Chr Mutation (hg38) CAid Gene Transcript Linkouts
4g.42962958A=CA1453073760GRXCR1c.451A= (p.Thr151=)
c.88A= (p.Thr30=)
4g.42962958A>CCA356792219GRXCR1c.451A>C (p.Thr151Pro)
c.88A>C (p.Thr30Pro)
4g.42962958A>GCA2904408GRXCR1c.451A>G (p.Thr151Ala)
c.88A>G (p.Thr30Ala)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.42962958A>TCA356792220GRXCR1c.451A>T (p.Thr151Ser)
c.88A>T (p.Thr30Ser)
4g.42962959C>ACA356792221GRXCR1c.452C>A (p.Thr151Lys)
c.89C>A (p.Thr30Lys)
4g.42962959C=CA1453073761GRXCR1c.452C= (p.Thr151=)
c.89C= (p.Thr30=)
4g.42962959C>GCA356792222GRXCR1c.452C>G (p.Thr151Arg)
c.89C>G (p.Thr30Arg)
4g.42962959C>TCA2904409GRXCR1c.452C>T (p.Thr151Ile)
c.89C>T (p.Thr30Ile)
 dbSNP ExAC gnomAD v2 gnomAD v4
4g.42962960A>CCA439191549GRXCR1c.453A>C (p.Thr151=)
c.90A>C (p.Thr30=)
4g.42962960A>GCA439191547GRXCR1c.453A>G (p.Thr151=)
c.90A>G (p.Thr30=)
4g.42962960A>TCA439191546GRXCR1c.453A>T (p.Thr151=)
c.90A>T (p.Thr30=)
4g.42962961A>CCA356792225GRXCR1c.454A>C (p.Thr152Pro)
c.91A>C (p.Thr31Pro)
4g.42962961A>GCA356792223GRXCR1c.454A>G (p.Thr152Ala)
c.91A>G (p.Thr31Ala)
4g.42962961A>TCA356792224GRXCR1c.454A>T (p.Thr152Ser)
c.91A>T (p.Thr31Ser)
4g.42962962C>ACA356792226GRXCR1c.455C>A (p.Thr152Asn)
c.92C>A (p.Thr31Asn)
4g.42962962C>GCA356792227GRXCR1c.455C>G (p.Thr152Ser)
c.92C>G (p.Thr31Ser)
4g.42962962C>TCA356792228GRXCR1c.455C>T (p.Thr152Ile)
c.92C>T (p.Thr31Ile)
 gnomAD v4 COSMIC
4g.42962963delCA2670496481GRXCR1c.456del (p.Phe153LeufsTer16)
c.93del (p.Phe32LeufsTer16)
 gnomAD v4
4g.42962963C>ACA439191552GRXCR1c.456C>A (p.Thr152=)
c.93C>A (p.Thr31=)
 dbSNP gnomAD v2 gnomAD v4
4g.42962963C=CA1453073762GRXCR1c.456C= (p.Thr152=)
c.93C= (p.Thr31=)
4g.42962963C>GCA439191553GRXCR1c.456C>G (p.Thr152=)
c.93C>G (p.Thr31=)
 dbSNP gnomAD v3 gnomAD v4
4g.42962963C>TCA2904410GRXCR1c.456C>T (p.Thr152=)
c.93C>T (p.Thr31=)
 dbSNP ExAC gnomAD v2
4g.42962963_42962964insACTCA2521723338GRXCR1c.456_457insACT (p.Thr152_Phe153insThr)
c.93_94insACT (p.Thr31_Phe32insThr)
4g.42962964T>ACA356792230GRXCR1c.457T>A (p.Phe153Ile)
c.94T>A (p.Phe32Ile)
4g.42962964T>CCA356792229GRXCR1c.457T>C (p.Phe153Leu)
c.94T>C (p.Phe32Leu)
4g.42962964T>GCA2904411GRXCR1c.457T>G (p.Phe153Val)
c.94T>G (p.Phe32Val)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.42962964T=CA1453073763GRXCR1c.457T= (p.Phe153=)
c.94T= (p.Phe32=)
4g.42962965T>ACA356792231GRXCR1c.458T>A (p.Phe153Tyr)
c.95T>A (p.Phe32Tyr)
4g.42962965T>CCA356792232GRXCR1c.458T>C (p.Phe153Ser)
c.95T>C (p.Phe32Ser)
4g.42962965T>GCA356792233GRXCR1c.458T>G (p.Phe153Cys)
c.95T>G (p.Phe32Cys)
4g.42962966T>ACA356792234GRXCR1c.459T>A (p.Phe153Leu)
c.96T>A (p.Phe32Leu)
4g.42962966T>CCA2904412GRXCR1c.459T>C (p.Phe153=)
c.96T>C (p.Phe32=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.42962966T>GCA356792235GRXCR1c.459T>G (p.Phe153Leu)
c.96T>G (p.Phe32Leu)
 gnomAD v4
4g.42962966T=CA1453073764GRXCR1c.459T= (p.Phe153=)
c.96T= (p.Phe32=)
4g.42962967G>ACA356792236GRXCR1c.460G>A (p.Glu154Lys)
c.97G>A (p.Glu33Lys)
 dbSNP
4g.42962967G>CCA356792238GRXCR1c.460G>C (p.Glu154Gln)
c.97G>C (p.Glu33Gln)
 dbSNP gnomAD v3 gnomAD v4
4g.42962967G=CA1453073765GRXCR1c.460G= (p.Glu154=)
c.97G= (p.Glu33=)
4g.42962967G>TCA356792237GRXCR1c.460G>T (p.Glu154Ter)
c.97G>T (p.Glu33Ter)
4g.42962968A>CCA356792239GRXCR1c.461A>C (p.Glu154Ala)
c.98A>C (p.Glu33Ala)
 gnomAD v4
4g.42962968A>GCA356792240GRXCR1c.461A>G (p.Glu154Gly)
c.98A>G (p.Glu33Gly)
4g.42962968A>TCA356792241GRXCR1c.461A>T (p.Glu154Val)
c.98A>T (p.Glu33Val)
4g.42962969A>CCA356792242GRXCR1c.462A>C (p.Glu154Asp)
c.99A>C (p.Glu33Asp)
4g.42962969A>GCA439191555GRXCR1c.462A>G (p.Glu154=)
c.99A>G (p.Glu33=)
4g.42962969A>TCA356792243GRXCR1c.462A>T (p.Glu154Asp)
c.99A>T (p.Glu33Asp)
4g.42962970A>CCA439191556GRXCR1c.463A>C (p.Arg155=)
c.100A>C (p.Arg34=)
4g.42962970A>GCA356792244GRXCR1c.463A>G (p.Arg155Gly)
c.100A>G (p.Arg34Gly)
4g.42962970A>TCA356792245GRXCR1c.463A>T (p.Arg155Ter)
c.100A>T (p.Arg34Ter)
4g.42962971G>ACA2904413GRXCR1c.464G>A (p.Arg155Lys)
c.101G>A (p.Arg34Lys)
 dbSNP ExAC gnomAD v2 gnomAD v4
4g.42962971G>CCA356792246GRXCR1c.464G>C (p.Arg155Thr)
c.101G>C (p.Arg34Thr)
 gnomAD v4
4g.42962971G=CA1453073766GRXCR1c.464G= (p.Arg155=)
c.101G= (p.Arg34=)
4g.42962971G>TCA356792247GRXCR1c.464G>T (p.Arg155Ile)
c.101G>T (p.Arg34Ile)
 COSMIC
4g.42962972A>CCA356792248GRXCR1c.465A>C (p.Arg155Ser)
c.102A>C (p.Arg34Ser)
4g.42962972A>GCA439191557GRXCR1c.465A>G (p.Arg155=)
c.102A>G (p.Arg34=)
4g.42962972A>TCA356792249GRXCR1c.465A>T (p.Arg155Ser)
c.102A>T (p.Arg34Ser)
4g.42962973T>ACA356792250GRXCR1c.466T>A (p.Cys156Ser)
c.103T>A (p.Cys35Ser)
 gnomAD v4
4g.42962973T>CCA2904414GRXCR1c.466T>C (p.Cys156Arg)
c.103T>C (p.Cys35Arg)
 dbSNP ExAC gnomAD v2 gnomAD v4
4g.42962973T>GCA356792251GRXCR1c.466T>G (p.Cys156Gly)
c.103T>G (p.Cys35Gly)
4g.42962973T=CA1453073767GRXCR1c.466T= (p.Cys156=)
c.103T= (p.Cys35=)
4g.42962974G>ACA356792252GRXCR1c.467G>A (p.Cys156Tyr)
c.104G>A (p.Cys35Tyr)
 gnomAD v4
4g.42962974G>CCA356792253GRXCR1c.467G>C (p.Cys156Ser)
c.104G>C (p.Cys35Ser)
4g.42962974G>TCA356792254GRXCR1c.467G>T (p.Cys156Phe)
c.104G>T (p.Cys35Phe)
4g.42962975T>ACA356792255GRXCR1c.468T>A (p.Cys156Ter)
c.105T>A (p.Cys35Ter)
4g.42962975T>CCA439191561GRXCR1c.468T>C (p.Cys156=)
c.105T>C (p.Cys35=)
4g.42962975T>GCA356792256GRXCR1c.468T>G (p.Cys156Trp)
c.105T>G (p.Cys35Trp)
4g.42962976G>ACA356792257GRXCR1c.469G>A (p.Glu157Lys)
c.106G>A (p.Glu36Lys)
4g.42962976G>CCA356792258GRXCR1c.469G>C (p.Glu157Gln)
c.106G>C (p.Glu36Gln)
 gnomAD v4
4g.42962976G=CA1453073768GRXCR1c.469G= (p.Glu157=)
c.106G= (p.Glu36=)
4g.42962976G>TCA2904415GRXCR1c.469G>T (p.Glu157Ter)
c.106G>T (p.Glu36Ter)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.42962977A>CCA356792259GRXCR1c.470A>C (p.Glu157Ala)
c.107A>C (p.Glu36Ala)
4g.42962977A>GCA356792260GRXCR1c.470A>G (p.Glu157Gly)
c.107A>G (p.Glu36Gly)
4g.42962977A>TCA356792261GRXCR1c.470A>T (p.Glu157Val)
c.107A>T (p.Glu36Val)
4g.42962978A=CA1453073769GRXCR1c.471A= (p.Glu157=)
c.108A= (p.Glu36=)
4g.42962978A>CCA356792262GRXCR1c.471A>C (p.Glu157Asp)
c.108A>C (p.Glu36Asp)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.42962978A>GCA439191565GRXCR1c.471A>G (p.Glu157=)
c.108A>G (p.Glu36=)
 dbSNP
4g.42962978A>TCA356792263GRXCR1c.471A>T (p.Glu157Asp)
c.108A>T (p.Glu36Asp)
4g.42962979C>ACA356792264GRXCR1c.472C>A (p.Leu158Met)
c.109C>A (p.Leu37Met)
 gnomAD v4
4g.42962979C>GCA356792265GRXCR1c.472C>G (p.Leu158Val)
c.109C>G (p.Leu37Val)
4g.42962979C>TCA439191568GRXCR1c.472C>T (p.Leu158=)
c.109C>T (p.Leu37=)
4g.42962980T>ACA356792266GRXCR1c.473T>A (p.Leu158Gln)
c.110T>A (p.Leu37Gln)
 gnomAD v4
4g.42962980T>CCA356792267GRXCR1c.473T>C (p.Leu158Pro)
c.110T>C (p.Leu37Pro)
4g.42962980T>GCA356792268GRXCR1c.473T>G (p.Leu158Arg)
c.110T>G (p.Leu37Arg)
4g.42962981G>ACA439191571GRXCR1c.474G>A (p.Leu158=)
c.111G>A (p.Leu37=)
4g.42962981G>CCA439191569GRXCR1c.474G>C (p.Leu158=)
c.111G>C (p.Leu37=)
 gnomAD v4
4g.42962981G>TCA439191570GRXCR1c.474G>T (p.Leu158=)
c.111G>T (p.Leu37=)
4g.42962982G>ACA96311683GRXCR1c.475G>A (p.Val159Ile)
c.112G>A (p.Val38Ile)
 dbSNP COSMIC
4g.42962982G>CCA356792269GRXCR1c.475G>C (p.Val159Leu)
c.112G>C (p.Val38Leu)
 gnomAD v4
4g.42962982G=CA1453073770GRXCR1c.475G= (p.Val159=)
c.112G= (p.Val38=)
4g.42962982G>TCA356792270GRXCR1c.475G>T (p.Val159Phe)
c.112G>T (p.Val38Phe)
4g.42962983T>ACA356792271GRXCR1c.476T>A (p.Val159Asp)
c.113T>A (p.Val38Asp)
4g.42962983T>CCA2904416GRXCR1c.476T>C (p.Val159Ala)
c.113T>C (p.Val38Ala)
 dbSNP ExAC gnomAD v2 gnomAD v4
4g.42962983T>GCA356792272GRXCR1c.476T>G (p.Val159Gly)
c.113T>G (p.Val38Gly)
4g.42962983T=CA1453073771GRXCR1c.476T= (p.Val159=)
c.113T= (p.Val38=)
4g.42962984T>ACA2904417GRXCR1c.477T>A (p.Val159=)
c.114T>A (p.Val38=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.42962984T>CCA439191578GRXCR1c.477T>C (p.Val159=)
c.114T>C (p.Val38=)
4g.42962984T>GCA439191580GRXCR1c.477T>G (p.Val159=)
c.114T>G (p.Val38=)
 gnomAD v4
4g.42962984T=CA1453073772GRXCR1c.477T= (p.Val159=)
c.114T= (p.Val38=)
4g.42962984_42962985delinsAGCA2499217214GRXCR1c.477_478delinsAG (p.Arg160Gly)
c.114_115delinsAG (p.Arg39Gly)
 ClinVar dbSNP
4g.42962985A=CA1453073773GRXCR1c.478A= (p.Arg160=)
c.115A= (p.Arg39=)
4g.42962985A>CCA439191581GRXCR1c.478A>C (p.Arg160=)
c.115A>C (p.Arg39=)
4g.42962985A>GCA2904418GRXCR1c.478A>G (p.Arg160Gly)
c.115A>G (p.Arg39Gly)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.42962985A>TCA356792273GRXCR1c.478A>T (p.Arg160Ter)
c.115A>T (p.Arg39Ter)
4g.42962986G>ACA356792276GRXCR1c.479G>A (p.Arg160Lys)
c.116G>A (p.Arg39Lys)
 COSMIC
4g.42962986G>CCA356792275GRXCR1c.479G>C (p.Arg160Thr)
c.116G>C (p.Arg39Thr)
4g.42962986G>TCA356792274GRXCR1c.479G>T (p.Arg160Ile)
c.116G>T (p.Arg39Ile)
4g.42962987A>CCA356792278GRXCR1c.480A>C (p.Arg160Ser)
c.117A>C (p.Arg39Ser)
4g.42962987A>GCA439191583GRXCR1c.480A>G (p.Arg160=)
c.117A>G (p.Arg39=)
 gnomAD v4
4g.42962987A>TCA356792277GRXCR1c.480A>T (p.Arg160Ser)
c.117A>T (p.Arg39Ser)
4g.42962988A=CA1453073774GRXCR1c.481A= (p.Lys161=)
c.118A= (p.Lys40=)
4g.42962988A>CCA356792281GRXCR1c.481A>C (p.Lys161Gln)
c.118A>C (p.Lys40Gln)
4g.42962988A>GCA356792279GRXCR1c.481A>G (p.Lys161Glu)
c.118A>G (p.Lys40Glu)
 dbSNP gnomAD v2 gnomAD v4
4g.42962988A>TCA356792280GRXCR1c.481A>T (p.Lys161Ter)
c.118A>T (p.Lys40Ter)
4g.42962989A>CCA356792282GRXCR1c.482A>C (p.Lys161Thr)
c.119A>C (p.Lys40Thr)
 ClinVar
4g.42962989A>GCA356792283GRXCR1c.482A>G (p.Lys161Arg)
c.119A>G (p.Lys40Arg)
 gnomAD v4
4g.42962989A>TCA356792284GRXCR1c.482A>T (p.Lys161Met)
c.119A>T (p.Lys40Met)
4g.42962990G>ACA439191584GRXCR1c.483G>A (p.Lys161=)
c.120G>A (p.Lys40=)
4g.42962990G>CCA2904419GRXCR1c.483G>C (p.Lys161Asn)
c.120G>C (p.Lys40Asn)
 dbSNP ExAC gnomAD v2 gnomAD v4
4g.42962990G=CA1453073775GRXCR1c.483G= (p.Lys161=)
c.120G= (p.Lys40=)
4g.42962990G>TCA356792285GRXCR1c.483G>T (p.Lys161Asn)
c.120G>T (p.Lys40Asn)
4g.42962991A>CCA356792286GRXCR1c.484A>C (p.Ile162Leu)
c.121A>C (p.Ile41Leu)
4g.42962991A>GCA356792287GRXCR1c.484A>G (p.Ile162Val)
c.121A>G (p.Ile41Val)
4g.42962991A>TCA356792288GRXCR1c.484A>T (p.Ile162Phe)
c.121A>T (p.Ile41Phe)
4g.42962992T>ACA356792289GRXCR1c.485T>A (p.Ile162Asn)
c.122T>A (p.Ile41Asn)
4g.42962992T>CCA356792290GRXCR1c.485T>C (p.Ile162Thr)
c.122T>C (p.Ile41Thr)
4g.42962992T>GCA356792291GRXCR1c.485T>G (p.Ile162Ser)
c.122T>G (p.Ile41Ser)
4g.42962993T>ACA439191587GRXCR1c.486T>A (p.Ile162=)
c.123T>A (p.Ile41=)
4g.42962993T>CCA2904420GRXCR1c.486T>C (p.Ile162=)
c.123T>C (p.Ile41=)
 dbSNP ExAC gnomAD v2 gnomAD v4
4g.42962993T>GCA356792292GRXCR1c.486T>G (p.Ile162Met)
c.123T>G (p.Ile41Met)
4g.42962993T=CA1453073776GRXCR1c.486T= (p.Ile162=)
c.123T= (p.Ile41=)
4g.42962994T>ACA356792293GRXCR1c.487T>A (p.Phe163Ile)
c.124T>A (p.Phe42Ile)
4g.42962994T>CCA356792294GRXCR1c.487T>C (p.Phe163Leu)
c.124T>C (p.Phe42Leu)
4g.42962994T>GCA356792295GRXCR1c.487T>G (p.Phe163Val)
c.124T>G (p.Phe42Val)
4g.42962995T>ACA356792296GRXCR1c.488T>A (p.Phe163Tyr)
c.125T>A (p.Phe42Tyr)
4g.42962995T>CCA356792297GRXCR1c.488T>C (p.Phe163Ser)
c.125T>C (p.Phe42Ser)
 dbSNP COSMIC
4g.42962995T>GCA356792298GRXCR1c.488T>G (p.Phe163Cys)
c.125T>G (p.Phe42Cys)
4g.42962995T=CA1453073777GRXCR1c.488T= (p.Phe163=)
c.125T= (p.Phe42=)
4g.42962996C>ACA356792299GRXCR1c.489C>A (p.Phe163Leu)
c.126C>A (p.Phe42Leu)
4g.42962996C>GCA356792300GRXCR1c.489C>G (p.Phe163Leu)
c.126C>G (p.Phe42Leu)
4g.42962996C>TCA439191591GRXCR1c.489C>T (p.Phe163=)
c.126C>T (p.Phe42=)
4g.42962997C>ACA356792301GRXCR1c.490C>A (p.Gln164Lys)
c.127C>A (p.Gln43Lys)
4g.42962997C>GCA356792302GRXCR1c.490C>G (p.Gln164Glu)
c.127C>G (p.Gln43Glu)
4g.42962997C>TCA356792303GRXCR1c.490C>T (p.Gln164Ter)
c.127C>T (p.Gln43Ter)
4g.42962998A>CCA356792305GRXCR1c.491A>C (p.Gln164Pro)
c.128A>C (p.Gln43Pro)
4g.42962998A>GCA356792306GRXCR1c.491A>G (p.Gln164Arg)
c.128A>G (p.Gln43Arg)
4g.42962998A>TCA356792304GRXCR1c.491A>T (p.Gln164Leu)
c.128A>T (p.Gln43Leu)
4g.42962999A>CCA356792307GRXCR1c.492A>C (p.Gln164His)
c.129A>C (p.Gln43His)
4g.42962999A>GCA439191593GRXCR1c.492A>G (p.Gln164=)
c.129A>G (p.Gln43=)
4g.42962999A>TCA356792308GRXCR1c.492A>T (p.Gln164His)
c.129A>T (p.Gln43His)
4g.42963000A>CCA356792309GRXCR1c.493A>C (p.Asn165His)
c.130A>C (p.Asn44His)
4g.42963000A>GCA356792310GRXCR1c.493A>G (p.Asn165Asp)
c.130A>G (p.Asn44Asp)
4g.42963000A>TCA356792311GRXCR1c.493A>T (p.Asn165Tyr)
c.130A>T (p.Asn44Tyr)
4g.42963001A=CA1453073778GRXCR1c.494A= (p.Asn165=)
c.131A= (p.Asn44=)
4g.42963001A>CCA356792312GRXCR1c.494A>C (p.Asn165Thr)
c.131A>C (p.Asn44Thr)
4g.42963001A>GCA2904421GRXCR1c.494A>G (p.Asn165Ser)
c.131A>G (p.Asn44Ser)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.42963001A>TCA356792313GRXCR1c.494A>T (p.Asn165Ile)
c.131A>T (p.Asn44Ile)
4g.42963002C>ACA356792314GRXCR1c.495C>A (p.Asn165Lys)
c.132C>A (p.Asn44Lys)
4g.42963002C=CA1453073779GRXCR1c.495C= (p.Asn165=)
c.132C= (p.Asn44=)
4g.42963002C>GCA356792315GRXCR1c.495C>G (p.Asn165Lys)
c.132C>G (p.Asn44Lys)
4g.42963002C>TCA439191594GRXCR1c.495C>T (p.Asn165=)
c.132C>T (p.Asn44=)
 dbSNP gnomAD v4
4g.42963003C>ACA356792316GRXCR1c.496C>A (p.His166Asn)
c.133C>A (p.His45Asn)
4g.42963003C=CA1453073780GRXCR1c.496C= (p.His166=)
c.133C= (p.His45=)
4g.42963003C>GCA356792317GRXCR1c.496C>G (p.His166Asp)
c.133C>G (p.His45Asp)
4g.42963003C>TCA356792318GRXCR1c.496C>T (p.His166Tyr)
c.133C>T (p.His45Tyr)
 dbSNP gnomAD v4
4g.42963004A=CA1453073781GRXCR1c.497A= (p.His166=)
c.134A= (p.His45=)
4g.42963004A>CCA356792320GRXCR1c.497A>C (p.His166Pro)
c.134A>C (p.His45Pro)
4g.42963004A>GCA2904422GRXCR1c.497A>G (p.His166Arg)
c.134A>G (p.His45Arg)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.42963004A>TCA356792319GRXCR1c.497A>T (p.His166Leu)
c.134A>T (p.His45Leu)
4g.42963005T>ACA356792321GRXCR1c.498T>A (p.His166Gln)
c.135T>A (p.His45Gln)
4g.42963005T>CCA439191596GRXCR1c.498T>C (p.His166=)
c.135T>C (p.His45=)
 dbSNP
4g.42963005T>GCA356792322GRXCR1c.498T>G (p.His166Gln)
c.135T>G (p.His45Gln)
4g.42963005T=CA1453073782GRXCR1c.498T= (p.His166=)
c.135T= (p.His45=)
4g.42963006C>ACA356792323GRXCR1c.499C>A (p.Arg167Ser)
c.136C>A (p.Arg46Ser)
 COSMIC
4g.42963006C=CA1453073783GRXCR1c.499C= (p.Arg167=)
c.136C= (p.Arg46=)
4g.42963006C>GCA356792324GRXCR1c.499C>G (p.Arg167Gly)
c.136C>G (p.Arg46Gly)
 dbSNP gnomAD v4
4g.42963006C>TCA2904423GRXCR1c.499C>T (p.Arg167Cys)
c.136C>T (p.Arg46Cys)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
4g.42963007G>ACA2904424GRXCR1c.500G>A (p.Arg167His)
c.137G>A (p.Arg46His)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
4g.42963007G>CCA356792325GRXCR1c.500G>C (p.Arg167Pro)
c.137G>C (p.Arg46Pro)
4g.42963007G=CA1453073784GRXCR1c.500G= (p.Arg167=)
c.137G= (p.Arg46=)
4g.42963007G>TCA356792326GRXCR1c.500G>T (p.Arg167Leu)
c.137G>T (p.Arg46Leu)
4g.42963008C>ACA439191599GRXCR1c.501C>A (p.Arg167=)
c.138C>A (p.Arg46=)
 dbSNP gnomAD v4
4g.42963008C=CA1453073785GRXCR1c.501C= (p.Arg167=)
c.138C= (p.Arg46=)
4g.42963008C>GCA439191601GRXCR1c.501C>G (p.Arg167=)
c.138C>G (p.Arg46=)
4g.42963008C>TCA439191600GRXCR1c.501C>T (p.Arg167=)
c.138C>T (p.Arg46=)
 dbSNP gnomAD v4
4g.42963009G>ACA2904425GRXCR1c.502G>A (p.Val168Ile)
c.139G>A (p.Val47Ile)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
4g.42963009G>CCA356792327GRXCR1c.502G>C (p.Val168Leu)
c.139G>C (p.Val47Leu)
4g.42963009G=CA1453073786GRXCR1c.502G= (p.Val168=)
c.139G= (p.Val47=)
4g.42963009G>TCA356792328GRXCR1c.502G>T (p.Val168Leu)
c.139G>T (p.Val47Leu)
 gnomAD v4
4g.42963010T>ACA356792329GRXCR1c.503T>A (p.Val168Glu)
c.140T>A (p.Val47Glu)
4g.42963010T>CCA356792330GRXCR1c.503T>C (p.Val168Ala)
c.140T>C (p.Val47Ala)
4g.42963010T>GCA356792331GRXCR1c.503T>G (p.Val168Gly)
c.140T>G (p.Val47Gly)
4g.42963011A>CCA439191605GRXCR1c.504A>C (p.Val168=)
c.141A>C (p.Val47=)
4g.42963011A>GCA439191604GRXCR1c.504A>G (p.Val168=)
c.141A>G (p.Val47=)
4g.42963011A>TCA439191603GRXCR1c.504A>T (p.Val168=)
c.141A>T (p.Val47=)
4g.42963012A>CCA356792333GRXCR1c.505A>C (p.Lys169Gln)
c.142A>C (p.Lys48Gln)
 COSMIC
4g.42963012A>GCA356792334GRXCR1c.505A>G (p.Lys169Glu)
c.142A>G (p.Lys48Glu)
4g.42963012A>TCA356792332GRXCR1c.505A>T (p.Lys169Ter)
c.142A>T (p.Lys48Ter)
4g.42963013A=CA1453073787GRXCR1c.506A= (p.Lys169=)
c.143A= (p.Lys48=)
4g.42963013A>CCA356792335GRXCR1c.506A>C (p.Lys169Thr)
c.143A>C (p.Lys48Thr)
 COSMIC
4g.42963013A>GCA356792336GRXCR1c.506A>G (p.Lys169Arg)
c.143A>G (p.Lys48Arg)
4g.42963013A>TCA2904426GRXCR1c.506A>T (p.Lys169Ile)
c.143A>T (p.Lys48Ile)
 dbSNP ExAC gnomAD v2 gnomAD v4
4g.42963014A>CCA356792337GRXCR1c.507A>C (p.Lys169Asn)
c.144A>C (p.Lys48Asn)
4g.42963014A>GCA439191608GRXCR1c.507A>G (p.Lys169=)
c.144A>G (p.Lys48=)
4g.42963014A>TCA356792338GRXCR1c.507A>T (p.Lys169Asn)
c.144A>T (p.Lys48Asn)
 ClinVar
4g.42963015T>ACA356792339GRXCR1c.508T>A (p.Phe170Ile)
c.145T>A (p.Phe49Ile)
 gnomAD v4
4g.42963015T>CCA356792340GRXCR1c.508T>C (p.Phe170Leu)
c.145T>C (p.Phe49Leu)
4g.42963015T>GCA356792341GRXCR1c.508T>G (p.Phe170Val)
c.145T>G (p.Phe49Val)
4g.42963016T>ACA356792342GRXCR1c.509T>A (p.Phe170Tyr)
c.146T>A (p.Phe49Tyr)
4g.42963016T>CCA356792343GRXCR1c.509T>C (p.Phe170Ser)
c.146T>C (p.Phe49Ser)
 dbSNP
4g.42963016T>GCA356792344GRXCR1c.509T>G (p.Phe170Cys)
c.146T>G (p.Phe49Cys)
 COSMIC
4g.42963016T=CA1453073788GRXCR1c.509T= (p.Phe170=)
c.146T= (p.Phe49=)
4g.42963017T>ACA356792345GRXCR1c.510T>A (p.Phe170Leu)
c.147T>A (p.Phe49Leu)
4g.42963017T>CCA439191612GRXCR1c.510T>C (p.Phe170=)
c.147T>C (p.Phe49=)
 gnomAD v4
4g.42963017T>GCA356792346GRXCR1c.510T>G (p.Phe170Leu)
c.147T>G (p.Phe49Leu)
4g.42963018G>ACA356792347GRXCR1c.511G>A (p.Glu171Lys)
c.148G>A (p.Glu50Lys)
4g.42963018G>CCA356792348GRXCR1c.511G>C (p.Glu171Gln)
c.148G>C (p.Glu50Gln)
4g.42963018G>TCA356792349GRXCR1c.511G>T (p.Glu171Ter)
c.148G>T (p.Glu50Ter)
4g.42963019A>CCA356792352GRXCR1c.512A>C (p.Glu171Ala)
c.149A>C (p.Glu50Ala)
4g.42963019A>GCA356792350GRXCR1c.512A>G (p.Glu171Gly)
c.149A>G (p.Glu50Gly)
4g.42963019A>TCA356792351GRXCR1c.512A>T (p.Glu171Val)
c.149A>T (p.Glu50Val)
4g.42963020A=CA1453073789GRXCR1c.513A= (p.Glu171=)
c.150A= (p.Glu50=)
4g.42963020A>CCA356792353GRXCR1c.513A>C (p.Glu171Asp)
c.150A>C (p.Glu50Asp)
4g.42963020A>GCA439191616GRXCR1c.513A>G (p.Glu171=)
c.150A>G (p.Glu50=)
 dbSNP gnomAD v3 gnomAD v4
4g.42963020A>TCA356792354GRXCR1c.513A>T (p.Glu171Asp)
c.150A>T (p.Glu50Asp)
4g.42963021G>ACA356792355GRXCR1c.514G>A (p.Glu172Lys)
c.151G>A (p.Glu51Lys)
 gnomAD v4
4g.42963021G>CCA356792356GRXCR1c.514G>C (p.Glu172Gln)
c.151G>C (p.Glu51Gln)
4g.42963021G>TCA356792357GRXCR1c.514G>T (p.Glu172Ter)
c.151G>T (p.Glu51Ter)
4g.42963022A=CA1453073790GRXCR1c.515A= (p.Glu172=)
c.152A= (p.Glu51=)
4g.42963022A>CCA356792358GRXCR1c.515A>C (p.Glu172Ala)
c.152A>C (p.Glu51Ala)
4g.42963022A>GCA356792359GRXCR1c.515A>G (p.Glu172Gly)
c.152A>G (p.Glu51Gly)
 dbSNP gnomAD v2 gnomAD v4
4g.42963022A>TCA356792360GRXCR1c.515A>T (p.Glu172Val)
c.152A>T (p.Glu51Val)
4g.42963023G>ACA439191620GRXCR1c.516G>A (p.Glu172=)
c.153G>A (p.Glu51=)
 dbSNP gnomAD v4
4g.42963023G>CCA356792361GRXCR1c.516G>C (p.Glu172Asp)
c.153G>C (p.Glu51Asp)
4g.42963023G=CA1453073791GRXCR1c.516G= (p.Glu172=)
c.153G= (p.Glu51=)
4g.42963023G>TCA356792362GRXCR1c.516G>T (p.Glu172Asp)
c.153G>T (p.Glu51Asp)
4g.42963024A>CCA356792364GRXCR1c.517A>C (p.Lys173Gln)
c.154A>C (p.Lys52Gln)
4g.42963024A>GCA356792365GRXCR1c.517A>G (p.Lys173Glu)
c.154A>G (p.Lys52Glu)
4g.42963024A>TCA356792363GRXCR1c.517A>T (p.Lys173Ter)
c.154A>T (p.Lys52Ter)
4g.42963028delCA2670496482GRXCR1c.521del (p.Asn174ThrfsTer2)
c.158del (p.Asn53ThrfsTer2)
 gnomAD v4
4g.42963025A>CCA356792366GRXCR1c.518A>C (p.Lys173Thr)
c.155A>C (p.Lys52Thr)
4g.42963025A>GCA356792367GRXCR1c.518A>G (p.Lys173Arg)
c.155A>G (p.Lys52Arg)
4g.42963025A>TCA356792368GRXCR1c.518A>T (p.Lys173Ile)
c.155A>T (p.Lys52Ile)
 COSMIC
4g.42963026A>CCA356792369GRXCR1c.519A>C (p.Lys173Asn)
c.156A>C (p.Lys52Asn)
4g.42963026A>GCA439191624GRXCR1c.519A>G (p.Lys173=)
c.156A>G (p.Lys52=)
4g.42963026A>TCA356792370GRXCR1c.519A>T (p.Lys173Asn)
c.156A>T (p.Lys52Asn)
4g.42963027A>CCA356792373GRXCR1c.520A>C (p.Asn174His)
c.157A>C (p.Asn53His)
4g.42963027A>GCA356792371GRXCR1c.520A>G (p.Asn174Asp)
c.157A>G (p.Asn53Asp)
4g.42963027A>TCA356792372GRXCR1c.520A>T (p.Asn174Tyr)
c.157A>T (p.Asn53Tyr)
4g.42963028A>CCA356792374GRXCR1c.521A>C (p.Asn174Thr)
c.158A>C (p.Asn53Thr)
4g.42963028A>GCA356792375GRXCR1c.521A>G (p.Asn174Ser)
c.158A>G (p.Asn53Ser)
 gnomAD v4
4g.42963028A>TCA356792376GRXCR1c.521A>T (p.Asn174Ile)
c.158A>T (p.Asn53Ile)
4g.42963029C>ACA356792377GRXCR1c.522C>A (p.Asn174Lys)
c.159C>A (p.Asn53Lys)
4g.42963029C>GCA356792378GRXCR1c.522C>G (p.Asn174Lys)
c.159C>G (p.Asn53Lys)
4g.42963029C>TCA439191626GRXCR1c.522C>T (p.Asn174=)
c.159C>T (p.Asn53=)
 COSMIC
4g.42963030A=CA1453073792GRXCR1c.523A= (p.Ile175=)
c.160A= (p.Ile54=)
4g.42963030A>CCA356792379GRXCR1c.523A>C (p.Ile175Leu)
c.160A>C (p.Ile54Leu)
4g.42963030A>GCA2904427GRXCR1c.523A>G (p.Ile175Val)
c.160A>G (p.Ile54Val)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.42963030A>TCA356792380GRXCR1c.523A>T (p.Ile175Leu)
c.160A>T (p.Ile54Leu)
 gnomAD v4
4g.42963031T>ACA356792381GRXCR1c.524T>A (p.Ile175Lys)
c.161T>A (p.Ile54Lys)
4g.42963031T>CCA2904428GRXCR1c.524T>C (p.Ile175Thr)
c.161T>C (p.Ile54Thr)
 dbSNP ExAC gnomAD v2 gnomAD v4
4g.42963031T>GCA356792382GRXCR1c.524T>G (p.Ile175Arg)
c.161T>G (p.Ile54Arg)
4g.42963031T=CA1453073793GRXCR1c.524T= (p.Ile175=)
c.161T= (p.Ile54=)
4g.42963031_42963036delinsTAGCCCCA1453073794GRXCR1c.524_529delinsTAGCCC (p.Ile175=)
c.161_166delinsTAGCCC (p.Ile54=)
4g.42963032A>CCA439191630GRXCR1c.525A>C (p.Ile175=)
c.162A>C (p.Ile54=)
4g.42963032A>GCA356792383GRXCR1c.525A>G (p.Ile175Met)
c.162A>G (p.Ile54Met)
4g.42963032A>TCA439191631GRXCR1c.525A>T (p.Ile175=)
c.162A>T (p.Ile54=)
4g.42963032_42963036delCA1453073795GRXCR1c.525_529del (p.Ala176GlufsTer3)
c.162_166del (p.Ala55GlufsTer3)
 dbSNP
4g.42963033G>ACA356792384GRXCR1c.526G>A (p.Ala176Thr)
c.163G>A (p.Ala55Thr)
 gnomAD v4
4g.42963033G>CCA356792385GRXCR1c.526G>C (p.Ala176Pro)
c.163G>C (p.Ala55Pro)
4g.42963033G=CA1453073796GRXCR1c.526G= (p.Ala176=)
c.163G= (p.Ala55=)
4g.42963033G>TCA356792386GRXCR1c.526G>T (p.Ala176Ser)
c.163G>T (p.Ala55Ser)
 dbSNP gnomAD v3 gnomAD v4
4g.42963034C>ACA356792387GRXCR1c.527C>A (p.Ala176Asp)
c.164C>A (p.Ala55Asp)
4g.42963034C=CA1453073797GRXCR1c.527C= (p.Ala176=)
c.164C= (p.Ala55=)
4g.42963034C>GCA356792388GRXCR1c.527C>G (p.Ala176Gly)
c.164C>G (p.Ala55Gly)
4g.42963034C>TCA2904429GRXCR1c.527C>T (p.Ala176Val)
c.164C>T (p.Ala55Val)
 dbSNP ExAC gnomAD v2 gnomAD v4
4g.42963035C>ACA439191633GRXCR1c.528C>A (p.Ala176=)
c.165C>A (p.Ala55=)
4g.42963035C=CA1453073798GRXCR1c.528C= (p.Ala176=)
c.165C= (p.Ala55=)
4g.42963035C>GCA439191635GRXCR1c.528C>G (p.Ala176=)
c.165C>G (p.Ala55=)
4g.42963035C>TCA439191634GRXCR1c.528C>T (p.Ala176=)
c.165C>T (p.Ala55=)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.42963036C>ACA2904430GRXCR1c.529C>A (p.Leu177Met)
c.166C>A (p.Leu56Met)
 dbSNP ExAC gnomAD v2 gnomAD v4
4g.42963036C=CA1453073799GRXCR1c.529C= (p.Leu177=)
c.166C= (p.Leu56=)
4g.42963036C>GCA356792389GRXCR1c.529C>G (p.Leu177Val)
c.166C>G (p.Leu56Val)
4g.42963036C>TCA439191636GRXCR1c.529C>T (p.Leu177=)
c.166C>T (p.Leu56=)
4g.42963037T>ACA356792390GRXCR1c.530T>A (p.Leu177Gln)
c.167T>A (p.Leu56Gln)
 COSMIC
4g.42963037T>CCA356792391GRXCR1c.530T>C (p.Leu177Pro)
c.167T>C (p.Leu56Pro)
4g.42963037T>GCA96311684GRXCR1c.530T>G (p.Leu177Arg)
c.167T>G (p.Leu56Arg)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.42963037T=CA1453073800GRXCR1c.530T= (p.Leu177=)
c.167T= (p.Leu56=)
4g.42963038G>ACA439191638GRXCR1c.531G>A (p.Leu177=)
c.168G>A (p.Leu56=)
4g.42963038G>CCA439191639GRXCR1c.531G>C (p.Leu177=)
c.168G>C (p.Leu56=)
 dbSNP
4g.42963038G=CA1453073801GRXCR1c.531G= (p.Leu177=)
c.168G= (p.Leu56=)
4g.42963038G>TCA439191640GRXCR1c.531G>T (p.Leu177=)
c.168G>T (p.Leu56=)
4g.42963039A>CCA356792392GRXCR1c.532A>C (p.Asn178His)
c.169A>C (p.Asn57His)
4g.42963039A>GCA356792393GRXCR1c.532A>G (p.Asn178Asp)
c.169A>G (p.Asn57Asp)
4g.42963039A>TCA356792394GRXCR1c.532A>T (p.Asn178Tyr)
c.169A>T (p.Asn57Tyr)
4g.42963040A=CA1453073802GRXCR1c.533A= (p.Asn178=)
c.170A= (p.Asn57=)
4g.42963040A>CCA356792395GRXCR1c.533A>C (p.Asn178Thr)
c.170A>C (p.Asn57Thr)
4g.42963040A>GCA356792396GRXCR1c.533A>G (p.Asn178Ser)
c.170A>G (p.Asn57Ser)
 dbSNP gnomAD v4
4g.42963040A>TCA356792397GRXCR1c.533A>T (p.Asn178Ile)
c.170A>T (p.Asn57Ile)
4g.42963041T>ACA356792399GRXCR1c.534T>A (p.Asn178Lys)
c.171T>A (p.Asn57Lys)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.42963041T>CCA439191644GRXCR1c.534T>C (p.Asn178=)
c.171T>C (p.Asn57=)
4g.42963041T>GCA356792398GRXCR1c.534T>G (p.Asn178Lys)
c.171T>G (p.Asn57Lys)
 gnomAD v4
4g.42963041T=CA1453073803GRXCR1c.534T= (p.Asn178=)
c.171T= (p.Asn57=)
4g.42963042G>ACA356792400GRXCR1c.535G>A (p.Gly179Ser)
c.172G>A (p.Gly58Ser)
 dbSNP gnomAD v2 gnomAD v4
4g.42963042G>CCA356792401GRXCR1c.535G>C (p.Gly179Arg)
c.172G>C (p.Gly58Arg)
4g.42963042G=CA1453073804GRXCR1c.535G= (p.Gly179=)
c.172G= (p.Gly58=)
4g.42963042G>TCA356792402GRXCR1c.535G>T (p.Gly179Cys)
c.172G>T (p.Gly58Cys)
 dbSNP
4g.42963043G>ACA356792403GRXCR1c.536G>A (p.Gly179Asp)
c.173G>A (p.Gly58Asp)
 dbSNP gnomAD v2 gnomAD v4
4g.42963043G>CCA356792404GRXCR1c.536G>C (p.Gly179Ala)
c.173G>C (p.Gly58Ala)
4g.42963043G=CA1453073805GRXCR1c.536G= (p.Gly179=)
c.173G= (p.Gly58=)
4g.42963043G>TCA356792405GRXCR1c.536G>T (p.Gly179Val)
c.173G>T (p.Gly58Val)
4g.42963044T>ACA439191648GRXCR1c.537T>A (p.Gly179=)
c.174T>A (p.Gly58=)
4g.42963044T>CCA439191646GRXCR1c.537T>C (p.Gly179=)
c.174T>C (p.Gly58=)
 gnomAD v4
4g.42963044T>GCA439191647GRXCR1c.537T>G (p.Gly179=)
c.174T>G (p.Gly58=)
4g.42963044_42963045insAACA2557343122GRXCR1c.537_538insAA (p.Glu180LysfsTer7)
c.174_175insAA (p.Glu59LysfsTer7)
4g.42963045G>ACA356792408GRXCR1c.538G>A (p.Glu180Lys)
c.175G>A (p.Glu59Lys)
 gnomAD v4
4g.42963045G>CCA356792406GRXCR1c.538G>C (p.Glu180Gln)
c.175G>C (p.Glu59Gln)
4g.42963045G>TCA356792407GRXCR1c.538G>T (p.Glu180Ter)
c.175G>T (p.Glu59Ter)
 COSMIC
4g.42963046A>CCA356792409GRXCR1c.539A>C (p.Glu180Ala)
c.176A>C (p.Glu59Ala)
4g.42963046A>GCA356792410GRXCR1c.539A>G (p.Glu180Gly)
c.176A>G (p.Glu59Gly)
4g.42963046A>TCA356792411GRXCR1c.539A>T (p.Glu180Val)
c.176A>T (p.Glu59Val)
4g.42963047A>CCA356792412GRXCR1c.540A>C (p.Glu180Asp)
c.177A>C (p.Glu59Asp)
4g.42963047A>GCA439191651GRXCR1c.540A>G (p.Glu180=)
c.177A>G (p.Glu59=)
 gnomAD v4
4g.42963047A>TCA356792413GRXCR1c.540A>T (p.Glu180Asp)
c.177A>T (p.Glu59Asp)
4g.42963049_42963050delCA2514245875GRXCR1c.542_543del (p.Tyr181TrpfsTer13)
c.179_180del (p.Tyr60TrpfsTer13)
4g.42963048T>ACA356792414GRXCR1c.541T>A (p.Tyr181Asn)
c.178T>A (p.Tyr60Asn)
4g.42963048T>CCA356792415GRXCR1c.541T>C (p.Tyr181His)
c.178T>C (p.Tyr60His)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.42963048T>GCA356792416GRXCR1c.541T>G (p.Tyr181Asp)
c.178T>G (p.Tyr60Asp)
4g.42963048T=CA1453073806GRXCR1c.541T= (p.Tyr181=)
c.178T= (p.Tyr60=)
4g.42963049A>CCA356792417GRXCR1c.542A>C (p.Tyr181Ser)
c.179A>C (p.Tyr60Ser)
4g.42963049A>GCA356792418GRXCR1c.542A>G (p.Tyr181Cys)
c.179A>G (p.Tyr60Cys)
4g.42963049A>TCA356792419GRXCR1c.542A>T (p.Tyr181Phe)
c.179A>T (p.Tyr60Phe)
4g.42963050T>ACA356792420GRXCR1c.543T>A (p.Tyr181Ter)
c.180T>A (p.Tyr60Ter)
4g.42963050T>CCA439191653GRXCR1c.543T>C (p.Tyr181=)
c.180T>C (p.Tyr60=)
 gnomAD v4 COSMIC
4g.42963050T>GCA356792421GRXCR1c.543T>G (p.Tyr181Ter)
c.180T>G (p.Tyr60Ter)
4g.42963051G>ACA356792422GRXCR1c.544G>A (p.Gly182Arg)
c.181G>A (p.Gly61Arg)
4g.42963051G>CCA356792424GRXCR1c.544G>C (p.Gly182Arg)
c.181G>C (p.Gly61Arg)
4g.42963051G>TCA356792423GRXCR1c.544G>T (p.Gly182Ter)
c.181G>T (p.Gly61Ter)
4g.42963052G>ACA356792425GRXCR1c.545G>A (p.Gly182Glu)
c.182G>A (p.Gly61Glu)
 dbSNP gnomAD v4 COSMIC
4g.42963052G>CCA356792426GRXCR1c.545G>C (p.Gly182Ala)
c.182G>C (p.Gly61Ala)
4g.42963052G=CA1453073807GRXCR1c.545G= (p.Gly182=)
c.182G= (p.Gly61=)
4g.42963052G>TCA356792427GRXCR1c.545G>T (p.Gly182Val)
c.182G>T (p.Gly61Val)
4g.42963053A>CCA439191656GRXCR1c.546A>C (p.Gly182=)
c.183A>C (p.Gly61=)
4g.42963053A>GCA439191657GRXCR1c.546A>G (p.Gly182=)
c.183A>G (p.Gly61=)
4g.42963053A>TCA439191658GRXCR1c.546A>T (p.Gly182=)
c.183A>T (p.Gly61=)
4g.42963056delCA2578076948GRXCR1c.549del (p.Glu184SerfsTer2)
c.186del (p.Glu63SerfsTer2)
4g.42963054A>CCA356792428GRXCR1c.547A>C (p.Lys183Gln)
c.184A>C (p.Lys62Gln)
4g.42963054A>GCA356792429GRXCR1c.547A>G (p.Lys183Glu)
c.184A>G (p.Lys62Glu)
4g.42963054A>TCA356792430GRXCR1c.547A>T (p.Lys183Ter)
c.184A>T (p.Lys62Ter)
4g.42963055A=CA1453073808GRXCR1c.548A= (p.Lys183=)
c.185A= (p.Lys62=)
4g.42963055A>CCA2904431GRXCR1c.548A>C (p.Lys183Thr)
c.185A>C (p.Lys62Thr)
 dbSNP ExAC gnomAD v2 gnomAD v4
4g.42963055A>GCA356792431GRXCR1c.548A>G (p.Lys183Arg)
c.185A>G (p.Lys62Arg)
 gnomAD v4
4g.42963055A>TCA356792432GRXCR1c.548A>T (p.Lys183Ile)
c.185A>T (p.Lys62Ile)
4g.42963056A=CA1453073809GRXCR1c.549A= (p.Lys183=)
c.186A= (p.Lys62=)
4g.42963056A>CCA356792433GRXCR1c.549A>C (p.Lys183Asn)
c.186A>C (p.Lys62Asn)
4g.42963056A>GCA2904432GRXCR1c.549A>G (p.Lys183=)
c.186A>G (p.Lys62=)
 dbSNP ExAC gnomAD v4
4g.42963056A>TCA356792434GRXCR1c.549A>T (p.Lys183Asn)
c.186A>T (p.Lys62Asn)
4g.42963057G>ACA356792437GRXCR1c.550G>A (p.Glu184Lys)
c.187G>A (p.Glu63Lys)
4g.42963057G>CCA356792436GRXCR1c.550G>C (p.Glu184Gln)
c.187G>C (p.Glu63Gln)
4g.42963057G>TCA356792435GRXCR1c.550G>T (p.Glu184Ter)
c.187G>T (p.Glu63Ter)
 ClinVar dbSNP
4g.42963058A=CA1453073810GRXCR1c.551A= (p.Glu184=)
c.188A= (p.Glu63=)
4g.42963058A>CCA356792438GRXCR1c.551A>C (p.Glu184Ala)
c.188A>C (p.Glu63Ala)
4g.42963058A>GCA356792439GRXCR1c.551A>G (p.Glu184Gly)
c.188A>G (p.Glu63Gly)
4g.42963058A>TCA10621111GRXCR1c.551A>T (p.Glu184Val)
c.188A>T (p.Glu63Val)
 ClinVar dbSNP gnomAD v2 gnomAD v4
4g.42963060_42963063delCA2670496483GRXCR1c.553_556del (p.Leu185ThrfsTer?)
c.190_193del (p.Leu64ThrfsTer?)
 gnomAD v4

Number of alleles fetched