Chr Mutation (hg38) CAid Gene Transcript Linkouts
4g.42962899_42962908delinsCAACTGATCTCA1453073731GRXCR1c.392_401delinsCAACTGATCT (p.Ser131=)
c.29_38delinsCAACTGATCT (p.Ser10=)
4g.42962901_42962909delCA795065018GRXCR1c.394_402del (p.Thr132_Leu134del)
c.31_39del (p.Thr11_Leu13del)
 dbSNP
4g.42962907C>ACA356792122GRXCR1c.400C>A (p.Leu134Ile)
c.37C>A (p.Leu13Ile)
4g.42962907C>GCA356792123GRXCR1c.400C>G (p.Leu134Val)
c.37C>G (p.Leu13Val)
 gnomAD v4
4g.42962907C>TCA439191476GRXCR1c.400C>T (p.Leu134=)
c.37C>T (p.Leu13=)
4g.42962908T>ACA356792124GRXCR1c.401T>A (p.Leu134Gln)
c.38T>A (p.Leu13Gln)
 gnomAD v4
4g.42962908T>CCA356792125GRXCR1c.401T>C (p.Leu134Pro)
c.38T>C (p.Leu13Pro)
4g.42962908T>GCA356792126GRXCR1c.401T>G (p.Leu134Arg)
c.38T>G (p.Leu13Arg)
4g.42962909A>CCA439191477GRXCR1c.402A>C (p.Leu134=)
c.39A>C (p.Leu13=)
4g.42962909A>GCA439191478GRXCR1c.402A>G (p.Leu134=)
c.39A>G (p.Leu13=)
4g.42962909A>TCA439191479GRXCR1c.402A>T (p.Leu134=)
c.39A>T (p.Leu13=)
4g.42962910G>ACA356792127GRXCR1c.403G>A (p.Glu135Lys)
c.40G>A (p.Glu14Lys)
 COSMIC
4g.42962910G>CCA2904396GRXCR1c.403G>C (p.Glu135Gln)
c.40G>C (p.Glu14Gln)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
4g.42962910G=CA1453073737GRXCR1c.403G= (p.Glu135=)
c.40G= (p.Glu14=)
4g.42962910G>TCA356792128GRXCR1c.403G>T (p.Glu135Ter)
c.40G>T (p.Glu14Ter)
 dbSNP gnomAD v3 gnomAD v4
4g.42962911A>CCA356792131GRXCR1c.404A>C (p.Glu135Ala)
c.41A>C (p.Glu14Ala)
4g.42962911A>GCA356792130GRXCR1c.404A>G (p.Glu135Gly)
c.41A>G (p.Glu14Gly)
 gnomAD v4
4g.42962911A>TCA356792129GRXCR1c.404A>T (p.Glu135Val)
c.41A>T (p.Glu14Val)
4g.42962912A>CCA356792132GRXCR1c.405A>C (p.Glu135Asp)
c.42A>C (p.Glu14Asp)
4g.42962912A>GCA439191482GRXCR1c.405A>G (p.Glu135=)
c.42A>G (p.Glu14=)
4g.42962912A>TCA356792133GRXCR1c.405A>T (p.Glu135Asp)
c.42A>T (p.Glu14Asp)
4g.42962913T>ACA356792134GRXCR1c.406T>A (p.Phe136Ile)
c.43T>A (p.Phe15Ile)
4g.42962913T>CCA356792135GRXCR1c.406T>C (p.Phe136Leu)
c.43T>C (p.Phe15Leu)
 gnomAD v4
4g.42962913T>GCA356792136GRXCR1c.406T>G (p.Phe136Val)
c.43T>G (p.Phe15Val)
4g.42962914T>ACA356792137GRXCR1c.407T>A (p.Phe136Tyr)
c.44T>A (p.Phe15Tyr)
4g.42962914T>CCA356792138GRXCR1c.407T>C (p.Phe136Ser)
c.44T>C (p.Phe15Ser)
4g.42962914T>GCA356792139GRXCR1c.407T>G (p.Phe136Cys)
c.44T>G (p.Phe15Cys)
4g.42962915T>ACA356792140GRXCR1c.408T>A (p.Phe136Leu)
c.45T>A (p.Phe15Leu)
4g.42962915T>CCA96311681GRXCR1c.408T>C (p.Phe136=)
c.45T>C (p.Phe15=)
 dbSNP gnomAD v4
4g.42962915T>GCA356792141GRXCR1c.408T>G (p.Phe136Leu)
c.45T>G (p.Phe15Leu)
4g.42962915T=CA1453073738GRXCR1c.408T= (p.Phe136=)
c.45T= (p.Phe15=)
4g.42962916G>ACA356792142GRXCR1c.409G>A (p.Asp137Asn)
c.46G>A (p.Asp16Asn)
 COSMIC
4g.42962916G>CCA356792143GRXCR1c.409G>C (p.Asp137His)
c.46G>C (p.Asp16His)
4g.42962916G>TCA356792144GRXCR1c.409G>T (p.Asp137Tyr)
c.46G>T (p.Asp16Tyr)
 gnomAD v4 COSMIC
4g.42962917A>CCA356792146GRXCR1c.410A>C (p.Asp137Ala)
c.47A>C (p.Asp16Ala)
4g.42962917A>GCA356792147GRXCR1c.410A>G (p.Asp137Gly)
c.47A>G (p.Asp16Gly)
4g.42962917A>TCA356792145GRXCR1c.410A>T (p.Asp137Val)
c.47A>T (p.Asp16Val)
4g.42962918C>ACA356792148GRXCR1c.411C>A (p.Asp137Glu)
c.48C>A (p.Asp16Glu)
4g.42962918C=CA1453073739GRXCR1c.411C= (p.Asp137=)
c.48C= (p.Asp16=)
4g.42962918C>GCA356792149GRXCR1c.411C>G (p.Asp137Glu)
c.48C>G (p.Asp16Glu)
4g.42962918C>TCA439191487GRXCR1c.411C>T (p.Asp137=)
c.48C>T (p.Asp16=)
 dbSNP gnomAD v3 gnomAD v4
4g.42962919C>ACA356792150GRXCR1c.412C>A (p.Arg138Ser)
c.49C>A (p.Arg17Ser)
4g.42962919C=CA1453073740GRXCR1c.412C= (p.Arg138=)
c.49C= (p.Arg17=)
4g.42962919C>GCA356792151GRXCR1c.412C>G (p.Arg138Gly)
c.49C>G (p.Arg17Gly)
4g.42962919C>TCA114035GRXCR1c.412C>T (p.Arg138Cys)
c.49C>T (p.Arg17Cys)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
4g.42962920G>ACA2904397GRXCR1c.413G>A (p.Arg138His)
c.50G>A (p.Arg17His)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
4g.42962920G>CCA356792152GRXCR1c.413G>C (p.Arg138Pro)
c.50G>C (p.Arg17Pro)
4g.42962920G=CA1453073741GRXCR1c.413G= (p.Arg138=)
c.50G= (p.Arg17=)
4g.42962920G>TCA356792153GRXCR1c.413G>T (p.Arg138Leu)
c.50G>T (p.Arg17Leu)
4g.42962921T>ACA439191491GRXCR1c.414T>A (p.Arg138=)
c.51T>A (p.Arg17=)
4g.42962921T>CCA439191492GRXCR1c.414T>C (p.Arg138=)
c.51T>C (p.Arg17=)
 dbSNP gnomAD v3 gnomAD v4
4g.42962921T>GCA439191493GRXCR1c.414T>G (p.Arg138=)
c.51T>G (p.Arg17=)
4g.42962921T=CA1453073742GRXCR1c.414T= (p.Arg138=)
c.51T= (p.Arg17=)
4g.42962922G>ACA356792154GRXCR1c.415G>A (p.Val139Ile)
c.52G>A (p.Val18Ile)
 dbSNP gnomAD v3 gnomAD v4
4g.42962922G>CCA356792155GRXCR1c.415G>C (p.Val139Leu)
c.52G>C (p.Val18Leu)
4g.42962922G=CA1453073743GRXCR1c.415G= (p.Val139=)
c.52G= (p.Val18=)
4g.42962922G>TCA356792156GRXCR1c.415G>T (p.Val139Leu)
c.52G>T (p.Val18Leu)
 COSMIC
4g.42962923T>ACA356792159GRXCR1c.416T>A (p.Val139Glu)
c.53T>A (p.Val18Glu)
4g.42962923T>CCA356792158GRXCR1c.416T>C (p.Val139Ala)
c.53T>C (p.Val18Ala)
 gnomAD v4
4g.42962923T>GCA356792157GRXCR1c.416T>G (p.Val139Gly)
c.53T>G (p.Val18Gly)
4g.42962924A>CCA439191495GRXCR1c.417A>C (p.Val139=)
c.54A>C (p.Val18=)
4g.42962924A>GCA439191496GRXCR1c.417A>G (p.Val139=)
c.54A>G (p.Val18=)
 gnomAD v4
4g.42962924A>TCA439191498GRXCR1c.417A>T (p.Val139=)
c.54A>T (p.Val18=)
4g.42962925G>ACA356792160GRXCR1c.418G>A (p.Val140Met)
c.55G>A (p.Val19Met)
4g.42962925G>CCA356792161GRXCR1c.418G>C (p.Val140Leu)
c.55G>C (p.Val19Leu)
4g.42962925G>TCA356792162GRXCR1c.418G>T (p.Val140Leu)
c.55G>T (p.Val19Leu)
4g.42962926T>ACA356792163GRXCR1c.419T>A (p.Val140Glu)
c.56T>A (p.Val19Glu)
4g.42962926T>CCA356792164GRXCR1c.419T>C (p.Val140Ala)
c.56T>C (p.Val19Ala)
4g.42962926T>GCA356792165GRXCR1c.419T>G (p.Val140Gly)
c.56T>G (p.Val19Gly)
4g.42962927G>ACA439191499GRXCR1c.420G>A (p.Val140=)
c.57G>A (p.Val19=)
 COSMIC
4g.42962927G>CCA439191500GRXCR1c.420G>C (p.Val140=)
c.57G>C (p.Val19=)
4g.42962927G=CA1453073744GRXCR1c.420G= (p.Val140=)
c.57G= (p.Val19=)
4g.42962927G>TCA439191501GRXCR1c.420G>T (p.Val140=)
c.57G>T (p.Val19=)
 dbSNP gnomAD v3 gnomAD v4 COSMIC
4g.42962928A>CCA356792166GRXCR1c.421A>C (p.Ile141Leu)
c.58A>C (p.Ile20Leu)
4g.42962928A>GCA356792167GRXCR1c.421A>G (p.Ile141Val)
c.58A>G (p.Ile20Val)
4g.42962928A>TCA356792168GRXCR1c.421A>T (p.Ile141Phe)
c.58A>T (p.Ile20Phe)
4g.42962929T>ACA356792169GRXCR1c.422T>A (p.Ile141Asn)
c.59T>A (p.Ile20Asn)
4g.42962929T>CCA356792170GRXCR1c.422T>C (p.Ile141Thr)
c.59T>C (p.Ile20Thr)
4g.42962929T>GCA356792171GRXCR1c.422T>G (p.Ile141Ser)
c.59T>G (p.Ile20Ser)
4g.42962931dupCA2670496480GRXCR1c.424dup (p.Tyr142LeufsTer13)
c.61dup (p.Tyr21LeufsTer13)
 gnomAD v4
4g.42962930T>ACA439191505GRXCR1c.423T>A (p.Ile141=)
c.60T>A (p.Ile20=)
 dbSNP gnomAD v2 gnomAD v4
4g.42962930T>CCA439191506GRXCR1c.423T>C (p.Ile141=)
c.60T>C (p.Ile20=)
4g.42962930T>GCA356792172GRXCR1c.423T>G (p.Ile141Met)
c.60T>G (p.Ile20Met)
4g.42962930T=CA1453073745GRXCR1c.423T= (p.Ile141=)
c.60T= (p.Ile20=)
4g.42962931T>ACA356792174GRXCR1c.424T>A (p.Tyr142Asn)
c.61T>A (p.Tyr21Asn)
4g.42962931T>CCA356792173GRXCR1c.424T>C (p.Tyr142His)
c.61T>C (p.Tyr21His)
4g.42962931T>GCA356792175GRXCR1c.424T>G (p.Tyr142Asp)
c.61T>G (p.Tyr21Asp)
 COSMIC
4g.42962932A=CA1453073746GRXCR1c.425A= (p.Tyr142=)
c.62A= (p.Tyr21=)
4g.42962932A>CCA356792176GRXCR1c.425A>C (p.Tyr142Ser)
c.62A>C (p.Tyr21Ser)
 dbSNP gnomAD v3 gnomAD v4
4g.42962932A>GCA2904398GRXCR1c.425A>G (p.Tyr142Cys)
c.62A>G (p.Tyr21Cys)
 dbSNP ExAC gnomAD v2 gnomAD v4
4g.42962932A>TCA356792177GRXCR1c.425A>T (p.Tyr142Phe)
c.62A>T (p.Tyr21Phe)
4g.42962933T>ACA356792178GRXCR1c.426T>A (p.Tyr142Ter)
c.63T>A (p.Tyr21Ter)
4g.42962933T>CCA439191508GRXCR1c.426T>C (p.Tyr142=)
c.63T>C (p.Tyr21=)
 dbSNP
4g.42962933T>GCA356792179GRXCR1c.426T>G (p.Tyr142Ter)
c.63T>G (p.Tyr21Ter)
4g.42962933T=CA1453073747GRXCR1c.426T= (p.Tyr142=)
c.63T= (p.Tyr21=)
4g.42962934A>CCA356792180GRXCR1c.427A>C (p.Thr143Pro)
c.64A>C (p.Thr22Pro)
4g.42962934A>GCA356792181GRXCR1c.427A>G (p.Thr143Ala)
c.64A>G (p.Thr22Ala)
4g.42962934A>TCA356792182GRXCR1c.427A>T (p.Thr143Ser)
c.64A>T (p.Thr22Ser)
4g.42962935C>ACA356792183GRXCR1c.428C>A (p.Thr143Asn)
c.65C>A (p.Thr22Asn)
4g.42962935C>GCA356792184GRXCR1c.428C>G (p.Thr143Ser)
c.65C>G (p.Thr22Ser)
4g.42962935C>TCA356792185GRXCR1c.428C>T (p.Thr143Ile)
c.65C>T (p.Thr22Ile)
4g.42962936C>ACA439191513GRXCR1c.429C>A (p.Thr143=)
c.66C>A (p.Thr22=)
4g.42962936C>GCA439191512GRXCR1c.429C>G (p.Thr143=)
c.66C>G (p.Thr22=)
4g.42962936C>TCA439191510GRXCR1c.429C>T (p.Thr143=)
c.66C>T (p.Thr22=)
4g.42962937A>CCA356792188GRXCR1c.430A>C (p.Thr144Pro)
c.67A>C (p.Thr23Pro)
4g.42962937A>GCA356792186GRXCR1c.430A>G (p.Thr144Ala)
c.67A>G (p.Thr23Ala)
 COSMIC
4g.42962937A>TCA356792187GRXCR1c.430A>T (p.Thr144Ser)
c.67A>T (p.Thr23Ser)
4g.42962938C>ACA356792189GRXCR1c.431C>A (p.Thr144Asn)
c.68C>A (p.Thr23Asn)
4g.42962938C>GCA356792190GRXCR1c.431C>G (p.Thr144Ser)
c.68C>G (p.Thr23Ser)
4g.42962938C>TCA356792191GRXCR1c.431C>T (p.Thr144Ile)
c.68C>T (p.Thr23Ile)
4g.42962939C>ACA439191515GRXCR1c.432C>A (p.Thr144=)
c.69C>A (p.Thr23=)
4g.42962939C>GCA439191517GRXCR1c.432C>G (p.Thr144=)
c.69C>G (p.Thr23=)
 dbSNP
4g.42962939C>TCA439191516GRXCR1c.432C>T (p.Thr144=)
c.69C>T (p.Thr23=)
4g.42962940T>ACA356792192GRXCR1c.433T>A (p.Cys145Ser)
c.70T>A (p.Cys24Ser)
 dbSNP gnomAD v3 gnomAD v4
4g.42962940T>CCA356792193GRXCR1c.433T>C (p.Cys145Arg)
c.70T>C (p.Cys24Arg)
4g.42962940T>GCA2904399GRXCR1c.433T>G (p.Cys145Gly)
c.70T>G (p.Cys24Gly)
 dbSNP ExAC gnomAD v2 gnomAD v4
4g.42962940T=CA1453073748GRXCR1c.433T= (p.Cys145=)
c.70T= (p.Cys24=)
4g.42962941G>ACA96311682GRXCR1c.434G>A (p.Cys145Tyr)
c.71G>A (p.Cys24Tyr)
 dbSNP gnomAD v3 gnomAD v4
4g.42962941G>CCA356792194GRXCR1c.434G>C (p.Cys145Ser)
c.71G>C (p.Cys24Ser)
4g.42962941G=CA1453073749GRXCR1c.434G= (p.Cys145=)
c.71G= (p.Cys24=)
4g.42962941G>TCA356792195GRXCR1c.434G>T (p.Cys145Phe)
c.71G>T (p.Cys24Phe)
4g.42962942C>ACA356792196GRXCR1c.435C>A (p.Cys145Ter)
c.72C>A (p.Cys24Ter)
4g.42962942C=CA1453073750GRXCR1c.435C= (p.Cys145=)
c.72C= (p.Cys24=)
4g.42962942C>GCA356792197GRXCR1c.435C>G (p.Cys145Trp)
c.72C>G (p.Cys24Trp)
4g.42962942C>TCA439191520GRXCR1c.435C>T (p.Cys145=)
c.72C>T (p.Cys24=)
 ClinVar dbSNP gnomAD v4
4g.42962943C>ACA356792199GRXCR1c.436C>A (p.Leu146Ile)
c.73C>A (p.Leu25Ile)
4g.42962943C>GCA356792200GRXCR1c.436C>G (p.Leu146Val)
c.73C>G (p.Leu25Val)
4g.42962943C>TCA356792198GRXCR1c.436C>T (p.Leu146Phe)
c.73C>T (p.Leu25Phe)
4g.42962944T>ACA356792201GRXCR1c.437T>A (p.Leu146His)
c.74T>A (p.Leu25His)
4g.42962944T>CCA2904400GRXCR1c.437T>C (p.Leu146Pro)
c.74T>C (p.Leu25Pro)
 dbSNP ExAC gnomAD v2
4g.42962944T>GCA356792202GRXCR1c.437T>G (p.Leu146Arg)
c.74T>G (p.Leu25Arg)
4g.42962944T=CA1453073751GRXCR1c.437T= (p.Leu146=)
c.74T= (p.Leu25=)
4g.42962945T>ACA439191523GRXCR1c.438T>A (p.Leu146=)
c.75T>A (p.Leu25=)
4g.42962945T>CCA439191525GRXCR1c.438T>C (p.Leu146=)
c.75T>C (p.Leu25=)
4g.42962945T>GCA439191526GRXCR1c.438T>G (p.Leu146=)
c.75T>G (p.Leu25=)
4g.42962946C>ACA356792203GRXCR1c.439C>A (p.Arg147Ser)
c.76C>A (p.Arg26Ser)
 gnomAD v4
4g.42962946C=CA1453073752GRXCR1c.439C= (p.Arg147=)
c.76C= (p.Arg26=)
4g.42962946C>GCA356792204GRXCR1c.439C>G (p.Arg147Gly)
c.76C>G (p.Arg26Gly)
4g.42962946C>TCA2904401GRXCR1c.439C>T (p.Arg147Cys)
c.76C>T (p.Arg26Cys)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
4g.42962947G>ACA2904403GRXCR1c.440G>A (p.Arg147His)
c.77G>A (p.Arg26His)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
4g.42962947G>CCA2904402GRXCR1c.440G>C (p.Arg147Pro)
c.77G>C (p.Arg26Pro)
 dbSNP ExAC gnomAD v2 gnomAD v4
4g.42962947G=CA1453073753GRXCR1c.440G= (p.Arg147=)
c.77G= (p.Arg26=)
4g.42962947G>TCA356792205GRXCR1c.440G>T (p.Arg147Leu)
c.77G>T (p.Arg26Leu)
 dbSNP COSMIC
4g.42962948T>ACA439191527GRXCR1c.441T>A (p.Arg147=)
c.78T>A (p.Arg26=)
4g.42962948T>CCA439191528GRXCR1c.441T>C (p.Arg147=)
c.78T>C (p.Arg26=)
4g.42962948T>GCA439191529GRXCR1c.441T>G (p.Arg147=)
c.78T>G (p.Arg26=)
4g.42962949G>ACA356792206GRXCR1c.442G>A (p.Val148Met)
c.79G>A (p.Val27Met)
 dbSNP gnomAD v2 gnomAD v4
4g.42962949G>CCA356792207GRXCR1c.442G>C (p.Val148Leu)
c.79G>C (p.Val27Leu)
4g.42962949G=CA1453073754GRXCR1c.442G= (p.Val148=)
c.79G= (p.Val27=)
4g.42962949G>TCA356792208GRXCR1c.442G>T (p.Val148Leu)
c.79G>T (p.Val27Leu)
4g.42962950T>ACA356792210GRXCR1c.443T>A (p.Val148Glu)
c.80T>A (p.Val27Glu)
4g.42962950T>CCA356792211GRXCR1c.443T>C (p.Val148Ala)
c.80T>C (p.Val27Ala)
4g.42962950T>GCA356792209GRXCR1c.443T>G (p.Val148Gly)
c.80T>G (p.Val27Gly)
4g.42962951G>ACA439191531GRXCR1c.444G>A (p.Val148=)
c.81G>A (p.Val27=)
4g.42962951G>CCA439191532GRXCR1c.444G>C (p.Val148=)
c.81G>C (p.Val27=)
 dbSNP
4g.42962951G=CA1453073755GRXCR1c.444G= (p.Val148=)
c.81G= (p.Val27=)
4g.42962951G>TCA439191533GRXCR1c.444G>T (p.Val148=)
c.81G>T (p.Val27=)
 COSMIC
4g.42962952G>ACA2904404GRXCR1c.445G>A (p.Val149Ile)
c.82G>A (p.Val28Ile)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.42962952G>CCA356792212GRXCR1c.445G>C (p.Val149Leu)
c.82G>C (p.Val28Leu)
4g.42962952G=CA1453073756GRXCR1c.445G= (p.Val149=)
c.82G= (p.Val28=)
4g.42962952G>TCA356792213GRXCR1c.445G>T (p.Val149Phe)
c.82G>T (p.Val28Phe)
 COSMIC
4g.42962953T>ACA356792214GRXCR1c.446T>A (p.Val149Asp)
c.83T>A (p.Val28Asp)
4g.42962953T>CCA2904405GRXCR1c.446T>C (p.Val149Ala)
c.83T>C (p.Val28Ala)
 dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
4g.42962953T>GCA356792215GRXCR1c.446T>G (p.Val149Gly)
c.83T>G (p.Val28Gly)
4g.42962953T=CA1453073757GRXCR1c.446T= (p.Val149=)
c.83T= (p.Val28=)
4g.42962954C>ACA439191534GRXCR1c.447C>A (p.Val149=)
c.84C>A (p.Val28=)
4g.42962954C>GCA439191537GRXCR1c.447C>G (p.Val149=)
c.84C>G (p.Val28=)
 gnomAD v4
4g.42962954C>TCA439191538GRXCR1c.447C>T (p.Val149=)
c.84C>T (p.Val28=)
4g.42962954_42962956delCA2526528602GRXCR1c.447_449del (p.Arg150del)
c.84_86del (p.Arg29del)
4g.42962955C>ACA439191539GRXCR1c.448C>A (p.Arg150=)
c.85C>A (p.Arg29=)
4g.42962955C=CA1453073758GRXCR1c.448C= (p.Arg150=)
c.85C= (p.Arg29=)
4g.42962955C>GCA356792216GRXCR1c.448C>G (p.Arg150Gly)
c.85C>G (p.Arg29Gly)
4g.42962955C>TCA2904406GRXCR1c.448C>T (p.Arg150Trp)
c.85C>T (p.Arg29Trp)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
4g.42962956G>ACA2904407GRXCR1c.449G>A (p.Arg150Gln)
c.86G>A (p.Arg29Gln)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.42962956G>CCA356792217GRXCR1c.449G>C (p.Arg150Pro)
c.86G>C (p.Arg29Pro)
4g.42962956G=CA1453073759GRXCR1c.449G= (p.Arg150=)
c.86G= (p.Arg29=)
4g.42962956G>TCA356792218GRXCR1c.449G>T (p.Arg150Leu)
c.86G>T (p.Arg29Leu)
4g.42962957G>ACA439191543GRXCR1c.450G>A (p.Arg150=)
c.87G>A (p.Arg29=)
 gnomAD v4
4g.42962957G>CCA439191544GRXCR1c.450G>C (p.Arg150=)
c.87G>C (p.Arg29=)
4g.42962957G>TCA439191545GRXCR1c.450G>T (p.Arg150=)
c.87G>T (p.Arg29=)
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)

Number of alleles fetched