ClinVar Miner

List of variants in gene AGRN reported as likely benign by Breakthrough Genomics, Breakthrough Genomics

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 62
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HGVS dbSNP gnomAD frequency
NM_198576.4(AGRN):c.4298+50G>T rs762581337 0.01825
NM_198576.4(AGRN):c.5651+58C>T rs113261977 0.01727
NM_198576.4(AGRN):c.3388+66C>T rs147362722 0.01412
NM_198576.4(AGRN):c.1178-42G>A rs114521679 0.01294
NM_198576.4(AGRN):c.4976+44G>A rs60267685 0.01257
NM_198576.4(AGRN):c.3570C>T (p.Arg1190=) rs75361935 0.01197
NM_198576.4(AGRN):c.2255-101G>A rs112752525 0.01114
NM_198576.4(AGRN):c.2025C>G (p.Gly675=) rs28484890 0.01053
NM_198576.4(AGRN):c.464-202G>A rs116522930 0.01035
NM_198576.4(AGRN):c.2406C>T (p.Gly802=) rs75774767 0.01029
NM_198576.4(AGRN):c.4452C>T (p.Thr1484=) rs75767981 0.00984
NM_198576.4(AGRN):c.4514+50C>G rs111525350 0.00947
NM_198576.4(AGRN):c.4879+92G>A rs111638438 0.00903
NM_198576.4(AGRN):c.1528G>A (p.Gly510Ser) rs138288952 0.00834
NM_198576.4(AGRN):c.4695G>C (p.Gln1565His) rs199876002 0.00827
NM_198576.4(AGRN):c.738C>T (p.Asp246=) rs536085218 0.00811
NM_198576.4(AGRN):c.3964C>T (p.Arg1322Trp) rs184970403 0.00750
NM_198576.4(AGRN):c.4540G>A (p.Ala1514Thr) rs111818381 0.00748
NM_198576.4(AGRN):c.5726G>C (p.Ser1909Thr) rs74685771 0.00724
NM_198576.4(AGRN):c.1660G>A (p.Val554Met) rs79016973 0.00706
NM_198576.4(AGRN):c.1177+71G>T rs1435024596 0.00693
NM_198576.4(AGRN):c.3077C>A (p.Thr1026Asn) rs3813188 0.00690
NM_198576.4(AGRN):c.1603+19G>A rs115191992 0.00678
NM_198576.4(AGRN):c.2536+45C>T rs183108359 0.00658
NM_198576.4(AGRN):c.5142-50C>T rs28545735 0.00633
NM_198576.4(AGRN):c.5352C>T (p.Phe1784=) rs112073270 0.00537
NM_198576.4(AGRN):c.1123G>T (p.Ala375Ser) rs138031468 0.00517
NM_198576.4(AGRN):c.4514+29C>T rs146377446 0.00485
NM_198576.4(AGRN):c.4352C>T (p.Pro1451Leu) rs144620006 0.00406
NM_198576.4(AGRN):c.3517-47G>A rs146562180 0.00401
NM_198576.4(AGRN):c.5896C>T (p.Leu1966=) rs115828965 0.00378
NM_198576.4(AGRN):c.5254-173G>A rs571906979 0.00344
NM_198576.4(AGRN):c.2067G>A (p.Gln689=) rs139886237 0.00282
NM_198576.4(AGRN):c.800C>T (p.Thr267Met) rs566673314 0.00265
NM_198576.4(AGRN):c.773C>T (p.Thr258Ile) rs200607541 0.00231
NM_198576.4(AGRN):c.4131C>T (p.Phe1377=) rs368555478 0.00225
NM_198576.4(AGRN):c.5466A>G (p.Ser1822=) rs149659540 0.00218
NM_198576.4(AGRN):c.494C>T (p.Pro165Leu) rs140954236 0.00196
NM_198576.4(AGRN):c.2805+7G>A rs190000918 0.00177
NM_198576.4(AGRN):c.6074A>G (p.His2025Arg) rs377296839 0.00141
NM_198576.4(AGRN):c.1188G>A (p.Pro396=) rs138841641 0.00105
NM_198576.4(AGRN):c.2266G>A (p.Ala756Thr) rs140764403 0.00089
NM_198576.4(AGRN):c.5564-11C>T rs191736727 0.00080
NM_198576.4(AGRN):c.2682C>T (p.Asp894=) rs118105080 0.00067
NM_198576.4(AGRN):c.4272G>A (p.Ala1424=) rs201470321 0.00061
NM_198576.4(AGRN):c.2796C>T (p.Asn932=) rs147153797 0.00034
NM_198576.4(AGRN):c.1198C>T (p.Arg400Trp) rs149636063 0.00032
NM_198576.4(AGRN):c.2277G>A (p.Pro759=) rs199985558 0.00032
NM_198576.4(AGRN):c.3003C>T (p.Pro1001=) rs375208869 0.00021
NM_198576.4(AGRN):c.2681-16C>G rs199785742 0.00018
NM_198576.4(AGRN):c.1395G>A (p.Pro465=) rs367601178 0.00014
NM_198576.4(AGRN):c.2400T>C (p.Ser800=) rs529944515 0.00011
NM_198576.4(AGRN):c.5925C>T (p.Thr1975=) rs376944871 0.00011
NM_198576.4(AGRN):c.2667G>A (p.Ala889=) rs144205055 0.00009
NM_198576.4(AGRN):c.3752-5G>A rs201733530 0.00009
NM_198576.4(AGRN):c.4488C>T (p.Gly1496=) rs748221306 0.00009
NM_198576.4(AGRN):c.5589C>T (p.Asp1863=) rs148105695 0.00007
NM_198576.4(AGRN):c.2148+8C>G rs747897478 0.00003
NM_198576.4(AGRN):c.201+138G>T rs555803746
NM_198576.4(AGRN):c.2457G>A (p.Gly819=) rs112039851
NM_198576.4(AGRN):c.2457G>C (p.Gly819=) rs112039851
NM_198576.4(AGRN):c.3264G>C (p.Leu1088Phe) rs150132566

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