Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
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 |
1 | g.1048098C>A | CA337852578 | AGRN | c.3838C>A (p.Pro1280Thr) c.3523C>A (p.Pro1175Thr) c.3424C>A (p.Pro1142Thr) c.2965C>A (p.Pro989Thr) c.2104C>A (p.Pro702Thr) n.3905C>A n.3909C>A | gnomAD v4 |
1 | g.1048098C= | CA1146649680 | AGRN | c.3838C= (p.Pro1280=) c.3523C= (p.Pro1175=) c.3424C= (p.Pro1142=) c.2965C= (p.Pro989=) c.2104C= (p.Pro702=) n.3905C= n.3909C= | |
1 | g.1048098C>G | CA337852581 | AGRN | c.3838C>G (p.Pro1280Ala) c.3523C>G (p.Pro1175Ala) c.3424C>G (p.Pro1142Ala) c.2965C>G (p.Pro989Ala) c.2104C>G (p.Pro702Ala) n.3905C>G n.3909C>G | gnomAD v4 |
1 | g.1048098C>T | CA16760185 | AGRN | c.3838C>T (p.Pro1280Ser) c.3523C>T (p.Pro1175Ser) c.3424C>T (p.Pro1142Ser) c.2965C>T (p.Pro989Ser) c.2104C>T (p.Pro702Ser) n.3905C>T n.3909C>T | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.1048099C>A | CA337852590 | AGRN | c.3839C>A (p.Pro1280Gln) c.3524C>A (p.Pro1175Gln) c.3425C>A (p.Pro1142Gln) c.2966C>A (p.Pro989Gln) c.2105C>A (p.Pro702Gln) n.3906C>A n.3910C>A | gnomAD v4 |
1 | g.1048099C= | CA1148803759 | AGRN | c.3839C= (p.Pro1280=) c.3524C= (p.Pro1175=) c.3425C= (p.Pro1142=) c.2966C= (p.Pro989=) c.2105C= (p.Pro702=) n.3906C= n.3910C= | |
1 | g.1048099C>G | CA337852602 | AGRN | c.3839C>G (p.Pro1280Arg) c.3524C>G (p.Pro1175Arg) c.3425C>G (p.Pro1142Arg) c.2966C>G (p.Pro989Arg) c.2105C>G (p.Pro702Arg) n.3906C>G n.3910C>G | |
1 | g.1048099C>T | CA509257 | AGRN | c.3839C>T (p.Pro1280Leu) c.3524C>T (p.Pro1175Leu) c.3425C>T (p.Pro1142Leu) c.2966C>T (p.Pro989Leu) c.2105C>T (p.Pro702Leu) n.3906C>T n.3910C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.1048100G>A | CA509258 | AGRN | c.3840G>A (p.Pro1280=) c.3525G>A (p.Pro1175=) c.3426G>A (p.Pro1142=) c.2967G>A (p.Pro989=) c.2106G>A (p.Pro702=) n.3907G>A n.3911G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.1048100G>C | CA415758104 | AGRN | c.3840G>C (p.Pro1280=) c.3525G>C (p.Pro1175=) c.3426G>C (p.Pro1142=) c.2967G>C (p.Pro989=) c.2106G>C (p.Pro702=) n.3907G>C n.3911G>C | |
1 | g.1048100G= | CA1148803768 | AGRN | c.3840G= (p.Pro1280=) c.3525G= (p.Pro1175=) c.3426G= (p.Pro1142=) c.2967G= (p.Pro989=) c.2106G= (p.Pro702=) n.3907G= n.3911G= | |
1 | g.1048100G>T | CA415758105 | AGRN | c.3840G>T (p.Pro1280=) c.3525G>T (p.Pro1175=) c.3426G>T (p.Pro1142=) c.2967G>T (p.Pro989=) c.2106G>T (p.Pro702=) n.3907G>T n.3911G>T | dbSNP gnomAD v2 gnomAD v4 |
1 | g.1048101T>A | CA337852607 | AGRN | c.3841T>A (p.Ser1281Thr) c.3526T>A (p.Ser1176Thr) c.3427T>A (p.Ser1143Thr) c.2968T>A (p.Ser990Thr) c.2107T>A (p.Ser703Thr) n.3908T>A n.3912T>A | |
1 | g.1048101T>C | CA337852611 | AGRN | c.3841T>C (p.Ser1281Pro) c.3526T>C (p.Ser1176Pro) c.3427T>C (p.Ser1143Pro) c.2968T>C (p.Ser990Pro) c.2107T>C (p.Ser703Pro) n.3908T>C n.3912T>C | gnomAD v4 |
1 | g.1048101T>G | CA337852613 | AGRN | c.3841T>G (p.Ser1281Ala) c.3526T>G (p.Ser1176Ala) c.3427T>G (p.Ser1143Ala) c.2968T>G (p.Ser990Ala) c.2107T>G (p.Ser703Ala) n.3908T>G n.3912T>G | |
1 | g.1048102C>A | CA337852616 | AGRN | c.3842C>A (p.Ser1281Tyr) c.3527C>A (p.Ser1176Tyr) c.3428C>A (p.Ser1143Tyr) c.2969C>A (p.Ser990Tyr) c.2108C>A (p.Ser703Tyr) n.3909C>A n.3913C>A | |
1 | g.1048102C= | CA1148803782 | AGRN | c.3842C= (p.Ser1281=) c.3527C= (p.Ser1176=) c.3428C= (p.Ser1143=) c.2969C= (p.Ser990=) c.2108C= (p.Ser703=) n.3909C= n.3913C= | |
1 | g.1048102C>G | CA337852619 | AGRN | c.3842C>G (p.Ser1281Cys) c.3527C>G (p.Ser1176Cys) c.3428C>G (p.Ser1143Cys) c.2969C>G (p.Ser990Cys) c.2108C>G (p.Ser703Cys) n.3909C>G n.3913C>G | |
1 | g.1048102C>T | CA337852621 | AGRN | c.3842C>T (p.Ser1281Phe) c.3527C>T (p.Ser1176Phe) c.3428C>T (p.Ser1143Phe) c.2969C>T (p.Ser990Phe) c.2108C>T (p.Ser703Phe) n.3909C>T n.3913C>T | dbSNP gnomAD v2 gnomAD v4 |
1 | g.1048102_1048104delinsCCT | CA1148803804 | AGRN | c.3842_3844delinsCCT (p.Ser1281=) c.3527_3529delinsCCT (p.Ser1176=) c.3428_3430delinsCCT (p.Ser1143=) c.2969_2971delinsCCT (p.Ser990=) c.2108_2110delinsCCT (p.Ser703=) n.3909_3911delinsCCT n.3913_3915delinsCCT | |
1 | g.1048103C>A | CA415758109 | AGRN | c.3843C>A (p.Ser1281=) c.3528C>A (p.Ser1176=) c.3429C>A (p.Ser1143=) c.2970C>A (p.Ser990=) c.2109C>A (p.Ser703=) n.3910C>A n.3914C>A | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.1048103C= | CA1148803812 | AGRN | c.3843C= (p.Ser1281=) c.3528C= (p.Ser1176=) c.3429C= (p.Ser1143=) c.2970C= (p.Ser990=) c.2109C= (p.Ser703=) n.3910C= n.3914C= | |
1 | g.1048103C>G | CA415758110 | AGRN | c.3843C>G (p.Ser1281=) c.3528C>G (p.Ser1176=) c.3429C>G (p.Ser1143=) c.2970C>G (p.Ser990=) c.2109C>G (p.Ser703=) n.3910C>G n.3914C>G | |
1 | g.1048103C>T | CA415758111 | AGRN | c.3843C>T (p.Ser1281=) c.3528C>T (p.Ser1176=) c.3429C>T (p.Ser1143=) c.2970C>T (p.Ser990=) c.2109C>T (p.Ser703=) n.3910C>T n.3914C>T | dbSNP gnomAD v4 |
1 | g.1048105_1048106del | CA884898092 | AGRN | c.3845_3846del (p.Ser1282CysfsTer?) c.3530_3531del (p.Ser1177CysfsTer?) c.3431_3432del (p.Ser1144CysfsTer?) c.2972_2973del (p.Ser991CysfsTer?) c.2111_2112del (p.Ser704CysfsTer?) n.3912_3913del n.3916_3917del | dbSNP |
1 | g.1048104T>A | CA337852626 | AGRN | c.3844T>A (p.Ser1282Thr) c.3529T>A (p.Ser1177Thr) c.3430T>A (p.Ser1144Thr) c.2971T>A (p.Ser991Thr) c.2110T>A (p.Ser704Thr) n.3911T>A n.3915T>A | |
1 | g.1048104T>C | CA337852635 | AGRN | c.3844T>C (p.Ser1282Pro) c.3529T>C (p.Ser1177Pro) c.3430T>C (p.Ser1144Pro) c.2971T>C (p.Ser991Pro) c.2110T>C (p.Ser704Pro) n.3911T>C n.3915T>C | ClinVar dbSNP |
1 | g.1048104T>G | CA337852638 | AGRN | c.3844T>G (p.Ser1282Ala) c.3529T>G (p.Ser1177Ala) c.3430T>G (p.Ser1144Ala) c.2971T>G (p.Ser991Ala) c.2110T>G (p.Ser704Ala) n.3911T>G n.3915T>G | |
1 | g.1048104T= | CA1148803830 | AGRN | c.3844T= (p.Ser1282=) c.3529T= (p.Ser1177=) c.3430T= (p.Ser1144=) c.2971T= (p.Ser991=) c.2110T= (p.Ser704=) n.3911T= n.3915T= | |
1 | g.1048105C>A | CA337852651 | AGRN | c.3845C>A (p.Ser1282Tyr) c.3530C>A (p.Ser1177Tyr) c.3431C>A (p.Ser1144Tyr) c.2972C>A (p.Ser991Tyr) c.2111C>A (p.Ser704Tyr) n.3912C>A n.3916C>A | gnomAD v4 |
1 | g.1048105C>G | CA337852655 | AGRN | c.3845C>G (p.Ser1282Cys) c.3530C>G (p.Ser1177Cys) c.3431C>G (p.Ser1144Cys) c.2972C>G (p.Ser991Cys) c.2111C>G (p.Ser704Cys) n.3912C>G n.3916C>G | |
1 | g.1048105C>T | CA337852641 | AGRN | c.3845C>T (p.Ser1282Phe) c.3530C>T (p.Ser1177Phe) c.3431C>T (p.Ser1144Phe) c.2972C>T (p.Ser991Phe) c.2111C>T (p.Ser704Phe) n.3912C>T n.3916C>T | |
1 | g.1048106T>A | CA415758122 | AGRN | c.3846T>A (p.Ser1282=) c.3531T>A (p.Ser1177=) c.3432T>A (p.Ser1144=) c.2973T>A (p.Ser991=) c.2112T>A (p.Ser704=) n.3913T>A n.3917T>A | |
1 | g.1048106T>C | CA415758121 | AGRN | c.3846T>C (p.Ser1282=) c.3531T>C (p.Ser1177=) c.3432T>C (p.Ser1144=) c.2973T>C (p.Ser991=) c.2112T>C (p.Ser704=) n.3913T>C n.3917T>C | |
1 | g.1048106T>G | CA415758120 | AGRN | c.3846T>G (p.Ser1282=) c.3531T>G (p.Ser1177=) c.3432T>G (p.Ser1144=) c.2973T>G (p.Ser991=) c.2112T>G (p.Ser704=) n.3913T>G n.3917T>G | gnomAD v4 |
1 | g.1048107G>A | CA337852657 | AGRN | c.3847G>A (p.Ala1283Thr) c.3532G>A (p.Ala1178Thr) c.3433G>A (p.Ala1145Thr) c.2974G>A (p.Ala992Thr) c.2113G>A (p.Ala705Thr) n.3914G>A n.3918G>A | dbSNP gnomAD v4 |
1 | g.1048107G>C | CA337852658 | AGRN | c.3847G>C (p.Ala1283Pro) c.3532G>C (p.Ala1178Pro) c.3433G>C (p.Ala1145Pro) c.2974G>C (p.Ala992Pro) c.2113G>C (p.Ala705Pro) n.3914G>C n.3918G>C | |
1 | g.1048107G= | CA1148803862 | AGRN | c.3847G= (p.Ala1283=) c.3532G= (p.Ala1178=) c.3433G= (p.Ala1145=) c.2974G= (p.Ala992=) c.2113G= (p.Ala705=) n.3914G= n.3918G= | |
1 | g.1048107G>T | CA509259 | AGRN | c.3847G>T (p.Ala1283Ser) c.3532G>T (p.Ala1178Ser) c.3433G>T (p.Ala1145Ser) c.2974G>T (p.Ala992Ser) c.2113G>T (p.Ala705Ser) n.3914G>T n.3918G>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.1048108C>A | CA337852661 | AGRN | c.3848C>A (p.Ala1283Asp) c.3533C>A (p.Ala1178Asp) c.3434C>A (p.Ala1145Asp) c.2975C>A (p.Ala992Asp) c.2114C>A (p.Ala705Asp) n.3915C>A n.3919C>A | gnomAD v4 |
1 | g.1048108C>G | CA337852663 | AGRN | c.3848C>G (p.Ala1283Gly) c.3533C>G (p.Ala1178Gly) c.3434C>G (p.Ala1145Gly) c.2975C>G (p.Ala992Gly) c.2114C>G (p.Ala705Gly) n.3915C>G n.3919C>G | |
1 | g.1048108C>T | CA337852664 | AGRN | c.3848C>T (p.Ala1283Val) c.3533C>T (p.Ala1178Val) c.3434C>T (p.Ala1145Val) c.2975C>T (p.Ala992Val) c.2114C>T (p.Ala705Val) n.3915C>T n.3919C>T | gnomAD v4 |
1 | g.1048109T>A | CA415758126 | AGRN | c.3849T>A (p.Ala1283=) c.3534T>A (p.Ala1178=) c.3435T>A (p.Ala1145=) c.2976T>A (p.Ala992=) c.2115T>A (p.Ala705=) n.3916T>A n.3920T>A | |
1 | g.1048109T>C | CA415758128 | AGRN | c.3849T>C (p.Ala1283=) c.3534T>C (p.Ala1178=) c.3435T>C (p.Ala1145=) c.2976T>C (p.Ala992=) c.2115T>C (p.Ala705=) n.3916T>C n.3920T>C | |
1 | g.1048109T>G | CA415758133 | AGRN | c.3849T>G (p.Ala1283=) c.3534T>G (p.Ala1178=) c.3435T>G (p.Ala1145=) c.2976T>G (p.Ala992=) c.2115T>G (p.Ala705=) n.3916T>G n.3920T>G | |
1 | g.1048110G>A | CA337852672 | AGRN | c.3850G>A (p.Val1284Met) c.3535G>A (p.Val1179Met) c.3436G>A (p.Val1146Met) c.2977G>A (p.Val993Met) c.2116G>A (p.Val706Met) n.3917G>A n.3921G>A | gnomAD v4 |
1 | g.1048110G>C | CA337852674 | AGRN | c.3850G>C (p.Val1284Leu) c.3535G>C (p.Val1179Leu) c.3436G>C (p.Val1146Leu) c.2977G>C (p.Val993Leu) c.2116G>C (p.Val706Leu) n.3917G>C n.3921G>C | |
1 | g.1048110G>T | CA337852679 | AGRN | c.3850G>T (p.Val1284Leu) c.3535G>T (p.Val1179Leu) c.3436G>T (p.Val1146Leu) c.2977G>T (p.Val993Leu) c.2116G>T (p.Val706Leu) n.3917G>T n.3921G>T | gnomAD v4 |
1 | g.1048111T>A | CA337852691 | AGRN | c.3851T>A (p.Val1284Glu) c.3536T>A (p.Val1179Glu) c.3437T>A (p.Val1146Glu) c.2978T>A (p.Val993Glu) c.2117T>A (p.Val706Glu) n.3918T>A n.3922T>A | |
1 | g.1048111T>C | CA337852694 | AGRN | c.3851T>C (p.Val1284Ala) c.3536T>C (p.Val1179Ala) c.3437T>C (p.Val1146Ala) c.2978T>C (p.Val993Ala) c.2117T>C (p.Val706Ala) n.3918T>C n.3922T>C | |
1 | g.1048111T>G | CA337852697 | AGRN | c.3851T>G (p.Val1284Gly) c.3536T>G (p.Val1179Gly) c.3437T>G (p.Val1146Gly) c.2978T>G (p.Val993Gly) c.2117T>G (p.Val706Gly) n.3918T>G n.3922T>G | |
1 | g.1048112G>A | CA415758142 | AGRN | c.3852G>A (p.Val1284=) c.3537G>A (p.Val1179=) c.3438G>A (p.Val1146=) c.2979G>A (p.Val993=) c.2118G>A (p.Val706=) n.3919G>A n.3923G>A | |
1 | g.1048112G>C | CA415758143 | AGRN | c.3852G>C (p.Val1284=) c.3537G>C (p.Val1179=) c.3438G>C (p.Val1146=) c.2979G>C (p.Val993=) c.2118G>C (p.Val706=) n.3919G>C n.3923G>C | |
1 | g.1048112G>T | CA415758144 | AGRN | c.3852G>T (p.Val1284=) c.3537G>T (p.Val1179=) c.3438G>T (p.Val1146=) c.2979G>T (p.Val993=) c.2118G>T (p.Val706=) n.3919G>T n.3923G>T | gnomAD v4 |
1 | g.1048113A>C | CA337852702 | AGRN | c.3853A>C (p.Thr1285Pro) c.3538A>C (p.Thr1180Pro) c.3439A>C (p.Thr1147Pro) c.2980A>C (p.Thr994Pro) c.2119A>C (p.Thr707Pro) n.3920A>C n.3924A>C | |
1 | g.1048113A>G | CA337852704 | AGRN | c.3853A>G (p.Thr1285Ala) c.3538A>G (p.Thr1180Ala) c.3439A>G (p.Thr1147Ala) c.2980A>G (p.Thr994Ala) c.2119A>G (p.Thr707Ala) n.3920A>G n.3924A>G | |
1 | g.1048113A>T | CA337852700 | AGRN | c.3853A>T (p.Thr1285Ser) c.3538A>T (p.Thr1180Ser) c.3439A>T (p.Thr1147Ser) c.2980A>T (p.Thr994Ser) c.2119A>T (p.Thr707Ser) n.3920A>T n.3924A>T | |
1 | g.1048114C>A | CA337852707 | AGRN | c.3854C>A (p.Thr1285Asn) c.3539C>A (p.Thr1180Asn) c.3440C>A (p.Thr1147Asn) c.2981C>A (p.Thr994Asn) c.2120C>A (p.Thr707Asn) n.3921C>A n.3925C>A | gnomAD v4 |
1 | g.1048114C= | CA1148803874 | AGRN | c.3854C= (p.Thr1285=) c.3539C= (p.Thr1180=) c.3440C= (p.Thr1147=) c.2981C= (p.Thr994=) c.2120C= (p.Thr707=) n.3921C= n.3925C= | |
1 | g.1048114C>G | CA337852708 | AGRN | c.3854C>G (p.Thr1285Ser) c.3539C>G (p.Thr1180Ser) c.3440C>G (p.Thr1147Ser) c.2981C>G (p.Thr994Ser) c.2120C>G (p.Thr707Ser) n.3921C>G n.3925C>G | |
1 | g.1048114C>T | CA337852710 | AGRN | c.3854C>T (p.Thr1285Ile) c.3539C>T (p.Thr1180Ile) c.3440C>T (p.Thr1147Ile) c.2981C>T (p.Thr994Ile) c.2120C>T (p.Thr707Ile) n.3921C>T n.3925C>T | dbSNP gnomAD v2 gnomAD v4 |
1 | g.1048115C>A | CA509260 | AGRN | c.3855C>A (p.Thr1285=) c.3540C>A (p.Thr1180=) c.3441C>A (p.Thr1147=) c.2982C>A (p.Thr994=) c.2121C>A (p.Thr707=) n.3922C>A n.3926C>A | dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.1048115C= | CA1148803877 | AGRN | c.3855C= (p.Thr1285=) c.3540C= (p.Thr1180=) c.3441C= (p.Thr1147=) c.2982C= (p.Thr994=) c.2121C= (p.Thr707=) n.3922C= n.3926C= | |
1 | g.1048115C>G | CA415758148 | AGRN | c.3855C>G (p.Thr1285=) c.3540C>G (p.Thr1180=) c.3441C>G (p.Thr1147=) c.2982C>G (p.Thr994=) c.2121C>G (p.Thr707=) n.3922C>G n.3926C>G | |
1 | g.1048115C>T | CA415758151 | AGRN | c.3855C>T (p.Thr1285=) c.3540C>T (p.Thr1180=) c.3441C>T (p.Thr1147=) c.2982C>T (p.Thr994=) c.2121C>T (p.Thr707=) n.3922C>T n.3926C>T | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.1048116C>A | CA337852711 | AGRN | c.3856C>A (p.Pro1286Thr) c.3541C>A (p.Pro1181Thr) c.3442C>A (p.Pro1148Thr) c.2983C>A (p.Pro995Thr) c.2122C>A (p.Pro708Thr) n.3923C>A n.3927C>A | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.1048116C= | CA1148803904 | AGRN | c.3856C= (p.Pro1286=) c.3541C= (p.Pro1181=) c.3442C= (p.Pro1148=) c.2983C= (p.Pro995=) c.2122C= (p.Pro708=) n.3923C= n.3927C= | |
1 | g.1048116C>G | CA337852713 | AGRN | c.3856C>G (p.Pro1286Ala) c.3541C>G (p.Pro1181Ala) c.3442C>G (p.Pro1148Ala) c.2983C>G (p.Pro995Ala) c.2122C>G (p.Pro708Ala) n.3923C>G n.3927C>G | |
1 | g.1048116C>T | CA509261 | AGRN | c.3856C>T (p.Pro1286Ser) c.3541C>T (p.Pro1181Ser) c.3442C>T (p.Pro1148Ser) c.2983C>T (p.Pro995Ser) c.2122C>T (p.Pro708Ser) n.3923C>T n.3927C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.1048117C>A | CA509262 | AGRN | c.3857C>A (p.Pro1286His) c.3542C>A (p.Pro1181His) c.3443C>A (p.Pro1148His) c.2984C>A (p.Pro995His) c.2123C>A (p.Pro708His) n.3924C>A n.3928C>A | dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.1048117C= | CA1148803911 | AGRN | c.3857C= (p.Pro1286=) c.3542C= (p.Pro1181=) c.3443C= (p.Pro1148=) c.2984C= (p.Pro995=) c.2123C= (p.Pro708=) n.3924C= n.3928C= | |
1 | g.1048117C>G | CA337852718 | AGRN | c.3857C>G (p.Pro1286Arg) c.3542C>G (p.Pro1181Arg) c.3443C>G (p.Pro1148Arg) c.2984C>G (p.Pro995Arg) c.2123C>G (p.Pro708Arg) n.3924C>G n.3928C>G | dbSNP gnomAD v4 |
1 | g.1048117C>T | CA337852716 | AGRN | c.3857C>T (p.Pro1286Leu) c.3542C>T (p.Pro1181Leu) c.3443C>T (p.Pro1148Leu) c.2984C>T (p.Pro995Leu) c.2123C>T (p.Pro708Leu) n.3924C>T n.3928C>T | |
1 | g.1048118T>A | CA415758156 | AGRN | c.3858T>A (p.Pro1286=) c.3543T>A (p.Pro1181=) c.3444T>A (p.Pro1148=) c.2985T>A (p.Pro995=) c.2124T>A (p.Pro708=) n.3925T>A n.3929T>A | |
1 | g.1048118T>C | CA415758159 | AGRN | c.3858T>C (p.Pro1286=) c.3543T>C (p.Pro1181=) c.3444T>C (p.Pro1148=) c.2985T>C (p.Pro995=) c.2124T>C (p.Pro708=) n.3925T>C n.3929T>C | gnomAD v4 |
1 | g.1048118T>G | CA415758158 | AGRN | c.3858T>G (p.Pro1286=) c.3543T>G (p.Pro1181=) c.3444T>G (p.Pro1148=) c.2985T>G (p.Pro995=) c.2124T>G (p.Pro708=) n.3925T>G n.3929T>G | |
1 | g.1048119C>A | CA415758162 | AGRN | c.3859C>A (p.Arg1287=) c.3544C>A (p.Arg1182=) c.3445C>A (p.Arg1149=) c.2986C>A (p.Arg996=) c.2125C>A (p.Arg709=) n.3926C>A n.3930C>A | gnomAD v4 |
1 | g.1048119C= | CA1148803921 | AGRN | c.3859C= (p.Arg1287=) c.3544C= (p.Arg1182=) c.3445C= (p.Arg1149=) c.2986C= (p.Arg996=) c.2125C= (p.Arg709=) n.3926C= n.3930C= | |
1 | g.1048119C>G | CA337852720 | AGRN | c.3859C>G (p.Arg1287Gly) c.3544C>G (p.Arg1182Gly) c.3445C>G (p.Arg1149Gly) c.2986C>G (p.Arg996Gly) c.2125C>G (p.Arg709Gly) n.3926C>G n.3930C>G | |
1 | g.1048119C>T | CA509263 | AGRN | c.3859C>T (p.Arg1287Trp) c.3544C>T (p.Arg1182Trp) c.3445C>T (p.Arg1149Trp) c.2986C>T (p.Arg996Trp) c.2125C>T (p.Arg709Trp) n.3926C>T n.3930C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.1048120G>A | CA337852723 | AGRN | c.3860G>A (p.Arg1287Gln) c.3545G>A (p.Arg1182Gln) c.3446G>A (p.Arg1149Gln) c.2987G>A (p.Arg996Gln) c.2126G>A (p.Arg709Gln) n.3927G>A n.3931G>A | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
1 | g.1048120G>C | CA337852725 | AGRN | c.3860G>C (p.Arg1287Pro) c.3545G>C (p.Arg1182Pro) c.3446G>C (p.Arg1149Pro) c.2987G>C (p.Arg996Pro) c.2126G>C (p.Arg709Pro) n.3927G>C n.3931G>C | |
1 | g.1048120G= | CA1148803938 | AGRN | c.3860G= (p.Arg1287=) c.3545G= (p.Arg1182=) c.3446G= (p.Arg1149=) c.2987G= (p.Arg996=) c.2126G= (p.Arg709=) n.3927G= n.3931G= | |
1 | g.1048120G>T | CA337852726 | AGRN | c.3860G>T (p.Arg1287Leu) c.3545G>T (p.Arg1182Leu) c.3446G>T (p.Arg1149Leu) c.2987G>T (p.Arg996Leu) c.2126G>T (p.Arg709Leu) n.3927G>T n.3931G>T | gnomAD v4 |
1 | g.1048121G>A | CA509264 | AGRN | c.3861G>A (p.Arg1287=) c.3546G>A (p.Arg1182=) c.3447G>A (p.Arg1149=) c.2988G>A (p.Arg996=) c.2127G>A (p.Arg709=) n.3928G>A n.3932G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.1048121G>C | CA415758169 | AGRN | c.3861G>C (p.Arg1287=) c.3546G>C (p.Arg1182=) c.3447G>C (p.Arg1149=) c.2988G>C (p.Arg996=) c.2127G>C (p.Arg709=) n.3928G>C n.3932G>C | gnomAD v4 |
1 | g.1048121G= | CA1148803965 | AGRN | c.3861G= (p.Arg1287=) c.3546G= (p.Arg1182=) c.3447G= (p.Arg1149=) c.2988G= (p.Arg996=) c.2127G= (p.Arg709=) n.3928G= n.3932G= | |
1 | g.1048121G>T | CA415758171 | AGRN | c.3861G>T (p.Arg1287=) c.3546G>T (p.Arg1182=) c.3447G>T (p.Arg1149=) c.2988G>T (p.Arg996=) c.2127G>T (p.Arg709=) n.3928G>T n.3932G>T | gnomAD v4 |
1 | g.1048122G>A | CA337852747 | AGRN | c.3862G>A (p.Ala1288Thr) c.3547G>A (p.Ala1183Thr) c.3448G>A (p.Ala1150Thr) c.2989G>A (p.Ala997Thr) c.2128G>A (p.Ala710Thr) n.3929G>A n.3933G>A | gnomAD v4 |
1 | g.1048122G>C | CA337852727 | AGRN | c.3862G>C (p.Ala1288Pro) c.3547G>C (p.Ala1183Pro) c.3448G>C (p.Ala1150Pro) c.2989G>C (p.Ala997Pro) c.2128G>C (p.Ala710Pro) n.3929G>C n.3933G>C | |
1 | g.1048122G>T | CA337852754 | AGRN | c.3862G>T (p.Ala1288Ser) c.3547G>T (p.Ala1183Ser) c.3448G>T (p.Ala1150Ser) c.2989G>T (p.Ala997Ser) c.2128G>T (p.Ala710Ser) n.3929G>T n.3933G>T | gnomAD v4 |
1 | g.1048123C>A | CA337852757 | AGRN | c.3863C>A (p.Ala1288Asp) c.3548C>A (p.Ala1183Asp) c.3449C>A (p.Ala1150Asp) c.2990C>A (p.Ala997Asp) c.2129C>A (p.Ala710Asp) n.3930C>A n.3934C>A | gnomAD v4 |
1 | g.1048123C>G | CA337852761 | AGRN | c.3863C>G (p.Ala1288Gly) c.3548C>G (p.Ala1183Gly) c.3449C>G (p.Ala1150Gly) c.2990C>G (p.Ala997Gly) c.2129C>G (p.Ala710Gly) n.3930C>G n.3934C>G | |
1 | g.1048123C>T | CA337852759 | AGRN | c.3863C>T (p.Ala1288Val) c.3548C>T (p.Ala1183Val) c.3449C>T (p.Ala1150Val) c.2990C>T (p.Ala997Val) c.2129C>T (p.Ala710Val) n.3930C>T n.3934C>T | gnomAD v4 |
1 | g.1048126del | CA2574258706 | AGRN | c.3866del (p.Pro1289ArgfsTer?) c.3551del (p.Pro1184ArgfsTer?) c.3452del (p.Pro1151ArgfsTer?) c.2993del (p.Pro998ArgfsTer?) c.2132del (p.Pro711ArgfsTer?) n.3933del n.3937del | gnomAD v4 |
1 | g.1048124C>A | CA415758173 | AGRN | c.3864C>A (p.Ala1288=) c.3549C>A (p.Ala1183=) c.3450C>A (p.Ala1150=) c.2991C>A (p.Ala997=) c.2130C>A (p.Ala710=) n.3931C>A n.3935C>A | |
1 | g.1048124C>G | CA415758175 | AGRN | c.3864C>G (p.Ala1288=) c.3549C>G (p.Ala1183=) c.3450C>G (p.Ala1150=) c.2991C>G (p.Ala997=) c.2130C>G (p.Ala710=) n.3931C>G n.3935C>G | |
1 | g.1048124C>T | CA415758176 | AGRN | c.3864C>T (p.Ala1288=) c.3549C>T (p.Ala1183=) c.3450C>T (p.Ala1150=) c.2991C>T (p.Ala997=) c.2130C>T (p.Ala710=) n.3931C>T n.3935C>T | ClinVar |
1 | g.1048125C>A | CA337852762 | AGRN | c.3865C>A (p.Pro1289Thr) c.3550C>A (p.Pro1184Thr) c.3451C>A (p.Pro1151Thr) c.2992C>A (p.Pro998Thr) c.2131C>A (p.Pro711Thr) n.3932C>A n.3936C>A | gnomAD v4 |
1 | g.1048125C>G | CA337852763 | AGRN | c.3865C>G (p.Pro1289Ala) c.3550C>G (p.Pro1184Ala) c.3451C>G (p.Pro1151Ala) c.2992C>G (p.Pro998Ala) c.2131C>G (p.Pro711Ala) n.3932C>G n.3936C>G | |
1 | g.1048125C>T | CA337852764 | AGRN | c.3865C>T (p.Pro1289Ser) c.3550C>T (p.Pro1184Ser) c.3451C>T (p.Pro1151Ser) c.2992C>T (p.Pro998Ser) c.2131C>T (p.Pro711Ser) n.3932C>T n.3936C>T | ClinVar dbSNP gnomAD v4 |
1 | g.1048126C>A | CA337852765 | AGRN | c.3866C>A (p.Pro1289Gln) c.3551C>A (p.Pro1184Gln) c.3452C>A (p.Pro1151Gln) c.2993C>A (p.Pro998Gln) c.2132C>A (p.Pro711Gln) n.3933C>A n.3937C>A | gnomAD v4 |
1 | g.1048126C= | CA1141670886 | AGRN | c.3866C= (p.Pro1289=) c.3551C= (p.Pro1184=) c.3452C= (p.Pro1151=) c.2993C= (p.Pro998=) c.2132C= (p.Pro711=) n.3933C= n.3937C= | |
1 | g.1048126C>G | CA337852766 | AGRN | c.3866C>G (p.Pro1289Arg) c.3551C>G (p.Pro1184Arg) c.3452C>G (p.Pro1151Arg) c.2993C>G (p.Pro998Arg) c.2132C>G (p.Pro711Arg) n.3933C>G n.3937C>G | gnomAD v4 |
1 | g.1048126C>T | CA151645 | AGRN | c.3866C>T (p.Pro1289Leu) c.3551C>T (p.Pro1184Leu) c.3452C>T (p.Pro1151Leu) c.2993C>T (p.Pro998Leu) c.2132C>T (p.Pro711Leu) n.3933C>T n.3937C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.1048127G>A | CA509265 | AGRN | c.3867G>A (p.Pro1289=) c.3552G>A (p.Pro1184=) c.3453G>A (p.Pro1151=) c.2994G>A (p.Pro998=) c.2133G>A (p.Pro711=) n.3934G>A n.3938G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.1048127G>C | CA415758185 | AGRN | c.3867G>C (p.Pro1289=) c.3552G>C (p.Pro1184=) c.3453G>C (p.Pro1151=) c.2994G>C (p.Pro998=) c.2133G>C (p.Pro711=) n.3934G>C n.3938G>C | |
1 | g.1048127G= | CA1143833067 | AGRN | c.3867G= (p.Pro1289=) c.3552G= (p.Pro1184=) c.3453G= (p.Pro1151=) c.2994G= (p.Pro998=) c.2133G= (p.Pro711=) n.3934G= n.3938G= | |
1 | g.1048127G>T | CA415758183 | AGRN | c.3867G>T (p.Pro1289=) c.3552G>T (p.Pro1184=) c.3453G>T (p.Pro1151=) c.2994G>T (p.Pro998=) c.2133G>T (p.Pro711=) n.3934G>T n.3938G>T | gnomAD v4 |
1 | g.1048128C>A | CA337852767 | AGRN | c.3868C>A (p.His1290Asn) c.3553C>A (p.His1185Asn) c.3454C>A (p.His1152Asn) c.2995C>A (p.His999Asn) c.2134C>A (p.His712Asn) n.3935C>A n.3939C>A | gnomAD v4 |
1 | g.1048128C>G | CA337852770 | AGRN | c.3868C>G (p.His1290Asp) c.3553C>G (p.His1185Asp) c.3454C>G (p.His1152Asp) c.2995C>G (p.His999Asp) c.2134C>G (p.His712Asp) n.3935C>G n.3939C>G | |
1 | g.1048128C>T | CA337852773 | AGRN | c.3868C>T (p.His1290Tyr) c.3553C>T (p.His1185Tyr) c.3454C>T (p.His1152Tyr) c.2995C>T (p.His999Tyr) c.2134C>T (p.His712Tyr) n.3935C>T n.3939C>T | |
1 | g.1048129A= | CA1148803998 | AGRN | c.3869A= (p.His1290=) c.3554A= (p.His1185=) c.3455A= (p.His1152=) c.2996A= (p.His999=) c.2135A= (p.His712=) n.3936A= n.3940A= | |
1 | g.1048129A>C | CA509266 | AGRN | c.3869A>C (p.His1290Pro) c.3554A>C (p.His1185Pro) c.3455A>C (p.His1152Pro) c.2996A>C (p.His999Pro) c.2135A>C (p.His712Pro) n.3936A>C n.3940A>C | dbSNP ExAC gnomAD v4 |
1 | g.1048129A>G | CA337852777 | AGRN | c.3869A>G (p.His1290Arg) c.3554A>G (p.His1185Arg) c.3455A>G (p.His1152Arg) c.2996A>G (p.His999Arg) c.2135A>G (p.His712Arg) n.3936A>G n.3940A>G | dbSNP gnomAD v2 gnomAD v4 |
1 | g.1048129A>T | CA337852774 | AGRN | c.3869A>T (p.His1290Leu) c.3554A>T (p.His1185Leu) c.3455A>T (p.His1152Leu) c.2996A>T (p.His999Leu) c.2135A>T (p.His712Leu) n.3936A>T n.3940A>T | |
1 | g.1048130C>A | CA337852794 | AGRN | c.3870C>A (p.His1290Gln) c.3555C>A (p.His1185Gln) c.3456C>A (p.His1152Gln) c.2997C>A (p.His999Gln) c.2136C>A (p.His712Gln) n.3937C>A n.3941C>A | ClinVar dbSNP |
1 | g.1048130C= | CA1148804004 | AGRN | c.3870C= (p.His1290=) c.3555C= (p.His1185=) c.3456C= (p.His1152=) c.2997C= (p.His999=) c.2136C= (p.His712=) n.3937C= n.3941C= | |
1 | g.1048130C>G | CA337852798 | AGRN | c.3870C>G (p.His1290Gln) c.3555C>G (p.His1185Gln) c.3456C>G (p.His1152Gln) c.2997C>G (p.His999Gln) c.2136C>G (p.His712Gln) n.3937C>G n.3941C>G | |
1 | g.1048130C>T | CA415758194 | AGRN | c.3870C>T (p.His1290=) c.3555C>T (p.His1185=) c.3456C>T (p.His1152=) c.2997C>T (p.His999=) c.2136C>T (p.His712=) n.3937C>T n.3941C>T | dbSNP gnomAD v3 gnomAD v4 |
1 | g.1048131C>A | CA337852799 | AGRN | c.3871C>A (p.Pro1291Thr) c.3556C>A (p.Pro1186Thr) c.3457C>A (p.Pro1153Thr) c.2998C>A (p.Pro1000Thr) c.2137C>A (p.Pro713Thr) n.3938C>A n.3942C>A | gnomAD v4 |
1 | g.1048131C>G | CA337852801 | AGRN | c.3871C>G (p.Pro1291Ala) c.3556C>G (p.Pro1186Ala) c.3457C>G (p.Pro1153Ala) c.2998C>G (p.Pro1000Ala) c.2137C>G (p.Pro713Ala) n.3938C>G n.3942C>G | gnomAD v4 |
1 | g.1048131C>T | CA337852803 | AGRN | c.3871C>T (p.Pro1291Ser) c.3556C>T (p.Pro1186Ser) c.3457C>T (p.Pro1153Ser) c.2998C>T (p.Pro1000Ser) c.2137C>T (p.Pro713Ser) n.3938C>T n.3942C>T | gnomAD v4 |
1 | g.1048132C>A | CA337852804 | AGRN | c.3872C>A (p.Pro1291His) c.3557C>A (p.Pro1186His) c.3458C>A (p.Pro1153His) c.2999C>A (p.Pro1000His) c.2138C>A (p.Pro713His) n.3939C>A n.3943C>A | gnomAD v4 |
1 | g.1048132C= | CA1148804029 | AGRN | c.3872C= (p.Pro1291=) c.3557C= (p.Pro1186=) c.3458C= (p.Pro1153=) c.2999C= (p.Pro1000=) c.2138C= (p.Pro713=) n.3939C= n.3943C= | |
1 | g.1048132C>G | CA337852805 | AGRN | c.3872C>G (p.Pro1291Arg) c.3557C>G (p.Pro1186Arg) c.3458C>G (p.Pro1153Arg) c.2999C>G (p.Pro1000Arg) c.2138C>G (p.Pro713Arg) n.3939C>G n.3943C>G | dbSNP gnomAD v2 |
1 | g.1048132C>T | CA337852806 | AGRN | c.3872C>T (p.Pro1291Leu) c.3557C>T (p.Pro1186Leu) c.3458C>T (p.Pro1153Leu) c.2999C>T (p.Pro1000Leu) c.2138C>T (p.Pro713Leu) n.3939C>T n.3943C>T | gnomAD v4 |
1 | g.1048133C>A | CA415758203 | AGRN | c.3873C>A (p.Pro1291=) c.3558C>A (p.Pro1186=) c.3459C>A (p.Pro1153=) c.3000C>A (p.Pro1000=) c.2139C>A (p.Pro713=) n.3940C>A n.3944C>A | gnomAD v4 |
1 | g.1048133C>G | CA415758206 | AGRN | c.3873C>G (p.Pro1291=) c.3558C>G (p.Pro1186=) c.3459C>G (p.Pro1153=) c.3000C>G (p.Pro1000=) c.2139C>G (p.Pro713=) n.3940C>G n.3944C>G | gnomAD v4 |
1 | g.1048133C>T | CA415758207 | AGRN | c.3873C>T (p.Pro1291=) c.3558C>T (p.Pro1186=) c.3459C>T (p.Pro1153=) c.3000C>T (p.Pro1000=) c.2139C>T (p.Pro713=) n.3940C>T n.3944C>T | gnomAD v4 |
1 | g.1048134A>C | CA337852807 | AGRN | c.3874A>C (p.Ser1292Arg) c.3559A>C (p.Ser1187Arg) c.3460A>C (p.Ser1154Arg) c.3001A>C (p.Ser1001Arg) c.2140A>C (p.Ser714Arg) n.3941A>C n.3945A>C | dbSNP |
1 | g.1048134A>G | CA337852808 | AGRN | c.3874A>G (p.Ser1292Gly) c.3559A>G (p.Ser1187Gly) c.3460A>G (p.Ser1154Gly) c.3001A>G (p.Ser1001Gly) c.2140A>G (p.Ser714Gly) n.3941A>G n.3945A>G | gnomAD v4 |
1 | g.1048134A>T | CA337852809 | AGRN | c.3874A>T (p.Ser1292Cys) c.3559A>T (p.Ser1187Cys) c.3460A>T (p.Ser1154Cys) c.3001A>T (p.Ser1001Cys) c.2140A>T (p.Ser714Cys) n.3941A>T n.3945A>T | |
1 | g.1048135G>A | CA337852812 | AGRN | c.3875G>A (p.Ser1292Asn) c.3560G>A (p.Ser1187Asn) c.3461G>A (p.Ser1154Asn) c.3002G>A (p.Ser1001Asn) c.2141G>A (p.Ser714Asn) n.3942G>A n.3946G>A | dbSNP gnomAD v2 |
1 | g.1048135G>C | CA337852814 | AGRN | c.3875G>C (p.Ser1292Thr) c.3560G>C (p.Ser1187Thr) c.3461G>C (p.Ser1154Thr) c.3002G>C (p.Ser1001Thr) c.2141G>C (p.Ser714Thr) n.3942G>C n.3946G>C | |
1 | g.1048135G= | CA1148804030 | AGRN | c.3875G= (p.Ser1292=) c.3560G= (p.Ser1187=) c.3461G= (p.Ser1154=) c.3002G= (p.Ser1001=) c.2141G= (p.Ser714=) n.3942G= n.3946G= | |
1 | g.1048135G>T | CA337852810 | AGRN | c.3875G>T (p.Ser1292Ile) c.3560G>T (p.Ser1187Ile) c.3461G>T (p.Ser1154Ile) c.3002G>T (p.Ser1001Ile) c.2141G>T (p.Ser714Ile) n.3942G>T n.3946G>T | gnomAD v4 |
1 | g.1048136T>A | CA337852816 | AGRN | c.3876T>A (p.Ser1292Arg) c.3561T>A (p.Ser1187Arg) c.3462T>A (p.Ser1154Arg) c.3003T>A (p.Ser1001Arg) c.2142T>A (p.Ser714Arg) n.3943T>A n.3947T>A | gnomAD v4 |
1 | g.1048136T>C | CA415758208 | AGRN | c.3876T>C (p.Ser1292=) c.3561T>C (p.Ser1187=) c.3462T>C (p.Ser1154=) c.3003T>C (p.Ser1001=) c.2142T>C (p.Ser714=) n.3943T>C n.3947T>C | gnomAD v4 |
1 | g.1048136T>G | CA337852818 | AGRN | c.3876T>G (p.Ser1292Arg) c.3561T>G (p.Ser1187Arg) c.3462T>G (p.Ser1154Arg) c.3003T>G (p.Ser1001Arg) c.2142T>G (p.Ser714Arg) n.3943T>G n.3947T>G | |
1 | g.1048136_1048138delinsTCA | CA1148804032 | AGRN | c.3876_3878delinsTCA (p.Ser1292=) c.3561_3563delinsTCA (p.Ser1187=) c.3462_3464delinsTCA (p.Ser1154=) c.3003_3005delinsTCA (p.Ser1001=) c.2142_2144delinsTCA (p.Ser714=) n.3943_3945delinsTCA n.3947_3949delinsTCA | |
1 | g.1048137C>A | CA337852823 | AGRN | c.3877C>A (p.His1293Asn) c.3562C>A (p.His1188Asn) c.3463C>A (p.His1155Asn) c.3004C>A (p.His1002Asn) c.2143C>A (p.His715Asn) n.3944C>A n.3948C>A | gnomAD v4 |
1 | g.1048137C>G | CA337852824 | AGRN | c.3877C>G (p.His1293Asp) c.3562C>G (p.His1188Asp) c.3463C>G (p.His1155Asp) c.3004C>G (p.His1002Asp) c.2143C>G (p.His715Asp) n.3944C>G n.3948C>G | |
1 | g.1048137C>T | CA337852826 | AGRN | c.3877C>T (p.His1293Tyr) c.3562C>T (p.His1188Tyr) c.3463C>T (p.His1155Tyr) c.3004C>T (p.His1002Tyr) c.2143C>T (p.His715Tyr) n.3944C>T n.3948C>T | gnomAD v4 |
1 | g.1048141_1048142del | CA997654956 | AGRN | c.3881_3882del (p.Thr1294LysfsTer?) c.3566_3567del (p.Thr1189LysfsTer?) c.3467_3468del (p.Thr1156LysfsTer?) c.3008_3009del (p.Thr1003LysfsTer?) c.2147_2148del (p.Thr716LysfsTer?) n.3948_3949del n.3952_3953del | dbSNP gnomAD v3 gnomAD v4 |
1 | g.1048138A>C | CA337852831 | AGRN | c.3878A>C (p.His1293Pro) c.3563A>C (p.His1188Pro) c.3464A>C (p.His1155Pro) c.3005A>C (p.His1002Pro) c.2144A>C (p.His715Pro) n.3945A>C n.3949A>C | |
1 | g.1048138A>G | CA337852827 | AGRN | c.3878A>G (p.His1293Arg) c.3563A>G (p.His1188Arg) c.3464A>G (p.His1155Arg) c.3005A>G (p.His1002Arg) c.2144A>G (p.His715Arg) n.3945A>G n.3949A>G | |
1 | g.1048138A>T | CA337852828 | AGRN | c.3878A>T (p.His1293Leu) c.3563A>T (p.His1188Leu) c.3464A>T (p.His1155Leu) c.3005A>T (p.His1002Leu) c.2144A>T (p.His715Leu) n.3945A>T n.3949A>T | gnomAD v4 |
1 | g.1048139C>A | CA337852833 | AGRN | c.3879C>A (p.His1293Gln) c.3564C>A (p.His1188Gln) c.3465C>A (p.His1155Gln) c.3006C>A (p.His1002Gln) c.2145C>A (p.His715Gln) n.3946C>A n.3950C>A | |
1 | g.1048139C>G | CA337852835 | AGRN | c.3879C>G (p.His1293Gln) c.3564C>G (p.His1188Gln) c.3465C>G (p.His1155Gln) c.3006C>G (p.His1002Gln) c.2145C>G (p.His715Gln) n.3946C>G n.3950C>G | |
1 | g.1048139C>T | CA415758217 | AGRN | c.3879C>T (p.His1293=) c.3564C>T (p.His1188=) c.3465C>T (p.His1155=) c.3006C>T (p.His1002=) c.2145C>T (p.His715=) n.3946C>T n.3950C>T | |
1 | g.1048140A>C | CA337852848 | AGRN | c.3880A>C (p.Thr1294Pro) c.3565A>C (p.Thr1189Pro) c.3466A>C (p.Thr1156Pro) c.3007A>C (p.Thr1003Pro) c.2146A>C (p.Thr716Pro) n.3947A>C n.3951A>C | |
1 | g.1048140A>G | CA337852850 | AGRN | c.3880A>G (p.Thr1294Ala) c.3565A>G (p.Thr1189Ala) c.3466A>G (p.Thr1156Ala) c.3007A>G (p.Thr1003Ala) c.2146A>G (p.Thr716Ala) n.3947A>G n.3951A>G | |
1 | g.1048140A>T | CA337852852 | AGRN | c.3880A>T (p.Thr1294Ser) c.3565A>T (p.Thr1189Ser) c.3466A>T (p.Thr1156Ser) c.3007A>T (p.Thr1003Ser) c.2146A>T (p.Thr716Ser) n.3947A>T n.3951A>T | |
1 | g.1048141C>A | CA337852854 | AGRN | c.3881C>A (p.Thr1294Lys) c.3566C>A (p.Thr1189Lys) c.3467C>A (p.Thr1156Lys) c.3008C>A (p.Thr1003Lys) c.2147C>A (p.Thr716Lys) n.3948C>A n.3952C>A | gnomAD v4 |
1 | g.1048141C= | CA1148804039 | AGRN | c.3881C= (p.Thr1294=) c.3566C= (p.Thr1189=) c.3467C= (p.Thr1156=) c.3008C= (p.Thr1003=) c.2147C= (p.Thr716=) n.3948C= n.3952C= | |
1 | g.1048141C>G | CA337852858 | AGRN | c.3881C>G (p.Thr1294Arg) c.3566C>G (p.Thr1189Arg) c.3467C>G (p.Thr1156Arg) c.3008C>G (p.Thr1003Arg) c.2147C>G (p.Thr716Arg) n.3948C>G n.3952C>G | ClinVar |
1 | g.1048141C>T | CA337852856 | AGRN | c.3881C>T (p.Thr1294Ile) c.3566C>T (p.Thr1189Ile) c.3467C>T (p.Thr1156Ile) c.3008C>T (p.Thr1003Ile) c.2147C>T (p.Thr716Ile) n.3948C>T n.3952C>T | dbSNP gnomAD v4 |
1 | g.1048142A= | CA1148804046 | AGRN | c.3882A= (p.Thr1294=) c.3567A= (p.Thr1189=) c.3468A= (p.Thr1156=) c.3009A= (p.Thr1003=) c.2148A= (p.Thr716=) n.3949A= n.3953A= | |
1 | g.1048142A>C | CA415758226 | AGRN | c.3882A>C (p.Thr1294=) c.3567A>C (p.Thr1189=) c.3468A>C (p.Thr1156=) c.3009A>C (p.Thr1003=) c.2148A>C (p.Thr716=) n.3949A>C n.3953A>C | |
1 | g.1048142A>G | CA415758224 | AGRN | c.3882A>G (p.Thr1294=) c.3567A>G (p.Thr1189=) c.3468A>G (p.Thr1156=) c.3009A>G (p.Thr1003=) c.2148A>G (p.Thr716=) n.3949A>G n.3953A>G | dbSNP gnomAD v3 gnomAD v4 |
1 | g.1048142A>T | CA415758223 | AGRN | c.3882A>T (p.Thr1294=) c.3567A>T (p.Thr1189=) c.3468A>T (p.Thr1156=) c.3009A>T (p.Thr1003=) c.2148A>T (p.Thr716=) n.3949A>T n.3953A>T | |
1 | g.1048143A>C | CA337852860 | AGRN | c.3883A>C (p.Ser1295Arg) c.3568A>C (p.Ser1190Arg) c.3469A>C (p.Ser1157Arg) c.3010A>C (p.Ser1004Arg) c.2149A>C (p.Ser717Arg) n.3950A>C n.3954A>C | |
1 | g.1048143A>G | CA337852861 | AGRN | c.3883A>G (p.Ser1295Gly) c.3568A>G (p.Ser1190Gly) c.3469A>G (p.Ser1157Gly) c.3010A>G (p.Ser1004Gly) c.2149A>G (p.Ser717Gly) n.3950A>G n.3954A>G | gnomAD v4 |
1 | g.1048143A>T | CA337852864 | AGRN | c.3883A>T (p.Ser1295Cys) c.3568A>T (p.Ser1190Cys) c.3469A>T (p.Ser1157Cys) c.3010A>T (p.Ser1004Cys) c.2149A>T (p.Ser717Cys) n.3950A>T n.3954A>T | |
1 | g.1048144G>A | CA337852869 | AGRN | c.3884G>A (p.Ser1295Asn) c.3569G>A (p.Ser1190Asn) c.3470G>A (p.Ser1157Asn) c.3011G>A (p.Ser1004Asn) c.2150G>A (p.Ser717Asn) n.3951G>A n.3955G>A | dbSNP gnomAD v3 gnomAD v4 |
1 | g.1048144G>C | CA509267 | AGRN | c.3884G>C (p.Ser1295Thr) c.3569G>C (p.Ser1190Thr) c.3470G>C (p.Ser1157Thr) c.3011G>C (p.Ser1004Thr) c.2150G>C (p.Ser717Thr) n.3951G>C n.3955G>C | dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.1048144G= | CA1148804089 | AGRN | c.3884G= (p.Ser1295=) c.3569G= (p.Ser1190=) c.3470G= (p.Ser1157=) c.3011G= (p.Ser1004=) c.2150G= (p.Ser717=) n.3951G= n.3955G= | |
1 | g.1048144G>T | CA337852879 | AGRN | c.3884G>T (p.Ser1295Ile) c.3569G>T (p.Ser1190Ile) c.3470G>T (p.Ser1157Ile) c.3011G>T (p.Ser1004Ile) c.2150G>T (p.Ser717Ile) n.3951G>T n.3955G>T | gnomAD v4 |
1 | g.1048145C>A | CA337852880 | AGRN | c.3885C>A (p.Ser1295Arg) c.3570C>A (p.Ser1190Arg) c.3471C>A (p.Ser1157Arg) c.3012C>A (p.Ser1004Arg) c.2151C>A (p.Ser717Arg) n.3952C>A n.3956C>A | gnomAD v4 |
1 | g.1048145C= | CA1148804098 | AGRN | c.3885C= (p.Ser1295=) c.3570C= (p.Ser1190=) c.3471C= (p.Ser1157=) c.3012C= (p.Ser1004=) c.2151C= (p.Ser717=) n.3952C= n.3956C= | |
1 | g.1048145C>G | CA337852881 | AGRN | c.3885C>G (p.Ser1295Arg) c.3570C>G (p.Ser1190Arg) c.3471C>G (p.Ser1157Arg) c.3012C>G (p.Ser1004Arg) c.2151C>G (p.Ser717Arg) n.3952C>G n.3956C>G | dbSNP gnomAD v2 |
1 | g.1048145C>T | CA509268 | AGRN | c.3885C>T (p.Ser1295=) c.3570C>T (p.Ser1190=) c.3471C>T (p.Ser1157=) c.3012C>T (p.Ser1004=) c.2151C>T (p.Ser717=) n.3952C>T n.3956C>T | dbSNP ExAC gnomAD v4 |
1 | g.1048146C>A | CA337852882 | AGRN | c.3886C>A (p.Gln1296Lys) c.3571C>A (p.Gln1191Lys) c.3472C>A (p.Gln1158Lys) c.3013C>A (p.Gln1005Lys) c.2152C>A (p.Gln718Lys) n.3953C>A n.3957C>A | gnomAD v4 |
1 | g.1048146C= | CA1148804104 | AGRN | c.3886C= (p.Gln1296=) c.3571C= (p.Gln1191=) c.3472C= (p.Gln1158=) c.3013C= (p.Gln1005=) c.2152C= (p.Gln718=) n.3953C= n.3957C= | |
1 | g.1048146C>G | CA337852884 | AGRN | c.3886C>G (p.Gln1296Glu) c.3571C>G (p.Gln1191Glu) c.3472C>G (p.Gln1158Glu) c.3013C>G (p.Gln1005Glu) c.2152C>G (p.Gln718Glu) n.3953C>G n.3957C>G | |
1 | g.1048146C>T | CA337852886 | AGRN | c.3886C>T (p.Gln1296Ter) c.3571C>T (p.Gln1191Ter) c.3472C>T (p.Gln1158Ter) c.3013C>T (p.Gln1005Ter) c.2152C>T (p.Gln718Ter) n.3953C>T n.3957C>T | dbSNP gnomAD v2 gnomAD v4 |
1 | g.1048147A>C | CA337852890 | AGRN | c.3887A>C (p.Gln1296Pro) c.3572A>C (p.Gln1191Pro) c.3473A>C (p.Gln1158Pro) c.3014A>C (p.Gln1005Pro) c.2153A>C (p.Gln718Pro) n.3954A>C n.3958A>C | |
1 | g.1048147A>G | CA337852894 | AGRN | c.3887A>G (p.Gln1296Arg) c.3572A>G (p.Gln1191Arg) c.3473A>G (p.Gln1158Arg) c.3014A>G (p.Gln1005Arg) c.2153A>G (p.Gln718Arg) n.3954A>G n.3958A>G | |
1 | g.1048147A>T | CA337852889 | AGRN | c.3887A>T (p.Gln1296Leu) c.3572A>T (p.Gln1191Leu) c.3473A>T (p.Gln1158Leu) c.3014A>T (p.Gln1005Leu) c.2153A>T (p.Gln718Leu) n.3954A>T n.3958A>T | |
1 | g.1048148G>A | CA415758239 | AGRN | c.3888G>A (p.Gln1296=) c.3573G>A (p.Gln1191=) c.3474G>A (p.Gln1158=) c.3015G>A (p.Gln1005=) c.2154G>A (p.Gln718=) n.3955G>A n.3959G>A | gnomAD v4 |
1 | g.1048148G>C | CA337852897 | AGRN | c.3888G>C (p.Gln1296His) c.3573G>C (p.Gln1191His) c.3474G>C (p.Gln1158His) c.3015G>C (p.Gln1005His) c.2154G>C (p.Gln718His) n.3955G>C n.3959G>C | |
1 | g.1048148G>T | CA337852900 | AGRN | c.3888G>T (p.Gln1296His) c.3573G>T (p.Gln1191His) c.3474G>T (p.Gln1158His) c.3015G>T (p.Gln1005His) c.2154G>T (p.Gln718His) n.3955G>T n.3959G>T | gnomAD v4 |
1 | g.1048149C>A | CA337852903 | AGRN | c.3889C>A (p.Pro1297Thr) c.3574C>A (p.Pro1192Thr) c.3475C>A (p.Pro1159Thr) c.3016C>A (p.Pro1006Thr) c.2155C>A (p.Pro719Thr) n.3956C>A n.3960C>A | gnomAD v4 |
1 | g.1048149C>G | CA337852906 | AGRN | c.3889C>G (p.Pro1297Ala) c.3574C>G (p.Pro1192Ala) c.3475C>G (p.Pro1159Ala) c.3016C>G (p.Pro1006Ala) c.2155C>G (p.Pro719Ala) n.3956C>G n.3960C>G | |
1 | g.1048149C>T | CA337852909 | AGRN | c.3889C>T (p.Pro1297Ser) c.3574C>T (p.Pro1192Ser) c.3475C>T (p.Pro1159Ser) c.3016C>T (p.Pro1006Ser) c.2155C>T (p.Pro719Ser) n.3956C>T n.3960C>T | dbSNP gnomAD v4 COSMIC |
1 | g.1048150C>A | CA337852918 | AGRN | c.3890C>A (p.Pro1297His) c.3575C>A (p.Pro1192His) c.3476C>A (p.Pro1159His) c.3017C>A (p.Pro1006His) c.2156C>A (p.Pro719His) n.3957C>A n.3961C>A | gnomAD v4 |
1 | g.1048150C>G | CA337852919 | AGRN | c.3890C>G (p.Pro1297Arg) c.3575C>G (p.Pro1192Arg) c.3476C>G (p.Pro1159Arg) c.3017C>G (p.Pro1006Arg) c.2156C>G (p.Pro719Arg) n.3957C>G n.3961C>G | |
1 | g.1048150C>T | CA337852920 | AGRN | c.3890C>T (p.Pro1297Leu) c.3575C>T (p.Pro1192Leu) c.3476C>T (p.Pro1159Leu) c.3017C>T (p.Pro1006Leu) c.2156C>T (p.Pro719Leu) n.3957C>T n.3961C>T | |
1 | g.1048151C>A | CA415758246 | AGRN | c.3891C>A (p.Pro1297=) c.3576C>A (p.Pro1192=) c.3477C>A (p.Pro1159=) c.3018C>A (p.Pro1006=) c.2157C>A (p.Pro719=) n.3958C>A n.3962C>A | dbSNP gnomAD v2 gnomAD v4 |
1 | g.1048151C= | CA1148804122 | AGRN | c.3891C= (p.Pro1297=) c.3576C= (p.Pro1192=) c.3477C= (p.Pro1159=) c.3018C= (p.Pro1006=) c.2157C= (p.Pro719=) n.3958C= n.3962C= | |
1 | g.1048151C>G | CA415758249 | AGRN | c.3891C>G (p.Pro1297=) c.3576C>G (p.Pro1192=) c.3477C>G (p.Pro1159=) c.3018C>G (p.Pro1006=) c.2157C>G (p.Pro719=) n.3958C>G n.3962C>G | |
1 | g.1048151C>T | CA16760233 | AGRN | c.3891C>T (p.Pro1297=) c.3576C>T (p.Pro1192=) c.3477C>T (p.Pro1159=) c.3018C>T (p.Pro1006=) c.2157C>T (p.Pro719=) n.3958C>T n.3962C>T | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.1048152G>A | CA16760236 | AGRN | c.3892G>A (p.Val1298Ile) c.3577G>A (p.Val1193Ile) c.3478G>A (p.Val1160Ile) c.3019G>A (p.Val1007Ile) c.2158G>A (p.Val720Ile) n.3959G>A n.3963G>A | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
1 | g.1048152G>C | CA337852921 | AGRN | c.3892G>C (p.Val1298Leu) c.3577G>C (p.Val1193Leu) c.3478G>C (p.Val1160Leu) c.3019G>C (p.Val1007Leu) c.2158G>C (p.Val720Leu) n.3959G>C n.3963G>C | |
1 | g.1048152G= | CA1148804129 | AGRN | c.3892G= (p.Val1298=) c.3577G= (p.Val1193=) c.3478G= (p.Val1160=) c.3019G= (p.Val1007=) c.2158G= (p.Val720=) n.3959G= n.3963G= | |
1 | g.1048152G>T | CA337852922 | AGRN | c.3892G>T (p.Val1298Phe) c.3577G>T (p.Val1193Phe) c.3478G>T (p.Val1160Phe) c.3019G>T (p.Val1007Phe) c.2158G>T (p.Val720Phe) n.3959G>T n.3963G>T | gnomAD v4 |
1 | g.1048153T>A | CA337852924 | AGRN | c.3893T>A (p.Val1298Asp) c.3578T>A (p.Val1193Asp) c.3479T>A (p.Val1160Asp) c.3020T>A (p.Val1007Asp) c.2159T>A (p.Val720Asp) n.3960T>A n.3964T>A | |
1 | g.1048153T>C | CA337852926 | AGRN | c.3893T>C (p.Val1298Ala) c.3578T>C (p.Val1193Ala) c.3479T>C (p.Val1160Ala) c.3020T>C (p.Val1007Ala) c.2159T>C (p.Val720Ala) n.3960T>C n.3964T>C | gnomAD v4 |
1 | g.1048153T>G | CA337852929 | AGRN | c.3893T>G (p.Val1298Gly) c.3578T>G (p.Val1193Gly) c.3479T>G (p.Val1160Gly) c.3020T>G (p.Val1007Gly) c.2159T>G (p.Val720Gly) n.3960T>G n.3964T>G | |
1 | g.1048154T>A | CA415758255 | AGRN | c.3894T>A (p.Val1298=) c.3579T>A (p.Val1193=) c.3480T>A (p.Val1160=) c.3021T>A (p.Val1007=) c.2160T>A (p.Val720=) n.3961T>A n.3965T>A | |
1 | g.1048154T>C | CA509270 | AGRN | c.3894T>C (p.Val1298=) c.3579T>C (p.Val1193=) c.3480T>C (p.Val1160=) c.3021T>C (p.Val1007=) c.2160T>C (p.Val720=) n.3961T>C n.3965T>C | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.1048154T>G | CA509269 | AGRN | c.3894T>G (p.Val1298=) c.3579T>G (p.Val1193=) c.3480T>G (p.Val1160=) c.3021T>G (p.Val1007=) c.2160T>G (p.Val720=) n.3961T>G n.3965T>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.1048154T= | CA1148804134 | AGRN | c.3894T= (p.Val1298=) c.3579T= (p.Val1193=) c.3480T= (p.Val1160=) c.3021T= (p.Val1007=) c.2160T= (p.Val720=) n.3961T= n.3965T= | |
1 | g.1048155G>A | CA16760241 | AGRN | c.3895G>A (p.Ala1299Thr) c.3580G>A (p.Ala1194Thr) c.3481G>A (p.Ala1161Thr) c.3022G>A (p.Ala1008Thr) c.2161G>A (p.Ala721Thr) n.3962G>A n.3966G>A | dbSNP gnomAD v2 gnomAD v4 |
1 | g.1048155G>C | CA337852934 | AGRN | c.3895G>C (p.Ala1299Pro) c.3580G>C (p.Ala1194Pro) c.3481G>C (p.Ala1161Pro) c.3022G>C (p.Ala1008Pro) c.2161G>C (p.Ala721Pro) n.3962G>C n.3966G>C | |
1 | g.1048155G= | CA1148804139 | AGRN | c.3895G= (p.Ala1299=) c.3580G= (p.Ala1194=) c.3481G= (p.Ala1161=) c.3022G= (p.Ala1008=) c.2161G= (p.Ala721=) n.3962G= n.3966G= | |
1 | g.1048155G>T | CA337852936 | AGRN | c.3895G>T (p.Ala1299Ser) c.3580G>T (p.Ala1194Ser) c.3481G>T (p.Ala1161Ser) c.3022G>T (p.Ala1008Ser) c.2161G>T (p.Ala721Ser) n.3962G>T n.3966G>T | gnomAD v4 |
1 | g.1048156C>A | CA337852938 | AGRN | c.3896C>A (p.Ala1299Asp) c.3581C>A (p.Ala1194Asp) c.3482C>A (p.Ala1161Asp) c.3023C>A (p.Ala1008Asp) c.2162C>A (p.Ala721Asp) n.3963C>A n.3967C>A | gnomAD v4 |
1 | g.1048156C>G | CA337852939 | AGRN | c.3896C>G (p.Ala1299Gly) c.3581C>G (p.Ala1194Gly) c.3482C>G (p.Ala1161Gly) c.3023C>G (p.Ala1008Gly) c.2162C>G (p.Ala721Gly) n.3963C>G n.3967C>G | |
1 | g.1048156C>T | CA337852941 | AGRN | c.3896C>T (p.Ala1299Val) c.3581C>T (p.Ala1194Val) c.3482C>T (p.Ala1161Val) c.3023C>T (p.Ala1008Val) c.2162C>T (p.Ala721Val) n.3963C>T n.3967C>T | gnomAD v4 |
1 | g.1048157C>A | CA415758261 | AGRN | c.3897C>A (p.Ala1299=) c.3582C>A (p.Ala1194=) c.3483C>A (p.Ala1161=) c.3024C>A (p.Ala1008=) c.2163C>A (p.Ala721=) n.3964C>A n.3968C>A | gnomAD v4 |
1 | g.1048157C= | CA1148804149 | AGRN | c.3897C= (p.Ala1299=) c.3582C= (p.Ala1194=) c.3483C= (p.Ala1161=) c.3024C= (p.Ala1008=) c.2163C= (p.Ala721=) n.3964C= n.3968C= | |
1 | g.1048157C>G | CA415758260 | AGRN | c.3897C>G (p.Ala1299=) c.3582C>G (p.Ala1194=) c.3483C>G (p.Ala1161=) c.3024C>G (p.Ala1008=) c.2163C>G (p.Ala721=) n.3964C>G n.3968C>G | dbSNP |
1 | g.1048157C>T | CA415758262 | AGRN | c.3897C>T (p.Ala1299=) c.3582C>T (p.Ala1194=) c.3483C>T (p.Ala1161=) c.3024C>T (p.Ala1008=) c.2163C>T (p.Ala721=) n.3964C>T n.3968C>T | gnomAD v4 |
1 | g.1048158A>C | CA337852947 | AGRN | c.3898A>C (p.Lys1300Gln) c.3583A>C (p.Lys1195Gln) c.3484A>C (p.Lys1162Gln) c.3025A>C (p.Lys1009Gln) c.2164A>C (p.Lys722Gln) n.3965A>C n.3969A>C | |
1 | g.1048158A>G | CA337852943 | AGRN | c.3898A>G (p.Lys1300Glu) c.3583A>G (p.Lys1195Glu) c.3484A>G (p.Lys1162Glu) c.3025A>G (p.Lys1009Glu) c.2164A>G (p.Lys722Glu) n.3965A>G n.3969A>G | |
1 | g.1048158A>T | CA337852945 | AGRN | c.3898A>T (p.Lys1300Ter) c.3583A>T (p.Lys1195Ter) c.3484A>T (p.Lys1162Ter) c.3025A>T (p.Lys1009Ter) c.2164A>T (p.Lys722Ter) n.3965A>T n.3969A>T | |
1 | g.1048159A>C | CA337852949 | AGRN | c.3899A>C (p.Lys1300Thr) c.3584A>C (p.Lys1195Thr) c.3485A>C (p.Lys1162Thr) c.3026A>C (p.Lys1009Thr) c.2165A>C (p.Lys722Thr) n.3966A>C n.3970A>C | |
1 | g.1048159A>G | CA337852951 | AGRN | c.3899A>G (p.Lys1300Arg) c.3584A>G (p.Lys1195Arg) c.3485A>G (p.Lys1162Arg) c.3026A>G (p.Lys1009Arg) c.2165A>G (p.Lys722Arg) n.3966A>G n.3970A>G | |
1 | g.1048159A>T | CA337852952 | AGRN | c.3899A>T (p.Lys1300Met) c.3584A>T (p.Lys1195Met) c.3485A>T (p.Lys1162Met) c.3026A>T (p.Lys1009Met) c.2165A>T (p.Lys722Met) n.3966A>T n.3970A>T | gnomAD v4 |
1 | g.1048160G>A | CA415758266 | AGRN | c.3900G>A (p.Lys1300=) c.3585G>A (p.Lys1195=) c.3486G>A (p.Lys1162=) c.3027G>A (p.Lys1009=) c.2166G>A (p.Lys722=) n.3967G>A n.3971G>A | |
1 | g.1048160G>C | CA337852954 | AGRN | c.3900G>C (p.Lys1300Asn) c.3585G>C (p.Lys1195Asn) c.3486G>C (p.Lys1162Asn) c.3027G>C (p.Lys1009Asn) c.2166G>C (p.Lys722Asn) n.3967G>C n.3971G>C | gnomAD v4 |
1 | g.1048160G>T | CA337852955 | AGRN | c.3900G>T (p.Lys1300Asn) c.3585G>T (p.Lys1195Asn) c.3486G>T (p.Lys1162Asn) c.3027G>T (p.Lys1009Asn) c.2166G>T (p.Lys722Asn) n.3967G>T n.3971G>T | gnomAD v4 |
1 | g.1048161A>C | CA337852958 | AGRN | c.3901A>C (p.Thr1301Pro) c.3586A>C (p.Thr1196Pro) c.3487A>C (p.Thr1163Pro) c.3028A>C (p.Thr1010Pro) c.2167A>C (p.Thr723Pro) n.3968A>C n.3972A>C | |
1 | g.1048161A>G | CA337852961 | AGRN | c.3901A>G (p.Thr1301Ala) c.3586A>G (p.Thr1196Ala) c.3487A>G (p.Thr1163Ala) c.3028A>G (p.Thr1010Ala) c.2167A>G (p.Thr723Ala) n.3968A>G n.3972A>G | |
1 | g.1048161A>T | CA337852960 | AGRN | c.3901A>T (p.Thr1301Ser) c.3586A>T (p.Thr1196Ser) c.3487A>T (p.Thr1163Ser) c.3028A>T (p.Thr1010Ser) c.2167A>T (p.Thr723Ser) n.3968A>T n.3972A>T | |
1 | g.1048162C>A | CA337852964 | AGRN | c.3902C>A (p.Thr1301Asn) c.3587C>A (p.Thr1196Asn) c.3488C>A (p.Thr1163Asn) c.3029C>A (p.Thr1010Asn) c.2168C>A (p.Thr723Asn) n.3969C>A n.3973C>A | dbSNP gnomAD v2 |
1 | g.1048162C= | CA1148804158 | AGRN | c.3902C= (p.Thr1301=) c.3587C= (p.Thr1196=) c.3488C= (p.Thr1163=) c.3029C= (p.Thr1010=) c.2168C= (p.Thr723=) n.3969C= n.3973C= | |
1 | g.1048162C>G | CA16760243 | AGRN | c.3902C>G (p.Thr1301Ser) c.3587C>G (p.Thr1196Ser) c.3488C>G (p.Thr1163Ser) c.3029C>G (p.Thr1010Ser) c.2168C>G (p.Thr723Ser) n.3969C>G n.3973C>G | dbSNP gnomAD v2 gnomAD v4 |
1 | g.1048162C>T | CA337852966 | AGRN | c.3902C>T (p.Thr1301Ile) c.3587C>T (p.Thr1196Ile) c.3488C>T (p.Thr1163Ile) c.3029C>T (p.Thr1010Ile) c.2168C>T (p.Thr723Ile) n.3969C>T n.3973C>T | gnomAD v4 |
1 | g.1048163del | CA2642492198 | AGRN | c.3903del (p.Thr1302ArgfsTer?) c.3588del (p.Thr1197ArgfsTer?) c.3489del (p.Thr1164ArgfsTer?) c.3030del (p.Thr1011ArgfsTer?) c.2169del (p.Thr724ArgfsTer?) n.3970del n.3974del | gnomAD v4 |
1 | g.1048163C>A | CA415758273 | AGRN | c.3903C>A (p.Thr1301=) c.3588C>A (p.Thr1196=) c.3489C>A (p.Thr1163=) c.3030C>A (p.Thr1010=) c.2169C>A (p.Thr723=) n.3970C>A n.3974C>A | gnomAD v4 |
1 | g.1048163C= | CA1148804161 | AGRN | c.3903C= (p.Thr1301=) c.3588C= (p.Thr1196=) c.3489C= (p.Thr1163=) c.3030C= (p.Thr1010=) c.2169C= (p.Thr723=) n.3970C= n.3974C= | |
1 | g.1048163C>G | CA415758274 | AGRN | c.3903C>G (p.Thr1301=) c.3588C>G (p.Thr1196=) c.3489C>G (p.Thr1163=) c.3030C>G (p.Thr1010=) c.2169C>G (p.Thr723=) n.3970C>G n.3974C>G | dbSNP gnomAD v3 gnomAD v4 |
1 | g.1048163C>T | CA415758275 | AGRN | c.3903C>T (p.Thr1301=) c.3588C>T (p.Thr1196=) c.3489C>T (p.Thr1163=) c.3030C>T (p.Thr1010=) c.2169C>T (p.Thr723=) n.3970C>T n.3974C>T | dbSNP gnomAD v2 gnomAD v4 |
1 | g.1048164A= | CA1148804168 | AGRN | c.3904A= (p.Thr1302=) c.3589A= (p.Thr1197=) c.3490A= (p.Thr1164=) c.3031A= (p.Thr1011=) c.2170A= (p.Thr724=) n.3971A= n.3975A= | |
1 | g.1048164A>C | CA337852969 | AGRN | c.3904A>C (p.Thr1302Pro) c.3589A>C (p.Thr1197Pro) c.3490A>C (p.Thr1164Pro) c.3031A>C (p.Thr1011Pro) c.2170A>C (p.Thr724Pro) n.3971A>C n.3975A>C | |
1 | g.1048164A>G | CA337852970 | AGRN | c.3904A>G (p.Thr1302Ala) c.3589A>G (p.Thr1197Ala) c.3490A>G (p.Thr1164Ala) c.3031A>G (p.Thr1011Ala) c.2170A>G (p.Thr724Ala) n.3971A>G n.3975A>G | dbSNP gnomAD v2 gnomAD v4 |
1 | g.1048164A>T | CA337852971 | AGRN | c.3904A>T (p.Thr1302Ser) c.3589A>T (p.Thr1197Ser) c.3490A>T (p.Thr1164Ser) c.3031A>T (p.Thr1011Ser) c.2170A>T (p.Thr724Ser) n.3971A>T n.3975A>T | |
1 | g.1048165C>A | CA337852973 | AGRN | c.3905C>A (p.Thr1302Lys) c.3590C>A (p.Thr1197Lys) c.3491C>A (p.Thr1164Lys) c.3032C>A (p.Thr1011Lys) c.2171C>A (p.Thr724Lys) n.3972C>A n.3976C>A | gnomAD v4 |
1 | g.1048165C= | CA1148269818 | AGRN | c.3905C= (p.Thr1302=) c.3590C= (p.Thr1197=) c.3491C= (p.Thr1164=) c.3032C= (p.Thr1011=) c.2171C= (p.Thr724=) n.3972C= n.3976C= | |
1 | g.1048165C>G | CA337852976 | AGRN | c.3905C>G (p.Thr1302Arg) c.3590C>G (p.Thr1197Arg) c.3491C>G (p.Thr1164Arg) c.3032C>G (p.Thr1011Arg) c.2171C>G (p.Thr724Arg) n.3972C>G n.3976C>G | dbSNP gnomAD v2 gnomAD v4 |
1 | g.1048165C>T | CA509271 | AGRN | c.3905C>T (p.Thr1302Met) c.3590C>T (p.Thr1197Met) c.3491C>T (p.Thr1164Met) c.3032C>T (p.Thr1011Met) c.2171C>T (p.Thr724Met) n.3972C>T n.3976C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.1048166G>A | CA16760245 | AGRN | c.3906G>A (p.Thr1302=) c.3591G>A (p.Thr1197=) c.3492G>A (p.Thr1164=) c.3033G>A (p.Thr1011=) c.2172G>A (p.Thr724=) n.3973G>A n.3977G>A | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.1048166G>C | CA415758281 | AGRN | c.3906G>C (p.Thr1302=) c.3591G>C (p.Thr1197=) c.3492G>C (p.Thr1164=) c.3033G>C (p.Thr1011=) c.2172G>C (p.Thr724=) n.3973G>C n.3977G>C | |
1 | g.1048166G= | CA1146051981 | AGRN | c.3906G= (p.Thr1302=) c.3591G= (p.Thr1197=) c.3492G= (p.Thr1164=) c.3033G= (p.Thr1011=) c.2172G= (p.Thr724=) n.3973G= n.3977G= | |
1 | g.1048166G>T | CA415758279 | AGRN | c.3906G>T (p.Thr1302=) c.3591G>T (p.Thr1197=) c.3492G>T (p.Thr1164=) c.3033G>T (p.Thr1011=) c.2172G>T (p.Thr724=) n.3973G>T n.3977G>T | gnomAD v4 |
1 | g.1048167G>A | CA337852980 | AGRN | c.3907G>A (p.Ala1303Thr) c.3592G>A (p.Ala1198Thr) c.3493G>A (p.Ala1165Thr) c.3034G>A (p.Ala1012Thr) c.2173G>A (p.Ala725Thr) n.3974G>A n.3978G>A | gnomAD v4 |
1 | g.1048167G>C | CA337852982 | AGRN | c.3907G>C (p.Ala1303Pro) c.3592G>C (p.Ala1198Pro) c.3493G>C (p.Ala1165Pro) c.3034G>C (p.Ala1012Pro) c.2173G>C (p.Ala725Pro) n.3974G>C n.3978G>C | |
1 | g.1048167G>T | CA337852983 | AGRN | c.3907G>T (p.Ala1303Ser) c.3592G>T (p.Ala1198Ser) c.3493G>T (p.Ala1165Ser) c.3034G>T (p.Ala1012Ser) c.2173G>T (p.Ala725Ser) n.3974G>T n.3978G>T | gnomAD v4 |
1 | g.1048168C>A | CA337852991 | AGRN | c.3908C>A (p.Ala1303Glu) c.3593C>A (p.Ala1198Glu) c.3494C>A (p.Ala1165Glu) c.3035C>A (p.Ala1012Glu) c.2174C>A (p.Ala725Glu) n.3975C>A n.3979C>A | gnomAD v4 |
1 | g.1048168C= | CA1148804184 | AGRN | c.3908C= (p.Ala1303=) c.3593C= (p.Ala1198=) c.3494C= (p.Ala1165=) c.3035C= (p.Ala1012=) c.2174C= (p.Ala725=) n.3975C= n.3979C= | |
1 | g.1048168C>G | CA337852985 | AGRN | c.3908C>G (p.Ala1303Gly) c.3593C>G (p.Ala1198Gly) c.3494C>G (p.Ala1165Gly) c.3035C>G (p.Ala1012Gly) c.2174C>G (p.Ala725Gly) n.3975C>G n.3979C>G | |
1 | g.1048168C>T | CA337852988 | AGRN | c.3908C>T (p.Ala1303Val) c.3593C>T (p.Ala1198Val) c.3494C>T (p.Ala1165Val) c.3035C>T (p.Ala1012Val) c.2174C>T (p.Ala725Val) n.3975C>T n.3979C>T | dbSNP gnomAD v2 gnomAD v4 |
1 | g.1048169A>C | CA415758288 | AGRN | c.3909A>C (p.Ala1303=) c.3594A>C (p.Ala1198=) c.3495A>C (p.Ala1165=) c.3036A>C (p.Ala1012=) c.2175A>C (p.Ala725=) n.3976A>C n.3980A>C | dbSNP |
1 | g.1048169A>G | CA415758289 | AGRN | c.3909A>G (p.Ala1303=) c.3594A>G (p.Ala1198=) c.3495A>G (p.Ala1165=) c.3036A>G (p.Ala1012=) c.2175A>G (p.Ala725=) n.3976A>G n.3980A>G | dbSNP |
1 | g.1048169A>T | CA415758290 | AGRN | c.3909A>T (p.Ala1303=) c.3594A>T (p.Ala1198=) c.3495A>T (p.Ala1165=) c.3036A>T (p.Ala1012=) c.2175A>T (p.Ala725=) n.3976A>T n.3980A>T | |
1 | g.1048170G>A | CA509272 | AGRN | c.3910G>A (p.Ala1304Thr) c.3595G>A (p.Ala1199Thr) c.3496G>A (p.Ala1166Thr) c.3037G>A (p.Ala1013Thr) c.2176G>A (p.Ala726Thr) n.3977G>A n.3981G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.1048170G>C | CA337852997 | AGRN | c.3910G>C (p.Ala1304Pro) c.3595G>C (p.Ala1199Pro) c.3496G>C (p.Ala1166Pro) c.3037G>C (p.Ala1013Pro) c.2176G>C (p.Ala726Pro) n.3977G>C n.3981G>C | gnomAD v4 |
1 | g.1048170G= | CA1144070224 | AGRN | c.3910G= (p.Ala1304=) c.3595G= (p.Ala1199=) c.3496G= (p.Ala1166=) c.3037G= (p.Ala1013=) c.2176G= (p.Ala726=) n.3977G= n.3981G= | |
1 | g.1048170G>T | CA337852998 | AGRN | c.3910G>T (p.Ala1304Ser) c.3595G>T (p.Ala1199Ser) c.3496G>T (p.Ala1166Ser) c.3037G>T (p.Ala1013Ser) c.2176G>T (p.Ala726Ser) n.3977G>T n.3981G>T | gnomAD v4 |
1 | g.1048171C>A | CA337853000 | AGRN | c.3911C>A (p.Ala1304Asp) c.3596C>A (p.Ala1199Asp) c.3497C>A (p.Ala1166Asp) c.3038C>A (p.Ala1013Asp) c.2177C>A (p.Ala726Asp) n.3978C>A n.3982C>A | gnomAD v4 |
1 | g.1048171C= | CA1148804193 | AGRN | c.3911C= (p.Ala1304=) c.3596C= (p.Ala1199=) c.3497C= (p.Ala1166=) c.3038C= (p.Ala1013=) c.2177C= (p.Ala726=) n.3978C= n.3982C= | |
1 | g.1048171C>G | CA337853003 | AGRN | c.3911C>G (p.Ala1304Gly) c.3596C>G (p.Ala1199Gly) c.3497C>G (p.Ala1166Gly) c.3038C>G (p.Ala1013Gly) c.2177C>G (p.Ala726Gly) n.3978C>G n.3982C>G | dbSNP gnomAD v4 |
1 | g.1048171C>T | CA337853006 | AGRN | c.3911C>T (p.Ala1304Val) c.3596C>T (p.Ala1199Val) c.3497C>T (p.Ala1166Val) c.3038C>T (p.Ala1013Val) c.2177C>T (p.Ala726Val) n.3978C>T n.3982C>T | dbSNP gnomAD v2 gnomAD v4 |
1 | g.1048175del | CA2574258711 | AGRN | c.3915del (p.Thr1306ProfsTer?) c.3600del (p.Thr1201ProfsTer?) c.3501del (p.Thr1168ProfsTer?) c.3042del (p.Thr1015ProfsTer?) c.2181del (p.Thr728ProfsTer?) n.3982del n.3986del | gnomAD v4 |
1 | g.1048181_1048198dup | CA2642492199 | AGRN | c.3921_3938dup (p.Thr1313_Ala1314insArgArgProProThrThr) c.3606_3623dup (p.Thr1208_Ala1209insArgArgProProThrThr) c.3507_3524dup (p.Thr1175_Ala1176insArgArgProProThrThr) c.3048_3065dup (p.Thr1022_Ala1023insArgArgProProThrThr) c.2187_2204dup (p.Thr735_Ala736insArgArgProProThrThr) n.3988_4005dup n.3992_4009dup | gnomAD v4 |
1 | g.1048181_1048198del | CA2642492200 | AGRN | c.3921_3938del (p.Arg1308_Thr1313del) c.3606_3623del (p.Arg1203_Thr1208del) c.3507_3524del (p.Arg1170_Thr1175del) c.3048_3065del (p.Arg1017_Thr1022del) c.2187_2204del (p.Arg730_Thr735del) n.3988_4005del n.3992_4009del | gnomAD v4 |
1 | g.1048172C>A | CA509273 | AGRN | c.3912C>A (p.Ala1304=) c.3597C>A (p.Ala1199=) c.3498C>A (p.Ala1166=) c.3039C>A (p.Ala1013=) c.2178C>A (p.Ala726=) n.3979C>A n.3983C>A | dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.1048172C= | CA1148804203 | AGRN | c.3912C= (p.Ala1304=) c.3597C= (p.Ala1199=) c.3498C= (p.Ala1166=) c.3039C= (p.Ala1013=) c.2178C= (p.Ala726=) n.3979C= n.3983C= | |
1 | g.1048172C>G | CA415758295 | AGRN | c.3912C>G (p.Ala1304=) c.3597C>G (p.Ala1199=) c.3498C>G (p.Ala1166=) c.3039C>G (p.Ala1013=) c.2178C>G (p.Ala726=) n.3979C>G n.3983C>G | |
1 | g.1048172C>T | CA415758297 | AGRN | c.3912C>T (p.Ala1304=) c.3597C>T (p.Ala1199=) c.3498C>T (p.Ala1166=) c.3039C>T (p.Ala1013=) c.2178C>T (p.Ala726=) n.3979C>T n.3983C>T | dbSNP gnomAD v3 gnomAD v4 |
1 | g.1048173C>A | CA16760255 | AGRN | c.3913C>A (p.Pro1305Thr) c.3598C>A (p.Pro1200Thr) c.3499C>A (p.Pro1167Thr) c.3040C>A (p.Pro1014Thr) c.2179C>A (p.Pro727Thr) n.3980C>A n.3984C>A | dbSNP gnomAD v4 |
1 | g.1048173C= | CA1148804209 | AGRN | c.3913C= (p.Pro1305=) c.3598C= (p.Pro1200=) c.3499C= (p.Pro1167=) c.3040C= (p.Pro1014=) c.2179C= (p.Pro727=) n.3980C= n.3984C= | |
1 | g.1048173C>G | CA337853010 | AGRN | c.3913C>G (p.Pro1305Ala) c.3598C>G (p.Pro1200Ala) c.3499C>G (p.Pro1167Ala) c.3040C>G (p.Pro1014Ala) c.2179C>G (p.Pro727Ala) n.3980C>G n.3984C>G | gnomAD v4 |
1 | g.1048173C>T | CA337853011 | AGRN | c.3913C>T (p.Pro1305Ser) c.3598C>T (p.Pro1200Ser) c.3499C>T (p.Pro1167Ser) c.3040C>T (p.Pro1014Ser) c.2179C>T (p.Pro727Ser) n.3980C>T n.3984C>T | gnomAD v4 |
1 | g.1048174C>A | CA337853013 | AGRN | c.3914C>A (p.Pro1305His) c.3599C>A (p.Pro1200His) c.3500C>A (p.Pro1167His) c.3041C>A (p.Pro1014His) c.2180C>A (p.Pro727His) n.3981C>A n.3985C>A | gnomAD v4 |
1 | g.1048174C>G | CA337853015 | AGRN | c.3914C>G (p.Pro1305Arg) c.3599C>G (p.Pro1200Arg) c.3500C>G (p.Pro1167Arg) c.3041C>G (p.Pro1014Arg) c.2180C>G (p.Pro727Arg) n.3981C>G n.3985C>G | |
1 | g.1048174C>T | CA337853017 | AGRN | c.3914C>T (p.Pro1305Leu) c.3599C>T (p.Pro1200Leu) c.3500C>T (p.Pro1167Leu) c.3041C>T (p.Pro1014Leu) c.2180C>T (p.Pro727Leu) n.3981C>T n.3985C>T | gnomAD v4 |
1 | g.1048175C>A | CA415758301 | AGRN | c.3915C>A (p.Pro1305=) c.3600C>A (p.Pro1200=) c.3501C>A (p.Pro1167=) c.3042C>A (p.Pro1014=) c.2181C>A (p.Pro727=) n.3982C>A n.3986C>A | gnomAD v4 |
1 | g.1048175C= | CA1148804214 | AGRN | c.3915C= (p.Pro1305=) c.3600C= (p.Pro1200=) c.3501C= (p.Pro1167=) c.3042C= (p.Pro1014=) c.2181C= (p.Pro727=) n.3982C= n.3986C= | |
1 | g.1048175C>G | CA415758302 | AGRN | c.3915C>G (p.Pro1305=) c.3600C>G (p.Pro1200=) c.3501C>G (p.Pro1167=) c.3042C>G (p.Pro1014=) c.2181C>G (p.Pro727=) n.3982C>G n.3986C>G | |
1 | g.1048175C>T | CA415758304 | AGRN | c.3915C>T (p.Pro1305=) c.3600C>T (p.Pro1200=) c.3501C>T (p.Pro1167=) c.3042C>T (p.Pro1014=) c.2181C>T (p.Pro727=) n.3982C>T n.3986C>T | dbSNP gnomAD v2 gnomAD v4 |
1 | g.1048176A>C | CA337853026 | AGRN | c.3916A>C (p.Thr1306Pro) c.3601A>C (p.Thr1201Pro) c.3502A>C (p.Thr1168Pro) c.3043A>C (p.Thr1015Pro) c.2182A>C (p.Thr728Pro) n.3983A>C n.3987A>C | dbSNP gnomAD v4 |
1 | g.1048176A>G | CA337853024 | AGRN | c.3916A>G (p.Thr1306Ala) c.3601A>G (p.Thr1201Ala) c.3502A>G (p.Thr1168Ala) c.3043A>G (p.Thr1015Ala) c.2182A>G (p.Thr728Ala) n.3983A>G n.3987A>G | ClinVar gnomAD v4 |
1 | g.1048176A>T | CA337853019 | AGRN | c.3916A>T (p.Thr1306Ser) c.3601A>T (p.Thr1201Ser) c.3502A>T (p.Thr1168Ser) c.3043A>T (p.Thr1015Ser) c.2182A>T (p.Thr728Ser) n.3983A>T n.3987A>T | |
1 | g.1048177C>A | CA337853029 | AGRN | c.3917C>A (p.Thr1306Asn) c.3602C>A (p.Thr1201Asn) c.3503C>A (p.Thr1168Asn) c.3044C>A (p.Thr1015Asn) c.2183C>A (p.Thr728Asn) n.3984C>A n.3988C>A | gnomAD v4 |
1 | g.1048177C>G | CA337853027 | AGRN | c.3917C>G (p.Thr1306Ser) c.3602C>G (p.Thr1201Ser) c.3503C>G (p.Thr1168Ser) c.3044C>G (p.Thr1015Ser) c.2183C>G (p.Thr728Ser) n.3984C>G n.3988C>G | |
1 | g.1048177C>T | CA337853030 | AGRN | c.3917C>T (p.Thr1306Ile) c.3602C>T (p.Thr1201Ile) c.3503C>T (p.Thr1168Ile) c.3044C>T (p.Thr1015Ile) c.2183C>T (p.Thr728Ile) n.3984C>T n.3988C>T | gnomAD v4 |