ClinVar Miner

List of variants in gene AGRN reported as likely benign by CeGaT Center for Human Genetics Tuebingen

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 44
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HGVS dbSNP gnomAD frequency
NM_198576.4(AGRN):c.5223C>T (p.Gly1741=) rs147681220 0.00805
NM_198576.4(AGRN):c.3465T>C (p.Ala1155=) rs146358566 0.00657
NM_198576.4(AGRN):c.3866C>T (p.Pro1289Leu) rs139294803 0.00637
NM_198576.4(AGRN):c.5025C>T (p.Gly1675=) rs147990356 0.00536
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.5896C>T (p.Leu1966=) rs115828965 0.00378
NM_198576.4(AGRN):c.579G>A (p.Ala193=) rs201301445 0.00331
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.2067G>A (p.Gln689=) rs139886237 0.00288
NM_198576.4(AGRN):c.4639G>A (p.Glu1547Lys) rs2799068 0.00284
NM_198576.4(AGRN):c.1434G>A (p.Thr478=) rs147346337 0.00281
NM_198576.4(AGRN):c.5095C>T (p.Arg1699Cys) rs148518738 0.00268
NM_198576.4(AGRN):c.3533G>A (p.Arg1178Gln) rs148430436 0.00264
NM_198576.4(AGRN):c.5254-5C>T rs34708466 0.00248
NM_198576.4(AGRN):c.4131C>T (p.Phe1377=) rs368555478 0.00225
NM_198576.4(AGRN):c.2805+7G>A rs190000918 0.00177
NM_198576.4(AGRN):c.6074A>G (p.His2025Arg) rs377296839 0.00151
NM_198576.4(AGRN):c.4840G>A (p.Glu1614Lys) rs147259096 0.00113
NM_198576.4(AGRN):c.1178-7G>A rs200932219 0.00106
NM_198576.4(AGRN):c.1188G>A (p.Pro396=) rs138841641 0.00103
NM_198576.4(AGRN):c.2013C>T (p.Ser671=) rs141603403 0.00093
NM_198576.4(AGRN):c.2681-4C>T rs186518388 0.00092
NM_198576.4(AGRN):c.2266G>A (p.Ala756Thr) rs140764403 0.00079
NM_198576.4(AGRN):c.4323G>A (p.Ala1441=) rs373287346 0.00066
NM_198576.4(AGRN):c.4272G>A (p.Ala1424=) rs201470321 0.00061
NM_198576.4(AGRN):c.4734C>T (p.Pro1578=) rs186574226 0.00049
NM_198576.4(AGRN):c.2796C>T (p.Asn932=) rs147153797 0.00031
NM_198576.4(AGRN):c.1209C>T (p.Ala403=) rs368625531 0.00028
NM_198576.4(AGRN):c.5814C>T (p.Pro1938=) rs369308183 0.00020
NM_198576.4(AGRN):c.4605G>T (p.Gly1535=) rs373097825 0.00015
NM_198576.4(AGRN):c.1395G>A (p.Pro465=) rs367601178 0.00014
NM_198576.4(AGRN):c.1557C>T (p.Ala519=) rs146185843 0.00012
NM_198576.4(AGRN):c.5589C>T (p.Asp1863=) rs148105695 0.00007
NM_198576.4(AGRN):c.3366C>T (p.Asp1122=) rs374090990 0.00004
NM_198576.4(AGRN):c.1902C>T (p.Ser634=) rs549820648 0.00002
NM_198576.4(AGRN):c.3522C>T (p.Asp1174=) rs374008359 0.00002
NM_198576.4(AGRN):c.5133G>A (p.Ala1711=) rs376535149 0.00002
NM_198576.4(AGRN):c.4470C>T (p.Asp1490=) rs547462192 0.00001
NM_198576.4(AGRN):c.1878C>A (p.Pro626=)
NM_198576.4(AGRN):c.3015C>T (p.Pro1005=) rs547720389
NM_198576.4(AGRN):c.3021T>C (p.Ala1007=)
NM_198576.4(AGRN):c.4497C>T (p.Pro1499=)

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