ClinVar Miner

List of variants in gene AGRN reported as benign by Invitae

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 60
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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.1434G>A (p.Thr478=) rs147346337
NM_198576.4(AGRN):c.1528G>A (p.Gly510Ser) rs138288952
NM_198576.4(AGRN):c.1603+10G>A rs60074964
NM_198576.4(AGRN):c.1660G>A (p.Val554Met) rs79016973
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.2183A>T (p.Glu728Val) rs113288277
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.2508C>T (p.Ile836=) rs148864199
NM_198576.4(AGRN):c.2555A>G (p.Gln852Arg) rs9697293
NM_198576.4(AGRN):c.261C>T (p.Asp87=) rs6657048
NM_198576.4(AGRN):c.2682C>T (p.Asp894=) rs118105080
NM_198576.4(AGRN):c.2805+7G>A rs190000918
NM_198576.4(AGRN):c.3039C>T (p.His1013=) rs549843700
NM_198576.4(AGRN):c.3077C>A (p.Thr1026Asn) rs3813188
NM_198576.4(AGRN):c.3264G>C (p.Leu1088Phe) rs150132566
NM_198576.4(AGRN):c.3276C>T (p.Ser1092=) rs201166586
NM_198576.4(AGRN):c.3353C>A (p.Thr1118Lys) rs149159118
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.3570C>T (p.Arg1190=) rs75361935
NM_198576.4(AGRN):c.3866C>T (p.Pro1289Leu) rs139294803
NM_198576.4(AGRN):c.3972G>A (p.Pro1324=) rs201483077
NM_198576.4(AGRN):c.4285C>T (p.Arg1429Cys) rs201346452
NM_198576.4(AGRN):c.4298+6C>T rs199977575
NM_198576.4(AGRN):c.4298+6_4298+88del rs1553177542
NM_198576.4(AGRN):c.4323G>A (p.Ala1441=) rs373287346
NM_198576.4(AGRN):c.4452C>T (p.Thr1484=) rs75767981
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.4740C>T (p.Arg1580=) rs115019873
NM_198576.4(AGRN):c.4821C>T (p.Pro1607=) rs149543827
NM_198576.4(AGRN):c.4839C>T (p.Cys1613=) rs113020870
NM_198576.4(AGRN):c.4893C>T (p.Asp1631=) rs139400715
NM_198576.4(AGRN):c.4977-10A>G rs142286944
NM_198576.4(AGRN):c.4996G>A (p.Val1666Ile) rs17160775
NM_198576.4(AGRN):c.5025C>T (p.Gly1675=) rs147990356
NM_198576.4(AGRN):c.5070C>T (p.Phe1690=) rs17160776
NM_198576.4(AGRN):c.5201G>A (p.Arg1734His) rs145444272
NM_198576.4(AGRN):c.5223C>T (p.Gly1741=) rs147681220
NM_198576.4(AGRN):c.5254-5C>T rs34708466
NM_198576.4(AGRN):c.5352C>T (p.Phe1784=) rs112073270
NM_198576.4(AGRN):c.5353G>A (p.Asp1785Asn) rs144245019
NM_198576.4(AGRN):c.5466A>G (p.Ser1822=) rs149659540
NM_198576.4(AGRN):c.5550G>A (p.Pro1850=) rs74045090
NM_198576.4(AGRN):c.5598C>T (p.Thr1866=) rs17778478
NM_198576.4(AGRN):c.5667G>A (p.Gln1889=) rs115061121
NM_198576.4(AGRN):c.5726G>C (p.Ser1909Thr) rs74685771
NM_198576.4(AGRN):c.579G>A (p.Ala193=) rs201301445
NM_198576.4(AGRN):c.5814C>T (p.Pro1938=) rs369308183
NM_198576.4(AGRN):c.5896C>T (p.Leu1966=) rs115828965
NM_198576.4(AGRN):c.67G>C (p.Val23Leu) rs201073369
NM_198576.4(AGRN):c.729C>G (p.Gly243=) rs191270495
NM_198576.4(AGRN):c.773C>T (p.Thr258Ile) rs200607541
NM_198576.4(AGRN):c.804C>T (p.Ala268=) rs113789806

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