Chr Mutation (hg38) CAid Gene Transcript Linkouts
16g.79598940G>ACA496508892MAFc.963C>T (p.Asn321=)
n.3013C>T
gnomAD v4
16g.79598940G>CCA396534849MAFc.963C>G (p.Asn321Lys)
n.3013C>G
dbSNP
16g.79598940G>TCA396534848MAFc.963C>A (p.Asn321Lys)
n.3013C>A
gnomAD v4
16g.79598941T>ACA396534850MAFc.962A>T (p.Asn321Ile)
n.3012A>T
16g.79598941T>CCA396534851MAFc.962A>G (p.Asn321Ser)
n.3012A>G
16g.79598941T>GCA396534852MAFc.962A>C (p.Asn321Thr)
n.3012A>C
16g.79598942T>ACA396534853MAFc.961A>T (p.Asn321Tyr)
n.3011A>T
16g.79598942T>CCA396534854MAFc.961A>G (p.Asn321Asp)
n.3011A>G
16g.79598942T>GCA396534855MAFc.961A>C (p.Asn321His)
n.3011A>C
16g.79598943C>ACA396534856MAFc.960G>T (p.Lys320Asn)
n.3010G>T
dbSNP gnomAD v2 gnomAD v4
16g.79598943C=CA2235930732MAFc.960G= (p.Lys320=)
n.3010G=
16g.79598943C>GCA396534857MAFc.960G>C (p.Lys320Asn)
n.3010G>C
dbSNP gnomAD v2
16g.79598943C>TCA8184000MAFc.960G>A (p.Lys320=)
n.3010G>A
dbSNP ExAC gnomAD v2 gnomAD v4
16g.79598944T>ACA396534858MAFc.959A>T (p.Lys320Met)
n.3009A>T
16g.79598944T>CCA396534859MAFc.959A>G (p.Lys320Arg)
n.3009A>G
ClinVar
16g.79598944T>GCA396534860MAFc.959A>C (p.Lys320Thr)
n.3009A>C
16g.79598945T>ACA396534861MAFc.958A>T (p.Lys320Ter)
n.3008A>T
16g.79598945T>CCA396534862MAFc.958A>G (p.Lys320Glu)
n.3008A>G
dbSNP gnomAD v2 gnomAD v4
16g.79598945T>GCA396534863MAFc.958A>C (p.Lys320Gln)
n.3008A>C
16g.79598945T=CA2235930739MAFc.958A= (p.Lys320=)
n.3008A=
16g.79598946C>ACA396534864MAFc.957G>T (p.Glu319Asp)
n.3007G>T
16g.79598946C=CA2235930742MAFc.957G= (p.Glu319=)
n.3007G=
16g.79598946C>GCA396534865MAFc.957G>C (p.Glu319Asp)
n.3007G>C
16g.79598946C>TCA496508893MAFc.957G>A (p.Glu319=)
n.3007G>A
dbSNP gnomAD v4
16g.79598947T>ACA396534866MAFc.956A>T (p.Glu319Val)
n.3006A>T
16g.79598947T>CCA396534867MAFc.956A>G (p.Glu319Gly)
n.3006A>G
16g.79598947T>GCA396534868MAFc.956A>C (p.Glu319Ala)
n.3006A>C
16g.79598948C>ACA396534871MAFc.955G>T (p.Glu319Ter)
n.3005G>T
16g.79598948C>GCA396534870MAFc.955G>C (p.Glu319Gln)
n.3005G>C
16g.79598948C>TCA396534869MAFc.955G>A (p.Glu319Lys)
n.3005G>A
gnomAD v4
16g.79598949C>ACA496508894MAFc.954G>T (p.Ser318=)
n.3004G>T
16g.79598949C=CA2235930748MAFc.954G= (p.Ser318=)
n.3004G=
16g.79598949C>GCA496508895MAFc.954G>C (p.Ser318=)
n.3004G>C
16g.79598949C>TCA8184001MAFc.954G>A (p.Ser318=)
n.3004G>A
dbSNP ExAC gnomAD v2 gnomAD v4
16g.79598950G>ACA8184002MAFc.953C>T (p.Ser318Leu)
n.3003C>T
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
16g.79598950G>CCA396534872MAFc.953C>G (p.Ser318Trp)
n.3003C>G
gnomAD v4
16g.79598950G=CA2235930752MAFc.953C= (p.Ser318=)
n.3003C=
16g.79598950G>TCA396534873MAFc.953C>A (p.Ser318Ter)
n.3003C>A
16g.79598951A>CCA396534874MAFc.952T>G (p.Ser318Ala)
n.3002T>G
16g.79598951A>GCA396534875MAFc.952T>C (p.Ser318Pro)
n.3002T>C
16g.79598951A>TCA396534876MAFc.952T>A (p.Ser318Thr)
n.3002T>A
16g.79598952C>ACA396534877MAFc.951G>T (p.Glu317Asp)
n.3001G>T
16g.79598952C>GCA396534878MAFc.951G>C (p.Glu317Asp)
n.3001G>C
16g.79598952C>TCA496508896MAFc.951G>A (p.Glu317=)
n.3001G>A
16g.79598953T>ACA396534879MAFc.950A>T (p.Glu317Val)
n.3000A>T
16g.79598953T>CCA396534880MAFc.950A>G (p.Glu317Gly)
n.3000A>G
16g.79598953T>GCA396534881MAFc.950A>C (p.Glu317Ala)
n.3000A>C
16g.79598954C>ACA396534882MAFc.949G>T (p.Glu317Ter)
n.2999G>T
16g.79598954C>GCA396534883MAFc.949G>C (p.Glu317Gln)
n.2999G>C
16g.79598954C>TCA396534884MAFc.949G>A (p.Glu317Lys)
n.2999G>A
COSMIC
16g.79598955C>ACA496508897MAFc.948G>T (p.Leu316=)
n.2998G>T
16g.79598955C=CA2235930759MAFc.948G= (p.Leu316=)
n.2998G=
16g.79598955C>GCA496508898MAFc.948G>C (p.Leu316=)
n.2998G>C
16g.79598955C>TCA8184003MAFc.948G>A (p.Leu316=)
n.2998G>A
dbSNP ExAC gnomAD v2 gnomAD v4
16g.79598956A>CCA396534887MAFc.947T>G (p.Leu316Arg)
n.2997T>G
16g.79598956A>GCA396534885MAFc.947T>C (p.Leu316Pro)
n.2997T>C
16g.79598956A>TCA396534886MAFc.947T>A (p.Leu316Gln)
n.2997T>A
16g.79598957G>ACA284127958MAFc.946C>T (p.Leu316=)
n.2996C>T
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.79598957G>CCA396534888MAFc.946C>G (p.Leu316Val)
n.2996C>G
16g.79598957G=CA2235930762MAFc.946C= (p.Leu316=)
n.2996C=
16g.79598957G>TCA396534889MAFc.946C>A (p.Leu316Met)
n.2996C>A
16g.79598958G>ACA496508899MAFc.945C>T (p.Val315=)
n.2995C>T
gnomAD v4
16g.79598958G>CCA496508901MAFc.945C>G (p.Val315=)
n.2995C>G
dbSNP gnomAD v3 gnomAD v4
16g.79598958G=CA2235930766MAFc.945C= (p.Val315=)
n.2995C=
16g.79598958G>TCA496508900MAFc.945C>A (p.Val315=)
n.2995C>A
16g.79598959A=CA2235930773MAFc.944T= (p.Val315=)
n.2994T=
16g.79598959A>CCA396534890MAFc.944T>G (p.Val315Gly)
n.2994T>G
dbSNP
16g.79598959A>GCA396534891MAFc.944T>C (p.Val315Ala)
n.2994T>C
dbSNP gnomAD v4
16g.79598959A>TCA396534892MAFc.944T>A (p.Val315Asp)
n.2994T>A
dbSNP gnomAD v4
16g.79598960C>ACA396534893MAFc.943G>T (p.Val315Phe)
n.2993G>T
COSMIC
16g.79598960C>GCA396534894MAFc.943G>C (p.Val315Leu)
n.2993G>C
16g.79598960C>TCA396534895MAFc.943G>A (p.Val315Ile)
n.2993G>A
16g.79598961G>ACA8184004MAFc.942C>T (p.His314=)
n.2992C>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.79598961G>CCA396534896MAFc.942C>G (p.His314Gln)
n.2992C>G
16g.79598961G=CA2235930781MAFc.942C= (p.His314=)
n.2992C=
16g.79598961G>TCA396534897MAFc.942C>A (p.His314Gln)
n.2992C>A
dbSNP
16g.79598962T>ACA396534900MAFc.941A>T (p.His314Leu)
n.2991A>T
16g.79598962T>CCA396534899MAFc.941A>G (p.His314Arg)
n.2991A>G
16g.79598962T>GCA396534898MAFc.941A>C (p.His314Pro)
n.2991A>C
ClinVar dbSNP
16g.79598962T=CA2235930800MAFc.941A= (p.His314=)
n.2991A=
16g.79598963G>ACA396534901MAFc.940C>T (p.His314Tyr)
n.2990C>T
16g.79598963G>CCA396534902MAFc.940C>G (p.His314Asp)
n.2990C>G
16g.79598963G>TCA396534903MAFc.940C>A (p.His314Asn)
n.2990C>A
16g.79598964T>ACA396534904MAFc.939A>T (p.Arg313Ser)
n.2989A>T
16g.79598964T>CCA496508902MAFc.939A>G (p.Arg313=)
n.2989A>G
ClinVar dbSNP gnomAD v4
16g.79598964T>GCA396534905MAFc.939A>C (p.Arg313Ser)
n.2989A>C
16g.79598964T=CA2235930808MAFc.939A= (p.Arg313=)
n.2989A=
16g.79598965C>ACA396534906MAFc.938G>T (p.Arg313Ile)
n.2988G>T
16g.79598965C>GCA396534907MAFc.938G>C (p.Arg313Thr)
n.2988G>C
dbSNP
16g.79598965C>TCA396534908MAFc.938G>A (p.Arg313Lys)
n.2988G>A
16g.79598966T>ACA396534909MAFc.937A>T (p.Arg313Ter)
n.2987A>T
16g.79598966T>CCA396534910MAFc.937A>G (p.Arg313Gly)
n.2987A>G
16g.79598966T>GCA496508903MAFc.937A>C (p.Arg313=)
n.2987A>C
16g.79598967C>ACA396534911MAFc.936G>T (p.Gln312His)
n.2986G>T
16g.79598967C>GCA396534912MAFc.936G>C (p.Gln312His)
n.2986G>C
gnomAD v4
16g.79598967C>TCA496508904MAFc.936G>A (p.Gln312=)
n.2986G>A
16g.79598968T>ACA396534915MAFc.935A>T (p.Gln312Leu)
n.2985A>T
16g.79598968T>CCA396534913MAFc.935A>G (p.Gln312Arg)
n.2985A>G
ClinVar
16g.79598968T>GCA396534914MAFc.935A>C (p.Gln312Pro)
n.2985A>C
16g.79598969G>ACA396534916MAFc.934C>T (p.Gln312Ter)
n.2984C>T
16g.79598969G>CCA396534917MAFc.934C>G (p.Gln312Glu)
n.2984C>G
16g.79598969G>TCA396534918MAFc.934C>A (p.Gln312Lys)
n.2984C>A
16g.79598970C>ACA396534919MAFc.933G>T (p.Gln311His)
n.2983G>T
dbSNP gnomAD v2 gnomAD v4
16g.79598970C=CA2235930813MAFc.933G= (p.Gln311=)
n.2983G=
16g.79598970C>GCA396534920MAFc.933G>C (p.Gln311His)
n.2983G>C
16g.79598970C>TCA496508905MAFc.933G>A (p.Gln311=)
n.2983G>A
dbSNP gnomAD v4
16g.79598971T>ACA396534921MAFc.932A>T (p.Gln311Leu)
n.2982A>T
16g.79598971T>CCA396534922MAFc.932A>G (p.Gln311Arg)
n.2982A>G
dbSNP
16g.79598971T>GCA396534923MAFc.932A>C (p.Gln311Pro)
n.2982A>C
16g.79598971T=CA2235930819MAFc.932A= (p.Gln311=)
n.2982A=
16g.79598972G>ACA396534924MAFc.931C>T (p.Gln311Ter)
n.2981C>T
dbSNP
16g.79598972G>CCA396534925MAFc.931C>G (p.Gln311Glu)
n.2981C>G
16g.79598972G>TCA396534926MAFc.931C>A (p.Gln311Lys)
n.2981C>A
16g.79598973C>ACA496508923MAFc.930G>T (p.Val310=)
n.2980G>T
16g.79598973C=CA2235930823MAFc.930G= (p.Val310=)
n.2980G=
16g.79598973C>GCA496508924MAFc.930G>C (p.Val310=)
n.2980G>C
16g.79598973C>TCA8184005MAFc.930G>A (p.Val310=)
n.2980G>A
dbSNP ExAC gnomAD v2
16g.79598974A=CA2235930830MAFc.929T= (p.Val310=)
n.2979T=
16g.79598974A>CCA396534928MAFc.929T>G (p.Val310Gly)
n.2979T>G
dbSNP
16g.79598974A>GCA396534929MAFc.929T>C (p.Val310Ala)
n.2979T>C
16g.79598974A>TCA396534927MAFc.929T>A (p.Val310Glu)
n.2979T>A
dbSNP
16g.79598975C>ACA396534930MAFc.928G>T (p.Val310Leu)
n.2978G>T
16g.79598975C>GCA396534931MAFc.928G>C (p.Val310Leu)
n.2978G>C
16g.79598975C>TCA396534932MAFc.928G>A (p.Val310Met)
n.2978G>A
16g.79598976C>ACA396534933MAFc.927G>T (p.Arg309Ser)
n.2977G>T
COSMIC
16g.79598976C=CA2235930838MAFc.927G= (p.Arg309=)
n.2977G=
16g.79598976C>GCA396534934MAFc.927G>C (p.Arg309Ser)
n.2977G>C
16g.79598976C>TCA496508925MAFc.927G>A (p.Arg309=)
n.2977G>A
dbSNP
16g.79598977C>ACA396534937MAFc.926G>T (p.Arg309Met)
n.2976G>T
dbSNP
16g.79598977C>GCA396534936MAFc.926G>C (p.Arg309Thr)
n.2976G>C
16g.79598977C>TCA396534935MAFc.926G>A (p.Arg309Lys)
n.2976G>A
16g.79598978T>ACA396534938MAFc.925A>T (p.Arg309Trp)
n.2975A>T
16g.79598978T>CCA396534939MAFc.925A>G (p.Arg309Gly)
n.2975A>G
16g.79598978T>GCA496508927MAFc.925A>C (p.Arg309=)
n.2975A>C
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.79598978T=CA2235930843MAFc.925A= (p.Arg309=)
n.2975A=
16g.79598979C>ACA396534940MAFc.924G>T (p.Lys308Asn)
n.2974G>T
16g.79598979C=CA2235930845MAFc.924G= (p.Lys308=)
n.2974G=
16g.79598979C>GCA8184006MAFc.924G>C (p.Lys308Asn)
n.2974G>C
dbSNP ExAC
16g.79598979C>TCA496508928MAFc.924G>A (p.Lys308=)
n.2974G>A
16g.79598980T>ACA396534941MAFc.923A>T (p.Lys308Met)
n.2973A>T
16g.79598980T>CCA396534942MAFc.923A>G (p.Lys308Arg)
n.2973A>G
16g.79598980T>GCA396534943MAFc.923A>C (p.Lys308Thr)
n.2973A>C
16g.79598981T>ACA396534944MAFc.922A>T (p.Lys308Ter)
n.2972A>T
16g.79598981T>CCA396534946MAFc.922A>G (p.Lys308Glu)
n.2972A>G
ClinVar
16g.79598981T>GCA396534945MAFc.922A>C (p.Lys308Gln)
n.2972A>C
16g.79598982G>ACA496508935MAFc.921C>T (p.Phe307=)
n.2971C>T
16g.79598982G>CCA396534947MAFc.921C>G (p.Phe307Leu)
n.2971C>G
16g.79598982G>TCA396534948MAFc.921C>A (p.Phe307Leu)
n.2971C>A
16g.79598983A>CCA396534949MAFc.920T>G (p.Phe307Cys)
n.2970T>G
16g.79598983A>GCA396534950MAFc.920T>C (p.Phe307Ser)
n.2970T>C
16g.79598983A>TCA396534951MAFc.920T>A (p.Phe307Tyr)
n.2970T>A
16g.79598984A>CCA396534952MAFc.919T>G (p.Phe307Val)
n.2969T>G
16g.79598984A>GCA396534953MAFc.919T>C (p.Phe307Leu)
n.2969T>C
16g.79598984A>TCA396534954MAFc.919T>A (p.Phe307Ile)
n.2969T>A
16g.79598985G>ACA8184007MAFc.918C>T (p.Arg306=)
n.2968C>T
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.79598985G>CCA496508942MAFc.918C>G (p.Arg306=)
n.2968C>G
dbSNP gnomAD v4
16g.79598985G=CA2235930847MAFc.918C= (p.Arg306=)
n.2968C=
16g.79598985G>TCA496508941MAFc.918C>A (p.Arg306=)
n.2968C>A
16g.79598986C>ACA396534955MAFc.917G>T (p.Arg306Leu)
n.2967G>T
dbSNP
16g.79598986C>GCA396534956MAFc.917G>C (p.Arg306Pro)
n.2967G>C
dbSNP
16g.79598986C>TCA396534957MAFc.917G>A (p.Arg306His)
n.2967G>A
COSMIC
16g.79598987G>ACA396534958MAFc.916C>T (p.Arg306Cys)
n.2966C>T
16g.79598987G>CCA396534960MAFc.916C>G (p.Arg306Gly)
n.2966C>G
ClinVar dbSNP
16g.79598987G=CA2235930855MAFc.916C= (p.Arg306=)
n.2966C=
16g.79598987G>TCA396534959MAFc.916C>A (p.Arg306Ser)
n.2966C>A
dbSNP
16g.79598988G>ACA278839MAFc.915C>T (p.Cys305=)
n.2965C>T
ClinVar dbSNP
16g.79598988G>CCA396534961MAFc.915C>G (p.Cys305Trp)
n.2965C>G
16g.79598988G=CA2235930859MAFc.915C= (p.Cys305=)
n.2965C=
16g.79598988G>TCA396534962MAFc.915C>A (p.Cys305Ter)
n.2965C>A
16g.79598989C>ACA396534963MAFc.914G>T (p.Cys305Phe)
n.2964G>T
ClinVar
16g.79598989C=CA2235930864MAFc.914G= (p.Cys305=)
n.2964G=
16g.79598989C>GCA396534964MAFc.914G>C (p.Cys305Ser)
n.2964G>C
16g.79598989C>TCA396534965MAFc.914G>A (p.Cys305Tyr)
n.2964G>A
ClinVar dbSNP gnomAD v4
16g.79598990A>CCA396534966MAFc.913T>G (p.Cys305Gly)
n.2963T>G
16g.79598990A>GCA396534967MAFc.913T>C (p.Cys305Arg)
n.2963T>C
16g.79598990A>TCA396534968MAFc.913T>A (p.Cys305Ser)
n.2963T>A
16g.79598991G>ACA496508948MAFc.912C>T (p.Ser304=)
n.2962C>T
16g.79598991G>CCA496508950MAFc.912C>G (p.Ser304=)
n.2962C>G
gnomAD v4
16g.79598991G>TCA496508949MAFc.912C>A (p.Ser304=)
n.2962C>A
16g.79598992G>ACA284128022MAFc.911C>T (p.Ser304Phe)
n.2961C>T
dbSNP
16g.79598992G>CCA396534969MAFc.911C>G (p.Ser304Cys)
n.2961C>G
16g.79598992G=CA2235930867MAFc.911C= (p.Ser304=)
n.2961C=
16g.79598992G>TCA396534970MAFc.911C>A (p.Ser304Tyr)
n.2961C>A
16g.79598993A>CCA396534973MAFc.910T>G (p.Ser304Ala)
n.2960T>G
16g.79598993A>GCA396534972MAFc.910T>C (p.Ser304Pro)
n.2960T>C
16g.79598993A>TCA396534971MAFc.910T>A (p.Ser304Thr)
n.2960T>A
16g.79598994C>ACA396534974MAFc.909G>T (p.Gln303His)
n.2959G>T
16g.79598994C=CA2235930874MAFc.909G= (p.Gln303=)
n.2959G=
16g.79598994C>GCA8184009MAFc.909G>C (p.Gln303His)
n.2959G>C
dbSNP ExAC gnomAD v2 gnomAD v4
16g.79598994C>TCA8184008MAFc.909G>A (p.Gln303=)
n.2959G>A
dbSNP ExAC gnomAD v2 gnomAD v4
16g.79598995T>ACA396534975MAFc.908A>T (p.Gln303Leu)
n.2958A>T
16g.79598995T>CCA396534976MAFc.908A>G (p.Gln303Arg)
n.2958A>G
16g.79598995T>GCA199636MAFc.908A>C (p.Gln303Pro)
n.2958A>C
ClinVar dbSNP
16g.79598995T=CA2235930880MAFc.908A= (p.Gln303=)
n.2958A=
16g.79598996G>ACA396534977MAFc.907C>T (p.Gln303Ter)
n.2957C>T
16g.79598996G>CCA396534978MAFc.907C>G (p.Gln303Glu)
n.2957C>G
16g.79598996G>TCA396534979MAFc.907C>A (p.Gln303Lys)
n.2957C>A
16g.79598997G>ACA496508957MAFc.906C>T (p.Ala302=)
n.2956C>T
gnomAD v4
16g.79598997G>CCA8184010MAFc.906C>G (p.Ala302=)
n.2956C>G
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.79598997G=CA2235930883MAFc.906C= (p.Ala302=)
n.2956C=
16g.79598997G>TCA496508961MAFc.906C>A (p.Ala302=)
n.2956C>A
16g.79598998G>ACA396534980MAFc.905C>T (p.Ala302Val)
n.2955C>T
ClinVar dbSNP gnomAD v2 COSMIC
16g.79598998G>CCA396534981MAFc.905C>G (p.Ala302Gly)
n.2955C>G
16g.79598998G=CA2235930888MAFc.905C= (p.Ala302=)
n.2955C=
16g.79598998G>TCA396534982MAFc.905C>A (p.Ala302Asp)
n.2955C>A
ClinVar dbSNP
16g.79598999delCA2634430781MAFc.904del (p.Ala302ProfsTer?)
n.2954del
gnomAD v4
16g.79598999C>ACA396534984MAFc.904G>T (p.Ala302Ser)
n.2954G>T
16g.79598999C>GCA396534985MAFc.904G>C (p.Ala302Pro)
n.2954G>C
16g.79598999C>TCA396534983MAFc.904G>A (p.Ala302Thr)
n.2954G>A
dbSNP
16g.79599000A>CCA396534987MAFc.903T>G (p.Tyr301Ter)
n.2953T>G
16g.79599000A>GCA496508967MAFc.903T>C (p.Tyr301=)
n.2953T>C
16g.79599000A>TCA396534986MAFc.903T>A (p.Tyr301Ter)
n.2953T>A
16g.79599001T>ACA396534990MAFc.902A>T (p.Tyr301Phe)
n.2952A>T
COSMIC
16g.79599001T>CCA396534988MAFc.902A>G (p.Tyr301Cys)
n.2952A>G
ClinVar
16g.79599001T>GCA396534989MAFc.902A>C (p.Tyr301Ser)
n.2952A>C
16g.79599002A>CCA396534991MAFc.901T>G (p.Tyr301Asp)
n.2951T>G
16g.79599002A>GCA396534992MAFc.901T>C (p.Tyr301His)
n.2951T>C
16g.79599002A>TCA396534993MAFc.901T>A (p.Tyr301Asn)
n.2951T>A
16g.79599003G>ACA496508975MAFc.900C>T (p.Gly300=)
n.2950C>T
16g.79599003G>CCA284128034MAFc.900C>G (p.Gly300=)
n.2950C>G
dbSNP gnomAD v4
16g.79599003G=CA2235930899MAFc.900C= (p.Gly300=)
n.2950C=
16g.79599003G>TCA496508978MAFc.900C>A (p.Gly300=)
n.2950C>A
16g.79599004C>ACA396534996MAFc.899G>T (p.Gly300Val)
n.2949G>T
gnomAD v4
16g.79599004C>GCA396534995MAFc.899G>C (p.Gly300Ala)
n.2949G>C
16g.79599004C>TCA396534994MAFc.899G>A (p.Gly300Asp)
n.2949G>A
ClinVar
16g.79599005C>ACA396534997MAFc.898G>T (p.Gly300Cys)
n.2948G>T
16g.79599005C>GCA396534998MAFc.898G>C (p.Gly300Arg)
n.2948G>C
dbSNP
16g.79599005C>TCA396534999MAFc.898G>A (p.Gly300Ser)
n.2948G>A
ClinVar dbSNP
16g.79599006G>ACA496508985MAFc.897C>T (p.Arg299=)
n.2947C>T
ClinVar dbSNP gnomAD v3 gnomAD v4
16g.79599006G>CCA496508986MAFc.897C>G (p.Arg299=)
n.2947C>G
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.79599006G=CA2235930903MAFc.897C= (p.Arg299=)
n.2947C=
16g.79599006G>TCA496508987MAFc.897C>A (p.Arg299=)
n.2947C>A
16g.79599007C>ACA396535000MAFc.896G>T (p.Arg299Leu)
n.2946G>T
16g.79599007C>GCA396535001MAFc.896G>C (p.Arg299Pro)
n.2946G>C
dbSNP
16g.79599007C>TCA396535002MAFc.896G>A (p.Arg299His)
n.2946G>A
COSMIC
16g.79599008G>ACA396535004MAFc.895C>T (p.Arg299Cys)
n.2945C>T
ClinVar dbSNP
16g.79599008G>CCA396535003MAFc.895C>G (p.Arg299Gly)
n.2945C>G
ClinVar
16g.79599008G=CA2235930908MAFc.895C= (p.Arg299=)
n.2945C=
16g.79599008G>TCA199634MAFc.895C>A (p.Arg299Ser)
n.2945C>A
ClinVar dbSNP gnomAD v3 gnomAD v4
16g.79599009G>ACA496508994MAFc.894C>T (p.Asn298=)
n.2944C>T
gnomAD v4
16g.79599009G>CCA396535005MAFc.894C>G (p.Asn298Lys)
n.2944C>G
16g.79599009G>TCA396535006MAFc.894C>A (p.Asn298Lys)
n.2944C>A
ClinVar gnomAD v4
16g.79599010T>ACA396535007MAFc.893A>T (p.Asn298Ile)
n.2943A>T
16g.79599010T>CCA396535008MAFc.893A>G (p.Asn298Ser)
n.2943A>G
16g.79599010T>GCA396535009MAFc.893A>C (p.Asn298Thr)
n.2943A>C
16g.79599011T>ACA396535010MAFc.892A>T (p.Asn298Tyr)
n.2942A>T
16g.79599011T>CCA396535011MAFc.892A>G (p.Asn298Asp)
n.2942A>G
16g.79599011T>GCA396535012MAFc.892A>C (p.Asn298His)
n.2942A>C
ClinVar
16g.79599012T>ACA396535013MAFc.891A>T (p.Lys297Asn)
n.2941A>T
16g.79599012T>CCA496509004MAFc.891A>G (p.Lys297=)
n.2941A>G
16g.79599012T>GCA396535014MAFc.891A>C (p.Lys297Asn)
n.2941A>C
16g.79599013T>ACA396535015MAFc.890A>T (p.Lys297Ile)
n.2940A>T
16g.79599013T>CCA122974MAFc.890A>G (p.Lys297Arg)
n.2940A>G
ClinVar dbSNP
16g.79599013T>GCA396535016MAFc.890A>C (p.Lys297Thr)
n.2940A>C
16g.79599013T=CA2235930913MAFc.890A= (p.Lys297=)
n.2940A=
16g.79599014T>ACA396535017MAFc.889A>T (p.Lys297Ter)
n.2939A>T
16g.79599014T>CCA396535019MAFc.889A>G (p.Lys297Glu)
n.2939A>G
16g.79599014T>GCA396535018MAFc.889A>C (p.Lys297Gln)
n.2939A>C
16g.79599015C>ACA496509008MAFc.888G>T (p.Leu296=)
n.2938G>T
16g.79599015C>GCA496509009MAFc.888G>C (p.Leu296=)
n.2938G>C
gnomAD v3 gnomAD v4
16g.79599015C>TCA496509012MAFc.888G>A (p.Leu296=)
n.2938G>A
16g.79599016A=CA2235930919MAFc.887T= (p.Leu296=)
n.2937T=
16g.79599016A>CCA396535020MAFc.887T>G (p.Leu296Arg)
n.2937T>G
16g.79599016A>GCA396535021MAFc.887T>C (p.Leu296Pro)
n.2937T>C
ClinVar dbSNP
16g.79599016A>TCA396535022MAFc.887T>A (p.Leu296Gln)
n.2937T>A
16g.79599017G>ACA496509014MAFc.886C>T (p.Leu296=)
n.2936C>T
dbSNP gnomAD v3 gnomAD v4
16g.79599017G>CCA396535023MAFc.886C>G (p.Leu296Val)
n.2936C>G
gnomAD v4
16g.79599017G=CA2235930923MAFc.886C= (p.Leu296=)
n.2936C=
16g.79599017G>TCA396535024MAFc.886C>A (p.Leu296Met)
n.2936C>A
16g.79599018G>ACA496509018MAFc.885C>T (p.Thr295=)
n.2935C>T
dbSNP gnomAD v2
16g.79599018G>CCA496509020MAFc.885C>G (p.Thr295=)
n.2935C>G
gnomAD v4
16g.79599018G=CA2235930924MAFc.885C= (p.Thr295=)
n.2935C=
16g.79599018G>TCA496509021MAFc.885C>A (p.Thr295=)
n.2935C>A
16g.79599019G>ACA396535025MAFc.884C>T (p.Thr295Ile)
n.2934C>T
16g.79599019G>CCA396535026MAFc.884C>G (p.Thr295Ser)
n.2934C>G
16g.79599019G>TCA396535027MAFc.884C>A (p.Thr295Asn)
n.2934C>A
16g.79599020T>ACA396535028MAFc.883A>T (p.Thr295Ser)
n.2933A>T
16g.79599020T>CCA396535029MAFc.883A>G (p.Thr295Ala)
n.2933A>G
16g.79599020T>GCA396535030MAFc.883A>C (p.Thr295Pro)
n.2933A>C
16g.79599021C>ACA496509029MAFc.882G>T (p.Arg294=)
n.2932G>T
16g.79599021C=CA2235930929MAFc.882G= (p.Arg294=)
n.2932G=
16g.79599021C>GCA496509028MAFc.882G>C (p.Arg294=)
n.2932G>C
16g.79599021C>TCA8184011MAFc.882G>A (p.Arg294=)
n.2932G>A
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.79599022C>ACA396535033MAFc.881G>T (p.Arg294Leu)
n.2931G>T
16g.79599022C=CA2235930937MAFc.881G= (p.Arg294=)
n.2931G=
16g.79599022C>GCA396535031MAFc.881G>C (p.Arg294Pro)
n.2931G>C
16g.79599022C>TCA396535032MAFc.881G>A (p.Arg294Gln)
n.2931G>A
ClinVar dbSNP
16g.79599023G>ACA278847MAFc.880C>T (p.Arg294Trp)
n.2930C>T
ClinVar dbSNP
16g.79599023G>CCA396535034MAFc.880C>G (p.Arg294Gly)
n.2930C>G
16g.79599023G=CA2235930947MAFc.880C= (p.Arg294=)
n.2930C=
16g.79599023G>TCA496509036MAFc.880C>A (p.Arg294=)
n.2930C>A
gnomAD v3 gnomAD v4
16g.79599024C>ACA396535035MAFc.879G>T (p.Arg293Ser)
n.2929G>T
16g.79599024C=CA2235930953MAFc.879G= (p.Arg293=)
n.2929G=
16g.79599024C>GCA396535036MAFc.879G>C (p.Arg293Ser)
n.2929G>C
16g.79599024C>TCA496509037MAFc.879G>A (p.Arg293=)
n.2929G>A
dbSNP
16g.79599025C>ACA396535037MAFc.878G>T (p.Arg293Met)
n.2928G>T
16g.79599025C>GCA396535038MAFc.878G>C (p.Arg293Thr)
n.2928G>C
16g.79599025C>TCA396535039MAFc.878G>A (p.Arg293Lys)
n.2928G>A
16g.79599026T>ACA396535040MAFc.877A>T (p.Arg293Trp)
n.2927A>T
16g.79599026T>CCA396535041MAFc.877A>G (p.Arg293Gly)
n.2927A>G
gnomAD v4
16g.79599026T>GCA496509043MAFc.877A>C (p.Arg293=)
n.2927A>C
16g.79599027C>ACA396535042MAFc.876G>T (p.Lys292Asn)
n.2926G>T
16g.79599027C>GCA396535043MAFc.876G>C (p.Lys292Asn)
n.2926G>C
16g.79599027C>TCA496509049MAFc.876G>A (p.Lys292=)
n.2926G>A
16g.79599028T>ACA396535046MAFc.875A>T (p.Lys292Met)
n.2925A>T
16g.79599028T>CCA396535045MAFc.875A>G (p.Lys292Arg)
n.2925A>G
gnomAD v4
16g.79599028T>GCA396535044MAFc.875A>C (p.Lys292Thr)
n.2925A>C
16g.79599029T>ACA396535047MAFc.874A>T (p.Lys292Ter)
n.2924A>T
16g.79599029T>CCA396535048MAFc.874A>G (p.Lys292Glu)
n.2924A>G
gnomAD v4
16g.79599029T>GCA396535049MAFc.874A>C (p.Lys292Gln)
n.2924A>C
16g.79599030C>ACA396535050MAFc.873G>T (p.Gln291His)
n.2923G>T
16g.79599030C>GCA396535051MAFc.873G>C (p.Gln291His)
n.2923G>C
COSMIC
16g.79599030C>TCA496509056MAFc.873G>A (p.Gln291=)
n.2923G>A
gnomAD v4 COSMIC
16g.79599031T>ACA396535054MAFc.872A>T (p.Gln291Leu)
n.2922A>T
16g.79599031T>CCA396535053MAFc.872A>G (p.Gln291Arg)
n.2922A>G
16g.79599031T>GCA396535052MAFc.872A>C (p.Gln291Pro)
n.2922A>C
16g.79599032G>ACA396535055MAFc.871C>T (p.Gln291Ter)
n.2921C>T
dbSNP
16g.79599032G>CCA396535056MAFc.871C>G (p.Gln291Glu)
n.2921C>G
ClinVar gnomAD v4
16g.79599032G>TCA396535057MAFc.871C>A (p.Gln291Lys)
n.2921C>A
gnomAD v4
16g.79599033C>ACA396535058MAFc.870G>T (p.Lys290Asn)
n.2920G>T
16g.79599033C=CA2235930955MAFc.870G= (p.Lys290=)
n.2920G=
16g.79599033C>GCA396535059MAFc.870G>C (p.Lys290Asn)
n.2920G>C
16g.79599033C>TCA8184012MAFc.870G>A (p.Lys290=)
n.2920G>A
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.79599034T>ACA396535062MAFc.869A>T (p.Lys290Met)
n.2919A>T
16g.79599034T>CCA396535060MAFc.869A>G (p.Lys290Arg)
n.2919A>G
16g.79599034T>GCA396535061MAFc.869A>C (p.Lys290Thr)
n.2919A>C
16g.79599035T>ACA396535063MAFc.868A>T (p.Lys290Ter)
n.2918A>T
16g.79599035T>CCA396535064MAFc.868A>G (p.Lys290Glu)
n.2918A>G
dbSNP
16g.79599035T>GCA396535065MAFc.868A>C (p.Lys290Gln)
n.2918A>C
16g.79599036C>ACA496509071MAFc.867G>T (p.Leu289=)
n.2917G>T
16g.79599036C=CA2235930959MAFc.867G= (p.Leu289=)
n.2917G=
16g.79599036C>GCA496509072MAFc.867G>C (p.Leu289=)
n.2917G>C
dbSNP
16g.79599036C>TCA496509074MAFc.867G>A (p.Leu289=)
n.2917G>A
dbSNP gnomAD v2 gnomAD v4
16g.79599037A=CA2235930961MAFc.866T= (p.Leu289=)
n.2916T=
16g.79599037A>CCA396535066MAFc.866T>G (p.Leu289Arg)
n.2916T>G
16g.79599037A>GCA396535067MAFc.866T>C (p.Leu289Pro)
n.2916T>C
16g.79599037A>TCA284128083MAFc.866T>A (p.Leu289Gln)
n.2916T>A
ClinVar dbSNP
16g.79599038G>ACA8184013MAFc.865C>T (p.Leu289=)
n.2915C>T
dbSNP ExAC gnomAD v2 gnomAD v4
16g.79599038G>CCA396535068MAFc.865C>G (p.Leu289Val)
n.2915C>G
16g.79599038G=CA2235930965MAFc.865C= (p.Leu289=)
n.2915C=
16g.79599038G>TCA396535069MAFc.865C>A (p.Leu289Met)
n.2915C>A
gnomAD v4
16g.79599039C>ACA496509082MAFc.864G>T (p.Arg288=)
n.2914G>T
16g.79599039C=CA2235930969MAFc.864G= (p.Arg288=)
n.2914G=
16g.79599039C>GCA496509084MAFc.864G>C (p.Arg288=)
n.2914G>C
16g.79599039C>TCA8184014MAFc.864G>A (p.Arg288=)
n.2914G>A
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.79599040C>ACA396535070MAFc.863G>T (p.Arg288Leu)
n.2913G>T
16g.79599040C=CA2235930976MAFc.863G= (p.Arg288=)
n.2913G=
16g.79599040C>GCA122972MAFc.863G>C (p.Arg288Pro)
n.2913G>C
ClinVar dbSNP
16g.79599040C>TCA8184015MAFc.863G>A (p.Arg288Gln)
n.2913G>A
dbSNP ExAC gnomAD v2 gnomAD v4

Number of alleles fetched