ClinVar Miner

List of variants in gene AGRN reported as likely benign for not specified

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 72
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HGVS dbSNP
NM_198576.4(AGRN):c.1058A>G (p.Gln353Arg) rs150359724
NM_198576.4(AGRN):c.1123G>T (p.Ala375Ser) rs138031468
NM_198576.4(AGRN):c.11G>C (p.Arg4Pro) rs539283387
NM_198576.4(AGRN):c.1394C>T (p.Pro465Leu) rs116586548
NM_198576.4(AGRN):c.1528G>A (p.Gly510Ser) rs138288952
NM_198576.4(AGRN):c.1603+19G>A rs115191992
NM_198576.4(AGRN):c.1993G>A (p.Glu665Lys) rs143324306
NM_198576.4(AGRN):c.2025C>G (p.Gly675=) rs28484890
NM_198576.4(AGRN):c.2067G>A (p.Gln689=) rs139886237
NM_198576.4(AGRN):c.2266G>A (p.Ala756Thr) rs140764403
NM_198576.4(AGRN):c.2271G>A (p.Pro757=) rs150123719
NM_198576.4(AGRN):c.2371+12A>G rs375177822
NM_198576.4(AGRN):c.2406C>T (p.Gly802=) rs75774767
NM_198576.4(AGRN):c.2457G>C (p.Gly819=) rs112039851
NM_198576.4(AGRN):c.2499T>C (p.Phe833=) rs753858864
NM_198576.4(AGRN):c.2536+45C>T rs183108359
NM_198576.4(AGRN):c.2589G>A (p.Thr863=) rs776485359
NM_198576.4(AGRN):c.261C>T (p.Asp87=) rs6657048
NM_198576.4(AGRN):c.2681-16C>G rs199785742
NM_198576.4(AGRN):c.2682C>T (p.Asp894=) rs118105080
NM_198576.4(AGRN):c.2796C>T (p.Asn932=) rs147153797
NM_198576.4(AGRN):c.2805+7G>A rs190000918
NM_198576.4(AGRN):c.3003C>T (p.Pro1001=) rs375208869
NM_198576.4(AGRN):c.3255C>T (p.Leu1085=) rs775823409
NM_198576.4(AGRN):c.3264G>C (p.Leu1088Phe) rs150132566
NM_198576.4(AGRN):c.3285C>G (p.Thr1095=) rs149957221
NM_198576.4(AGRN):c.3388+19G>A rs749958717
NM_198576.4(AGRN):c.3404A>G (p.Gln1135Arg) rs142416636
NM_198576.4(AGRN):c.3465T>C (p.Ala1155=) rs146358566
NM_198576.4(AGRN):c.3516+10G>C rs76264143
NM_198576.4(AGRN):c.3516+8G>A rs199620555
NM_198576.4(AGRN):c.3570C>T (p.Arg1190=) rs75361935
NM_198576.4(AGRN):c.3719C>T (p.Pro1240Leu) rs142620337
NM_198576.4(AGRN):c.3732C>T (p.His1244=) rs536657086
NM_198576.4(AGRN):c.3819C>T (p.Ala1273=) rs142597617
NM_198576.4(AGRN):c.3866C>T (p.Pro1289Leu) rs139294803
NM_198576.4(AGRN):c.3964C>T (p.Arg1322Trp) rs184970403
NM_198576.4(AGRN):c.3972G>A (p.Pro1324=) rs201483077
NM_198576.4(AGRN):c.4116C>T (p.Ala1372=) rs200170414
NM_198576.4(AGRN):c.4131C>T (p.Phe1377=) rs368555478
NM_198576.4(AGRN):c.4285C>T (p.Arg1429Cys) rs201346452
NM_198576.4(AGRN):c.4298+11A>T rs369279324
NM_198576.4(AGRN):c.4298+6C>T rs199977575
NM_198576.4(AGRN):c.4352C>T (p.Pro1451Leu) rs144620006
NM_198576.4(AGRN):c.4452C>T (p.Thr1484=) rs75767981
NM_198576.4(AGRN):c.4518G>A (p.Ala1506=) rs376592885
NM_198576.4(AGRN):c.4540G>A (p.Ala1514Thr) rs111818381
NM_198576.4(AGRN):c.4695G>C (p.Gln1565His) rs199876002
NM_198576.4(AGRN):c.4731G>A (p.Pro1577=) rs115885544
NM_198576.4(AGRN):c.4734C>T (p.Pro1578=) rs186574226
NM_198576.4(AGRN):c.4740C>T (p.Arg1580=) rs115019873
NM_198576.4(AGRN):c.4839C>T (p.Cys1613=) rs113020870
NM_198576.4(AGRN):c.4879+17T>A rs535286672
NM_198576.4(AGRN):c.4996G>A (p.Val1666Ile) rs17160775
NM_198576.4(AGRN):c.5201G>A (p.Arg1734His) rs145444272
NM_198576.4(AGRN):c.5254-5C>T rs34708466
NM_198576.4(AGRN):c.526C>T (p.Leu176=) rs544749044
NM_198576.4(AGRN):c.5337C>T (p.Ala1779=) rs141463750
NM_198576.4(AGRN):c.5358T>C (p.Gly1786=) rs17160781
NM_198576.4(AGRN):c.5370+11G>A rs373058941
NM_198576.4(AGRN):c.5413C>T (p.Leu1805=) rs751461791
NM_198576.4(AGRN):c.5598C>T (p.Thr1866=) rs17778478
NM_198576.4(AGRN):c.5643G>A (p.Val1881=) rs142242736
NM_198576.4(AGRN):c.5651+14C>T rs766872717
NM_198576.4(AGRN):c.5726G>C (p.Ser1909Thr) rs74685771
NM_198576.4(AGRN):c.5832C>T (p.Thr1944=) rs143373928
NM_198576.4(AGRN):c.5877-17C>A rs199552967
NM_198576.4(AGRN):c.5896C>T (p.Leu1966=) rs115828965
NM_198576.4(AGRN):c.6054G>A (p.Arg2018=) rs754185719
NM_198576.4(AGRN):c.6074A>G (p.His2025Arg) rs377296839
NM_198576.4(AGRN):c.67G>C (p.Val23Leu) rs201073369
NM_198576.4(AGRN):c.773C>T (p.Thr258Ile) rs200607541

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