)
dbSNP gnomAD v4
4g.67753822C>ACA357054290GNRHRc.514G>T (p.Gly172Ter)
4g.67753822C=CA1465420441GNRHRc.514G= (p.Gly172=)
4g.67753822C>GCA357054291GNRHRc.514G>C (p.Gly172Arg)
4g.67753822C>TCA2938927GNRHRc.514G>A (p.Gly172Arg)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.67753823T>ACA439928808GNRHRc.513A>T (p.Ala171=)
4g.67753823T>CCA439928815GNRHRc.513A>G (p.Ala171=)
dbSNP gnomAD v4
4g.67753823T>GCA439928812GNRHRc.513A>C (p.Ala171=)
4g.67753824G>ACA357054292GNRHRc.512C>T (p.Ala171Val)
4g.67753824G>CCA357054293GNRHRc.512C>G (p.Ala171Gly)
4g.67753824G=CA1465420445GNRHRc.512C= (p.Ala171=)
4g.67753824G>TCA357054294GNRHRc.512C>A (p.Ala171Glu)
dbSNP gnomAD v2 gnomAD v4
4g.67753825C>ACA98671906GNRHRc.511G>T (p.Ala171Ser)
dbSNP
4g.67753825C=CA1465420451GNRHRc.511G= (p.Ala171=)
4g.67753825C>GCA357054295GNRHRc.511G>C (p.Ala171Pro)
4g.67753825C>TCA130210GNRHRc.511G>A (p.Ala171Thr)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
4g.67753826A=CA1465420457GNRHRc.510T= (p.Phe170=)
4g.67753826A>CCA357054296GNRHRc.510T>G (p.Phe170Leu)
4g.67753826A>GCA439928838GNRHRc.510T>C (p.Phe170=)
dbSNP gnomAD v4
4g.67753826A>TCA357054297GNRHRc.510T>A (p.Phe170Leu)
4g.67753827A>CCA357054298GNRHRc.509T>G (p.Phe170Cys)
4g.67753827A>GCA357054299GNRHRc.509T>C (p.Phe170Ser)
4g.67753827A>TCA357054300GNRHRc.509T>A (p.Phe170Tyr)
4g.67753828A>CCA357054301GNRHRc.508T>G (p.Phe170Val)
4g.67753828A>GCA357054303GNRHRc.508T>C (p.Phe170Leu)
4g.67753828A>TCA357054302GNRHRc.508T>A (p.Phe170Ile)
4g.67753829G>ACA439928871GNRHRc.507C>T (p.Val169=)
4g.67753829G>CCA439928880GNRHRc.507C>G (p.Val169=)
4g.67753829G>TCA439928883GNRHRc.507C>A (p.Val169=)
4g.67753830A=CA1465420461GNRHRc.506T= (p.Val169=)
4g.67753830A>CCA357054304GNRHRc.506T>G (p.Val169Gly)
dbSNP gnomAD v2 gnomAD v4
4g.67753830A>GCA357054305GNRHRc.506T>C (p.Val169Ala)
gnomAD v4
4g.67753830A>TCA357054306GNRHRc.506T>A (p.Val169Asp)
4g.67753831C>ACA357054307GNRHRc.505G>T (p.Val169Phe)
4g.67753831C>GCA357054308GNRHRc.505G>C (p.Val169Leu)
4g.67753831C>TCA357054309GNRHRc.505G>A (p.Val169Ile)
gnomAD v4
4g.67753832A=CA1465420468GNRHRc.504T= (p.Ser168=)
4g.67753832A>CCA357054310GNRHRc.504T>G (p.Ser168Arg)
4g.67753832A>GCA439928918GNRHRc.504T>C (p.Ser168=)
4g.67753832A>TCA130205GNRHRc.504T>A (p.Ser168Arg)
ClinVar dbSNP
4g.67753833C>ACA357054312GNRHRc.503G>T (p.Ser168Ile)
4g.67753833C=CA1465420472GNRHRc.503G= (p.Ser168=)
4g.67753833C>GCA357054313GNRHRc.503G>C (p.Ser168Thr)
4g.67753833C>TCA357054311GNRHRc.503G>A (p.Ser168Asn)
dbSNP gnomAD v4
4g.67753834T>ACA357054314GNRHRc.502A>T (p.Ser168Cys)
4g.67753834T>CCA357054315GNRHRc.502A>G (p.Ser168Gly)
4g.67753834T>GCA357054316GNRHRc.502A>C (p.Ser168Arg)
4g.67753835A=CA1465420477GNRHRc.501T= (p.Ser167=)
4g.67753835A>CCA98671910GNRHRc.501T>G (p.Ser167Arg)
dbSNP
4g.67753835A>GCA439928941GNRHRc.501T>C (p.Ser167=)
gnomAD v4
4g.67753835A>TCA357054317GNRHRc.501T>A (p.Ser167Arg)
dbSNP
4g.67753836C>ACA357054318GNRHRc.500G>T (p.Ser167Ile)
4g.67753836C=CA1465420479GNRHRc.500G= (p.Ser167=)
4g.67753836C>GCA357054319GNRHRc.500G>C (p.Ser167Thr)
4g.67753836C>TCA357054320GNRHRc.500G>A (p.Ser167Asn)
dbSNP gnomAD v2 gnomAD v4
4g.67753837T>ACA357054321GNRHRc.499A>T (p.Ser167Cys)
4g.67753837T>CCA357054322GNRHRc.499A>G (p.Ser167Gly)
4g.67753837T>GCA357054323GNRHRc.499A>C (p.Ser167Arg)
4g.67753838G>ACA439928968GNRHRc.498C>T (p.Leu166=)
4g.67753838G>CCA439928971GNRHRc.498C>G (p.Leu166=)
dbSNP gnomAD v2
4g.67753838G=CA1465420482GNRHRc.498C= (p.Leu166=)
4g.67753838G>TCA439928973GNRHRc.498C>A (p.Leu166=)
COSMIC
4g.67753839A>CCA357054326GNRHRc.497T>G (p.Leu166Arg)
4g.67753839A>GCA357054325GNRHRc.497T>C (p.Leu166Pro)
gnomAD v4
4g.67753839A>TCA357054324GNRHRc.497T>A (p.Leu166His)
4g.67753840G>ACA2938928GNRHRc.496C>T (p.Leu166Phe)
dbSNP ExAC gnomAD v2 gnomAD v4
4g.67753840G>CCA357054327GNRHRc.496C>G (p.Leu166Val)
4g.67753840G=CA1465420486GNRHRc.496C= (p.Leu166=)
4g.67753840G>TCA357054328GNRHRc.496C>A (p.Leu166Ile)
4g.67753841G>ACA439928993GNRHRc.495C>T (p.Ile165=)
4g.67753841G>CCA357054329GNRHRc.495C>G (p.Ile165Met)
4g.67753841G>TCA439928996GNRHRc.495C>A (p.Ile165=)
gnomAD v4
4g.67753842A>CCA357054330GNRHRc.494T>G (p.Ile165Ser)
4g.67753842A>GCA357054331GNRHRc.494T>C (p.Ile165Thr)
4g.67753842A>TCA357054332GNRHRc.494T>A (p.Ile165Asn)
4g.67753843T>ACA357054333GNRHRc.493A>T (p.Ile165Phe)
4g.67753843T>CCA357054334GNRHRc.493A>G (p.Ile165Val)
4g.67753843T>GCA357054335GNRHRc.493A>C (p.Ile165Leu)
4g.67753844C>ACA357054336GNRHRc.492G>T (p.Trp164Cys)
4g.67753844C>GCA357054337GNRHRc.492G>C (p.Trp164Cys)
4g.67753844C>TCA357054338GNRHRc.492G>A (p.Trp164Ter)
4g.67753845C>ACA357054340GNRHRc.491G>T (p.Trp164Leu)
dbSNP
4g.67753845C=CA1465420489GNRHRc.491G= (p.Trp164=)
4g.67753845C>GCA357054341GNRHRc.491G>C (p.Trp164Ser)
4g.67753845C>TCA357054339GNRHRc.491G>A (p.Trp164Ter)
4g.67753846A=CA1465420493GNRHRc.490T= (p.Trp164=)
4g.67753846A>CCA357054344GNRHRc.490T>G (p.Trp164Gly)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.67753846A>GCA357054342GNRHRc.490T>C (p.Trp164Arg)
4g.67753846A>TCA357054343GNRHRc.490T>A (p.Trp164Arg)
4g.67753847G>ACA439929041GNRHRc.489C>T (p.Ala163=)
4g.67753847G>CCA439929042GNRHRc.489C>G (p.Ala163=)
4g.67753847G>TCA439929044GNRHRc.489C>A (p.Ala163=)
4g.67753848G>ACA357054345GNRHRc.488C>T (p.Ala163Val)
4g.67753848G>CCA357054346GNRHRc.488C>G (p.Ala163Gly)
4g.67753848G=CA1465420497GNRHRc.488C= (p.Ala163=)
4g.67753848G>TCA357054347GNRHRc.488C>A (p.Ala163Asp)
dbSNP gnomAD v3 gnomAD v4
4g.67753849C>ACA357054348GNRHRc.487G>T (p.Ala163Ser)
gnomAD v4
4g.67753849C=CA1465420500GNRHRc.487G= (p.Ala163=)
4g.67753849C>GCA357054349GNRHRc.487G>C (p.Ala163Pro)
4g.67753849C>TCA357054350GNRHRc.487G>A (p.Ala163Thr)
dbSNP
4g.67753850C>ACA439930255GNRHRc.486G>T (p.Leu162=)
4g.67753850C>GCA439930257GNRHRc.486G>C (p.Leu162=)
4g.67753850C>TCA439930259GNRHRc.486G>A (p.Leu162=)
4g.67753851A>CCA357054351GNRHRc.485T>G (p.Leu162Arg)
4g.67753851A>GCA357054352GNRHRc.485T>C (p.Leu162Pro)
4g.67753851A>TCA357054353GNRHRc.485T>A (p.Leu162Gln)
4g.67753852G>ACA439930267GNRHRc.484C>T (p.Leu162=)
4g.67753852G>CCA357054354GNRHRc.484C>G (p.Leu162Val)
4g.67753852G>TCA357054355GNRHRc.484C>A (p.Leu162Met)
4g.67753853delCA2670820607GNRHRc.484del (p.Leu162TrpfsTer19)
c.484del (p.Leu162TrpfsTer?)
gnomAD v4
4g.67753853G>ACA2938929GNRHRc.483C>T (p.Gly161=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.67753853G>CCA439930275GNRHRc.483C>G (p.Gly161=)
4g.67753853G=CA1465420504GNRHRc.483C= (p.Gly161=)
4g.67753853G>TCA439930277GNRHRc.483C>A (p.Gly161=)
gnomAD v4
4g.67753854C>ACA357054356GNRHRc.482G>T (p.Gly161Val)
dbSNP gnomAD v2 gnomAD v4
4g.67753854C=CA1465420507GNRHRc.482G= (p.Gly161=)
4g.67753854C>GCA98671914GNRHRc.482G>C (p.Gly161Ala)
dbSNP gnomAD v3 gnomAD v4
4g.67753854C>TCA357054357GNRHRc.482G>A (p.Gly161Asp)
gnomAD v4
4g.67753855C>ACA357054358GNRHRc.481G>T (p.Gly161Cys)
4g.67753855C>GCA357054359GNRHRc.481G>C (p.Gly161Arg)
4g.67753855C>TCA357054360GNRHRc.481G>A (p.Gly161Ser)
4g.67753856A>CCA439930289GNRHRc.480T>G (p.Val160=)
4g.67753856A>GCA439930291GNRHRc.480T>C (p.Val160=)
4g.67753856A>TCA439930292GNRHRc.480T>A (p.Val160=)
4g.67753857A=CA1465420510GNRHRc.479T= (p.Val160=)
4g.67753857A>CCA357054361GNRHRc.479T>G (p.Val160Gly)
4g.67753857A>GCA357054362GNRHRc.479T>C (p.Val160Ala)
gnomAD v4
4g.67753857A>TCA357054363GNRHRc.479T>A (p.Val160Asp)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.67753858C>ACA357054364GNRHRc.478G>T (p.Val160Phe)
4g.67753858C=CA1465420511GNRHRc.478G= (p.Val160=)
4g.67753858C>GCA357054365GNRHRc.478G>C (p.Val160Leu)
4g.67753858C>TCA98671917GNRHRc.478G>A (p.Val160Ile)
dbSNP gnomAD v2 gnomAD v4
4g.67753859C>ACA357054367GNRHRc.477G>T (p.Met159Ile)
4g.67753859C>GCA357054368GNRHRc.477G>C (p.Met159Ile)
4g.67753859C>TCA357054366GNRHRc.477G>A (p.Met159Ile)
dbSNP gnomAD v4 COSMIC
4g.67753860A>CCA357054369GNRHRc.476T>G (p.Met159Arg)
4g.67753860A>GCA357054370GNRHRc.476T>C (p.Met159Thr)
gnomAD v4 COSMIC
4g.67753860A>TCA357054371GNRHRc.476T>A (p.Met159Lys)
gnomAD v4
4g.67753861T>ACA357054372GNRHRc.475A>T (p.Met159Leu)
4g.67753861T>CCA357054373GNRHRc.475A>G (p.Met159Val)
4g.67753861T>GCA357054374GNRHRc.475A>C (p.Met159Leu)
4g.67753862G>ACA439930325GNRHRc.474C>T (p.Ser158=)
4g.67753862G>CCA439930327GNRHRc.474C>G (p.Ser158=)
4g.67753862G>TCA439930330GNRHRc.474C>A (p.Ser158=)
4g.67753863G>ACA357054377GNRHRc.473C>T (p.Ser158Phe)
4g.67753863G>CCA357054375GNRHRc.473C>G (p.Ser158Cys)
4g.67753863G=CA1465420513GNRHRc.473C= (p.Ser158=)
4g.67753863G>TCA357054376GNRHRc.473C>A (p.Ser158Tyr)
dbSNP gnomAD v3 gnomAD v4
4g.67753864A>CCA357054378GNRHRc.472T>G (p.Ser158Ala)
4g.67753864A>GCA357054379GNRHRc.472T>C (p.Ser158Pro)
4g.67753864A>TCA357054380GNRHRc.472T>A (p.Ser158Thr)

Number of alleles fetched