ClinVar Miner

List of variants in gene AGRN reported as likely benign by Ambry Genetics

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Gene type:
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Total variants: 24
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HGVS dbSNP gnomAD frequency
NM_198576.4(AGRN):c.4139G>A (p.Arg1380His) rs183686622 0.00183
NM_198576.4(AGRN):c.3926G>A (p.Arg1309Gln) rs199680125 0.00143
NM_198576.4(AGRN):c.6074A>G (p.His2025Arg) rs377296839 0.00141
NM_198576.4(AGRN):c.2219G>A (p.Arg740Gln) rs146863919 0.00025
NM_198576.4(AGRN):c.2306C>T (p.Thr769Met) rs148837216 0.00008
NM_198576.4(AGRN):c.4090G>A (p.Ala1364Thr) rs375639071 0.00008
NM_198576.4(AGRN):c.1478C>T (p.Ala493Val) rs1295689490 0.00004
NM_198576.4(AGRN):c.3056C>T (p.Pro1019Leu) rs756489447 0.00004
NM_198576.4(AGRN):c.3971C>T (p.Pro1324Leu) rs770876851 0.00004
NM_198576.4(AGRN):c.1199G>A (p.Arg400Gln) rs748219640 0.00003
NM_198576.4(AGRN):c.5096G>A (p.Arg1699His) rs777269140 0.00003
NM_198576.4(AGRN):c.6119G>A (p.Arg2040Gln) rs527639453 0.00003
NM_198576.4(AGRN):c.2404G>A (p.Gly802Ser) rs762481817 0.00002
NM_198576.4(AGRN):c.3004G>A (p.Gly1002Ser) rs757677789 0.00002
NM_198576.4(AGRN):c.3068G>A (p.Arg1023Gln) rs775442981 0.00002
NM_198576.4(AGRN):c.5387G>A (p.Arg1796His) rs774881136 0.00002
NM_198576.4(AGRN):c.5459G>A (p.Arg1820Gln) rs1170138989 0.00002
NM_198576.4(AGRN):c.1685T>C (p.Leu562Ser) rs771414620 0.00001
NM_198576.4(AGRN):c.2216A>G (p.Gln739Arg) rs938948615 0.00001
NM_198576.4(AGRN):c.2276C>T (p.Pro759Leu) rs1214623286 0.00001
NM_198576.4(AGRN):c.4739G>A (p.Arg1580His) rs780013869 0.00001
NM_198576.4(AGRN):c.4869C>A (p.Phe1623Leu) rs748076659 0.00001
NM_198576.4(AGRN):c.2282T>C (p.Val761Ala)
NM_198576.4(AGRN):c.5444G>A (p.Gly1815Asp) rs1270329202

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