Chr Mutation (hg38) CAid Gene Transcript Linkouts
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)
4g.67740654T>ACA357048077GNRHRc.813A>T (p.Ala271=)
c.685A>T (p.Ile229Phe)
4g.67740654T>CCA2938849GNRHRc.813A>G (p.Ala271=)
c.685A>G (p.Ile229Val)
 dbSNP ExAC gnomAD v2 gnomAD v4
4g.67740654T>GCA357048069GNRHRc.813A>C (p.Ala271=)
c.685A>C (p.Ile229Leu)
4g.67740654T=CA1465409145GNRHRc.813A= (p.Ala271=)
c.685A= (p.Ile229=)
4g.67740655G>ACA357048084GNRHRc.812C>T (p.Ala271Val)
c.684C>T (p.Cys228=)
4g.67740655G>CCA357048086GNRHRc.812C>G (p.Ala271Gly)
c.684C>G (p.Cys228Trp)
4g.67740655G>TCA357048088GNRHRc.812C>A (p.Ala271Glu)
c.684C>A (p.Cys228Ter)
4g.67740656C>ACA357048091GNRHRc.811G>T (p.Ala271Ser)
c.683G>T (p.Cys228Phe)
4g.67740656C=CA1465409148GNRHRc.811G= (p.Ala271=)
c.683G= (p.Cys228=)
4g.67740656C>GCA2938850GNRHRc.811G>C (p.Ala271Pro)
c.683G>C (p.Cys228Ser)
 dbSNP ExAC gnomAD v2 gnomAD v4
4g.67740656C>TCA357048102GNRHRc.811G>A (p.Ala271Thr)
c.683G>A (p.Cys228Tyr)
4g.67740657A>CCA357048103GNRHRc.810T>G (p.Val270=)
c.682T>G (p.Cys228Gly)
4g.67740657A>GCA357048104GNRHRc.810T>C (p.Val270=)
c.682T>C (p.Cys228Arg)
4g.67740657A>TCA357048107GNRHRc.810T>A (p.Val270=)
c.682T>A (p.Cys228Ser)
4g.67740658A>CCA357048114GNRHRc.809T>G (p.Val270Gly)
c.681T>G (p.Gly227=)
4g.67740658A>GCA357048112GNRHRc.809T>C (p.Val270Ala)
c.681T>C (p.Gly227=)
 gnomAD v4
4g.67740658A>TCA357048109GNRHRc.809T>A (p.Val270Asp)
c.681T>A (p.Gly227=)
4g.67740659C>ACA357048120GNRHRc.808G>T (p.Val270Phe)
c.680G>T (p.Gly227Val)
4g.67740659C=CA1465409152GNRHRc.808G= (p.Val270=)
c.680G= (p.Gly227=)
4g.67740659C>GCA357048122GNRHRc.808G>C (p.Val270Leu)
c.680G>C (p.Gly227Ala)
4g.67740659C>TCA357048127GNRHRc.808G>A (p.Val270Ile)
c.680G>A (p.Gly227Asp)
 dbSNP gnomAD v3 gnomAD v4 COSMIC
4g.67740660C>ACA357048131GNRHRc.807G>T (p.Thr269=)
c.679G>T (p.Gly227Cys)
4g.67740660C=CA1465409159GNRHRc.807G= (p.Thr269=)
c.679G= (p.Gly227=)
4g.67740660C>GCA357048133GNRHRc.807G>C (p.Thr269=)
c.679G>C (p.Gly227Arg)
4g.67740660C>TCA2938851GNRHRc.807G>A (p.Thr269=)
c.679G>A (p.Gly227Ser)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.67740661G>ACA269995GNRHRc.806C>T (p.Thr269Met)
c.678C>T (p.Asp226=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.67740661G>CCA357048142GNRHRc.806C>G (p.Thr269Arg)
c.678C>G (p.Asp226Glu)
4g.67740661G=CA1465409163GNRHRc.806C= (p.Thr269=)
c.678C= (p.Asp226=)
4g.67740661G>TCA357048147GNRHRc.806C>A (p.Thr269Lys)
c.678C>A (p.Asp226Glu)
 gnomAD v4
4g.67740662T>ACA357048149GNRHRc.805A>T (p.Thr269Ser)
c.677A>T (p.Asp226Val)
4g.67740662T>CCA357048153GNRHRc.805A>G (p.Thr269Ala)
c.677A>G (p.Asp226Gly)
4g.67740662T>GCA357048156GNRHRc.805A>C (p.Thr269Pro)
c.677A>C (p.Asp226Ala)
4g.67740663C>ACA357048163GNRHRc.804G>T (p.Met268Ile)
c.676G>T (p.Asp226Tyr)
4g.67740663C>GCA357048164GNRHRc.804G>C (p.Met268Ile)
c.676G>C (p.Asp226His)
4g.67740663C>TCA357048160GNRHRc.804G>A (p.Met268Ile)
c.676G>A (p.Asp226Asn)
4g.67740664A=CA1465409166GNRHRc.803T= (p.Met268=)
c.675T= (p.Asn225=)
4g.67740664A>CCA357048165GNRHRc.803T>G (p.Met268Arg)
c.675T>G (p.Asn225Lys)
4g.67740664A>GCA2938852GNRHRc.803T>C (p.Met268Thr)
c.675T>C (p.Asn225=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.67740664A>TCA357048166GNRHRc.803T>A (p.Met268Lys)
c.675T>A (p.Asn225Lys)
 dbSNP
4g.67740665T>ACA357048167GNRHRc.802A>T (p.Met268Leu)
c.674A>T (p.Asn225Ile)
4g.67740665T>CCA357048168GNRHRc.802A>G (p.Met268Val)
c.674A>G (p.Asn225Ser)
4g.67740665T>GCA357048171GNRHRc.802A>C (p.Met268Leu)
c.674A>C (p.Asn225Thr)
 dbSNP
4g.67740665T=CA1465409169GNRHRc.802A= (p.Met268=)
c.674A= (p.Asn225=)
4g.67740666T>ACA357048173GNRHRc.801A>T (p.Lys267Asn)
c.673A>T (p.Asn225Tyr)
4g.67740666T>CCA357048174GNRHRc.801A>G (p.Lys267=)
c.673A>G (p.Asn225Asp)
4g.67740666T>GCA357048176GNRHRc.801A>C (p.Lys267Asn)
c.673A>C (p.Asn225His)
4g.67740667T>ACA357048181GNRHRc.800A>T (p.Lys267Ile)
c.672A>T (p.Lys224Asn)
4g.67740667T>CCA357048188GNRHRc.800A>G (p.Lys267Arg)
c.672A>G (p.Lys224=)
4g.67740667T>GCA357048190GNRHRc.800A>C (p.Lys267Thr)
c.672A>C (p.Lys224Asn)
4g.67740668T>ACA357048197GNRHRc.799A>T (p.Lys267Ter)
c.671A>T (p.Lys224Ile)
4g.67740668T>CCA357048199GNRHRc.799A>G (p.Lys267Glu)
c.671A>G (p.Lys224Arg)
4g.67740668T>GCA357048194GNRHRc.799A>C (p.Lys267Gln)
c.671A>C (p.Lys224Thr)
4g.67740669T>ACA357048204GNRHRc.798A>T (p.Leu266=)
c.670A>T (p.Lys224Ter)
4g.67740669T>CCA357048206GNRHRc.798A>G (p.Leu266=)
c.670A>G (p.Lys224Glu)
4g.67740669T>GCA357048209GNRHRc.798A>C (p.Leu266=)
c.670A>C (p.Lys224Gln)
4g.67740669T=CA1465409172GNRHRc.798A= (p.Leu266=)
c.670A= (p.Lys224=)
4g.67740669_67740671delinsTAGCA1465409175GNRHRc.796_798delinsCTA (p.Leu266=)
c.668_670delinsCTA (p.Ser223=)
4g.67740670A=CA1465409183GNRHRc.797T= (p.Leu266=)
c.669T= (p.Ser223=)
4g.67740670A>CCA2938853GNRHRc.797T>G (p.Leu266Arg)
c.669T>G (p.Ser223=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.67740670A>GCA357048213GNRHRc.797T>C (p.Leu266Pro)
c.669T>C (p.Ser223=)
 gnomAD v4
4g.67740670A>TCA357048218GNRHRc.797T>A (p.Leu266Gln)
c.669T>A (p.Ser223=)
4g.67740670dupCA1465409181GNRHRc.797dup (p.Met268AsnfsTer26)
c.669dup (p.Lys224Ter)
 dbSNP
4g.67740670_67740671delinsAGCA1465409185GNRHRc.796_797delinsCT (p.Leu266=)
c.668_669delinsCT (p.Ser223=)
4g.67740672_67740673delCA645518038GNRHRc.796_797del (p.Leu266LysfsTer27)
c.668_669del (p.Ser223Ter)
 dbSNP COSMIC
4g.67740671delCA1465409188GNRHRc.796del (p.Leu266Ter)
c.668del (p.Ser223LeufsTer?)
 dbSNP
4g.67740671G>ACA98667567GNRHRc.796C>T (p.Leu266=)
c.668C>T (p.Ser223Phe)
 dbSNP
4g.67740671G>CCA98667570GNRHRc.796C>G (p.Leu266Val)
c.668C>G (p.Ser223Cys)
 dbSNP gnomAD v4
4g.67740671G=CA1465409189GNRHRc.796C= (p.Leu266=)
c.668C= (p.Ser223=)
4g.67740671G>TCA357048223GNRHRc.796C>A (p.Leu266Ile)
c.668C>A (p.Ser223Tyr)
 gnomAD v4
4g.67740672A>CCA357048236GNRHRc.795T>G (p.Thr265=)
c.667T>G (p.Ser223Ala)
4g.67740672A>GCA357048237GNRHRc.795T>C (p.Thr265=)
c.667T>C (p.Ser223Pro)
4g.67740672A>TCA357048238GNRHRc.795T>A (p.Thr265=)
c.667T>A (p.Ser223Thr)
4g.67740672_67740678delinsAGTCTTCCA1465409194GNRHRc.789_795delinsGAAGACT (p.Leu263=)
c.661_667delinsGAAGACT (p.Glu221=)
4g.67740673G>ACA357048240GNRHRc.794C>T (p.Thr265Ile)
c.666C>T (p.Asp222=)
4g.67740673G>CCA357048243GNRHRc.794C>G (p.Thr265Ser)
c.666C>G (p.Asp222Glu)
4g.67740673G>TCA357048246GNRHRc.794C>A (p.Thr265Asn)
c.666C>A (p.Asp222Glu)
 gnomAD v4
4g.67740673_67740678delCA1465409196GNRHRc.789_794del (p.Lys264_Thr265del)
c.661_666del (p.Glu221_Asp222del)
 dbSNP
4g.67740674T>ACA357048260GNRHRc.793A>T (p.Thr265Ser)
c.665A>T (p.Asp222Val)
4g.67740674T>CCA357048265GNRHRc.793A>G (p.Thr265Ala)
c.665A>G (p.Asp222Gly)
4g.67740674T>GCA357048249GNRHRc.793A>C (p.Thr265Pro)
c.665A>C (p.Asp222Ala)
4g.67740675C>ACA357048280GNRHRc.792G>T (p.Lys264Asn)
c.664G>T (p.Asp222Tyr)
4g.67740675C>GCA357048267GNRHRc.792G>C (p.Lys264Asn)
c.664G>C (p.Asp222His)
4g.67740675C>TCA357048276GNRHRc.792G>A (p.Lys264=)
c.664G>A (p.Asp222Asn)
4g.67740676T>ACA357048282GNRHRc.791A>T (p.Lys264Met)
c.663A>T (p.Glu221Asp)
4g.67740676T>CCA357048285GNRHRc.791A>G (p.Lys264Arg)
c.663A>G (p.Glu221=)
4g.67740676T>GCA357048288GNRHRc.791A>C (p.Lys264Thr)
c.663A>C (p.Glu221Asp)
4g.67740677T>ACA357048292GNRHRc.790A>T (p.Lys264Ter)
c.662A>T (p.Glu221Val)
4g.67740677T>CCA357048291GNRHRc.790A>G (p.Lys264Glu)
c.662A>G (p.Glu221Gly)
4g.67740677T>GCA357048290GNRHRc.790A>C (p.Lys264Gln)
c.662A>C (p.Glu221Ala)
4g.67740678C>ACA357048293GNRHRc.789G>T (p.Leu263=)
c.661G>T (p.Glu221Ter)
4g.67740678C>GCA357048295GNRHRc.789G>C (p.Leu263=)
c.661G>C (p.Glu221Gln)
4g.67740678C>TCA357048296GNRHRc.789G>A (p.Leu263=)
c.661G>A (p.Glu221Lys)
4g.67740679A>CCA357048298GNRHRc.788T>G (p.Leu263Arg)
c.660T>G (p.Ala220=)
4g.67740679A>GCA357048301GNRHRc.788T>C (p.Leu263Pro)
c.660T>C (p.Ala220=)
4g.67740679A>TCA357048304GNRHRc.788T>A (p.Leu263Gln)
c.660T>A (p.Ala220=)
4g.67740680G>ACA357048309GNRHRc.787C>T (p.Leu263=)
c.659C>T (p.Ala220Val)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.67740680G>CCA357048306GNRHRc.787C>G (p.Leu263Val)
c.659C>G (p.Ala220Gly)
 dbSNP
4g.67740680G=CA1465409202GNRHRc.787C= (p.Leu263=)
c.659C= (p.Ala220=)
4g.67740680G>TCA357048308GNRHRc.787C>A (p.Leu263Met)
c.659C>A (p.Ala220Asp)
 gnomAD v4
4g.67740681C>ACA357048311GNRHRc.786G>T (p.Arg262=)
c.658G>T (p.Ala220Ser)
4g.67740681C>GCA357048314GNRHRc.786G>C (p.Arg262=)
c.658G>C (p.Ala220Pro)
4g.67740681C>TCA357048318GNRHRc.786G>A (p.Arg262=)
c.658G>A (p.Ala220Thr)
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=)

Number of alleles fetched