ClinVar Miner

List of variants in gene AGRN studied for not provided

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Gene type:
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Total variants: 73
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HGVS dbSNP
GRCh37/hg19 1p36.33(chr1:957640-964438)x0
GRCh37/hg19 1p36.33(chr1:963864-964438)x1
GRCh37/hg19 1p36.33(chr1:963864-986737)x0
GRCh37/hg19 1p36.33(chr1:963938-964438)x1
GRCh37/hg19 1p36.33(chr1:963938-985900)x1
NC_000001.11:g.1019833T>C
NM_198576.4(AGRN):c.1123G>T (p.Ala375Ser) rs138031468
NM_198576.4(AGRN):c.1177+109_1178-99del
NM_198576.4(AGRN):c.1177+121G>C
NM_198576.4(AGRN):c.1384+238C>T
NM_198576.4(AGRN):c.1384+28G>A rs2710876
NM_198576.4(AGRN):c.1434G>A (p.Thr478=) rs147346337
NM_198576.4(AGRN):c.1507G>A (p.Gly503Ser) rs776919703
NM_198576.4(AGRN):c.1660G>A (p.Val554Met) rs79016973
NM_198576.4(AGRN):c.1865G>A (p.Arg622Gln) rs140789461
NM_198576.4(AGRN):c.1906G>A (p.Gly636Ser) rs1042435801
NM_198576.4(AGRN):c.1993G>A (p.Glu665Lys) rs143324306
NM_198576.4(AGRN):c.2013C>T (p.Ser671=) rs141603403
NM_198576.4(AGRN):c.2241G>C (p.Gln747His) rs144361725
NM_198576.4(AGRN):c.2255-81G>A
NM_198576.4(AGRN):c.2306C>T (p.Thr769Met) rs148837216
NM_198576.4(AGRN):c.2501G>A (p.Arg834Gln) rs146243145
NM_198576.4(AGRN):c.2537-26A>G rs3128098
NM_198576.4(AGRN):c.2650C>T (p.Arg884Cys) rs539990009
NM_198576.4(AGRN):c.2690C>T (p.Ala897Val) rs116836855
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.3388+107A>G
NM_198576.4(AGRN):c.3388+125T>C
NM_198576.4(AGRN):c.3388+176T>C
NM_198576.4(AGRN):c.3697C>T (p.Arg1233Trp) rs147673996
NM_198576.4(AGRN):c.3765G>A (p.Ala1255=)
NM_198576.4(AGRN):c.4021G>C (p.Gly1341Arg)
NM_198576.4(AGRN):c.4105+180C>A
NM_198576.4(AGRN):c.4106-145G>A
NM_198576.4(AGRN):c.4106-186C>T
NM_198576.4(AGRN):c.4106-214C>T
NM_198576.4(AGRN):c.4106-231G>A
NM_198576.4(AGRN):c.4106-45A>G
NM_198576.4(AGRN):c.4106-75_4106-74del
NM_198576.4(AGRN):c.4120G>T (p.Val1374Leu) rs1057523585
NM_198576.4(AGRN):c.4131C>T (p.Phe1377=) rs368555478
NM_198576.4(AGRN):c.4272G>A (p.Ala1424=) rs201470321
NM_198576.4(AGRN):c.44C>G (p.Pro15Arg) rs764659938
NM_198576.4(AGRN):c.4514+57A>G
NM_198576.4(AGRN):c.4540G>A (p.Ala1514Thr) rs111818381
NM_198576.4(AGRN):c.4621C>T (p.Arg1541Ter) rs750176911
NM_198576.4(AGRN):c.463+56G>T
NM_198576.4(AGRN):c.464-240A>C
NM_198576.4(AGRN):c.4745-44C>T
NM_198576.4(AGRN):c.4779_4793del (p.Gln1593_Cys1597del) rs769494139
NM_198576.4(AGRN):c.4839C>T (p.Cys1613=) rs113020870
NM_198576.4(AGRN):c.4869C>A (p.Phe1623Leu) rs748076659
NM_198576.4(AGRN):c.4879+43T>C
NM_198576.4(AGRN):c.4967G>A (p.Arg1656Gln) rs374905300
NM_198576.4(AGRN):c.498G>A (p.Pro166=)
NM_198576.4(AGRN):c.49C>T (p.Leu17Phe) rs1057523287
NM_198576.4(AGRN):c.511+132G>A
NM_198576.4(AGRN):c.5141+28G>T
NM_198576.4(AGRN):c.5253+68C>T
NM_198576.4(AGRN):c.5254-190C>T
NM_198576.4(AGRN):c.5312dup (p.Ser1772fs) rs1553178276
NM_198576.4(AGRN):c.5353G>A (p.Asp1785Asn) rs144245019
NM_198576.4(AGRN):c.5387G>A (p.Arg1796His) rs774881136
NM_198576.4(AGRN):c.5615G>A (p.Arg1872Gln) rs767076670
NM_198576.4(AGRN):c.5652-201G>C
NM_198576.4(AGRN):c.5743C>T (p.Arg1915Trp) rs140892896
NM_198576.4(AGRN):c.5990C>T (p.Pro1997Leu) rs144091542
NM_198576.4(AGRN):c.6019A>G (p.Lys2007Glu) rs1057522367
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.752T>C (p.Val251Ala) rs779170859
NM_198576.4(AGRN):c.804C>T (p.Ala268=) rs113789806

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