Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
1 | g.1047896_1048011del | CA2742134874 | AGRN | c.3751+1_3752-1del c.3436+1_3437-1del c.3337+1_3338-1del c.2878+1_2879-1del c.2017+1_2018-1del n.3818+1_3819-1del n.3822+1_3823-1del | |
1 | g.1047998C>A | CA2642492055 | AGRN | c.3752-14C>A (n.3752-14C>A) c.3437-14C>A (n.3437-14C>A) c.3338-14C>A (n.3338-14C>A) c.2879-14C>A (n.2879-14C>A) c.2018-14C>A (n.2018-14C>A) n.3819-14C>A n.3823-14C>A | gnomAD v4 |
1 | g.1047998C>T | CA2642492056 | AGRN | c.3752-14C>T (n.3752-14C>T) c.3437-14C>T (n.3437-14C>T) c.3338-14C>T (n.3338-14C>T) c.2879-14C>T (n.2879-14C>T) c.2018-14C>T (n.2018-14C>T) n.3819-14C>T n.3823-14C>T | gnomAD v4 |
1 | g.1047999C>A | CA2642492057 | AGRN | c.3752-13C>A (n.3752-13C>A) c.3437-13C>A (n.3437-13C>A) c.3338-13C>A (n.3338-13C>A) c.2879-13C>A (n.2879-13C>A) c.2018-13C>A (n.2018-13C>A) n.3819-13C>A n.3823-13C>A | gnomAD v4 |
1 | g.1047999C>T | CA2642492058 | AGRN | c.3752-13C>T (n.3752-13C>T) c.3437-13C>T (n.3437-13C>T) c.3338-13C>T (n.3338-13C>T) c.2879-13C>T (n.2879-13C>T) c.2018-13C>T (n.2018-13C>T) n.3819-13C>T n.3823-13C>T | gnomAD v4 |
1 | g.1048000C>A | CA2642492059 | AGRN | c.3752-12C>A (n.3752-12C>A) c.3437-12C>A (n.3437-12C>A) c.3338-12C>A (n.3338-12C>A) c.2879-12C>A (n.2879-12C>A) c.2018-12C>A (n.2018-12C>A) n.3819-12C>A n.3823-12C>A | gnomAD v4 |
1 | g.1048000C= | CA1148803095 | AGRN | c.3752-12C= (n.3752-12C=) c.3437-12C= (n.3437-12C=) c.3338-12C= (n.3338-12C=) c.2879-12C= (n.2879-12C=) c.2018-12C= (n.2018-12C=) n.3819-12C= n.3823-12C= | |
1 | g.1048000C>G | CA2642492060 | AGRN | c.3752-12C>G (n.3752-12C>G) c.3437-12C>G (n.3437-12C>G) c.3338-12C>G (n.3338-12C>G) c.2879-12C>G (n.2879-12C>G) c.2018-12C>G (n.2018-12C>G) n.3819-12C>G n.3823-12C>G | gnomAD v4 |
1 | g.1048000C>T | CA520659133 | AGRN | c.3752-12C>T (n.3752-12C>T) c.3437-12C>T (n.3437-12C>T) c.3338-12C>T (n.3338-12C>T) c.2879-12C>T (n.2879-12C>T) c.2018-12C>T (n.2018-12C>T) n.3819-12C>T n.3823-12C>T | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.1048001T>C | CA997654846 | AGRN | c.3752-11T>C (n.3752-11T>C) c.3437-11T>C (n.3437-11T>C) c.3338-11T>C (n.3338-11T>C) c.2879-11T>C (n.2879-11T>C) c.2018-11T>C (n.2018-11T>C) n.3819-11T>C n.3823-11T>C | dbSNP gnomAD v3 gnomAD v4 |
1 | g.1048001T= | CA1148803098 | AGRN | c.3752-11T= (n.3752-11T=) c.3437-11T= (n.3437-11T=) c.3338-11T= (n.3338-11T=) c.2879-11T= (n.2879-11T=) c.2018-11T= (n.2018-11T=) n.3819-11T= n.3823-11T= | |
1 | g.1048002G>A | CA509230 | AGRN | c.3752-10G>A (n.3752-10G>A) c.3437-10G>A (n.3437-10G>A) c.3338-10G>A (n.3338-10G>A) c.2879-10G>A (n.2879-10G>A) c.2018-10G>A (n.2018-10G>A) n.3819-10G>A n.3823-10G>A | dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.1048002G>C | CA2642492061 | AGRN | c.3752-10G>C (n.3752-10G>C) c.3437-10G>C (n.3437-10G>C) c.3338-10G>C (n.3338-10G>C) c.2879-10G>C (n.2879-10G>C) c.2018-10G>C (n.2018-10G>C) n.3819-10G>C n.3823-10G>C | gnomAD v4 |
1 | g.1048002G= | CA1148803100 | AGRN | c.3752-10G= (n.3752-10G=) c.3437-10G= (n.3437-10G=) c.3338-10G= (n.3338-10G=) c.2879-10G= (n.2879-10G=) c.2018-10G= (n.2018-10G=) n.3819-10G= n.3823-10G= | |
1 | g.1048002G>T | CA2642492062 | AGRN | c.3752-10G>T (n.3752-10G>T) c.3437-10G>T (n.3437-10G>T) c.3338-10G>T (n.3338-10G>T) c.2879-10G>T (n.2879-10G>T) c.2018-10G>T (n.2018-10G>T) n.3819-10G>T n.3823-10G>T | gnomAD v4 |
1 | g.1048003T>C | CA1148803110 | AGRN | c.3752-9T>C (n.3752-9T>C) c.3437-9T>C (n.3437-9T>C) c.3338-9T>C (n.3338-9T>C) c.2879-9T>C (n.2879-9T>C) c.2018-9T>C (n.2018-9T>C) n.3819-9T>C n.3823-9T>C | dbSNP |
1 | g.1048003T= | CA1148803104 | AGRN | c.3752-9T= (n.3752-9T=) c.3437-9T= (n.3437-9T=) c.3338-9T= (n.3338-9T=) c.2879-9T= (n.2879-9T=) c.2018-9T= (n.2018-9T=) n.3819-9T= n.3823-9T= | |
1 | g.1048004G>A | CA2574258704 | AGRN | c.3752-8G>A (n.3752-8G>A) c.3437-8G>A (n.3437-8G>A) c.3338-8G>A (n.3338-8G>A) c.2879-8G>A (n.2879-8G>A) c.2018-8G>A (n.2018-8G>A) n.3819-8G>A n.3823-8G>A | gnomAD v4 |
1 | g.1048004G>T | CA2642492064 | AGRN | c.3752-8G>T (n.3752-8G>T) c.3437-8G>T (n.3437-8G>T) c.3338-8G>T (n.3338-8G>T) c.2879-8G>T (n.2879-8G>T) c.2018-8G>T (n.2018-8G>T) n.3819-8G>T n.3823-8G>T | gnomAD v4 |
1 | g.1048005C>A | CA2642492065 | AGRN | c.3752-7C>A (n.3752-7C>A) c.3437-7C>A (n.3437-7C>A) c.3338-7C>A (n.3338-7C>A) c.2879-7C>A (n.2879-7C>A) c.2018-7C>A (n.2018-7C>A) n.3819-7C>A n.3823-7C>A | gnomAD v4 |
1 | g.1048005C= | CA1148803137 | AGRN | c.3752-7C= (n.3752-7C=) c.3437-7C= (n.3437-7C=) c.3338-7C= (n.3338-7C=) c.2879-7C= (n.2879-7C=) c.2018-7C= (n.2018-7C=) n.3819-7C= n.3823-7C= | |
1 | g.1048005C>T | CA509231 | AGRN | c.3752-7C>T (n.3752-7C>T) c.3437-7C>T (n.3437-7C>T) c.3338-7C>T (n.3338-7C>T) c.2879-7C>T (n.2879-7C>T) c.2018-7C>T (n.2018-7C>T) n.3819-7C>T n.3823-7C>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.1048006C>A | CA2642492066 | AGRN | c.3752-6C>A (n.3752-6C>A) c.3437-6C>A (n.3437-6C>A) c.3338-6C>A (n.3338-6C>A) c.2879-6C>A (n.2879-6C>A) c.2018-6C>A (n.2018-6C>A) n.3819-6C>A n.3823-6C>A | gnomAD v4 |
1 | g.1048006C= | CA1148803150 | AGRN | c.3752-6C= (n.3752-6C=) c.3437-6C= (n.3437-6C=) c.3338-6C= (n.3338-6C=) c.2879-6C= (n.2879-6C=) c.2018-6C= (n.2018-6C=) n.3819-6C= n.3823-6C= | |
1 | g.1048006C>T | CA205851 | AGRN | c.3752-6C>T (n.3752-6C>T) c.3437-6C>T (n.3437-6C>T) c.3338-6C>T (n.3338-6C>T) c.2879-6C>T (n.2879-6C>T) c.2018-6C>T (n.2018-6C>T) n.3819-6C>T n.3823-6C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.1048007G>A | CA509232 | AGRN | c.3752-5G>A (n.3752-5G>A) c.3437-5G>A (n.3437-5G>A) c.3338-5G>A (n.3338-5G>A) c.2879-5G>A (n.2879-5G>A) c.2018-5G>A (n.2018-5G>A) n.3819-5G>A n.3823-5G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.1048007G>C | CA1148803161 | AGRN | c.3752-5G>C (n.3752-5G>C) c.3437-5G>C (n.3437-5G>C) c.3338-5G>C (n.3338-5G>C) c.2879-5G>C (n.2879-5G>C) c.2018-5G>C (n.2018-5G>C) n.3819-5G>C n.3823-5G>C | dbSNP |
1 | g.1048007G= | CA1143501605 | AGRN | c.3752-5G= (n.3752-5G=) c.3437-5G= (n.3437-5G=) c.3338-5G= (n.3338-5G=) c.2879-5G= (n.2879-5G=) c.2018-5G= (n.2018-5G=) n.3819-5G= n.3823-5G= | |
1 | g.1048007G>T | CA2642492067 | AGRN | c.3752-5G>T (n.3752-5G>T) c.3437-5G>T (n.3437-5G>T) c.3338-5G>T (n.3338-5G>T) c.2879-5G>T (n.2879-5G>T) c.2018-5G>T (n.2018-5G>T) n.3819-5G>T n.3823-5G>T | gnomAD v4 |
1 | g.1048008G>A | CA1148803178 | AGRN | c.3752-4G>A (n.3752-4G>A) c.3437-4G>A (n.3437-4G>A) c.3338-4G>A (n.3338-4G>A) c.2879-4G>A (n.2879-4G>A) c.2018-4G>A (n.2018-4G>A) n.3819-4G>A n.3823-4G>A | dbSNP gnomAD v4 |
1 | g.1048008G= | CA1148803174 | AGRN | c.3752-4G= (n.3752-4G=) c.3437-4G= (n.3437-4G=) c.3338-4G= (n.3338-4G=) c.2879-4G= (n.2879-4G=) c.2018-4G= (n.2018-4G=) n.3819-4G= n.3823-4G= | |
1 | g.1048008G>T | CA2642492068 | AGRN | c.3752-4G>T (n.3752-4G>T) c.3437-4G>T (n.3437-4G>T) c.3338-4G>T (n.3338-4G>T) c.2879-4G>T (n.2879-4G>T) c.2018-4G>T (n.2018-4G>T) n.3819-4G>T n.3823-4G>T | gnomAD v4 |
1 | g.1048009C>A | CA2642492069 | AGRN | c.3752-3C>A (n.3752-3C>A) c.3437-3C>A (n.3437-3C>A) c.3338-3C>A (n.3338-3C>A) c.2879-3C>A (n.2879-3C>A) c.2018-3C>A (n.2018-3C>A) n.3819-3C>A n.3823-3C>A | gnomAD v4 |
1 | g.1048009C>T | CA2642492070 | AGRN | c.3752-3C>T (n.3752-3C>T) c.3437-3C>T (n.3437-3C>T) c.3338-3C>T (n.3338-3C>T) c.2879-3C>T (n.2879-3C>T) c.2018-3C>T (n.2018-3C>T) n.3819-3C>T n.3823-3C>T | gnomAD v4 |
1 | g.1048010A>C | CA337852096 | AGRN | c.3752-2A>C (n.3752-2A>C) c.3437-2A>C (n.3437-2A>C) c.3338-2A>C (n.3338-2A>C) c.2879-2A>C (n.2879-2A>C) c.2018-2A>C (n.2018-2A>C) n.3819-2A>C n.3823-2A>C | |
1 | g.1048010A>G | CA337852097 | AGRN | c.3752-2A>G (n.3752-2A>G) c.3437-2A>G (n.3437-2A>G) c.3338-2A>G (n.3338-2A>G) c.2879-2A>G (n.2879-2A>G) c.2018-2A>G (n.2018-2A>G) n.3819-2A>G n.3823-2A>G | gnomAD v4 |
1 | g.1048010A>T | CA337852098 | AGRN | c.3752-2A>T (n.3752-2A>T) c.3437-2A>T (n.3437-2A>T) c.3338-2A>T (n.3338-2A>T) c.2879-2A>T (n.2879-2A>T) c.2018-2A>T (n.2018-2A>T) n.3819-2A>T n.3823-2A>T | |
1 | g.1048011G>A | CA337852099 | AGRN | c.3752-1G>A (n.3752-1G>A) c.3437-1G>A (n.3437-1G>A) c.3338-1G>A (n.3338-1G>A) c.2879-1G>A (n.2879-1G>A) c.2018-1G>A (n.2018-1G>A) n.3819-1G>A n.3823-1G>A | |
1 | g.1048011G>C | CA337852100 | AGRN | c.3752-1G>C (n.3752-1G>C) c.3437-1G>C (n.3437-1G>C) c.3338-1G>C (n.3338-1G>C) c.2879-1G>C (n.2879-1G>C) c.2018-1G>C (n.2018-1G>C) n.3819-1G>C n.3823-1G>C | |
1 | g.1048011G>T | CA337852101 | AGRN | c.3752-1G>T (n.3752-1G>T) c.3437-1G>T (n.3437-1G>T) c.3338-1G>T (n.3338-1G>T) c.2879-1G>T (n.2879-1G>T) c.2018-1G>T (n.2018-1G>T) n.3819-1G>T n.3823-1G>T | gnomAD v4 |
1 | g.1048012A>C | CA337852104 | AGRN | c.3752A>C (p.Asp1251Ala) c.3437A>C (p.Asp1146Ala) c.3338A>C (p.Asp1113Ala) c.2879A>C (p.Asp960Ala) c.2018A>C (p.Asp673Ala) n.3819A>C n.3823A>C | |
1 | g.1048012A>G | CA337852105 | AGRN | c.3752A>G (p.Asp1251Gly) c.3437A>G (p.Asp1146Gly) c.3338A>G (p.Asp1113Gly) c.2879A>G (p.Asp960Gly) c.2018A>G (p.Asp673Gly) n.3819A>G n.3823A>G | gnomAD v4 |
1 | g.1048012A>T | CA337852106 | AGRN | c.3752A>T (p.Asp1251Val) c.3437A>T (p.Asp1146Val) c.3338A>T (p.Asp1113Val) c.2879A>T (p.Asp960Val) c.2018A>T (p.Asp673Val) n.3819A>T n.3823A>T | |
1 | g.1048013C>A | CA337852107 | AGRN | c.3753C>A (p.Asp1251Glu) c.3438C>A (p.Asp1146Glu) c.3339C>A (p.Asp1113Glu) c.2880C>A (p.Asp960Glu) c.2019C>A (p.Asp673Glu) n.3820C>A n.3824C>A | gnomAD v4 |
1 | g.1048013C= | CA1148803183 | AGRN | c.3753C= (p.Asp1251=) c.3438C= (p.Asp1146=) c.3339C= (p.Asp1113=) c.2880C= (p.Asp960=) c.2019C= (p.Asp673=) n.3820C= n.3824C= | |
1 | g.1048013C>G | CA337852108 | AGRN | c.3753C>G (p.Asp1251Glu) c.3438C>G (p.Asp1146Glu) c.3339C>G (p.Asp1113Glu) c.2880C>G (p.Asp960Glu) c.2019C>G (p.Asp673Glu) n.3820C>G n.3824C>G | dbSNP gnomAD v2 gnomAD v4 |
1 | g.1048013C>T | CA415758243 | AGRN | c.3753C>T (p.Asp1251=) c.3438C>T (p.Asp1146=) c.3339C>T (p.Asp1113=) c.2880C>T (p.Asp960=) c.2019C>T (p.Asp673=) n.3820C>T n.3824C>T | gnomAD v4 |
1 | g.1048014T>A | CA337852116 | AGRN | c.3754T>A (p.Trp1252Arg) c.3439T>A (p.Trp1147Arg) c.3340T>A (p.Trp1114Arg) c.2881T>A (p.Trp961Arg) c.2020T>A (p.Trp674Arg) n.3821T>A n.3825T>A | |
1 | g.1048014T>C | CA337852111 | AGRN | c.3754T>C (p.Trp1252Arg) c.3439T>C (p.Trp1147Arg) c.3340T>C (p.Trp1114Arg) c.2881T>C (p.Trp961Arg) c.2020T>C (p.Trp674Arg) n.3821T>C n.3825T>C | |
1 | g.1048014T>G | CA337852112 | AGRN | c.3754T>G (p.Trp1252Gly) c.3439T>G (p.Trp1147Gly) c.3340T>G (p.Trp1114Gly) c.2881T>G (p.Trp961Gly) c.2020T>G (p.Trp674Gly) n.3821T>G n.3825T>G | |
1 | g.1048015G>A | CA337852119 | AGRN | c.3755G>A (p.Trp1252Ter) c.3440G>A (p.Trp1147Ter) c.3341G>A (p.Trp1114Ter) c.2882G>A (p.Trp961Ter) c.2021G>A (p.Trp674Ter) n.3822G>A n.3826G>A | gnomAD v4 |
1 | g.1048015G>C | CA337852122 | AGRN | c.3755G>C (p.Trp1252Ser) c.3440G>C (p.Trp1147Ser) c.3341G>C (p.Trp1114Ser) c.2882G>C (p.Trp961Ser) c.2021G>C (p.Trp674Ser) n.3822G>C n.3826G>C | |
1 | g.1048015G>T | CA337852125 | AGRN | c.3755G>T (p.Trp1252Leu) c.3440G>T (p.Trp1147Leu) c.3341G>T (p.Trp1114Leu) c.2882G>T (p.Trp961Leu) c.2021G>T (p.Trp674Leu) n.3822G>T n.3826G>T | gnomAD v4 |
1 | g.1048016G>A | CA337852127 | AGRN | c.3756G>A (p.Trp1252Ter) c.3441G>A (p.Trp1147Ter) c.3342G>A (p.Trp1114Ter) c.2883G>A (p.Trp961Ter) c.2022G>A (p.Trp674Ter) n.3823G>A n.3827G>A | gnomAD v4 |
1 | g.1048016G>C | CA337852130 | AGRN | c.3756G>C (p.Trp1252Cys) c.3441G>C (p.Trp1147Cys) c.3342G>C (p.Trp1114Cys) c.2883G>C (p.Trp961Cys) c.2022G>C (p.Trp674Cys) n.3823G>C n.3827G>C | |
1 | g.1048016G>T | CA337852131 | AGRN | c.3756G>T (p.Trp1252Cys) c.3441G>T (p.Trp1147Cys) c.3342G>T (p.Trp1114Cys) c.2883G>T (p.Trp961Cys) c.2022G>T (p.Trp674Cys) n.3823G>T n.3827G>T | gnomAD v4 |
1 | g.1048017T>A | CA337852133 | AGRN | c.3757T>A (p.Phe1253Ile) c.3442T>A (p.Phe1148Ile) c.3343T>A (p.Phe1115Ile) c.2884T>A (p.Phe962Ile) c.2023T>A (p.Phe675Ile) n.3824T>A n.3828T>A | |
1 | g.1048017T>C | CA337852143 | AGRN | c.3757T>C (p.Phe1253Leu) c.3442T>C (p.Phe1148Leu) c.3343T>C (p.Phe1115Leu) c.2884T>C (p.Phe962Leu) c.2023T>C (p.Phe675Leu) n.3824T>C n.3828T>C | |
1 | g.1048017T>G | CA337852147 | AGRN | c.3757T>G (p.Phe1253Val) c.3442T>G (p.Phe1148Val) c.3343T>G (p.Phe1115Val) c.2884T>G (p.Phe962Val) c.2023T>G (p.Phe675Val) n.3824T>G n.3828T>G | |
1 | g.1048018T>A | CA337852152 | AGRN | c.3758T>A (p.Phe1253Tyr) c.3443T>A (p.Phe1148Tyr) c.3344T>A (p.Phe1115Tyr) c.2885T>A (p.Phe962Tyr) c.2024T>A (p.Phe675Tyr) n.3825T>A n.3829T>A | |
1 | g.1048018T>C | CA337852155 | AGRN | c.3758T>C (p.Phe1253Ser) c.3443T>C (p.Phe1148Ser) c.3344T>C (p.Phe1115Ser) c.2885T>C (p.Phe962Ser) c.2024T>C (p.Phe675Ser) n.3825T>C n.3829T>C | gnomAD v4 |
1 | g.1048018T>G | CA337852157 | AGRN | c.3758T>G (p.Phe1253Cys) c.3443T>G (p.Phe1148Cys) c.3344T>G (p.Phe1115Cys) c.2885T>G (p.Phe962Cys) c.2024T>G (p.Phe675Cys) n.3825T>G n.3829T>G | |
1 | g.1048019T>A | CA337852162 | AGRN | c.3759T>A (p.Phe1253Leu) c.3444T>A (p.Phe1148Leu) c.3345T>A (p.Phe1115Leu) c.2886T>A (p.Phe962Leu) c.2025T>A (p.Phe675Leu) n.3826T>A n.3830T>A | |
1 | g.1048019T>C | CA415758265 | AGRN | c.3759T>C (p.Phe1253=) c.3444T>C (p.Phe1148=) c.3345T>C (p.Phe1115=) c.2886T>C (p.Phe962=) c.2025T>C (p.Phe675=) n.3826T>C n.3830T>C | |
1 | g.1048019T>G | CA337852160 | AGRN | c.3759T>G (p.Phe1253Leu) c.3444T>G (p.Phe1148Leu) c.3345T>G (p.Phe1115Leu) c.2886T>G (p.Phe962Leu) c.2025T>G (p.Phe675Leu) n.3826T>G n.3830T>G | |
1 | g.1048020C>A | CA337852163 | AGRN | c.3760C>A (p.Pro1254Thr) c.3445C>A (p.Pro1149Thr) c.3346C>A (p.Pro1116Thr) c.2887C>A (p.Pro963Thr) c.2026C>A (p.Pro676Thr) n.3827C>A n.3831C>A | gnomAD v4 |
1 | g.1048020C= | CA1148803188 | AGRN | c.3760C= (p.Pro1254=) c.3445C= (p.Pro1149=) c.3346C= (p.Pro1116=) c.2887C= (p.Pro963=) c.2026C= (p.Pro676=) n.3827C= n.3831C= | |
1 | g.1048020C>G | CA337852167 | AGRN | c.3760C>G (p.Pro1254Ala) c.3445C>G (p.Pro1149Ala) c.3346C>G (p.Pro1116Ala) c.2887C>G (p.Pro963Ala) c.2026C>G (p.Pro676Ala) n.3827C>G n.3831C>G | |
1 | g.1048020C>T | CA337852173 | AGRN | c.3760C>T (p.Pro1254Ser) c.3445C>T (p.Pro1149Ser) c.3346C>T (p.Pro1116Ser) c.2887C>T (p.Pro963Ser) c.2026C>T (p.Pro676Ser) n.3827C>T n.3831C>T | ClinVar dbSNP gnomAD v4 |
1 | g.1048021C>A | CA337852176 | AGRN | c.3761C>A (p.Pro1254His) c.3446C>A (p.Pro1149His) c.3347C>A (p.Pro1116His) c.2888C>A (p.Pro963His) c.2027C>A (p.Pro676His) n.3828C>A n.3832C>A | |
1 | g.1048021C>G | CA337852178 | AGRN | c.3761C>G (p.Pro1254Arg) c.3446C>G (p.Pro1149Arg) c.3347C>G (p.Pro1116Arg) c.2888C>G (p.Pro963Arg) c.2027C>G (p.Pro676Arg) n.3828C>G n.3832C>G | |
1 | g.1048021C>T | CA337852180 | AGRN | c.3761C>T (p.Pro1254Leu) c.3446C>T (p.Pro1149Leu) c.3347C>T (p.Pro1116Leu) c.2888C>T (p.Pro963Leu) c.2027C>T (p.Pro676Leu) n.3828C>T n.3832C>T | ClinVar dbSNP gnomAD v4 |
1 | g.1048022T>A | CA415758272 | AGRN | c.3762T>A (p.Pro1254=) c.3447T>A (p.Pro1149=) c.3348T>A (p.Pro1116=) c.2889T>A (p.Pro963=) c.2028T>A (p.Pro676=) n.3829T>A n.3833T>A | |
1 | g.1048022T>C | CA415758276 | AGRN | c.3762T>C (p.Pro1254=) c.3447T>C (p.Pro1149=) c.3348T>C (p.Pro1116=) c.2889T>C (p.Pro963=) c.2028T>C (p.Pro676=) n.3829T>C n.3833T>C | ClinVar dbSNP gnomAD v3 gnomAD v4 |
1 | g.1048022T>G | CA415758277 | AGRN | c.3762T>G (p.Pro1254=) c.3447T>G (p.Pro1149=) c.3348T>G (p.Pro1116=) c.2889T>G (p.Pro963=) c.2028T>G (p.Pro676=) n.3829T>G n.3833T>G | |
1 | g.1048022T= | CA1148803192 | AGRN | c.3762T= (p.Pro1254=) c.3447T= (p.Pro1149=) c.3348T= (p.Pro1116=) c.2889T= (p.Pro963=) c.2028T= (p.Pro676=) n.3829T= n.3833T= | |
1 | g.1048023G>A | CA337852183 | AGRN | c.3763G>A (p.Ala1255Thr) c.3448G>A (p.Ala1150Thr) c.3349G>A (p.Ala1117Thr) c.2890G>A (p.Ala964Thr) c.2029G>A (p.Ala677Thr) n.3830G>A n.3834G>A | gnomAD v4 COSMIC |
1 | g.1048023G>C | CA337852184 | AGRN | c.3763G>C (p.Ala1255Pro) c.3448G>C (p.Ala1150Pro) c.3349G>C (p.Ala1117Pro) c.2890G>C (p.Ala964Pro) c.2029G>C (p.Ala677Pro) n.3830G>C n.3834G>C | |
1 | g.1048023G>T | CA337852186 | AGRN | c.3763G>T (p.Ala1255Ser) c.3448G>T (p.Ala1150Ser) c.3349G>T (p.Ala1117Ser) c.2890G>T (p.Ala964Ser) c.2029G>T (p.Ala677Ser) n.3830G>T n.3834G>T | gnomAD v4 |
1 | g.1048024C>A | CA337852190 | AGRN | c.3764C>A (p.Ala1255Glu) c.3449C>A (p.Ala1150Glu) c.3350C>A (p.Ala1117Glu) c.2891C>A (p.Ala964Glu) c.2030C>A (p.Ala677Glu) n.3831C>A n.3835C>A | gnomAD v4 |
1 | g.1048024C= | CA1141587484 | AGRN | c.3764C= (p.Ala1255=) c.3449C= (p.Ala1150=) c.3350C= (p.Ala1117=) c.2891C= (p.Ala964=) c.2030C= (p.Ala677=) n.3831C= n.3835C= | |
1 | g.1048024C>G | CA337852197 | AGRN | c.3764C>G (p.Ala1255Gly) c.3449C>G (p.Ala1150Gly) c.3350C>G (p.Ala1117Gly) c.2891C>G (p.Ala964Gly) c.2030C>G (p.Ala677Gly) n.3831C>G n.3835C>G | |
1 | g.1048024C>T | CA509233 | AGRN | c.3764C>T (p.Ala1255Val) c.3449C>T (p.Ala1150Val) c.3350C>T (p.Ala1117Val) c.2891C>T (p.Ala964Val) c.2030C>T (p.Ala677Val) n.3831C>T n.3835C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.1048025G>A | CA509234 | AGRN | c.3765G>A (p.Ala1255=) c.3450G>A (p.Ala1150=) c.3351G>A (p.Ala1117=) c.2892G>A (p.Ala964=) c.2031G>A (p.Ala677=) n.3832G>A n.3836G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.1048025G>C | CA415758287 | AGRN | c.3765G>C (p.Ala1255=) c.3450G>C (p.Ala1150=) c.3351G>C (p.Ala1117=) c.2892G>C (p.Ala964=) c.2031G>C (p.Ala677=) n.3832G>C n.3836G>C | |
1 | g.1048025G= | CA1142305248 | AGRN | c.3765G= (p.Ala1255=) c.3450G= (p.Ala1150=) c.3351G= (p.Ala1117=) c.2892G= (p.Ala964=) c.2031G= (p.Ala677=) n.3832G= n.3836G= | |
1 | g.1048025G>T | CA415758286 | AGRN | c.3765G>T (p.Ala1255=) c.3450G>T (p.Ala1150=) c.3351G>T (p.Ala1117=) c.2892G>T (p.Ala964=) c.2031G>T (p.Ala677=) n.3832G>T n.3836G>T | |
1 | g.1048026T>A | CA337852205 | AGRN | c.3766T>A (p.Phe1256Ile) c.3451T>A (p.Phe1151Ile) c.3352T>A (p.Phe1118Ile) c.2893T>A (p.Phe965Ile) c.2032T>A (p.Phe678Ile) n.3833T>A n.3837T>A | |
1 | g.1048026T>C | CA337852204 | AGRN | c.3766T>C (p.Phe1256Leu) c.3451T>C (p.Phe1151Leu) c.3352T>C (p.Phe1118Leu) c.2893T>C (p.Phe965Leu) c.2032T>C (p.Phe678Leu) n.3833T>C n.3837T>C | |
1 | g.1048026T>G | CA337852203 | AGRN | c.3766T>G (p.Phe1256Val) c.3451T>G (p.Phe1151Val) c.3352T>G (p.Phe1118Val) c.2893T>G (p.Phe965Val) c.2032T>G (p.Phe678Val) n.3833T>G n.3837T>G | |
1 | g.1048028del | CA2642492071 | AGRN | c.3768del (p.Phe1256LeufsTer29) c.3453del (p.Phe1151LeufsTer29) c.3354del (p.Phe1118LeufsTer29) c.2895del (p.Phe965LeufsTer29) c.2034del (p.Phe678LeufsTer29) n.3835del n.3839del | gnomAD v4 |
1 | g.1048027T>A | CA337852207 | AGRN | c.3767T>A (p.Phe1256Tyr) c.3452T>A (p.Phe1151Tyr) c.3353T>A (p.Phe1118Tyr) c.2894T>A (p.Phe965Tyr) c.2033T>A (p.Phe678Tyr) n.3834T>A n.3838T>A | |
1 | g.1048027T>C | CA337852209 | AGRN | c.3767T>C (p.Phe1256Ser) c.3452T>C (p.Phe1151Ser) c.3353T>C (p.Phe1118Ser) c.2894T>C (p.Phe965Ser) c.2033T>C (p.Phe678Ser) n.3834T>C n.3838T>C | gnomAD v4 |
1 | g.1048027T>G | CA337852213 | AGRN | c.3767T>G (p.Phe1256Cys) c.3452T>G (p.Phe1151Cys) c.3353T>G (p.Phe1118Cys) c.2894T>G (p.Phe965Cys) c.2033T>G (p.Phe678Cys) n.3834T>G n.3838T>G | |
1 | g.1048028T>A | CA337852217 | AGRN | c.3768T>A (p.Phe1256Leu) c.3453T>A (p.Phe1151Leu) c.3354T>A (p.Phe1118Leu) c.2895T>A (p.Phe965Leu) c.2034T>A (p.Phe678Leu) n.3835T>A n.3839T>A | |
1 | g.1048028T>C | CA415758293 | AGRN | c.3768T>C (p.Phe1256=) c.3453T>C (p.Phe1151=) c.3354T>C (p.Phe1118=) c.2895T>C (p.Phe965=) c.2034T>C (p.Phe678=) n.3835T>C n.3839T>C | |
1 | g.1048028T>G | CA337852218 | AGRN | c.3768T>G (p.Phe1256Leu) c.3453T>G (p.Phe1151Leu) c.3354T>G (p.Phe1118Leu) c.2895T>G (p.Phe965Leu) c.2034T>G (p.Phe678Leu) n.3835T>G n.3839T>G | |
1 | g.1048029A>C | CA337852220 | AGRN | c.3769A>C (p.Ile1257Leu) c.3454A>C (p.Ile1152Leu) c.3355A>C (p.Ile1119Leu) c.2896A>C (p.Ile966Leu) c.2035A>C (p.Ile679Leu) n.3836A>C n.3840A>C | |
1 | g.1048029A>G | CA337852222 | AGRN | c.3769A>G (p.Ile1257Val) c.3454A>G (p.Ile1152Val) c.3355A>G (p.Ile1119Val) c.2896A>G (p.Ile966Val) c.2035A>G (p.Ile679Val) n.3836A>G n.3840A>G | |
1 | g.1048029A>T | CA337852223 | AGRN | c.3769A>T (p.Ile1257Phe) c.3454A>T (p.Ile1152Phe) c.3355A>T (p.Ile1119Phe) c.2896A>T (p.Ile966Phe) c.2035A>T (p.Ile679Phe) n.3836A>T n.3840A>T | |
1 | g.1048030T>A | CA337852225 | AGRN | c.3770T>A (p.Ile1257Asn) c.3455T>A (p.Ile1152Asn) c.3356T>A (p.Ile1119Asn) c.2897T>A (p.Ile966Asn) c.2036T>A (p.Ile679Asn) n.3837T>A n.3841T>A | |
1 | g.1048030T>C | CA337852226 | AGRN | c.3770T>C (p.Ile1257Thr) c.3455T>C (p.Ile1152Thr) c.3356T>C (p.Ile1119Thr) c.2897T>C (p.Ile966Thr) c.2036T>C (p.Ile679Thr) n.3837T>C n.3841T>C | gnomAD v4 |
1 | g.1048030T>G | CA337852227 | AGRN | c.3770T>G (p.Ile1257Ser) c.3455T>G (p.Ile1152Ser) c.3356T>G (p.Ile1119Ser) c.2897T>G (p.Ile966Ser) c.2036T>G (p.Ile679Ser) n.3837T>G n.3841T>G | |
1 | g.1048031C>A | CA509235 | AGRN | c.3771C>A (p.Ile1257=) c.3456C>A (p.Ile1152=) c.3357C>A (p.Ile1119=) c.2898C>A (p.Ile966=) c.2037C>A (p.Ile679=) n.3838C>A n.3842C>A | dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.1048031C= | CA1148430682 | AGRN | c.3771C= (p.Ile1257=) c.3456C= (p.Ile1152=) c.3357C= (p.Ile1119=) c.2898C= (p.Ile966=) c.2037C= (p.Ile679=) n.3838C= n.3842C= | |
1 | g.1048031C>G | CA337852228 | AGRN | c.3771C>G (p.Ile1257Met) c.3456C>G (p.Ile1152Met) c.3357C>G (p.Ile1119Met) c.2898C>G (p.Ile966Met) c.2037C>G (p.Ile679Met) n.3838C>G n.3842C>G | |
1 | g.1048031C>T | CA415758306 | AGRN | c.3771C>T (p.Ile1257=) c.3456C>T (p.Ile1152=) c.3357C>T (p.Ile1119=) c.2898C>T (p.Ile966=) c.2037C>T (p.Ile679=) n.3838C>T n.3842C>T | dbSNP gnomAD v4 |
1 | g.1048032A>C | CA337852232 | AGRN | c.3772A>C (p.Thr1258Pro) c.3457A>C (p.Thr1153Pro) c.3358A>C (p.Thr1120Pro) c.2899A>C (p.Thr967Pro) c.2038A>C (p.Thr680Pro) n.3839A>C n.3843A>C | |
1 | g.1048032A>G | CA337852235 | AGRN | c.3772A>G (p.Thr1258Ala) c.3457A>G (p.Thr1153Ala) c.3358A>G (p.Thr1120Ala) c.2899A>G (p.Thr967Ala) c.2038A>G (p.Thr680Ala) n.3839A>G n.3843A>G | gnomAD v4 |
1 | g.1048032A>T | CA337852230 | AGRN | c.3772A>T (p.Thr1258Ser) c.3457A>T (p.Thr1153Ser) c.3358A>T (p.Thr1120Ser) c.2899A>T (p.Thr967Ser) c.2038A>T (p.Thr680Ser) n.3839A>T n.3843A>T | |
1 | g.1048033C>A | CA337852237 | AGRN | c.3773C>A (p.Thr1258Lys) c.3458C>A (p.Thr1153Lys) c.3359C>A (p.Thr1120Lys) c.2900C>A (p.Thr967Lys) c.2039C>A (p.Thr680Lys) n.3840C>A n.3844C>A | gnomAD v4 |
1 | g.1048033C= | CA1141829645 | AGRN | c.3773C= (p.Thr1258=) c.3458C= (p.Thr1153=) c.3359C= (p.Thr1120=) c.2900C= (p.Thr967=) c.2039C= (p.Thr680=) n.3840C= n.3844C= | |
1 | g.1048033C>G | CA337852242 | AGRN | c.3773C>G (p.Thr1258Arg) c.3458C>G (p.Thr1153Arg) c.3359C>G (p.Thr1120Arg) c.2900C>G (p.Thr967Arg) c.2039C>G (p.Thr680Arg) n.3840C>G n.3844C>G | |
1 | g.1048033C>T | CA509236 | AGRN | c.3773C>T (p.Thr1258Met) c.3458C>T (p.Thr1153Met) c.3359C>T (p.Thr1120Met) c.2900C>T (p.Thr967Met) c.2039C>T (p.Thr680Met) n.3840C>T n.3844C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.1048037_1048063del | CA2642492074 | AGRN | c.3777_3803del (p.Ala1260_Gly1268del) c.3462_3488del (p.Ala1155_Gly1163del) c.3363_3389del (p.Ala1122_Gly1130del) c.2904_2930del (p.Ala969_Gly977del) c.2043_2069del (p.Ala682_Gly690del) n.3844_3870del n.3848_3874del | gnomAD v4 |
1 | g.1048034G>A | CA509237 | AGRN | c.3774G>A (p.Thr1258=) c.3459G>A (p.Thr1153=) c.3360G>A (p.Thr1120=) c.2901G>A (p.Thr967=) c.2040G>A (p.Thr680=) n.3841G>A n.3845G>A | dbSNP ExAC gnomAD v4 |
1 | g.1048034G>C | CA415758312 | AGRN | c.3774G>C (p.Thr1258=) c.3459G>C (p.Thr1153=) c.3360G>C (p.Thr1120=) c.2901G>C (p.Thr967=) c.2040G>C (p.Thr680=) n.3841G>C n.3845G>C | gnomAD v4 |
1 | g.1048034G= | CA1148803216 | AGRN | c.3774G= (p.Thr1258=) c.3459G= (p.Thr1153=) c.3360G= (p.Thr1120=) c.2901G= (p.Thr967=) c.2040G= (p.Thr680=) n.3841G= n.3845G= | |
1 | g.1048034G>T | CA415758313 | AGRN | c.3774G>T (p.Thr1258=) c.3459G>T (p.Thr1153=) c.3360G>T (p.Thr1120=) c.2901G>T (p.Thr967=) c.2040G>T (p.Thr680=) n.3841G>T n.3845G>T | gnomAD v4 |
1 | g.1048038del | CA2642492075 | AGRN | c.3778del (p.Ala1260ProfsTer25) c.3463del (p.Ala1155ProfsTer25) c.3364del (p.Ala1122ProfsTer25) c.2905del (p.Ala969ProfsTer25) c.2044del (p.Ala682ProfsTer25) n.3845del n.3849del | gnomAD v4 |
1 | g.1048035G>A | CA337852254 | AGRN | c.3775G>A (p.Gly1259Arg) c.3460G>A (p.Gly1154Arg) c.3361G>A (p.Gly1121Arg) c.2902G>A (p.Gly968Arg) c.2041G>A (p.Gly681Arg) n.3842G>A n.3846G>A | gnomAD v4 |
1 | g.1048035G>C | CA337852256 | AGRN | c.3775G>C (p.Gly1259Arg) c.3460G>C (p.Gly1154Arg) c.3361G>C (p.Gly1121Arg) c.2902G>C (p.Gly968Arg) c.2041G>C (p.Gly681Arg) n.3842G>C n.3846G>C | |
1 | g.1048035G>T | CA337852257 | AGRN | c.3775G>T (p.Gly1259Trp) c.3460G>T (p.Gly1154Trp) c.3361G>T (p.Gly1121Trp) c.2902G>T (p.Gly968Trp) c.2041G>T (p.Gly681Trp) n.3842G>T n.3846G>T | gnomAD v4 |
1 | g.1048036G>A | CA337852258 | AGRN | c.3776G>A (p.Gly1259Glu) c.3461G>A (p.Gly1154Glu) c.3362G>A (p.Gly1121Glu) c.2903G>A (p.Gly968Glu) c.2042G>A (p.Gly681Glu) n.3843G>A n.3847G>A | dbSNP gnomAD v2 |
1 | g.1048036G>C | CA337852259 | AGRN | c.3776G>C (p.Gly1259Ala) c.3461G>C (p.Gly1154Ala) c.3362G>C (p.Gly1121Ala) c.2903G>C (p.Gly968Ala) c.2042G>C (p.Gly681Ala) n.3843G>C n.3847G>C | |
1 | g.1048036G= | CA1148803222 | AGRN | c.3776G= (p.Gly1259=) c.3461G= (p.Gly1154=) c.3362G= (p.Gly1121=) c.2903G= (p.Gly968=) c.2042G= (p.Gly681=) n.3843G= n.3847G= | |
1 | g.1048036G>T | CA337852260 | AGRN | c.3776G>T (p.Gly1259Val) c.3461G>T (p.Gly1154Val) c.3362G>T (p.Gly1121Val) c.2903G>T (p.Gly968Val) c.2042G>T (p.Gly681Val) n.3843G>T n.3847G>T | gnomAD v4 |
1 | g.1048037G>A | CA415758319 | AGRN | c.3777G>A (p.Gly1259=) c.3462G>A (p.Gly1154=) c.3363G>A (p.Gly1121=) c.2904G>A (p.Gly968=) c.2043G>A (p.Gly681=) n.3844G>A n.3848G>A | gnomAD v4 |
1 | g.1048037G>C | CA415758320 | AGRN | c.3777G>C (p.Gly1259=) c.3462G>C (p.Gly1154=) c.3363G>C (p.Gly1121=) c.2904G>C (p.Gly968=) c.2043G>C (p.Gly681=) n.3844G>C n.3848G>C | |
1 | g.1048037G>T | CA415758321 | AGRN | c.3777G>T (p.Gly1259=) c.3462G>T (p.Gly1154=) c.3363G>T (p.Gly1121=) c.2904G>T (p.Gly968=) c.2043G>T (p.Gly681=) n.3844G>T n.3848G>T | gnomAD v4 |
1 | g.1048038G>A | CA337852261 | AGRN | c.3778G>A (p.Ala1260Thr) c.3463G>A (p.Ala1155Thr) c.3364G>A (p.Ala1122Thr) c.2905G>A (p.Ala969Thr) c.2044G>A (p.Ala682Thr) n.3845G>A n.3849G>A | dbSNP gnomAD v4 |
1 | g.1048038G>C | CA337852262 | AGRN | c.3778G>C (p.Ala1260Pro) c.3463G>C (p.Ala1155Pro) c.3364G>C (p.Ala1122Pro) c.2905G>C (p.Ala969Pro) c.2044G>C (p.Ala682Pro) n.3845G>C n.3849G>C | |
1 | g.1048038G= | CA1148803233 | AGRN | c.3778G= (p.Ala1260=) c.3463G= (p.Ala1155=) c.3364G= (p.Ala1122=) c.2905G= (p.Ala969=) c.2044G= (p.Ala682=) n.3845G= n.3849G= | |
1 | g.1048038G>T | CA337852263 | AGRN | c.3778G>T (p.Ala1260Ser) c.3463G>T (p.Ala1155Ser) c.3364G>T (p.Ala1122Ser) c.2905G>T (p.Ala969Ser) c.2044G>T (p.Ala682Ser) n.3845G>T n.3849G>T | gnomAD v4 |
1 | g.1048039C>A | CA337852273 | AGRN | c.3779C>A (p.Ala1260Asp) c.3464C>A (p.Ala1155Asp) c.3365C>A (p.Ala1122Asp) c.2906C>A (p.Ala969Asp) c.2045C>A (p.Ala682Asp) n.3846C>A n.3850C>A | gnomAD v4 |
1 | g.1048039C= | CA1148803243 | AGRN | c.3779C= (p.Ala1260=) c.3464C= (p.Ala1155=) c.3365C= (p.Ala1122=) c.2906C= (p.Ala969=) c.2045C= (p.Ala682=) n.3846C= n.3850C= | |
1 | g.1048039C>G | CA337852270 | AGRN | c.3779C>G (p.Ala1260Gly) c.3464C>G (p.Ala1155Gly) c.3365C>G (p.Ala1122Gly) c.2906C>G (p.Ala969Gly) c.2045C>G (p.Ala682Gly) n.3846C>G n.3850C>G | |
1 | g.1048039C>T | CA337852265 | AGRN | c.3779C>T (p.Ala1260Val) c.3464C>T (p.Ala1155Val) c.3365C>T (p.Ala1122Val) c.2906C>T (p.Ala969Val) c.2045C>T (p.Ala682Val) n.3846C>T n.3850C>T | dbSNP gnomAD v4 |
1 | g.1048040C>A | CA415758331 | AGRN | c.3780C>A (p.Ala1260=) c.3465C>A (p.Ala1155=) c.3366C>A (p.Ala1122=) c.2907C>A (p.Ala969=) c.2046C>A (p.Ala682=) n.3847C>A n.3851C>A | gnomAD v4 |
1 | g.1048040C>G | CA415758332 | AGRN | c.3780C>G (p.Ala1260=) c.3465C>G (p.Ala1155=) c.3366C>G (p.Ala1122=) c.2907C>G (p.Ala969=) c.2046C>G (p.Ala682=) n.3847C>G n.3851C>G | |
1 | g.1048040C>T | CA415758335 | AGRN | c.3780C>T (p.Ala1260=) c.3465C>T (p.Ala1155=) c.3366C>T (p.Ala1122=) c.2907C>T (p.Ala969=) c.2046C>T (p.Ala682=) n.3847C>T n.3851C>T | gnomAD v4 |
1 | g.1048041A= | CA1148803249 | AGRN | c.3781A= (p.Thr1261=) c.3466A= (p.Thr1156=) c.3367A= (p.Thr1123=) c.2908A= (p.Thr970=) c.2047A= (p.Thr683=) n.3848A= n.3852A= | |
1 | g.1048041A>C | CA337852277 | AGRN | c.3781A>C (p.Thr1261Pro) c.3466A>C (p.Thr1156Pro) c.3367A>C (p.Thr1123Pro) c.2908A>C (p.Thr970Pro) c.2047A>C (p.Thr683Pro) n.3848A>C n.3852A>C | |
1 | g.1048041A>G | CA337852280 | AGRN | c.3781A>G (p.Thr1261Ala) c.3466A>G (p.Thr1156Ala) c.3367A>G (p.Thr1123Ala) c.2908A>G (p.Thr970Ala) c.2047A>G (p.Thr683Ala) n.3848A>G n.3852A>G | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.1048041A>T | CA337852281 | AGRN | c.3781A>T (p.Thr1261Ser) c.3466A>T (p.Thr1156Ser) c.3367A>T (p.Thr1123Ser) c.2908A>T (p.Thr970Ser) c.2047A>T (p.Thr683Ser) n.3848A>T n.3852A>T | |
1 | g.1048042C>A | CA337852284 | AGRN | c.3782C>A (p.Thr1261Lys) c.3467C>A (p.Thr1156Lys) c.3368C>A (p.Thr1123Lys) c.2909C>A (p.Thr970Lys) c.2048C>A (p.Thr683Lys) n.3849C>A n.3853C>A | gnomAD v4 |
1 | g.1048042C= | CA1148803256 | AGRN | c.3782C= (p.Thr1261=) c.3467C= (p.Thr1156=) c.3368C= (p.Thr1123=) c.2909C= (p.Thr970=) c.2048C= (p.Thr683=) n.3849C= n.3853C= | |
1 | g.1048042C>G | CA337852288 | AGRN | c.3782C>G (p.Thr1261Arg) c.3467C>G (p.Thr1156Arg) c.3368C>G (p.Thr1123Arg) c.2909C>G (p.Thr970Arg) c.2048C>G (p.Thr683Arg) n.3849C>G n.3853C>G | |
1 | g.1048042C>T | CA337852291 | AGRN | c.3782C>T (p.Thr1261Met) c.3467C>T (p.Thr1156Met) c.3368C>T (p.Thr1123Met) c.2909C>T (p.Thr970Met) c.2048C>T (p.Thr683Met) n.3849C>T n.3853C>T | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.1048043G>A | CA509238 | AGRN | c.3783G>A (p.Thr1261=) c.3468G>A (p.Thr1156=) c.3369G>A (p.Thr1123=) c.2910G>A (p.Thr970=) c.2049G>A (p.Thr683=) n.3850G>A n.3854G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.1048043G>C | CA415758351 | AGRN | c.3783G>C (p.Thr1261=) c.3468G>C (p.Thr1156=) c.3369G>C (p.Thr1123=) c.2910G>C (p.Thr970=) c.2049G>C (p.Thr683=) n.3850G>C n.3854G>C | gnomAD v4 |
1 | g.1048043G= | CA1144124552 | AGRN | c.3783G= (p.Thr1261=) c.3468G= (p.Thr1156=) c.3369G= (p.Thr1123=) c.2910G= (p.Thr970=) c.2049G= (p.Thr683=) n.3850G= n.3854G= | |
1 | g.1048043G>T | CA415758352 | AGRN | c.3783G>T (p.Thr1261=) c.3468G>T (p.Thr1156=) c.3369G>T (p.Thr1123=) c.2910G>T (p.Thr970=) c.2049G>T (p.Thr683=) n.3850G>T n.3854G>T | gnomAD v4 |
1 | g.1048044T>A | CA337852295 | AGRN | c.3784T>A (p.Ser1262Thr) c.3469T>A (p.Ser1157Thr) c.3370T>A (p.Ser1124Thr) c.2911T>A (p.Ser971Thr) c.2050T>A (p.Ser684Thr) n.3851T>A n.3855T>A | |
1 | g.1048044T>C | CA337852297 | AGRN | c.3784T>C (p.Ser1262Pro) c.3469T>C (p.Ser1157Pro) c.3370T>C (p.Ser1124Pro) c.2911T>C (p.Ser971Pro) c.2050T>C (p.Ser684Pro) n.3851T>C n.3855T>C | gnomAD v4 |
1 | g.1048044T>G | CA337852300 | AGRN | c.3784T>G (p.Ser1262Ala) c.3469T>G (p.Ser1157Ala) c.3370T>G (p.Ser1124Ala) c.2911T>G (p.Ser971Ala) c.2050T>G (p.Ser684Ala) n.3851T>G n.3855T>G | |
1 | g.1048045C>A | CA337852302 | AGRN | c.3785C>A (p.Ser1262Ter) c.3470C>A (p.Ser1157Ter) c.3371C>A (p.Ser1124Ter) c.2912C>A (p.Ser971Ter) c.2051C>A (p.Ser684Ter) n.3852C>A n.3856C>A | gnomAD v4 |
1 | g.1048045C>G | CA337852303 | AGRN | c.3785C>G (p.Ser1262Ter) c.3470C>G (p.Ser1157Ter) c.3371C>G (p.Ser1124Ter) c.2912C>G (p.Ser971Ter) c.2051C>G (p.Ser684Ter) n.3852C>G n.3856C>G | |
1 | g.1048045C>T | CA337852304 | AGRN | c.3785C>T (p.Ser1262Leu) c.3470C>T (p.Ser1157Leu) c.3371C>T (p.Ser1124Leu) c.2912C>T (p.Ser971Leu) c.2051C>T (p.Ser684Leu) n.3852C>T n.3856C>T | gnomAD v4 |
1 | g.1048046A= | CA1148803267 | AGRN | c.3786A= (p.Ser1262=) c.3471A= (p.Ser1157=) c.3372A= (p.Ser1124=) c.2913A= (p.Ser971=) c.2052A= (p.Ser684=) n.3853A= n.3857A= | |
1 | g.1048046A>C | CA415758359 | AGRN | c.3786A>C (p.Ser1262=) c.3471A>C (p.Ser1157=) c.3372A>C (p.Ser1124=) c.2913A>C (p.Ser971=) c.2052A>C (p.Ser684=) n.3853A>C n.3857A>C | |
1 | g.1048046A>G | CA415758363 | AGRN | c.3786A>G (p.Ser1262=) c.3471A>G (p.Ser1157=) c.3372A>G (p.Ser1124=) c.2913A>G (p.Ser971=) c.2052A>G (p.Ser684=) n.3853A>G n.3857A>G | dbSNP gnomAD v2 gnomAD v4 |
1 | g.1048046A>T | CA415758361 | AGRN | c.3786A>T (p.Ser1262=) c.3471A>T (p.Ser1157=) c.3372A>T (p.Ser1124=) c.2913A>T (p.Ser971=) c.2052A>T (p.Ser684=) n.3853A>T n.3857A>T | gnomAD v4 |
1 | g.1048048_1048050del | CA2642492078 | AGRN | c.3788_3790del (p.Gly1263del) c.3473_3475del (p.Gly1158del) c.3374_3376del (p.Gly1125del) c.2915_2917del (p.Gly972del) c.2054_2056del (p.Gly685del) n.3855_3857del n.3859_3861del | gnomAD v4 |
1 | g.1048047G>A | CA337852306 | AGRN | c.3787G>A (p.Gly1263Arg) c.3472G>A (p.Gly1158Arg) c.3373G>A (p.Gly1125Arg) c.2914G>A (p.Gly972Arg) c.2053G>A (p.Gly685Arg) n.3854G>A n.3858G>A | dbSNP gnomAD v4 |
1 | g.1048047G>C | CA337852307 | AGRN | c.3787G>C (p.Gly1263Arg) c.3472G>C (p.Gly1158Arg) c.3373G>C (p.Gly1125Arg) c.2914G>C (p.Gly972Arg) c.2053G>C (p.Gly685Arg) n.3854G>C n.3858G>C | |
1 | g.1048047G= | CA1148803270 | AGRN | c.3787G= (p.Gly1263=) c.3472G= (p.Gly1158=) c.3373G= (p.Gly1125=) c.2914G= (p.Gly972=) c.2053G= (p.Gly685=) n.3854G= n.3858G= | |
1 | g.1048047G>T | CA337852305 | AGRN | c.3787G>T (p.Gly1263Ter) c.3472G>T (p.Gly1158Ter) c.3373G>T (p.Gly1125Ter) c.2914G>T (p.Gly972Ter) c.2053G>T (p.Gly685Ter) n.3854G>T n.3858G>T | gnomAD v4 |
1 | g.1048048G>A | CA337852308 | AGRN | c.3788G>A (p.Gly1263Glu) c.3473G>A (p.Gly1158Glu) c.3374G>A (p.Gly1125Glu) c.2915G>A (p.Gly972Glu) c.2054G>A (p.Gly685Glu) n.3855G>A n.3859G>A | |
1 | g.1048048G>C | CA509240 | AGRN | c.3788G>C (p.Gly1263Ala) c.3473G>C (p.Gly1158Ala) c.3374G>C (p.Gly1125Ala) c.2915G>C (p.Gly972Ala) c.2054G>C (p.Gly685Ala) n.3855G>C n.3859G>C | dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.1048048G= | CA1148803278 | AGRN | c.3788G= (p.Gly1263=) c.3473G= (p.Gly1158=) c.3374G= (p.Gly1125=) c.2915G= (p.Gly972=) c.2054G= (p.Gly685=) n.3855G= n.3859G= | |
1 | g.1048048G>T | CA509239 | AGRN | c.3788G>T (p.Gly1263Val) c.3473G>T (p.Gly1158Val) c.3374G>T (p.Gly1125Val) c.2915G>T (p.Gly972Val) c.2054G>T (p.Gly685Val) n.3855G>T n.3859G>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.1048049A>C | CA415758372 | AGRN | c.3789A>C (p.Gly1263=) c.3474A>C (p.Gly1158=) c.3375A>C (p.Gly1125=) c.2916A>C (p.Gly972=) c.2055A>C (p.Gly685=) n.3856A>C n.3860A>C | |
1 | g.1048049A>G | CA415758376 | AGRN | c.3789A>G (p.Gly1263=) c.3474A>G (p.Gly1158=) c.3375A>G (p.Gly1125=) c.2916A>G (p.Gly972=) c.2055A>G (p.Gly685=) n.3856A>G n.3860A>G | gnomAD v4 |
1 | g.1048049A>T | CA415758377 | AGRN | c.3789A>T (p.Gly1263=) c.3474A>T (p.Gly1158=) c.3375A>T (p.Gly1125=) c.2916A>T (p.Gly972=) c.2055A>T (p.Gly685=) n.3856A>T n.3860A>T | |
1 | g.1048050G>A | CA16760130 | AGRN | c.3790G>A (p.Ala1264Thr) c.3475G>A (p.Ala1159Thr) c.3376G>A (p.Ala1126Thr) c.2917G>A (p.Ala973Thr) c.2056G>A (p.Ala686Thr) n.3857G>A n.3861G>A | dbSNP gnomAD v2 gnomAD v4 |
1 | g.1048050G>C | CA337852314 | AGRN | c.3790G>C (p.Ala1264Pro) c.3475G>C (p.Ala1159Pro) c.3376G>C (p.Ala1126Pro) c.2917G>C (p.Ala973Pro) c.2056G>C (p.Ala686Pro) n.3857G>C n.3861G>C | |
1 | g.1048050G= | CA1148803291 | AGRN | c.3790G= (p.Ala1264=) c.3475G= (p.Ala1159=) c.3376G= (p.Ala1126=) c.2917G= (p.Ala973=) c.2056G= (p.Ala686=) n.3857G= n.3861G= | |
1 | g.1048050G>T | CA337852315 | AGRN | c.3790G>T (p.Ala1264Ser) c.3475G>T (p.Ala1159Ser) c.3376G>T (p.Ala1126Ser) c.2917G>T (p.Ala973Ser) c.2056G>T (p.Ala686Ser) n.3857G>T n.3861G>T | ClinVar dbSNP gnomAD v2 gnomAD v4 |
1 | g.1048051C>A | CA337852317 | AGRN | c.3791C>A (p.Ala1264Asp) c.3476C>A (p.Ala1159Asp) c.3377C>A (p.Ala1126Asp) c.2918C>A (p.Ala973Asp) c.2057C>A (p.Ala686Asp) n.3858C>A n.3862C>A | gnomAD v4 |
1 | g.1048051C= | CA1148803295 | AGRN | c.3791C= (p.Ala1264=) c.3476C= (p.Ala1159=) c.3377C= (p.Ala1126=) c.2918C= (p.Ala973=) c.2057C= (p.Ala686=) n.3858C= n.3862C= | |
1 | g.1048051C>G | CA337852320 | AGRN | c.3791C>G (p.Ala1264Gly) c.3476C>G (p.Ala1159Gly) c.3377C>G (p.Ala1126Gly) c.2918C>G (p.Ala973Gly) c.2057C>G (p.Ala686Gly) n.3858C>G n.3862C>G | |
1 | g.1048051C>T | CA16760131 | AGRN | c.3791C>T (p.Ala1264Val) c.3476C>T (p.Ala1159Val) c.3377C>T (p.Ala1126Val) c.2918C>T (p.Ala973Val) c.2057C>T (p.Ala686Val) n.3858C>T n.3862C>T | dbSNP gnomAD v2 gnomAD v4 |
1 | g.1048052C>A | CA509241 | AGRN | c.3792C>A (p.Ala1264=) c.3477C>A (p.Ala1159=) c.3378C>A (p.Ala1126=) c.2919C>A (p.Ala973=) c.2058C>A (p.Ala686=) n.3859C>A n.3863C>A | dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.1048052C= | CA1148803317 | AGRN | c.3792C= (p.Ala1264=) c.3477C= (p.Ala1159=) c.3378C= (p.Ala1126=) c.2919C= (p.Ala973=) c.2058C= (p.Ala686=) n.3859C= n.3863C= | |
1 | g.1048052C>G | CA415758383 | AGRN | c.3792C>G (p.Ala1264=) c.3477C>G (p.Ala1159=) c.3378C>G (p.Ala1126=) c.2919C>G (p.Ala973=) c.2058C>G (p.Ala686=) n.3859C>G n.3863C>G | |
1 | g.1048052C>T | CA415758384 | AGRN | c.3792C>T (p.Ala1264=) c.3477C>T (p.Ala1159=) c.3378C>T (p.Ala1126=) c.2919C>T (p.Ala973=) c.2058C>T (p.Ala686=) n.3859C>T n.3863C>T | gnomAD v4 |
1 | g.1048053A= | CA1148803322 | AGRN | c.3793A= (p.Ile1265=) c.3478A= (p.Ile1160=) c.3379A= (p.Ile1127=) c.2920A= (p.Ile974=) c.2059A= (p.Ile687=) n.3860A= n.3864A= | |
1 | g.1048053A>C | CA337852332 | AGRN | c.3793A>C (p.Ile1265Leu) c.3478A>C (p.Ile1160Leu) c.3379A>C (p.Ile1127Leu) c.2920A>C (p.Ile974Leu) c.2059A>C (p.Ile687Leu) n.3860A>C n.3864A>C | |
1 | g.1048053A>G | CA337852334 | AGRN | c.3793A>G (p.Ile1265Val) c.3478A>G (p.Ile1160Val) c.3379A>G (p.Ile1127Val) c.2920A>G (p.Ile974Val) c.2059A>G (p.Ile687Val) n.3860A>G n.3864A>G | dbSNP gnomAD v4 |
1 | g.1048053A>T | CA337852335 | AGRN | c.3793A>T (p.Ile1265Phe) c.3478A>T (p.Ile1160Phe) c.3379A>T (p.Ile1127Phe) c.2920A>T (p.Ile974Phe) c.2059A>T (p.Ile687Phe) n.3860A>T n.3864A>T | |
1 | g.1048054T>A | CA337852338 | AGRN | c.3794T>A (p.Ile1265Asn) c.3479T>A (p.Ile1160Asn) c.3380T>A (p.Ile1127Asn) c.2921T>A (p.Ile974Asn) c.2060T>A (p.Ile687Asn) n.3861T>A n.3865T>A | gnomAD v4 |
1 | g.1048054T>C | CA337852343 | AGRN | c.3794T>C (p.Ile1265Thr) c.3479T>C (p.Ile1160Thr) c.3380T>C (p.Ile1127Thr) c.2921T>C (p.Ile974Thr) c.2060T>C (p.Ile687Thr) n.3861T>C n.3865T>C | |
1 | g.1048054T>G | CA337852341 | AGRN | c.3794T>G (p.Ile1265Ser) c.3479T>G (p.Ile1160Ser) c.3380T>G (p.Ile1127Ser) c.2921T>G (p.Ile974Ser) c.2060T>G (p.Ile687Ser) n.3861T>G n.3865T>G | |
1 | g.1048055T>A | CA509242 | AGRN | c.3795T>A (p.Ile1265=) c.3480T>A (p.Ile1160=) c.3381T>A (p.Ile1127=) c.2922T>A (p.Ile974=) c.2061T>A (p.Ile687=) n.3862T>A n.3866T>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.1048055T>C | CA415758389 | AGRN | c.3795T>C (p.Ile1265=) c.3480T>C (p.Ile1160=) c.3381T>C (p.Ile1127=) c.2922T>C (p.Ile974=) c.2061T>C (p.Ile687=) n.3862T>C n.3866T>C | |
1 | g.1048055T>G | CA337852345 | AGRN | c.3795T>G (p.Ile1265Met) c.3480T>G (p.Ile1160Met) c.3381T>G (p.Ile1127Met) c.2922T>G (p.Ile974Met) c.2061T>G (p.Ile687Met) n.3862T>G n.3866T>G | |
1 | g.1048055T= | CA1148803351 | AGRN | c.3795T= (p.Ile1265=) c.3480T= (p.Ile1160=) c.3381T= (p.Ile1127=) c.2922T= (p.Ile974=) c.2061T= (p.Ile687=) n.3862T= n.3866T= | |
1 | g.1048056G>A | CA337852347 | AGRN | c.3796G>A (p.Ala1266Thr) c.3481G>A (p.Ala1161Thr) c.3382G>A (p.Ala1128Thr) c.2923G>A (p.Ala975Thr) c.2062G>A (p.Ala688Thr) n.3863G>A n.3867G>A | |
1 | g.1048056G>C | CA337852348 | AGRN | c.3796G>C (p.Ala1266Pro) c.3481G>C (p.Ala1161Pro) c.3382G>C (p.Ala1128Pro) c.2923G>C (p.Ala975Pro) c.2062G>C (p.Ala688Pro) n.3863G>C n.3867G>C | gnomAD v4 |
1 | g.1048056G= | CA1148803375 | AGRN | c.3796G= (p.Ala1266=) c.3481G= (p.Ala1161=) c.3382G= (p.Ala1128=) c.2923G= (p.Ala975=) c.2062G= (p.Ala688=) n.3863G= n.3867G= | |
1 | g.1048056G>T | CA337852356 | AGRN | c.3796G>T (p.Ala1266Ser) c.3481G>T (p.Ala1161Ser) c.3382G>T (p.Ala1128Ser) c.2923G>T (p.Ala975Ser) c.2062G>T (p.Ala688Ser) n.3863G>T n.3867G>T | dbSNP gnomAD v4 |
1 | g.1048057C>A | CA337852361 | AGRN | c.3797C>A (p.Ala1266Asp) c.3482C>A (p.Ala1161Asp) c.3383C>A (p.Ala1128Asp) c.2924C>A (p.Ala975Asp) c.2063C>A (p.Ala688Asp) n.3864C>A n.3868C>A | gnomAD v4 |
1 | g.1048057C= | CA1148803384 | AGRN | c.3797C= (p.Ala1266=) c.3482C= (p.Ala1161=) c.3383C= (p.Ala1128=) c.2924C= (p.Ala975=) c.2063C= (p.Ala688=) n.3864C= n.3868C= | |
1 | g.1048057C>G | CA337852363 | AGRN | c.3797C>G (p.Ala1266Gly) c.3482C>G (p.Ala1161Gly) c.3383C>G (p.Ala1128Gly) c.2924C>G (p.Ala975Gly) c.2063C>G (p.Ala688Gly) n.3864C>G n.3868C>G | |
1 | g.1048057C>T | CA509243 | AGRN | c.3797C>T (p.Ala1266Val) c.3482C>T (p.Ala1161Val) c.3383C>T (p.Ala1128Val) c.2924C>T (p.Ala975Val) c.2063C>T (p.Ala688Val) n.3864C>T n.3868C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.1048058T>A | CA415758395 | AGRN | c.3798T>A (p.Ala1266=) c.3483T>A (p.Ala1161=) c.3384T>A (p.Ala1128=) c.2925T>A (p.Ala975=) c.2064T>A (p.Ala688=) n.3865T>A n.3869T>A | |
1 | g.1048058T>C | CA415758396 | AGRN | c.3798T>C (p.Ala1266=) c.3483T>C (p.Ala1161=) c.3384T>C (p.Ala1128=) c.2925T>C (p.Ala975=) c.2064T>C (p.Ala688=) n.3865T>C n.3869T>C | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.1048058T>G | CA415758397 | AGRN | c.3798T>G (p.Ala1266=) c.3483T>G (p.Ala1161=) c.3384T>G (p.Ala1128=) c.2925T>G (p.Ala975=) c.2064T>G (p.Ala688=) n.3865T>G n.3869T>G | |
1 | g.1048058T= | CA1148803392 | AGRN | c.3798T= (p.Ala1266=) c.3483T= (p.Ala1161=) c.3384T= (p.Ala1128=) c.2925T= (p.Ala975=) c.2064T= (p.Ala688=) n.3865T= n.3869T= | |
1 | g.1048059G>A | CA337852366 | AGRN | c.3799G>A (p.Ala1267Thr) c.3484G>A (p.Ala1162Thr) c.3385G>A (p.Ala1129Thr) c.2926G>A (p.Ala976Thr) c.2065G>A (p.Ala689Thr) n.3866G>A n.3870G>A | gnomAD v4 |
1 | g.1048059G>C | CA337852373 | AGRN | c.3799G>C (p.Ala1267Pro) c.3484G>C (p.Ala1162Pro) c.3385G>C (p.Ala1129Pro) c.2926G>C (p.Ala976Pro) c.2065G>C (p.Ala689Pro) n.3866G>C n.3870G>C | |
1 | g.1048059G>T | CA337852377 | AGRN | c.3799G>T (p.Ala1267Ser) c.3484G>T (p.Ala1162Ser) c.3385G>T (p.Ala1129Ser) c.2926G>T (p.Ala976Ser) c.2065G>T (p.Ala689Ser) n.3866G>T n.3870G>T | gnomAD v4 |
1 | g.1048060_1048062del | CA2642492083 | AGRN | c.3800_3802del (p.Ala1267del) c.3485_3487del (p.Ala1162del) c.3386_3388del (p.Ala1129del) c.2927_2929del (p.Ala976del) c.2066_2068del (p.Ala689del) n.3867_3869del n.3871_3873del | gnomAD v4 |
1 | g.1048060C>A | CA337852384 | AGRN | c.3800C>A (p.Ala1267Glu) c.3485C>A (p.Ala1162Glu) c.3386C>A (p.Ala1129Glu) c.2927C>A (p.Ala976Glu) c.2066C>A (p.Ala689Glu) n.3867C>A n.3871C>A | gnomAD v4 |
1 | g.1048060C= | CA1148803399 | AGRN | c.3800C= (p.Ala1267=) c.3485C= (p.Ala1162=) c.3386C= (p.Ala1129=) c.2927C= (p.Ala976=) c.2066C= (p.Ala689=) n.3867C= n.3871C= | |
1 | g.1048060C>G | CA337852387 | AGRN | c.3800C>G (p.Ala1267Gly) c.3485C>G (p.Ala1162Gly) c.3386C>G (p.Ala1129Gly) c.2927C>G (p.Ala976Gly) c.2066C>G (p.Ala689Gly) n.3867C>G n.3871C>G | dbSNP gnomAD v2 gnomAD v4 |
1 | g.1048060C>T | CA509244 | AGRN | c.3800C>T (p.Ala1267Val) c.3485C>T (p.Ala1162Val) c.3386C>T (p.Ala1129Val) c.2927C>T (p.Ala976Val) c.2066C>T (p.Ala689Val) n.3867C>T n.3871C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.1048061G>A | CA509245 | AGRN | c.3801G>A (p.Ala1267=) c.3486G>A (p.Ala1162=) c.3387G>A (p.Ala1129=) c.2928G>A (p.Ala976=) c.2067G>A (p.Ala689=) n.3868G>A n.3872G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.1048061G>C | CA415758406 | AGRN | c.3801G>C (p.Ala1267=) c.3486G>C (p.Ala1162=) c.3387G>C (p.Ala1129=) c.2928G>C (p.Ala976=) c.2067G>C (p.Ala689=) n.3868G>C n.3872G>C | gnomAD v4 |
1 | g.1048061G= | CA1142242683 | AGRN | c.3801G= (p.Ala1267=) c.3486G= (p.Ala1162=) c.3387G= (p.Ala1129=) c.2928G= (p.Ala976=) c.2067G= (p.Ala689=) n.3868G= n.3872G= | |
1 | g.1048061G>T | CA509246 | AGRN | c.3801G>T (p.Ala1267=) c.3486G>T (p.Ala1162=) c.3387G>T (p.Ala1129=) c.2928G>T (p.Ala976=) c.2067G>T (p.Ala689=) n.3868G>T n.3872G>T | dbSNP ExAC gnomAD v4 |
1 | g.1048062G>A | CA337852393 | AGRN | c.3802G>A (p.Gly1268Arg) c.3487G>A (p.Gly1163Arg) c.3388G>A (p.Gly1130Arg) c.2929G>A (p.Gly977Arg) c.2068G>A (p.Gly690Arg) n.3869G>A n.3873G>A | gnomAD v4 |
1 | g.1048062G>C | CA337852391 | AGRN | c.3802G>C (p.Gly1268Arg) c.3487G>C (p.Gly1163Arg) c.3388G>C (p.Gly1130Arg) c.2929G>C (p.Gly977Arg) c.2068G>C (p.Gly690Arg) n.3869G>C n.3873G>C | |
1 | g.1048062G>T | CA337852396 | AGRN | c.3802G>T (p.Gly1268Ter) c.3487G>T (p.Gly1163Ter) c.3388G>T (p.Gly1130Ter) c.2929G>T (p.Gly977Ter) c.2068G>T (p.Gly690Ter) n.3869G>T n.3873G>T | gnomAD v4 |
1 | g.1048062_1048073dup | CA2574258705 | AGRN | c.3802_3813dup (p.Ala1271_Arg1272insGlyAlaThrAla) c.3487_3498dup (p.Ala1166_Arg1167insGlyAlaThrAla) c.3388_3399dup (p.Ala1133_Arg1134insGlyAlaThrAla) c.2929_2940dup (p.Ala980_Arg981insGlyAlaThrAla) c.2068_2079dup (p.Ala693_Arg694insGlyAlaThrAla) n.3869_3880dup n.3873_3884dup | |
1 | g.1048063G>A | CA509247 | AGRN | c.3803G>A (p.Gly1268Glu) c.3488G>A (p.Gly1163Glu) c.3389G>A (p.Gly1130Glu) c.2930G>A (p.Gly977Glu) c.2069G>A (p.Gly690Glu) n.3870G>A n.3874G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
1 | g.1048063G>C | CA337852400 | AGRN | c.3803G>C (p.Gly1268Ala) c.3488G>C (p.Gly1163Ala) c.3389G>C (p.Gly1130Ala) c.2930G>C (p.Gly977Ala) c.2069G>C (p.Gly690Ala) n.3870G>C n.3874G>C | gnomAD v4 |
1 | g.1048063G= | CA1148803424 | AGRN | c.3803G= (p.Gly1268=) c.3488G= (p.Gly1163=) c.3389G= (p.Gly1130=) c.2930G= (p.Gly977=) c.2069G= (p.Gly690=) n.3870G= n.3874G= | |
1 | g.1048063G>T | CA337852401 | AGRN | c.3803G>T (p.Gly1268Val) c.3488G>T (p.Gly1163Val) c.3389G>T (p.Gly1130Val) c.2930G>T (p.Gly977Val) c.2069G>T (p.Gly690Val) n.3870G>T n.3874G>T | gnomAD v4 |
1 | g.1048064A>C | CA415758409 | AGRN | c.3804A>C (p.Gly1268=) c.3489A>C (p.Gly1163=) c.3390A>C (p.Gly1130=) c.2931A>C (p.Gly977=) c.2070A>C (p.Gly690=) n.3871A>C n.3875A>C | |
1 | g.1048064A>G | CA415758410 | AGRN | c.3804A>G (p.Gly1268=) c.3489A>G (p.Gly1163=) c.3390A>G (p.Gly1130=) c.2931A>G (p.Gly977=) c.2070A>G (p.Gly690=) n.3871A>G n.3875A>G | gnomAD v4 |
1 | g.1048064A>T | CA415758411 | AGRN | c.3804A>T (p.Gly1268=) c.3489A>T (p.Gly1163=) c.3390A>T (p.Gly1130=) c.2931A>T (p.Gly977=) c.2070A>T (p.Gly690=) n.3871A>T n.3875A>T | |
1 | g.1048065G>A | CA337852402 | AGRN | c.3805G>A (p.Ala1269Thr) c.3490G>A (p.Ala1164Thr) c.3391G>A (p.Ala1131Thr) c.2932G>A (p.Ala978Thr) c.2071G>A (p.Ala691Thr) n.3872G>A n.3876G>A | gnomAD v4 |
1 | g.1048065G>C | CA337852403 | AGRN | c.3805G>C (p.Ala1269Pro) c.3490G>C (p.Ala1164Pro) c.3391G>C (p.Ala1131Pro) c.2932G>C (p.Ala978Pro) c.2071G>C (p.Ala691Pro) n.3872G>C n.3876G>C | gnomAD v4 |
1 | g.1048065G>T | CA337852404 | AGRN | c.3805G>T (p.Ala1269Ser) c.3490G>T (p.Ala1164Ser) c.3391G>T (p.Ala1131Ser) c.2932G>T (p.Ala978Ser) c.2071G>T (p.Ala691Ser) n.3872G>T n.3876G>T | gnomAD v4 |
1 | g.1048066C>A | CA337852405 | AGRN | c.3806C>A (p.Ala1269Asp) c.3491C>A (p.Ala1164Asp) c.3392C>A (p.Ala1131Asp) c.2933C>A (p.Ala978Asp) c.2072C>A (p.Ala691Asp) n.3873C>A n.3877C>A | ClinVar gnomAD v4 |
1 | g.1048066C= | CA1148803441 | AGRN | c.3806C= (p.Ala1269=) c.3491C= (p.Ala1164=) c.3392C= (p.Ala1131=) c.2933C= (p.Ala978=) c.2072C= (p.Ala691=) n.3873C= n.3877C= | |
1 | g.1048066C>G | CA337852406 | AGRN | c.3806C>G (p.Ala1269Gly) c.3491C>G (p.Ala1164Gly) c.3392C>G (p.Ala1131Gly) c.2933C>G (p.Ala978Gly) c.2072C>G (p.Ala691Gly) n.3873C>G n.3877C>G | |
1 | g.1048066C>T | CA337852408 | AGRN | c.3806C>T (p.Ala1269Val) c.3491C>T (p.Ala1164Val) c.3392C>T (p.Ala1131Val) c.2933C>T (p.Ala978Val) c.2072C>T (p.Ala691Val) n.3873C>T n.3877C>T | dbSNP gnomAD v4 |
1 | g.1048067C>A | CA415757973 | AGRN | c.3807C>A (p.Ala1269=) c.3492C>A (p.Ala1164=) c.3393C>A (p.Ala1131=) c.2934C>A (p.Ala978=) c.2073C>A (p.Ala691=) n.3874C>A n.3878C>A | |
1 | g.1048067C>G | CA415757975 | AGRN | c.3807C>G (p.Ala1269=) c.3492C>G (p.Ala1164=) c.3393C>G (p.Ala1131=) c.2934C>G (p.Ala978=) c.2073C>G (p.Ala691=) n.3874C>G n.3878C>G | |
1 | g.1048067C>T | CA415757977 | AGRN | c.3807C>T (p.Ala1269=) c.3492C>T (p.Ala1164=) c.3393C>T (p.Ala1131=) c.2934C>T (p.Ala978=) c.2073C>T (p.Ala691=) n.3874C>T n.3878C>T | |
1 | g.1048068A= | CA1148803443 | AGRN | c.3808A= (p.Thr1270=) c.3493A= (p.Thr1165=) c.3394A= (p.Thr1132=) c.2935A= (p.Thr979=) c.2074A= (p.Thr692=) n.3875A= n.3879A= | |
1 | g.1048068A>C | CA337852410 | AGRN | c.3808A>C (p.Thr1270Pro) c.3493A>C (p.Thr1165Pro) c.3394A>C (p.Thr1132Pro) c.2935A>C (p.Thr979Pro) c.2074A>C (p.Thr692Pro) n.3875A>C n.3879A>C | |
1 | g.1048068A>G | CA16760145 | AGRN | c.3808A>G (p.Thr1270Ala) c.3493A>G (p.Thr1165Ala) c.3394A>G (p.Thr1132Ala) c.2935A>G (p.Thr979Ala) c.2074A>G (p.Thr692Ala) n.3875A>G n.3879A>G | dbSNP |
1 | g.1048068A>T | CA337852412 | AGRN | c.3808A>T (p.Thr1270Ser) c.3493A>T (p.Thr1165Ser) c.3394A>T (p.Thr1132Ser) c.2935A>T (p.Thr979Ser) c.2074A>T (p.Thr692Ser) n.3875A>T n.3879A>T | |
1 | g.1048069C>A | CA337852423 | AGRN | c.3809C>A (p.Thr1270Lys) c.3494C>A (p.Thr1165Lys) c.3395C>A (p.Thr1132Lys) c.2936C>A (p.Thr979Lys) c.2075C>A (p.Thr692Lys) n.3876C>A n.3880C>A | dbSNP gnomAD v4 |
1 | g.1048069C= | CA1148803446 | AGRN | c.3809C= (p.Thr1270=) c.3494C= (p.Thr1165=) c.3395C= (p.Thr1132=) c.2936C= (p.Thr979=) c.2075C= (p.Thr692=) n.3876C= n.3880C= | |
1 | g.1048069C>G | CA337852417 | AGRN | c.3809C>G (p.Thr1270Arg) c.3494C>G (p.Thr1165Arg) c.3395C>G (p.Thr1132Arg) c.2936C>G (p.Thr979Arg) c.2075C>G (p.Thr692Arg) n.3876C>G n.3880C>G | gnomAD v4 |
1 | g.1048069C>T | CA509248 | AGRN | c.3809C>T (p.Thr1270Met) c.3494C>T (p.Thr1165Met) c.3395C>T (p.Thr1132Met) c.2936C>T (p.Thr979Met) c.2075C>T (p.Thr692Met) n.3876C>T n.3880C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.1048070G>A | CA509249 | AGRN | c.3810G>A (p.Thr1270=) c.3495G>A (p.Thr1165=) c.3396G>A (p.Thr1132=) c.2937G>A (p.Thr979=) c.2076G>A (p.Thr692=) n.3877G>A n.3881G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.1048070G>C | CA415757981 | AGRN | c.3810G>C (p.Thr1270=) c.3495G>C (p.Thr1165=) c.3396G>C (p.Thr1132=) c.2937G>C (p.Thr979=) c.2076G>C (p.Thr692=) n.3877G>C n.3881G>C | gnomAD v4 |
1 | g.1048070G= | CA1143654242 | AGRN | c.3810G= (p.Thr1270=) c.3495G= (p.Thr1165=) c.3396G= (p.Thr1132=) c.2937G= (p.Thr979=) c.2076G= (p.Thr692=) n.3877G= n.3881G= | |
1 | g.1048070G>T | CA415757982 | AGRN | c.3810G>T (p.Thr1270=) c.3495G>T (p.Thr1165=) c.3396G>T (p.Thr1132=) c.2937G>T (p.Thr979=) c.2076G>T (p.Thr692=) n.3877G>T n.3881G>T | gnomAD v4 |
1 | g.1048071del | CA2642492089 | AGRN | c.3811del (p.Ala1271ProfsTer14) c.3496del (p.Ala1166ProfsTer14) c.3397del (p.Ala1133ProfsTer14) c.2938del (p.Ala980ProfsTer14) c.2077del (p.Ala693ProfsTer14) n.3878del n.3882del | gnomAD v4 |
1 | g.1048071G>A | CA337852429 | AGRN | c.3811G>A (p.Ala1271Thr) c.3496G>A (p.Ala1166Thr) c.3397G>A (p.Ala1133Thr) c.2938G>A (p.Ala980Thr) c.2077G>A (p.Ala693Thr) n.3878G>A n.3882G>A | gnomAD v4 |
1 | g.1048071G>C | CA337852432 | AGRN | c.3811G>C (p.Ala1271Pro) c.3496G>C (p.Ala1166Pro) c.3397G>C (p.Ala1133Pro) c.2938G>C (p.Ala980Pro) c.2077G>C (p.Ala693Pro) n.3878G>C n.3882G>C | |
1 | g.1048071G>T | CA337852434 | AGRN | c.3811G>T (p.Ala1271Ser) c.3496G>T (p.Ala1166Ser) c.3397G>T (p.Ala1133Ser) c.2938G>T (p.Ala980Ser) c.2077G>T (p.Ala693Ser) n.3878G>T n.3882G>T | |
1 | g.1048072C>A | CA337852437 | AGRN | c.3812C>A (p.Ala1271Asp) c.3497C>A (p.Ala1166Asp) c.3398C>A (p.Ala1133Asp) c.2939C>A (p.Ala980Asp) c.2078C>A (p.Ala693Asp) n.3879C>A n.3883C>A | gnomAD v4 |
1 | g.1048072C= | CA1148803458 | AGRN | c.3812C= (p.Ala1271=) c.3497C= (p.Ala1166=) c.3398C= (p.Ala1133=) c.2939C= (p.Ala980=) c.2078C= (p.Ala693=) n.3879C= n.3883C= | |
1 | g.1048072C>G | CA509250 | AGRN | c.3812C>G (p.Ala1271Gly) c.3497C>G (p.Ala1166Gly) c.3398C>G (p.Ala1133Gly) c.2939C>G (p.Ala980Gly) c.2078C>G (p.Ala693Gly) n.3879C>G n.3883C>G | dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.1048072C>T | CA337852441 | AGRN | c.3812C>T (p.Ala1271Val) c.3497C>T (p.Ala1166Val) c.3398C>T (p.Ala1133Val) c.2939C>T (p.Ala980Val) c.2078C>T (p.Ala693Val) n.3879C>T n.3883C>T | gnomAD v4 |
1 | g.1048073C>A | CA415757998 | AGRN | c.3813C>A (p.Ala1271=) c.3498C>A (p.Ala1166=) c.3399C>A (p.Ala1133=) c.2940C>A (p.Ala980=) c.2079C>A (p.Ala693=) n.3880C>A n.3884C>A | gnomAD v4 |
1 | g.1048073C>G | CA415758000 | AGRN | c.3813C>G (p.Ala1271=) c.3498C>G (p.Ala1166=) c.3399C>G (p.Ala1133=) c.2940C>G (p.Ala980=) c.2079C>G (p.Ala693=) n.3880C>G n.3884C>G | gnomAD v4 |
1 | g.1048073C>T | CA415758002 | AGRN | c.3813C>T (p.Ala1271=) c.3498C>T (p.Ala1166=) c.3399C>T (p.Ala1133=) c.2940C>T (p.Ala980=) c.2079C>T (p.Ala693=) n.3880C>T n.3884C>T | gnomAD v4 |
1 | g.1048074A>C | CA415758004 | AGRN | c.3814A>C (p.Arg1272=) c.3499A>C (p.Arg1167=) c.3400A>C (p.Arg1134=) c.2941A>C (p.Arg981=) c.2080A>C (p.Arg694=) n.3881A>C n.3885A>C | |
1 | g.1048074A>G | CA337852443 | AGRN | c.3814A>G (p.Arg1272Gly) c.3499A>G (p.Arg1167Gly) c.3400A>G (p.Arg1134Gly) c.2941A>G (p.Arg981Gly) c.2080A>G (p.Arg694Gly) n.3881A>G n.3885A>G | |
1 | g.1048074A>T | CA337852444 | AGRN | c.3814A>T (p.Arg1272Ter) c.3499A>T (p.Arg1167Ter) c.3400A>T (p.Arg1134Ter) c.2941A>T (p.Arg981Ter) c.2080A>T (p.Arg694Ter) n.3881A>T n.3885A>T | |
1 | g.1048075G>A | CA337852445 | AGRN | c.3815G>A (p.Arg1272Lys) c.3500G>A (p.Arg1167Lys) c.3401G>A (p.Arg1134Lys) c.2942G>A (p.Arg981Lys) c.2081G>A (p.Arg694Lys) n.3882G>A n.3886G>A | ClinVar dbSNP gnomAD v4 |
1 | g.1048075G>C | CA337852446 | AGRN | c.3815G>C (p.Arg1272Thr) c.3500G>C (p.Arg1167Thr) c.3401G>C (p.Arg1134Thr) c.2942G>C (p.Arg981Thr) c.2081G>C (p.Arg694Thr) n.3882G>C n.3886G>C | gnomAD v4 |
1 | g.1048075G= | CA1148803467 | AGRN | c.3815G= (p.Arg1272=) c.3500G= (p.Arg1167=) c.3401G= (p.Arg1134=) c.2942G= (p.Arg981=) c.2081G= (p.Arg694=) n.3882G= n.3886G= | |
1 | g.1048075G>T | CA337852447 | AGRN | c.3815G>T (p.Arg1272Ile) c.3500G>T (p.Arg1167Ile) c.3401G>T (p.Arg1134Ile) c.2942G>T (p.Arg981Ile) c.2081G>T (p.Arg694Ile) n.3882G>T n.3886G>T | gnomAD v4 |
1 | g.1048076A= | CA1148803475 | AGRN | c.3816A= (p.Arg1272=) c.3501A= (p.Arg1167=) c.3402A= (p.Arg1134=) c.2943A= (p.Arg981=) c.2082A= (p.Arg694=) n.3883A= n.3887A= | |
1 | g.1048076A>C | CA337852452 | AGRN | c.3816A>C (p.Arg1272Ser) c.3501A>C (p.Arg1167Ser) c.3402A>C (p.Arg1134Ser) c.2943A>C (p.Arg981Ser) c.2082A>C (p.Arg694Ser) n.3883A>C n.3887A>C | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.1048076A>G | CA415758013 | AGRN | c.3816A>G (p.Arg1272=) c.3501A>G (p.Arg1167=) c.3402A>G (p.Arg1134=) c.2943A>G (p.Arg981=) c.2082A>G (p.Arg694=) n.3883A>G n.3887A>G | gnomAD v4 |
1 | g.1048076A>T | CA337852449 | AGRN | c.3816A>T (p.Arg1272Ser) c.3501A>T (p.Arg1167Ser) c.3402A>T (p.Arg1134Ser) c.2943A>T (p.Arg981Ser) c.2082A>T (p.Arg694Ser) n.3883A>T n.3887A>T | |
1 | g.1048077G>A | CA337852454 | AGRN | c.3817G>A (p.Ala1273Thr) c.3502G>A (p.Ala1168Thr) c.3403G>A (p.Ala1135Thr) c.2944G>A (p.Ala982Thr) c.2083G>A (p.Ala695Thr) n.3884G>A n.3888G>A | gnomAD v4 |
1 | g.1048077G>C | CA337852455 | AGRN | c.3817G>C (p.Ala1273Pro) c.3502G>C (p.Ala1168Pro) c.3403G>C (p.Ala1135Pro) c.2944G>C (p.Ala982Pro) c.2083G>C (p.Ala695Pro) n.3884G>C n.3888G>C | |
1 | g.1048077G>T | CA337852457 | AGRN | c.3817G>T (p.Ala1273Ser) c.3502G>T (p.Ala1168Ser) c.3403G>T (p.Ala1135Ser) c.2944G>T (p.Ala982Ser) c.2083G>T (p.Ala695Ser) n.3884G>T n.3888G>T | gnomAD v4 |
1 | g.1048078C>A | CA337852459 | AGRN | c.3818C>A (p.Ala1273Asp) c.3503C>A (p.Ala1168Asp) c.3404C>A (p.Ala1135Asp) c.2945C>A (p.Ala982Asp) c.2084C>A (p.Ala695Asp) n.3885C>A n.3889C>A | gnomAD v4 |
1 | g.1048078C>G | CA337852461 | AGRN | c.3818C>G (p.Ala1273Gly) c.3503C>G (p.Ala1168Gly) c.3404C>G (p.Ala1135Gly) c.2945C>G (p.Ala982Gly) c.2084C>G (p.Ala695Gly) n.3885C>G n.3889C>G | |
1 | g.1048078C>T | CA337852462 | AGRN | c.3818C>T (p.Ala1273Val) c.3503C>T (p.Ala1168Val) c.3404C>T (p.Ala1135Val) c.2945C>T (p.Ala982Val) c.2084C>T (p.Ala695Val) n.3885C>T n.3889C>T | gnomAD v4 |
1 | g.1048079C>A | CA415758024 | AGRN | c.3819C>A (p.Ala1273=) c.3504C>A (p.Ala1168=) c.3405C>A (p.Ala1135=) c.2946C>A (p.Ala982=) c.2085C>A (p.Ala695=) n.3886C>A n.3890C>A | |
1 | g.1048079C= | CA1141876286 | AGRN | c.3819C= (p.Ala1273=) c.3504C= (p.Ala1168=) c.3405C= (p.Ala1135=) c.2946C= (p.Ala982=) c.2085C= (p.Ala695=) n.3886C= n.3890C= | |
1 | g.1048079C>G | CA415758025 | AGRN | c.3819C>G (p.Ala1273=) c.3504C>G (p.Ala1168=) c.3405C>G (p.Ala1135=) c.2946C>G (p.Ala982=) c.2085C>G (p.Ala695=) n.3886C>G n.3890C>G | |
1 | g.1048079C>T | CA509251 | AGRN | c.3819C>T (p.Ala1273=) c.3504C>T (p.Ala1168=) c.3405C>T (p.Ala1135=) c.2946C>T (p.Ala982=) c.2085C>T (p.Ala695=) n.3886C>T n.3890C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.1048080A= | CA1148803486 | AGRN | c.3820A= (p.Thr1274=) c.3505A= (p.Thr1169=) c.3406A= (p.Thr1136=) c.2947A= (p.Thr983=) c.2086A= (p.Thr696=) n.3887A= n.3891A= | |
1 | g.1048080A>C | CA337852467 | AGRN | c.3820A>C (p.Thr1274Pro) c.3505A>C (p.Thr1169Pro) c.3406A>C (p.Thr1136Pro) c.2947A>C (p.Thr983Pro) c.2086A>C (p.Thr696Pro) n.3887A>C n.3891A>C | dbSNP |
1 | g.1048080A>G | CA337852468 | AGRN | c.3820A>G (p.Thr1274Ala) c.3505A>G (p.Thr1169Ala) c.3406A>G (p.Thr1136Ala) c.2947A>G (p.Thr983Ala) c.2086A>G (p.Thr696Ala) n.3887A>G n.3891A>G | dbSNP gnomAD v4 |
1 | g.1048080A>T | CA337852470 | AGRN | c.3820A>T (p.Thr1274Ser) c.3505A>T (p.Thr1169Ser) c.3406A>T (p.Thr1136Ser) c.2947A>T (p.Thr983Ser) c.2086A>T (p.Thr696Ser) n.3887A>T n.3891A>T | |
1 | g.1048081C>A | CA337852472 | AGRN | c.3821C>A (p.Thr1274Asn) c.3506C>A (p.Thr1169Asn) c.3407C>A (p.Thr1136Asn) c.2948C>A (p.Thr983Asn) c.2087C>A (p.Thr696Asn) n.3888C>A n.3892C>A | ClinVar dbSNP gnomAD v4 |
1 | g.1048081C= | CA1148803554 | AGRN | c.3821C= (p.Thr1274=) c.3506C= (p.Thr1169=) c.3407C= (p.Thr1136=) c.2948C= (p.Thr983=) c.2087C= (p.Thr696=) n.3888C= n.3892C= | |
1 | g.1048081C>G | CA337852474 | AGRN | c.3821C>G (p.Thr1274Ser) c.3506C>G (p.Thr1169Ser) c.3407C>G (p.Thr1136Ser) c.2948C>G (p.Thr983Ser) c.2087C>G (p.Thr696Ser) n.3888C>G n.3892C>G | gnomAD v4 |
1 | g.1048081C>T | CA337852475 | AGRN | c.3821C>T (p.Thr1274Ile) c.3506C>T (p.Thr1169Ile) c.3407C>T (p.Thr1136Ile) c.2948C>T (p.Thr983Ile) c.2087C>T (p.Thr696Ile) n.3888C>T n.3892C>T | gnomAD v4 |
1 | g.1048082C>A | CA415758040 | AGRN | c.3822C>A (p.Thr1274=) c.3507C>A (p.Thr1169=) c.3408C>A (p.Thr1136=) c.2949C>A (p.Thr983=) c.2088C>A (p.Thr696=) n.3889C>A n.3893C>A | gnomAD v4 |
1 | g.1048082C= | CA1148803582 | AGRN | c.3822C= (p.Thr1274=) c.3507C= (p.Thr1169=) c.3408C= (p.Thr1136=) c.2949C= (p.Thr983=) c.2088C= (p.Thr696=) n.3889C= n.3893C= | |
1 | g.1048082C>G | CA415758039 | AGRN | c.3822C>G (p.Thr1274=) c.3507C>G (p.Thr1169=) c.3408C>G (p.Thr1136=) c.2949C>G (p.Thr983=) c.2088C>G (p.Thr696=) n.3889C>G n.3893C>G | gnomAD v4 |
1 | g.1048082C>T | CA415758038 | AGRN | c.3822C>T (p.Thr1274=) c.3507C>T (p.Thr1169=) c.3408C>T (p.Thr1136=) c.2949C>T (p.Thr983=) c.2088C>T (p.Thr696=) n.3889C>T n.3893C>T | dbSNP gnomAD v3 gnomAD v4 |
1 | g.1048083A>C | CA337852479 | AGRN | c.3823A>C (p.Thr1275Pro) c.3508A>C (p.Thr1170Pro) c.3409A>C (p.Thr1137Pro) c.2950A>C (p.Thr984Pro) c.2089A>C (p.Thr697Pro) n.3890A>C n.3894A>C | |
1 | g.1048083A>G | CA337852477 | AGRN | c.3823A>G (p.Thr1275Ala) c.3508A>G (p.Thr1170Ala) c.3409A>G (p.Thr1137Ala) c.2950A>G (p.Thr984Ala) c.2089A>G (p.Thr697Ala) n.3890A>G n.3894A>G | gnomAD v4 |
1 | g.1048083A>T | CA337852478 | AGRN | c.3823A>T (p.Thr1275Ser) c.3508A>T (p.Thr1170Ser) c.3409A>T (p.Thr1137Ser) c.2950A>T (p.Thr984Ser) c.2089A>T (p.Thr697Ser) n.3890A>T n.3894A>T | |
1 | g.1048084C>A | CA337852483 | AGRN | c.3824C>A (p.Thr1275Asn) c.3509C>A (p.Thr1170Asn) c.3410C>A (p.Thr1137Asn) c.2951C>A (p.Thr984Asn) c.2090C>A (p.Thr697Asn) n.3891C>A n.3895C>A | gnomAD v4 |
1 | g.1048084C>G | CA337852485 | AGRN | c.3824C>G (p.Thr1275Ser) c.3509C>G (p.Thr1170Ser) c.3410C>G (p.Thr1137Ser) c.2951C>G (p.Thr984Ser) c.2090C>G (p.Thr697Ser) n.3891C>G n.3895C>G | |
1 | g.1048084C>T | CA337852487 | AGRN | c.3824C>T (p.Thr1275Ile) c.3509C>T (p.Thr1170Ile) c.3410C>T (p.Thr1137Ile) c.2951C>T (p.Thr984Ile) c.2090C>T (p.Thr697Ile) n.3891C>T n.3895C>T | |
1 | g.1048085T>A | CA415758053 | AGRN | c.3825T>A (p.Thr1275=) c.3510T>A (p.Thr1170=) c.3411T>A (p.Thr1137=) c.2952T>A (p.Thr984=) c.2091T>A (p.Thr697=) n.3892T>A n.3896T>A | |
1 | g.1048085T>C | CA415758054 | AGRN | c.3825T>C (p.Thr1275=) c.3510T>C (p.Thr1170=) c.3411T>C (p.Thr1137=) c.2952T>C (p.Thr984=) c.2091T>C (p.Thr697=) n.3892T>C n.3896T>C | ClinVar gnomAD v4 |
1 | g.1048085T>G | CA415758055 | AGRN | c.3825T>G (p.Thr1275=) c.3510T>G (p.Thr1170=) c.3411T>G (p.Thr1137=) c.2952T>G (p.Thr984=) c.2091T>G (p.Thr697=) n.3892T>G n.3896T>G | |
1 | g.1048086G>A | CA337852489 | AGRN | c.3826G>A (p.Ala1276Thr) c.3511G>A (p.Ala1171Thr) c.3412G>A (p.Ala1138Thr) c.2953G>A (p.Ala985Thr) c.2092G>A (p.Ala698Thr) n.3893G>A n.3897G>A | gnomAD v4 |
1 | g.1048086G>C | CA337852492 | AGRN | c.3826G>C (p.Ala1276Pro) c.3511G>C (p.Ala1171Pro) c.3412G>C (p.Ala1138Pro) c.2953G>C (p.Ala985Pro) c.2092G>C (p.Ala698Pro) n.3893G>C n.3897G>C | gnomAD v4 |
1 | g.1048086G>T | CA337852501 | AGRN | c.3826G>T (p.Ala1276Ser) c.3511G>T (p.Ala1171Ser) c.3412G>T (p.Ala1138Ser) c.2953G>T (p.Ala985Ser) c.2092G>T (p.Ala698Ser) n.3893G>T n.3897G>T | gnomAD v4 |
1 | g.1048087C>A | CA337852502 | AGRN | c.3827C>A (p.Ala1276Glu) c.3512C>A (p.Ala1171Glu) c.3413C>A (p.Ala1138Glu) c.2954C>A (p.Ala985Glu) c.2093C>A (p.Ala698Glu) n.3894C>A n.3898C>A | gnomAD v4 |
1 | g.1048087C= | CA1148803602 | AGRN | c.3827C= (p.Ala1276=) c.3512C= (p.Ala1171=) c.3413C= (p.Ala1138=) c.2954C= (p.Ala985=) c.2093C= (p.Ala698=) n.3894C= n.3898C= | |
1 | g.1048087C>G | CA337852504 | AGRN | c.3827C>G (p.Ala1276Gly) c.3512C>G (p.Ala1171Gly) c.3413C>G (p.Ala1138Gly) c.2954C>G (p.Ala985Gly) c.2093C>G (p.Ala698Gly) n.3894C>G n.3898C>G | |
1 | g.1048087C>T | CA337852505 | AGRN | c.3827C>T (p.Ala1276Val) c.3512C>T (p.Ala1171Val) c.3413C>T (p.Ala1138Val) c.2954C>T (p.Ala985Val) c.2093C>T (p.Ala698Val) n.3894C>T n.3898C>T | dbSNP gnomAD v2 gnomAD v4 |
1 | g.1048088A= | CA1148803609 | AGRN | c.3828A= (p.Ala1276=) c.3513A= (p.Ala1171=) c.3414A= (p.Ala1138=) c.2955A= (p.Ala985=) c.2094A= (p.Ala698=) n.3895A= n.3899A= | |
1 | g.1048088A>C | CA415758065 | AGRN | c.3828A>C (p.Ala1276=) c.3513A>C (p.Ala1171=) c.3414A>C (p.Ala1138=) c.2955A>C (p.Ala985=) c.2094A>C (p.Ala698=) n.3895A>C n.3899A>C | |
1 | g.1048088A>G | CA16760178 | AGRN | c.3828A>G (p.Ala1276=) c.3513A>G (p.Ala1171=) c.3414A>G (p.Ala1138=) c.2955A>G (p.Ala985=) c.2094A>G (p.Ala698=) n.3895A>G n.3899A>G | ClinVar dbSNP gnomAD v2 gnomAD v4 |
1 | g.1048088A>T | CA415758068 | AGRN | c.3828A>T (p.Ala1276=) c.3513A>T (p.Ala1171=) c.3414A>T (p.Ala1138=) c.2955A>T (p.Ala985=) c.2094A>T (p.Ala698=) n.3895A>T n.3899A>T | gnomAD v4 |
1 | g.1048089T>A | CA337852514 | AGRN | c.3829T>A (p.Ser1277Thr) c.3514T>A (p.Ser1172Thr) c.3415T>A (p.Ser1139Thr) c.2956T>A (p.Ser986Thr) c.2095T>A (p.Ser699Thr) n.3896T>A n.3900T>A | |
1 | g.1048089T>C | CA337852516 | AGRN | c.3829T>C (p.Ser1277Pro) c.3514T>C (p.Ser1172Pro) c.3415T>C (p.Ser1139Pro) c.2956T>C (p.Ser986Pro) c.2095T>C (p.Ser699Pro) n.3896T>C n.3900T>C | dbSNP gnomAD v2 gnomAD v4 |
1 | g.1048089T>G | CA337852519 | AGRN | c.3829T>G (p.Ser1277Ala) c.3514T>G (p.Ser1172Ala) c.3415T>G (p.Ser1139Ala) c.2956T>G (p.Ser986Ala) c.2095T>G (p.Ser699Ala) n.3896T>G n.3900T>G | |
1 | g.1048089T= | CA1148803616 | AGRN | c.3829T= (p.Ser1277=) c.3514T= (p.Ser1172=) c.3415T= (p.Ser1139=) c.2956T= (p.Ser986=) c.2095T= (p.Ser699=) n.3896T= n.3900T= | |
1 | g.1048090C>A | CA337852528 | AGRN | c.3830C>A (p.Ser1277Ter) c.3515C>A (p.Ser1172Ter) c.3416C>A (p.Ser1139Ter) c.2957C>A (p.Ser986Ter) c.2096C>A (p.Ser699Ter) n.3897C>A n.3901C>A | gnomAD v4 |
1 | g.1048090C= | CA1148436635 | AGRN | c.3830C= (p.Ser1277=) c.3515C= (p.Ser1172=) c.3416C= (p.Ser1139=) c.2957C= (p.Ser986=) c.2096C= (p.Ser699=) n.3897C= n.3901C= | |
1 | g.1048090C>G | CA337852525 | AGRN | c.3830C>G (p.Ser1277Trp) c.3515C>G (p.Ser1172Trp) c.3416C>G (p.Ser1139Trp) c.2957C>G (p.Ser986Trp) c.2096C>G (p.Ser699Trp) n.3897C>G n.3901C>G | gnomAD v4 |
1 | g.1048090C>T | CA509252 | AGRN | c.3830C>T (p.Ser1277Leu) c.3515C>T (p.Ser1172Leu) c.3416C>T (p.Ser1139Leu) c.2957C>T (p.Ser986Leu) c.2096C>T (p.Ser699Leu) n.3897C>T n.3901C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.1048091G>A | CA415758077 | AGRN | c.3831G>A (p.Ser1277=) c.3516G>A (p.Ser1172=) c.3417G>A (p.Ser1139=) c.2958G>A (p.Ser986=) c.2097G>A (p.Ser699=) n.3898G>A n.3902G>A | ClinVar dbSNP gnomAD v2 gnomAD v4 |
1 | g.1048091G>C | CA415758079 | AGRN | c.3831G>C (p.Ser1277=) c.3516G>C (p.Ser1172=) c.3417G>C (p.Ser1139=) c.2958G>C (p.Ser986=) c.2097G>C (p.Ser699=) n.3898G>C n.3902G>C | |
1 | g.1048091G= | CA1148803646 | AGRN | c.3831G= (p.Ser1277=) c.3516G= (p.Ser1172=) c.3417G= (p.Ser1139=) c.2958G= (p.Ser986=) c.2097G= (p.Ser699=) n.3898G= n.3902G= | |
1 | g.1048091G>T | CA415758080 | AGRN | c.3831G>T (p.Ser1277=) c.3516G>T (p.Ser1172=) c.3417G>T (p.Ser1139=) c.2958G>T (p.Ser986=) c.2097G>T (p.Ser699=) n.3898G>T n.3902G>T | gnomAD v4 |
1 | g.1048092C>A | CA337852531 | AGRN | c.3832C>A (p.Arg1278Ser) c.3517C>A (p.Arg1173Ser) c.3418C>A (p.Arg1140Ser) c.2959C>A (p.Arg987Ser) c.2098C>A (p.Arg700Ser) n.3899C>A n.3903C>A | gnomAD v4 |
1 | g.1048092C= | CA1148803662 | AGRN | c.3832C= (p.Arg1278=) c.3517C= (p.Arg1173=) c.3418C= (p.Arg1140=) c.2959C= (p.Arg987=) c.2098C= (p.Arg700=) n.3899C= n.3903C= | |
1 | g.1048092C>G | CA337852536 | AGRN | c.3832C>G (p.Arg1278Gly) c.3517C>G (p.Arg1173Gly) c.3418C>G (p.Arg1140Gly) c.2959C>G (p.Arg987Gly) c.2098C>G (p.Arg700Gly) n.3899C>G n.3903C>G | gnomAD v4 |
1 | g.1048092C>T | CA509253 | AGRN | c.3832C>T (p.Arg1278Cys) c.3517C>T (p.Arg1173Cys) c.3418C>T (p.Arg1140Cys) c.2959C>T (p.Arg987Cys) c.2098C>T (p.Arg700Cys) n.3899C>T n.3903C>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.1048093G>A | CA509255 | AGRN | c.3833G>A (p.Arg1278His) c.3518G>A (p.Arg1173His) c.3419G>A (p.Arg1140His) c.2960G>A (p.Arg987His) c.2099G>A (p.Arg700His) n.3900G>A n.3904G>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
1 | g.1048093G>C | CA337852552 | AGRN | c.3833G>C (p.Arg1278Pro) c.3518G>C (p.Arg1173Pro) c.3419G>C (p.Arg1140Pro) c.2960G>C (p.Arg987Pro) c.2099G>C (p.Arg700Pro) n.3900G>C n.3904G>C | |
1 | g.1048093G= | CA1145406299 | AGRN | c.3833G= (p.Arg1278=) c.3518G= (p.Arg1173=) c.3419G= (p.Arg1140=) c.2960G= (p.Arg987=) c.2099G= (p.Arg700=) n.3900G= n.3904G= | |
1 | g.1048093G>T | CA509254 | AGRN | c.3833G>T (p.Arg1278Leu) c.3518G>T (p.Arg1173Leu) c.3419G>T (p.Arg1140Leu) c.2960G>T (p.Arg987Leu) c.2099G>T (p.Arg700Leu) n.3900G>T n.3904G>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.1048094C>A | CA415758086 | AGRN | c.3834C>A (p.Arg1278=) c.3519C>A (p.Arg1173=) c.3420C>A (p.Arg1140=) c.2961C>A (p.Arg987=) c.2100C>A (p.Arg700=) n.3901C>A n.3905C>A | gnomAD v4 |
1 | g.1048094C= | CA1148803675 | AGRN | c.3834C= (p.Arg1278=) c.3519C= (p.Arg1173=) c.3420C= (p.Arg1140=) c.2961C= (p.Arg987=) c.2100C= (p.Arg700=) n.3901C= n.3905C= | |
1 | g.1048094C>G | CA415758088 | AGRN | c.3834C>G (p.Arg1278=) c.3519C>G (p.Arg1173=) c.3420C>G (p.Arg1140=) c.2961C>G (p.Arg987=) c.2100C>G (p.Arg700=) n.3901C>G n.3905C>G | |
1 | g.1048094C>T | CA509256 | AGRN | c.3834C>T (p.Arg1278=) c.3519C>T (p.Arg1173=) c.3420C>T (p.Arg1140=) c.2961C>T (p.Arg987=) c.2100C>T (p.Arg700=) n.3901C>T n.3905C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.1048095C>A | CA337852560 | AGRN | c.3835C>A (p.Leu1279Met) c.3520C>A (p.Leu1174Met) c.3421C>A (p.Leu1141Met) c.2962C>A (p.Leu988Met) c.2101C>A (p.Leu701Met) n.3902C>A n.3906C>A | gnomAD v4 |
1 | g.1048095C= | CA1148803728 | AGRN | c.3835C= (p.Leu1279=) c.3520C= (p.Leu1174=) c.3421C= (p.Leu1141=) c.2962C= (p.Leu988=) c.2101C= (p.Leu701=) n.3902C= n.3906C= | |
1 | g.1048095C>G | CA337852562 | AGRN | c.3835C>G (p.Leu1279Val) c.3520C>G (p.Leu1174Val) c.3421C>G (p.Leu1141Val) c.2962C>G (p.Leu988Val) c.2101C>G (p.Leu701Val) n.3902C>G n.3906C>G | |
1 | g.1048095C>T | CA415758090 | AGRN | c.3835C>T (p.Leu1279=) c.3520C>T (p.Leu1174=) c.3421C>T (p.Leu1141=) c.2962C>T (p.Leu988=) c.2101C>T (p.Leu701=) n.3902C>T n.3906C>T | dbSNP gnomAD v3 gnomAD v4 |
1 | g.1048096T>A | CA337852569 | AGRN | c.3836T>A (p.Leu1279Gln) c.3521T>A (p.Leu1174Gln) c.3422T>A (p.Leu1141Gln) c.2963T>A (p.Leu988Gln) c.2102T>A (p.Leu701Gln) n.3903T>A n.3907T>A | dbSNP gnomAD v2 gnomAD v4 |
1 | g.1048096T>C | CA337852570 | AGRN | c.3836T>C (p.Leu1279Pro) c.3521T>C (p.Leu1174Pro) c.3422T>C (p.Leu1141Pro) c.2963T>C (p.Leu988Pro) c.2102T>C (p.Leu701Pro) n.3903T>C n.3907T>C | gnomAD v4 |
1 | g.1048096T>G | CA337852575 | AGRN | c.3836T>G (p.Leu1279Arg) c.3521T>G (p.Leu1174Arg) c.3422T>G (p.Leu1141Arg) c.2963T>G (p.Leu988Arg) c.2102T>G (p.Leu701Arg) n.3903T>G n.3907T>G | |
1 | g.1048096T= | CA1148803736 | AGRN | c.3836T= (p.Leu1279=) c.3521T= (p.Leu1174=) c.3422T= (p.Leu1141=) c.2963T= (p.Leu988=) c.2102T= (p.Leu701=) n.3903T= n.3907T= | |
1 | g.1048097G>A | CA415758101 | AGRN | c.3837G>A (p.Leu1279=) c.3522G>A (p.Leu1174=) c.3423G>A (p.Leu1141=) c.2964G>A (p.Leu988=) c.2103G>A (p.Leu701=) n.3904G>A n.3908G>A | gnomAD v4 |
1 | g.1048097G>C | CA415758098 | AGRN | c.3837G>C (p.Leu1279=) c.3522G>C (p.Leu1174=) c.3423G>C (p.Leu1141=) c.2964G>C (p.Leu988=) c.2103G>C (p.Leu701=) n.3904G>C n.3908G>C | |
1 | g.1048097G>T | CA415758100 | AGRN | c.3837G>T (p.Leu1279=) c.3522G>T (p.Leu1174=) c.3423G>T (p.Leu1141=) c.2964G>T (p.Leu988=) c.2103G>T (p.Leu701=) n.3904G>T n.3908G>T | gnomAD v4 |