ClinVar Miner

List of variants in gene AGRN reported as likely benign by PreventionGenetics, part of Exact Sciences

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Gene type:
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Total variants: 67
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HGVS dbSNP gnomAD frequency
NM_198576.4(AGRN):c.5726G>C (p.Ser1909Thr) rs74685771 0.00700
NM_198576.4(AGRN):c.2536+45C>T rs183108359 0.00533
NM_198576.4(AGRN):c.1123G>T (p.Ala375Ser) rs138031468 0.00517
NM_198576.4(AGRN):c.4352C>T (p.Pro1451Leu) rs144620006 0.00426
NM_198576.4(AGRN):c.4839C>T (p.Cys1613=) rs113020870 0.00302
NM_198576.4(AGRN):c.1993G>A (p.Glu665Lys) rs143324306 0.00297
NM_198576.4(AGRN):c.4639G>A (p.Glu1547Lys) rs2799068 0.00284
NM_198576.4(AGRN):c.1394C>T (p.Pro465Leu) rs116586548 0.00216
NM_198576.4(AGRN):c.2690C>T (p.Ala897Val) rs116836855 0.00203
NM_198576.4(AGRN):c.3719C>T (p.Pro1240Leu) rs142620337 0.00191
NM_198576.4(AGRN):c.4879+17T>A rs535286672 0.00170
NM_198576.4(AGRN):c.2155G>A (p.Gly719Ser) rs149594498 0.00158
NM_198576.4(AGRN):c.6074A>G (p.His2025Arg) rs377296839 0.00151
NM_198576.4(AGRN):c.752T>C (p.Val251Ala) rs779170859 0.00125
NM_198576.4(AGRN):c.1570C>T (p.Arg524Trp) rs144164397 0.00119
NM_198576.4(AGRN):c.3765G>A (p.Ala1255=) rs149490453 0.00113
NM_198576.4(AGRN):c.5370+11G>A rs373058941 0.00104
NM_198576.4(AGRN):c.2501G>A (p.Arg834Gln) rs146243145 0.00094
NM_198576.4(AGRN):c.5877-17C>A rs199552967 0.00083
NM_198576.4(AGRN):c.2266G>A (p.Ala756Thr) rs140764403 0.00079
NM_198576.4(AGRN):c.5643G>A (p.Val1881=) rs142242736 0.00074
NM_198576.4(AGRN):c.3819C>T (p.Ala1273=) rs142597617 0.00070
NM_198576.4(AGRN):c.4298+7G>A rs201995572 0.00066
NM_198576.4(AGRN):c.4272G>A (p.Ala1424=) rs201470321 0.00061
NM_198576.4(AGRN):c.2028T>A (p.Ser676=) rs144713799 0.00035
NM_198576.4(AGRN):c.5337C>T (p.Ala1779=) rs141463750 0.00035
NM_198576.4(AGRN):c.2796C>T (p.Asn932=) rs147153797 0.00031
NM_198576.4(AGRN):c.2601G>A (p.Ser867=) rs144794590 0.00025
NM_198576.4(AGRN):c.2271G>A (p.Pro757=) rs150123719 0.00020
NM_198576.4(AGRN):c.1107C>T (p.Val369=) rs369413947 0.00018
NM_198576.4(AGRN):c.2681-16C>G rs199785742 0.00018
NM_198576.4(AGRN):c.3732C>T (p.His1244=) rs536657086 0.00017
NM_198576.4(AGRN):c.1470C>T (p.Cys490=) rs372048253 0.00014
NM_198576.4(AGRN):c.2681-10C>T rs368080332 0.00014
NM_198576.4(AGRN):c.3003C>T (p.Pro1001=) rs375208869 0.00014
NM_198576.4(AGRN):c.1384+6C>T rs763495287 0.00013
NM_198576.4(AGRN):c.4518G>A (p.Ala1506=) rs376592885 0.00013
NM_198576.4(AGRN):c.3033C>T (p.Thr1011=) rs377422616 0.00009
NM_198576.4(AGRN):c.4228C>T (p.Leu1410=) rs544008933 0.00009
NM_198576.4(AGRN):c.1281C>T (p.Pro427=) rs767153644 0.00008
NM_198576.4(AGRN):c.1539C>T (p.Cys513=) rs370615022 0.00006
NM_198576.4(AGRN):c.3388+19G>A rs749958717 0.00006
NM_198576.4(AGRN):c.4989G>A (p.Ala1663=) rs371635309 0.00006
NM_198576.4(AGRN):c.5370+9G>A rs774988688 0.00006
NM_198576.4(AGRN):c.2647G>A (p.Gly883Ser) rs145162376 0.00005
NM_198576.4(AGRN):c.526C>T (p.Leu176=) rs544749044 0.00005
NM_198576.4(AGRN):c.1518C>T (p.Gly506=) rs139594136 0.00003
NM_198576.4(AGRN):c.6054G>A (p.Arg2018=) rs754185719 0.00003
NM_198576.4(AGRN):c.3522C>T (p.Asp1174=) rs374008359 0.00002
NM_198576.4(AGRN):c.2589G>A (p.Thr863=) rs776485359 0.00001
NM_198576.4(AGRN):c.3251-10G>A rs368963266 0.00001
NM_198576.4(AGRN):c.114G>T (p.Arg38=)
NM_198576.4(AGRN):c.1603+3C>T
NM_198576.4(AGRN):c.1650C>T (p.Thr550=) rs201719609
NM_198576.4(AGRN):c.1920C>T (p.Gly640=) rs763833644
NM_198576.4(AGRN):c.3015C>T (p.Pro1005=) rs547720389
NM_198576.4(AGRN):c.3039C>T (p.His1013=) rs549843700
NM_198576.4(AGRN):c.3517-10C>T
NM_198576.4(AGRN):c.3894T>G (p.Val1298=)
NM_198576.4(AGRN):c.4021G>A (p.Gly1341Arg) rs372543866
NM_198576.4(AGRN):c.464-617C>T
NM_198576.4(AGRN):c.4977-6C>T
NM_198576.4(AGRN):c.5112C>T (p.Tyr1704=)
NM_198576.4(AGRN):c.5253+189G>A
NM_198576.4(AGRN):c.5652-302T>G
NM_198576.4(AGRN):c.5837C>T (p.Pro1946Leu) rs771364268
NM_198576.4(AGRN):c.828C>T (p.Cys276=)

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