Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
16 | g.79598940G>A | CA496508892 | MAF | c.963C>T (p.Asn321=) n.3013C>T | gnomAD v4 |
16 | g.79598940G>C | CA396534849 | MAF | c.963C>G (p.Asn321Lys) n.3013C>G | dbSNP |
16 | g.79598940G>T | CA396534848 | MAF | c.963C>A (p.Asn321Lys) n.3013C>A | gnomAD v4 |
16 | g.79598941T>A | CA396534850 | MAF | c.962A>T (p.Asn321Ile) n.3012A>T | |
16 | g.79598941T>C | CA396534851 | MAF | c.962A>G (p.Asn321Ser) n.3012A>G | |
16 | g.79598941T>G | CA396534852 | MAF | c.962A>C (p.Asn321Thr) n.3012A>C | |
16 | g.79598942T>A | CA396534853 | MAF | c.961A>T (p.Asn321Tyr) n.3011A>T | |
16 | g.79598942T>C | CA396534854 | MAF | c.961A>G (p.Asn321Asp) n.3011A>G | |
16 | g.79598942T>G | CA396534855 | MAF | c.961A>C (p.Asn321His) n.3011A>C | |
16 | g.79598943C>A | CA396534856 | MAF | c.960G>T (p.Lys320Asn) n.3010G>T | dbSNP gnomAD v2 gnomAD v4 |
16 | g.79598943C= | CA2235930732 | MAF | c.960G= (p.Lys320=) n.3010G= | |
16 | g.79598943C>G | CA396534857 | MAF | c.960G>C (p.Lys320Asn) n.3010G>C | dbSNP gnomAD v2 |
16 | g.79598943C>T | CA8184000 | MAF | c.960G>A (p.Lys320=) n.3010G>A | dbSNP ExAC gnomAD v2 gnomAD v4 |
16 | g.79598944T>A | CA396534858 | MAF | c.959A>T (p.Lys320Met) n.3009A>T | |
16 | g.79598944T>C | CA396534859 | MAF | c.959A>G (p.Lys320Arg) n.3009A>G | ClinVar |
16 | g.79598944T>G | CA396534860 | MAF | c.959A>C (p.Lys320Thr) n.3009A>C | |
16 | g.79598945T>A | CA396534861 | MAF | c.958A>T (p.Lys320Ter) n.3008A>T | |
16 | g.79598945T>C | CA396534862 | MAF | c.958A>G (p.Lys320Glu) n.3008A>G | dbSNP gnomAD v2 gnomAD v4 |
16 | g.79598945T>G | CA396534863 | MAF | c.958A>C (p.Lys320Gln) n.3008A>C | |
16 | g.79598945T= | CA2235930739 | MAF | c.958A= (p.Lys320=) n.3008A= | |
16 | g.79598946C>A | CA396534864 | MAF | c.957G>T (p.Glu319Asp) n.3007G>T | |
16 | g.79598946C= | CA2235930742 | MAF | c.957G= (p.Glu319=) n.3007G= | |
16 | g.79598946C>G | CA396534865 | MAF | c.957G>C (p.Glu319Asp) n.3007G>C | |
16 | g.79598946C>T | CA496508893 | MAF | c.957G>A (p.Glu319=) n.3007G>A | dbSNP gnomAD v4 |
16 | g.79598947T>A | CA396534866 | MAF | c.956A>T (p.Glu319Val) n.3006A>T | |
16 | g.79598947T>C | CA396534867 | MAF | c.956A>G (p.Glu319Gly) n.3006A>G | |
16 | g.79598947T>G | CA396534868 | MAF | c.956A>C (p.Glu319Ala) n.3006A>C | |
16 | g.79598948C>A | CA396534871 | MAF | c.955G>T (p.Glu319Ter) n.3005G>T | |
16 | g.79598948C>G | CA396534870 | MAF | c.955G>C (p.Glu319Gln) n.3005G>C | |
16 | g.79598948C>T | CA396534869 | MAF | c.955G>A (p.Glu319Lys) n.3005G>A | gnomAD v4 |
16 | g.79598949C>A | CA496508894 | MAF | c.954G>T (p.Ser318=) n.3004G>T | |
16 | g.79598949C= | CA2235930748 | MAF | c.954G= (p.Ser318=) n.3004G= | |
16 | g.79598949C>G | CA496508895 | MAF | c.954G>C (p.Ser318=) n.3004G>C | |
16 | g.79598949C>T | CA8184001 | MAF | c.954G>A (p.Ser318=) n.3004G>A | dbSNP ExAC gnomAD v2 gnomAD v4 |
16 | g.79598950G>A | CA8184002 | MAF | c.953C>T (p.Ser318Leu) n.3003C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
16 | g.79598950G>C | CA396534872 | MAF | c.953C>G (p.Ser318Trp) n.3003C>G | gnomAD v4 |
16 | g.79598950G= | CA2235930752 | MAF | c.953C= (p.Ser318=) n.3003C= | |
16 | g.79598950G>T | CA396534873 | MAF | c.953C>A (p.Ser318Ter) n.3003C>A | |
16 | g.79598951A>C | CA396534874 | MAF | c.952T>G (p.Ser318Ala) n.3002T>G | |
16 | g.79598951A>G | CA396534875 | MAF | c.952T>C (p.Ser318Pro) n.3002T>C | |
16 | g.79598951A>T | CA396534876 | MAF | c.952T>A (p.Ser318Thr) n.3002T>A | |
16 | g.79598952C>A | CA396534877 | MAF | c.951G>T (p.Glu317Asp) n.3001G>T | |
16 | g.79598952C>G | CA396534878 | MAF | c.951G>C (p.Glu317Asp) n.3001G>C | |
16 | g.79598952C>T | CA496508896 | MAF | c.951G>A (p.Glu317=) n.3001G>A | |
16 | g.79598953T>A | CA396534879 | MAF | c.950A>T (p.Glu317Val) n.3000A>T | |
16 | g.79598953T>C | CA396534880 | MAF | c.950A>G (p.Glu317Gly) n.3000A>G | |
16 | g.79598953T>G | CA396534881 | MAF | c.950A>C (p.Glu317Ala) n.3000A>C | |
16 | g.79598954C>A | CA396534882 | MAF | c.949G>T (p.Glu317Ter) n.2999G>T | |
16 | g.79598954C>G | CA396534883 | MAF | c.949G>C (p.Glu317Gln) n.2999G>C | |
16 | g.79598954C>T | CA396534884 | MAF | c.949G>A (p.Glu317Lys) n.2999G>A | COSMIC |
16 | g.79598955C>A | CA496508897 | MAF | c.948G>T (p.Leu316=) n.2998G>T | |
16 | g.79598955C= | CA2235930759 | MAF | c.948G= (p.Leu316=) n.2998G= | |
16 | g.79598955C>G | CA496508898 | MAF | c.948G>C (p.Leu316=) n.2998G>C | |
16 | g.79598955C>T | CA8184003 | MAF | c.948G>A (p.Leu316=) n.2998G>A | dbSNP ExAC gnomAD v2 gnomAD v4 |
16 | g.79598956A>C | CA396534887 | MAF | c.947T>G (p.Leu316Arg) n.2997T>G | |
16 | g.79598956A>G | CA396534885 | MAF | c.947T>C (p.Leu316Pro) n.2997T>C | |
16 | g.79598956A>T | CA396534886 | MAF | c.947T>A (p.Leu316Gln) n.2997T>A | |
16 | g.79598957G>A | CA284127958 | MAF | c.946C>T (p.Leu316=) n.2996C>T | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.79598957G>C | CA396534888 | MAF | c.946C>G (p.Leu316Val) n.2996C>G | |
16 | g.79598957G= | CA2235930762 | MAF | c.946C= (p.Leu316=) n.2996C= | |
16 | g.79598957G>T | CA396534889 | MAF | c.946C>A (p.Leu316Met) n.2996C>A | |
16 | g.79598958G>A | CA496508899 | MAF | c.945C>T (p.Val315=) n.2995C>T | gnomAD v4 |
16 | g.79598958G>C | CA496508901 | MAF | c.945C>G (p.Val315=) n.2995C>G | dbSNP gnomAD v3 gnomAD v4 |
16 | g.79598958G= | CA2235930766 | MAF | c.945C= (p.Val315=) n.2995C= | |
16 | g.79598958G>T | CA496508900 | MAF | c.945C>A (p.Val315=) n.2995C>A | |
16 | g.79598959A= | CA2235930773 | MAF | c.944T= (p.Val315=) n.2994T= | |
16 | g.79598959A>C | CA396534890 | MAF | c.944T>G (p.Val315Gly) n.2994T>G | dbSNP |
16 | g.79598959A>G | CA396534891 | MAF | c.944T>C (p.Val315Ala) n.2994T>C | dbSNP gnomAD v4 |
16 | g.79598959A>T | CA396534892 | MAF | c.944T>A (p.Val315Asp) n.2994T>A | dbSNP gnomAD v4 |
16 | g.79598960C>A | CA396534893 | MAF | c.943G>T (p.Val315Phe) n.2993G>T | COSMIC |
16 | g.79598960C>G | CA396534894 | MAF | c.943G>C (p.Val315Leu) n.2993G>C | |
16 | g.79598960C>T | CA396534895 | MAF | c.943G>A (p.Val315Ile) n.2993G>A | |
16 | g.79598961G>A | CA8184004 | MAF | c.942C>T (p.His314=) n.2992C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.79598961G>C | CA396534896 | MAF | c.942C>G (p.His314Gln) n.2992C>G | |
16 | g.79598961G= | CA2235930781 | MAF | c.942C= (p.His314=) n.2992C= | |
16 | g.79598961G>T | CA396534897 | MAF | c.942C>A (p.His314Gln) n.2992C>A | dbSNP |
16 | g.79598962T>A | CA396534900 | MAF | c.941A>T (p.His314Leu) n.2991A>T | |
16 | g.79598962T>C | CA396534899 | MAF | c.941A>G (p.His314Arg) n.2991A>G | |
16 | g.79598962T>G | CA396534898 | MAF | c.941A>C (p.His314Pro) n.2991A>C | ClinVar dbSNP |
16 | g.79598962T= | CA2235930800 | MAF | c.941A= (p.His314=) n.2991A= | |
16 | g.79598963G>A | CA396534901 | MAF | c.940C>T (p.His314Tyr) n.2990C>T | |
16 | g.79598963G>C | CA396534902 | MAF | c.940C>G (p.His314Asp) n.2990C>G | |
16 | g.79598963G>T | CA396534903 | MAF | c.940C>A (p.His314Asn) n.2990C>A | |
16 | g.79598964T>A | CA396534904 | MAF | c.939A>T (p.Arg313Ser) n.2989A>T | |
16 | g.79598964T>C | CA496508902 | MAF | c.939A>G (p.Arg313=) n.2989A>G | ClinVar dbSNP gnomAD v4 |
16 | g.79598964T>G | CA396534905 | MAF | c.939A>C (p.Arg313Ser) n.2989A>C | |
16 | g.79598964T= | CA2235930808 | MAF | c.939A= (p.Arg313=) n.2989A= | |
16 | g.79598965C>A | CA396534906 | MAF | c.938G>T (p.Arg313Ile) n.2988G>T | |
16 | g.79598965C>G | CA396534907 | MAF | c.938G>C (p.Arg313Thr) n.2988G>C | dbSNP |
16 | g.79598965C>T | CA396534908 | MAF | c.938G>A (p.Arg313Lys) n.2988G>A | |
16 | g.79598966T>A | CA396534909 | MAF | c.937A>T (p.Arg313Ter) n.2987A>T | |
16 | g.79598966T>C | CA396534910 | MAF | c.937A>G (p.Arg313Gly) n.2987A>G | |
16 | g.79598966T>G | CA496508903 | MAF | c.937A>C (p.Arg313=) n.2987A>C | |
16 | g.79598967C>A | CA396534911 | MAF | c.936G>T (p.Gln312His) n.2986G>T | |
16 | g.79598967C>G | CA396534912 | MAF | c.936G>C (p.Gln312His) n.2986G>C | gnomAD v4 |
16 | g.79598967C>T | CA496508904 | MAF | c.936G>A (p.Gln312=) n.2986G>A | |
16 | g.79598968T>A | CA396534915 | MAF | c.935A>T (p.Gln312Leu) n.2985A>T | |
16 | g.79598968T>C | CA396534913 | MAF | c.935A>G (p.Gln312Arg) n.2985A>G | ClinVar |
16 | g.79598968T>G | CA396534914 | MAF | c.935A>C (p.Gln312Pro) n.2985A>C | |
16 | g.79598969G>A | CA396534916 | MAF | c.934C>T (p.Gln312Ter) n.2984C>T | |
16 | g.79598969G>C | CA396534917 | MAF | c.934C>G (p.Gln312Glu) n.2984C>G | |
16 | g.79598969G>T | CA396534918 | MAF | c.934C>A (p.Gln312Lys) n.2984C>A | |
16 | g.79598970C>A | CA396534919 | MAF | c.933G>T (p.Gln311His) n.2983G>T | dbSNP gnomAD v2 gnomAD v4 |
16 | g.79598970C= | CA2235930813 | MAF | c.933G= (p.Gln311=) n.2983G= | |
16 | g.79598970C>G | CA396534920 | MAF | c.933G>C (p.Gln311His) n.2983G>C | |
16 | g.79598970C>T | CA496508905 | MAF | c.933G>A (p.Gln311=) n.2983G>A | dbSNP gnomAD v4 |
16 | g.79598971T>A | CA396534921 | MAF | c.932A>T (p.Gln311Leu) n.2982A>T | |
16 | g.79598971T>C | CA396534922 | MAF | c.932A>G (p.Gln311Arg) n.2982A>G | dbSNP |
16 | g.79598971T>G | CA396534923 | MAF | c.932A>C (p.Gln311Pro) n.2982A>C | |
16 | g.79598971T= | CA2235930819 | MAF | c.932A= (p.Gln311=) n.2982A= | |
16 | g.79598972G>A | CA396534924 | MAF | c.931C>T (p.Gln311Ter) n.2981C>T | dbSNP |
16 | g.79598972G>C | CA396534925 | MAF | c.931C>G (p.Gln311Glu) n.2981C>G | |
16 | g.79598972G>T | CA396534926 | MAF | c.931C>A (p.Gln311Lys) n.2981C>A | |
16 | g.79598973C>A | CA496508923 | MAF | c.930G>T (p.Val310=) n.2980G>T | |
16 | g.79598973C= | CA2235930823 | MAF | c.930G= (p.Val310=) n.2980G= | |
16 | g.79598973C>G | CA496508924 | MAF | c.930G>C (p.Val310=) n.2980G>C | |
16 | g.79598973C>T | CA8184005 | MAF | c.930G>A (p.Val310=) n.2980G>A | dbSNP ExAC gnomAD v2 |
16 | g.79598974A= | CA2235930830 | MAF | c.929T= (p.Val310=) n.2979T= | |
16 | g.79598974A>C | CA396534928 | MAF | c.929T>G (p.Val310Gly) n.2979T>G | dbSNP |
16 | g.79598974A>G | CA396534929 | MAF | c.929T>C (p.Val310Ala) n.2979T>C | |
16 | g.79598974A>T | CA396534927 | MAF | c.929T>A (p.Val310Glu) n.2979T>A | dbSNP |
16 | g.79598975C>A | CA396534930 | MAF | c.928G>T (p.Val310Leu) n.2978G>T | |
16 | g.79598975C>G | CA396534931 | MAF | c.928G>C (p.Val310Leu) n.2978G>C | |
16 | g.79598975C>T | CA396534932 | MAF | c.928G>A (p.Val310Met) n.2978G>A | |
16 | g.79598976C>A | CA396534933 | MAF | c.927G>T (p.Arg309Ser) n.2977G>T | COSMIC |
16 | g.79598976C= | CA2235930838 | MAF | c.927G= (p.Arg309=) n.2977G= | |
16 | g.79598976C>G | CA396534934 | MAF | c.927G>C (p.Arg309Ser) n.2977G>C | |
16 | g.79598976C>T | CA496508925 | MAF | c.927G>A (p.Arg309=) n.2977G>A | dbSNP |
16 | g.79598977C>A | CA396534937 | MAF | c.926G>T (p.Arg309Met) n.2976G>T | dbSNP |
16 | g.79598977C>G | CA396534936 | MAF | c.926G>C (p.Arg309Thr) n.2976G>C | |
16 | g.79598977C>T | CA396534935 | MAF | c.926G>A (p.Arg309Lys) n.2976G>A | |
16 | g.79598978T>A | CA396534938 | MAF | c.925A>T (p.Arg309Trp) n.2975A>T | |
16 | g.79598978T>C | CA396534939 | MAF | c.925A>G (p.Arg309Gly) n.2975A>G | |
16 | g.79598978T>G | CA496508927 | MAF | c.925A>C (p.Arg309=) n.2975A>C | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.79598978T= | CA2235930843 | MAF | c.925A= (p.Arg309=) n.2975A= | |
16 | g.79598979C>A | CA396534940 | MAF | c.924G>T (p.Lys308Asn) n.2974G>T | |
16 | g.79598979C= | CA2235930845 | MAF | c.924G= (p.Lys308=) n.2974G= | |
16 | g.79598979C>G | CA8184006 | MAF | c.924G>C (p.Lys308Asn) n.2974G>C | dbSNP ExAC |
16 | g.79598979C>T | CA496508928 | MAF | c.924G>A (p.Lys308=) n.2974G>A | |
16 | g.79598980T>A | CA396534941 | MAF | c.923A>T (p.Lys308Met) n.2973A>T | |
16 | g.79598980T>C | CA396534942 | MAF | c.923A>G (p.Lys308Arg) n.2973A>G | |
16 | g.79598980T>G | CA396534943 | MAF | c.923A>C (p.Lys308Thr) n.2973A>C | |
16 | g.79598981T>A | CA396534944 | MAF | c.922A>T (p.Lys308Ter) n.2972A>T | |
16 | g.79598981T>C | CA396534946 | MAF | c.922A>G (p.Lys308Glu) n.2972A>G | ClinVar |
16 | g.79598981T>G | CA396534945 | MAF | c.922A>C (p.Lys308Gln) n.2972A>C | |
16 | g.79598982G>A | CA496508935 | MAF | c.921C>T (p.Phe307=) n.2971C>T | |
16 | g.79598982G>C | CA396534947 | MAF | c.921C>G (p.Phe307Leu) n.2971C>G | |
16 | g.79598982G>T | CA396534948 | MAF | c.921C>A (p.Phe307Leu) n.2971C>A | |
16 | g.79598983A>C | CA396534949 | MAF | c.920T>G (p.Phe307Cys) n.2970T>G | |
16 | g.79598983A>G | CA396534950 | MAF | c.920T>C (p.Phe307Ser) n.2970T>C | |
16 | g.79598983A>T | CA396534951 | MAF | c.920T>A (p.Phe307Tyr) n.2970T>A | |
16 | g.79598984A>C | CA396534952 | MAF | c.919T>G (p.Phe307Val) n.2969T>G | |
16 | g.79598984A>G | CA396534953 | MAF | c.919T>C (p.Phe307Leu) n.2969T>C | |
16 | g.79598984A>T | CA396534954 | MAF | c.919T>A (p.Phe307Ile) n.2969T>A | |
16 | g.79598985G>A | CA8184007 | MAF | c.918C>T (p.Arg306=) n.2968C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.79598985G>C | CA496508942 | MAF | c.918C>G (p.Arg306=) n.2968C>G | dbSNP gnomAD v4 |
16 | g.79598985G= | CA2235930847 | MAF | c.918C= (p.Arg306=) n.2968C= | |
16 | g.79598985G>T | CA496508941 | MAF | c.918C>A (p.Arg306=) n.2968C>A | |
16 | g.79598986C>A | CA396534955 | MAF | c.917G>T (p.Arg306Leu) n.2967G>T | dbSNP |
16 | g.79598986C>G | CA396534956 | MAF | c.917G>C (p.Arg306Pro) n.2967G>C | dbSNP |
16 | g.79598986C>T | CA396534957 | MAF | c.917G>A (p.Arg306His) n.2967G>A | COSMIC |
16 | g.79598987G>A | CA396534958 | MAF | c.916C>T (p.Arg306Cys) n.2966C>T | |
16 | g.79598987G>C | CA396534960 | MAF | c.916C>G (p.Arg306Gly) n.2966C>G | ClinVar dbSNP |
16 | g.79598987G= | CA2235930855 | MAF | c.916C= (p.Arg306=) n.2966C= | |
16 | g.79598987G>T | CA396534959 | MAF | c.916C>A (p.Arg306Ser) n.2966C>A | dbSNP |
16 | g.79598988G>A | CA278839 | MAF | c.915C>T (p.Cys305=) n.2965C>T | ClinVar dbSNP |
16 | g.79598988G>C | CA396534961 | MAF | c.915C>G (p.Cys305Trp) n.2965C>G | |
16 | g.79598988G= | CA2235930859 | MAF | c.915C= (p.Cys305=) n.2965C= | |
16 | g.79598988G>T | CA396534962 | MAF | c.915C>A (p.Cys305Ter) n.2965C>A | |
16 | g.79598989C>A | CA396534963 | MAF | c.914G>T (p.Cys305Phe) n.2964G>T | ClinVar |
16 | g.79598989C= | CA2235930864 | MAF | c.914G= (p.Cys305=) n.2964G= | |
16 | g.79598989C>G | CA396534964 | MAF | c.914G>C (p.Cys305Ser) n.2964G>C | |
16 | g.79598989C>T | CA396534965 | MAF | c.914G>A (p.Cys305Tyr) n.2964G>A | ClinVar dbSNP gnomAD v4 |
16 | g.79598990A>C | CA396534966 | MAF | c.913T>G (p.Cys305Gly) n.2963T>G | |
16 | g.79598990A>G | CA396534967 | MAF | c.913T>C (p.Cys305Arg) n.2963T>C | |
16 | g.79598990A>T | CA396534968 | MAF | c.913T>A (p.Cys305Ser) n.2963T>A | |
16 | g.79598991G>A | CA496508948 | MAF | c.912C>T (p.Ser304=) n.2962C>T | |
16 | g.79598991G>C | CA496508950 | MAF | c.912C>G (p.Ser304=) n.2962C>G | gnomAD v4 |
16 | g.79598991G>T | CA496508949 | MAF | c.912C>A (p.Ser304=) n.2962C>A | |
16 | g.79598992G>A | CA284128022 | MAF | c.911C>T (p.Ser304Phe) n.2961C>T | dbSNP |
16 | g.79598992G>C | CA396534969 | MAF | c.911C>G (p.Ser304Cys) n.2961C>G | |
16 | g.79598992G= | CA2235930867 | MAF | c.911C= (p.Ser304=) n.2961C= | |
16 | g.79598992G>T | CA396534970 | MAF | c.911C>A (p.Ser304Tyr) n.2961C>A | |
16 | g.79598993A>C | CA396534973 | MAF | c.910T>G (p.Ser304Ala) n.2960T>G | |
16 | g.79598993A>G | CA396534972 | MAF | c.910T>C (p.Ser304Pro) n.2960T>C | |
16 | g.79598993A>T | CA396534971 | MAF | c.910T>A (p.Ser304Thr) n.2960T>A | |
16 | g.79598994C>A | CA396534974 | MAF | c.909G>T (p.Gln303His) n.2959G>T | |
16 | g.79598994C= | CA2235930874 | MAF | c.909G= (p.Gln303=) n.2959G= | |
16 | g.79598994C>G | CA8184009 | MAF | c.909G>C (p.Gln303His) n.2959G>C | dbSNP ExAC gnomAD v2 gnomAD v4 |
16 | g.79598994C>T | CA8184008 | MAF | c.909G>A (p.Gln303=) n.2959G>A | dbSNP ExAC gnomAD v2 gnomAD v4 |
16 | g.79598995T>A | CA396534975 | MAF | c.908A>T (p.Gln303Leu) n.2958A>T | |
16 | g.79598995T>C | CA396534976 | MAF | c.908A>G (p.Gln303Arg) n.2958A>G | |
16 | g.79598995T>G | CA199636 | MAF | c.908A>C (p.Gln303Pro) n.2958A>C | ClinVar dbSNP |
16 | g.79598995T= | CA2235930880 | MAF | c.908A= (p.Gln303=) n.2958A= | |
16 | g.79598996G>A | CA396534977 | MAF | c.907C>T (p.Gln303Ter) n.2957C>T | |
16 | g.79598996G>C | CA396534978 | MAF | c.907C>G (p.Gln303Glu) n.2957C>G | |
16 | g.79598996G>T | CA396534979 | MAF | c.907C>A (p.Gln303Lys) n.2957C>A | |
16 | g.79598997G>A | CA496508957 | MAF | c.906C>T (p.Ala302=) n.2956C>T | gnomAD v4 |
16 | g.79598997G>C | CA8184010 | MAF | c.906C>G (p.Ala302=) n.2956C>G | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.79598997G= | CA2235930883 | MAF | c.906C= (p.Ala302=) n.2956C= | |
16 | g.79598997G>T | CA496508961 | MAF | c.906C>A (p.Ala302=) n.2956C>A | |
16 | g.79598998G>A | CA396534980 | MAF | c.905C>T (p.Ala302Val) n.2955C>T | ClinVar dbSNP gnomAD v2 COSMIC |
16 | g.79598998G>C | CA396534981 | MAF | c.905C>G (p.Ala302Gly) n.2955C>G | |
16 | g.79598998G= | CA2235930888 | MAF | c.905C= (p.Ala302=) n.2955C= | |
16 | g.79598998G>T | CA396534982 | MAF | c.905C>A (p.Ala302Asp) n.2955C>A | ClinVar dbSNP |
16 | g.79598999del | CA2634430781 | MAF | c.904del (p.Ala302ProfsTer?) n.2954del | gnomAD v4 |
16 | g.79598999C>A | CA396534984 | MAF | c.904G>T (p.Ala302Ser) n.2954G>T | |
16 | g.79598999C>G | CA396534985 | MAF | c.904G>C (p.Ala302Pro) n.2954G>C | |
16 | g.79598999C>T | CA396534983 | MAF | c.904G>A (p.Ala302Thr) n.2954G>A | dbSNP |
16 | g.79599000A>C | CA396534987 | MAF | c.903T>G (p.Tyr301Ter) n.2953T>G | |
16 | g.79599000A>G | CA496508967 | MAF | c.903T>C (p.Tyr301=) n.2953T>C | |
16 | g.79599000A>T | CA396534986 | MAF | c.903T>A (p.Tyr301Ter) n.2953T>A | |
16 | g.79599001T>A | CA396534990 | MAF | c.902A>T (p.Tyr301Phe) n.2952A>T | COSMIC |
16 | g.79599001T>C | CA396534988 | MAF | c.902A>G (p.Tyr301Cys) n.2952A>G | ClinVar |
16 | g.79599001T>G | CA396534989 | MAF | c.902A>C (p.Tyr301Ser) n.2952A>C | |
16 | g.79599002A>C | CA396534991 | MAF | c.901T>G (p.Tyr301Asp) n.2951T>G | |
16 | g.79599002A>G | CA396534992 | MAF | c.901T>C (p.Tyr301His) n.2951T>C | |
16 | g.79599002A>T | CA396534993 | MAF | c.901T>A (p.Tyr301Asn) n.2951T>A | |
16 | g.79599003G>A | CA496508975 | MAF | c.900C>T (p.Gly300=) n.2950C>T | |
16 | g.79599003G>C | CA284128034 | MAF | c.900C>G (p.Gly300=) n.2950C>G | dbSNP gnomAD v4 |
16 | g.79599003G= | CA2235930899 | MAF | c.900C= (p.Gly300=) n.2950C= | |
16 | g.79599003G>T | CA496508978 | MAF | c.900C>A (p.Gly300=) n.2950C>A | |
16 | g.79599004C>A | CA396534996 | MAF | c.899G>T (p.Gly300Val) n.2949G>T | gnomAD v4 |
16 | g.79599004C>G | CA396534995 | MAF | c.899G>C (p.Gly300Ala) n.2949G>C | |
16 | g.79599004C>T | CA396534994 | MAF | c.899G>A (p.Gly300Asp) n.2949G>A | ClinVar |
16 | g.79599005C>A | CA396534997 | MAF | c.898G>T (p.Gly300Cys) n.2948G>T | |
16 | g.79599005C>G | CA396534998 | MAF | c.898G>C (p.Gly300Arg) n.2948G>C | dbSNP |
16 | g.79599005C>T | CA396534999 | MAF | c.898G>A (p.Gly300Ser) n.2948G>A | ClinVar dbSNP |
16 | g.79599006G>A | CA496508985 | MAF | c.897C>T (p.Arg299=) n.2947C>T | ClinVar dbSNP gnomAD v3 gnomAD v4 |
16 | g.79599006G>C | CA496508986 | MAF | c.897C>G (p.Arg299=) n.2947C>G | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.79599006G= | CA2235930903 | MAF | c.897C= (p.Arg299=) n.2947C= | |
16 | g.79599006G>T | CA496508987 | MAF | c.897C>A (p.Arg299=) n.2947C>A | |
16 | g.79599007C>A | CA396535000 | MAF | c.896G>T (p.Arg299Leu) n.2946G>T | |
16 | g.79599007C>G | CA396535001 | MAF | c.896G>C (p.Arg299Pro) n.2946G>C | dbSNP |
16 | g.79599007C>T | CA396535002 | MAF | c.896G>A (p.Arg299His) n.2946G>A | COSMIC |
16 | g.79599008G>A | CA396535004 | MAF | c.895C>T (p.Arg299Cys) n.2945C>T | ClinVar dbSNP |
16 | g.79599008G>C | CA396535003 | MAF | c.895C>G (p.Arg299Gly) n.2945C>G | ClinVar |
16 | g.79599008G= | CA2235930908 | MAF | c.895C= (p.Arg299=) n.2945C= | |
16 | g.79599008G>T | CA199634 | MAF | c.895C>A (p.Arg299Ser) n.2945C>A | ClinVar dbSNP gnomAD v3 gnomAD v4 |
16 | g.79599009G>A | CA496508994 | MAF | c.894C>T (p.Asn298=) n.2944C>T | gnomAD v4 |
16 | g.79599009G>C | CA396535005 | MAF | c.894C>G (p.Asn298Lys) n.2944C>G | |
16 | g.79599009G>T | CA396535006 | MAF | c.894C>A (p.Asn298Lys) n.2944C>A | ClinVar gnomAD v4 |
16 | g.79599010T>A | CA396535007 | MAF | c.893A>T (p.Asn298Ile) n.2943A>T | |
16 | g.79599010T>C | CA396535008 | MAF | c.893A>G (p.Asn298Ser) n.2943A>G | |
16 | g.79599010T>G | CA396535009 | MAF | c.893A>C (p.Asn298Thr) n.2943A>C | |
16 | g.79599011T>A | CA396535010 | MAF | c.892A>T (p.Asn298Tyr) n.2942A>T | |
16 | g.79599011T>C | CA396535011 | MAF | c.892A>G (p.Asn298Asp) n.2942A>G | |
16 | g.79599011T>G | CA396535012 | MAF | c.892A>C (p.Asn298His) n.2942A>C | ClinVar |
16 | g.79599012T>A | CA396535013 | MAF | c.891A>T (p.Lys297Asn) n.2941A>T | |
16 | g.79599012T>C | CA496509004 | MAF | c.891A>G (p.Lys297=) n.2941A>G | |
16 | g.79599012T>G | CA396535014 | MAF | c.891A>C (p.Lys297Asn) n.2941A>C | |
16 | g.79599013T>A | CA396535015 | MAF | c.890A>T (p.Lys297Ile) n.2940A>T | |
16 | g.79599013T>C | CA122974 | MAF | c.890A>G (p.Lys297Arg) n.2940A>G | ClinVar dbSNP |
16 | g.79599013T>G | CA396535016 | MAF | c.890A>C (p.Lys297Thr) n.2940A>C | |
16 | g.79599013T= | CA2235930913 | MAF | c.890A= (p.Lys297=) n.2940A= | |
16 | g.79599014T>A | CA396535017 | MAF | c.889A>T (p.Lys297Ter) n.2939A>T | |
16 | g.79599014T>C | CA396535019 | MAF | c.889A>G (p.Lys297Glu) n.2939A>G | |
16 | g.79599014T>G | CA396535018 | MAF | c.889A>C (p.Lys297Gln) n.2939A>C | |
16 | g.79599015C>A | CA496509008 | MAF | c.888G>T (p.Leu296=) n.2938G>T | |
16 | g.79599015C>G | CA496509009 | MAF | c.888G>C (p.Leu296=) n.2938G>C | gnomAD v3 gnomAD v4 |
16 | g.79599015C>T | CA496509012 | MAF | c.888G>A (p.Leu296=) n.2938G>A | |
16 | g.79599016A= | CA2235930919 | MAF | c.887T= (p.Leu296=) n.2937T= | |
16 | g.79599016A>C | CA396535020 | MAF | c.887T>G (p.Leu296Arg) n.2937T>G | |
16 | g.79599016A>G | CA396535021 | MAF | c.887T>C (p.Leu296Pro) n.2937T>C | ClinVar dbSNP |
16 | g.79599016A>T | CA396535022 | MAF | c.887T>A (p.Leu296Gln) n.2937T>A | |
16 | g.79599017G>A | CA496509014 | MAF | c.886C>T (p.Leu296=) n.2936C>T | dbSNP gnomAD v3 gnomAD v4 |
16 | g.79599017G>C | CA396535023 | MAF | c.886C>G (p.Leu296Val) n.2936C>G | gnomAD v4 |
16 | g.79599017G= | CA2235930923 | MAF | c.886C= (p.Leu296=) n.2936C= | |
16 | g.79599017G>T | CA396535024 | MAF | c.886C>A (p.Leu296Met) n.2936C>A | |
16 | g.79599018G>A | CA496509018 | MAF | c.885C>T (p.Thr295=) n.2935C>T | dbSNP gnomAD v2 |
16 | g.79599018G>C | CA496509020 | MAF | c.885C>G (p.Thr295=) n.2935C>G | gnomAD v4 |
16 | g.79599018G= | CA2235930924 | MAF | c.885C= (p.Thr295=) n.2935C= | |
16 | g.79599018G>T | CA496509021 | MAF | c.885C>A (p.Thr295=) n.2935C>A | |
16 | g.79599019G>A | CA396535025 | MAF | c.884C>T (p.Thr295Ile) n.2934C>T | |
16 | g.79599019G>C | CA396535026 | MAF | c.884C>G (p.Thr295Ser) n.2934C>G | |
16 | g.79599019G>T | CA396535027 | MAF | c.884C>A (p.Thr295Asn) n.2934C>A | |
16 | g.79599020T>A | CA396535028 | MAF | c.883A>T (p.Thr295Ser) n.2933A>T | |
16 | g.79599020T>C | CA396535029 | MAF | c.883A>G (p.Thr295Ala) n.2933A>G | |
16 | g.79599020T>G | CA396535030 | MAF | c.883A>C (p.Thr295Pro) n.2933A>C | |
16 | g.79599021C>A | CA496509029 | MAF | c.882G>T (p.Arg294=) n.2932G>T | |
16 | g.79599021C= | CA2235930929 | MAF | c.882G= (p.Arg294=) n.2932G= | |
16 | g.79599021C>G | CA496509028 | MAF | c.882G>C (p.Arg294=) n.2932G>C | |
16 | g.79599021C>T | CA8184011 | MAF | c.882G>A (p.Arg294=) n.2932G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.79599022C>A | CA396535033 | MAF | c.881G>T (p.Arg294Leu) n.2931G>T | |
16 | g.79599022C= | CA2235930937 | MAF | c.881G= (p.Arg294=) n.2931G= | |
16 | g.79599022C>G | CA396535031 | MAF | c.881G>C (p.Arg294Pro) n.2931G>C | |
16 | g.79599022C>T | CA396535032 | MAF | c.881G>A (p.Arg294Gln) n.2931G>A | ClinVar dbSNP |
16 | g.79599023G>A | CA278847 | MAF | c.880C>T (p.Arg294Trp) n.2930C>T | ClinVar dbSNP |
16 | g.79599023G>C | CA396535034 | MAF | c.880C>G (p.Arg294Gly) n.2930C>G | |
16 | g.79599023G= | CA2235930947 | MAF | c.880C= (p.Arg294=) n.2930C= | |
16 | g.79599023G>T | CA496509036 | MAF | c.880C>A (p.Arg294=) n.2930C>A | gnomAD v3 gnomAD v4 |
16 | g.79599024C>A | CA396535035 | MAF | c.879G>T (p.Arg293Ser) n.2929G>T | |
16 | g.79599024C= | CA2235930953 | MAF | c.879G= (p.Arg293=) n.2929G= | |
16 | g.79599024C>G | CA396535036 | MAF | c.879G>C (p.Arg293Ser) n.2929G>C | |
16 | g.79599024C>T | CA496509037 | MAF | c.879G>A (p.Arg293=) n.2929G>A | dbSNP |
16 | g.79599025C>A | CA396535037 | MAF | c.878G>T (p.Arg293Met) n.2928G>T | |
16 | g.79599025C>G | CA396535038 | MAF | c.878G>C (p.Arg293Thr) n.2928G>C | |
16 | g.79599025C>T | CA396535039 | MAF | c.878G>A (p.Arg293Lys) n.2928G>A | |
16 | g.79599026T>A | CA396535040 | MAF | c.877A>T (p.Arg293Trp) n.2927A>T | |
16 | g.79599026T>C | CA396535041 | MAF | c.877A>G (p.Arg293Gly) n.2927A>G | gnomAD v4 |
16 | g.79599026T>G | CA496509043 | MAF | c.877A>C (p.Arg293=) n.2927A>C | |
16 | g.79599027C>A | CA396535042 | MAF | c.876G>T (p.Lys292Asn) n.2926G>T | |
16 | g.79599027C>G | CA396535043 | MAF | c.876G>C (p.Lys292Asn) n.2926G>C | |
16 | g.79599027C>T | CA496509049 | MAF | c.876G>A (p.Lys292=) n.2926G>A | |
16 | g.79599028T>A | CA396535046 | MAF | c.875A>T (p.Lys292Met) n.2925A>T | |
16 | g.79599028T>C | CA396535045 | MAF | c.875A>G (p.Lys292Arg) n.2925A>G | gnomAD v4 |
16 | g.79599028T>G | CA396535044 | MAF | c.875A>C (p.Lys292Thr) n.2925A>C | |
16 | g.79599029T>A | CA396535047 | MAF | c.874A>T (p.Lys292Ter) n.2924A>T | |
16 | g.79599029T>C | CA396535048 | MAF | c.874A>G (p.Lys292Glu) n.2924A>G | gnomAD v4 |
16 | g.79599029T>G | CA396535049 | MAF | c.874A>C (p.Lys292Gln) n.2924A>C | |
16 | g.79599030C>A | CA396535050 | MAF | c.873G>T (p.Gln291His) n.2923G>T | |
16 | g.79599030C>G | CA396535051 | MAF | c.873G>C (p.Gln291His) n.2923G>C | COSMIC |
16 | g.79599030C>T | CA496509056 | MAF | c.873G>A (p.Gln291=) n.2923G>A | gnomAD v4 COSMIC |
16 | g.79599031T>A | CA396535054 | MAF | c.872A>T (p.Gln291Leu) n.2922A>T | |
16 | g.79599031T>C | CA396535053 | MAF | c.872A>G (p.Gln291Arg) n.2922A>G | |
16 | g.79599031T>G | CA396535052 | MAF | c.872A>C (p.Gln291Pro) n.2922A>C | |
16 | g.79599032G>A | CA396535055 | MAF | c.871C>T (p.Gln291Ter) n.2921C>T | dbSNP |
16 | g.79599032G>C | CA396535056 | MAF | c.871C>G (p.Gln291Glu) n.2921C>G | ClinVar gnomAD v4 |
16 | g.79599032G>T | CA396535057 | MAF | c.871C>A (p.Gln291Lys) n.2921C>A | gnomAD v4 |
16 | g.79599033C>A | CA396535058 | MAF | c.870G>T (p.Lys290Asn) n.2920G>T | |
16 | g.79599033C= | CA2235930955 | MAF | c.870G= (p.Lys290=) n.2920G= | |
16 | g.79599033C>G | CA396535059 | MAF | c.870G>C (p.Lys290Asn) n.2920G>C | |
16 | g.79599033C>T | CA8184012 | MAF | c.870G>A (p.Lys290=) n.2920G>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.79599034T>A | CA396535062 | MAF | c.869A>T (p.Lys290Met) n.2919A>T | |
16 | g.79599034T>C | CA396535060 | MAF | c.869A>G (p.Lys290Arg) n.2919A>G | |
16 | g.79599034T>G | CA396535061 | MAF | c.869A>C (p.Lys290Thr) n.2919A>C | |
16 | g.79599035T>A | CA396535063 | MAF | c.868A>T (p.Lys290Ter) n.2918A>T | |
16 | g.79599035T>C | CA396535064 | MAF | c.868A>G (p.Lys290Glu) n.2918A>G | dbSNP |
16 | g.79599035T>G | CA396535065 | MAF | c.868A>C (p.Lys290Gln) n.2918A>C | |
16 | g.79599036C>A | CA496509071 | MAF | c.867G>T (p.Leu289=) n.2917G>T | |
16 | g.79599036C= | CA2235930959 | MAF | c.867G= (p.Leu289=) n.2917G= | |
16 | g.79599036C>G | CA496509072 | MAF | c.867G>C (p.Leu289=) n.2917G>C | dbSNP |
16 | g.79599036C>T | CA496509074 | MAF | c.867G>A (p.Leu289=) n.2917G>A | dbSNP gnomAD v2 gnomAD v4 |
16 | g.79599037A= | CA2235930961 | MAF | c.866T= (p.Leu289=) n.2916T= | |
16 | g.79599037A>C | CA396535066 | MAF | c.866T>G (p.Leu289Arg) n.2916T>G | |
16 | g.79599037A>G | CA396535067 | MAF | c.866T>C (p.Leu289Pro) n.2916T>C | |
16 | g.79599037A>T | CA284128083 | MAF | c.866T>A (p.Leu289Gln) n.2916T>A | ClinVar dbSNP |
16 | g.79599038G>A | CA8184013 | MAF | c.865C>T (p.Leu289=) n.2915C>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
16 | g.79599038G>C | CA396535068 | MAF | c.865C>G (p.Leu289Val) n.2915C>G | |
16 | g.79599038G= | CA2235930965 | MAF | c.865C= (p.Leu289=) n.2915C= | |
16 | g.79599038G>T | CA396535069 | MAF | c.865C>A (p.Leu289Met) n.2915C>A | gnomAD v4 |
16 | g.79599039C>A | CA496509082 | MAF | c.864G>T (p.Arg288=) n.2914G>T | |
16 | g.79599039C= | CA2235930969 | MAF | c.864G= (p.Arg288=) n.2914G= | |
16 | g.79599039C>G | CA496509084 | MAF | c.864G>C (p.Arg288=) n.2914G>C | |
16 | g.79599039C>T | CA8184014 | MAF | c.864G>A (p.Arg288=) n.2914G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.79599040C>A | CA396535070 | MAF | c.863G>T (p.Arg288Leu) n.2913G>T | |
16 | g.79599040C= | CA2235930976 | MAF | c.863G= (p.Arg288=) n.2913G= | |
16 | g.79599040C>G | CA122972 | MAF | c.863G>C (p.Arg288Pro) n.2913G>C | ClinVar dbSNP |
16 | g.79599040C>T | CA8184015 | MAF | c.863G>A (p.Arg288Gln) n.2913G>A | dbSNP ExAC gnomAD v2 gnomAD v4 |