ClinVar Miner

List of variants in gene PRKG1 reported as likely benign for not specified

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Total variants: 24
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HGVS dbSNP gnomAD frequency
NM_006258.4(PRKG1):c.845A>G (p.Asn282Ser) rs34997494 0.03846
NM_006258.4(PRKG1):c.1525C>T (p.His509Tyr) rs139646798 0.00109
NM_006258.4(PRKG1):c.312-12C>G rs371409852 0.00086
NM_006258.4(PRKG1):c.1963-16T>G rs376174664 0.00052
NM_006258.4(PRKG1):c.1002-9G>A rs200218082 0.00022
NM_006258.4(PRKG1):c.1710-20C>T rs370461631 0.00004
NM_006258.4(PRKG1):c.2049T>C (p.Asp683=) rs771700923 0.00004
NM_006258.4(PRKG1):c.1101C>T (p.Phe367=) rs752325371 0.00002
NM_006258.4(PRKG1):c.1962T>C (p.Ser654=) rs767330363 0.00002
NM_006258.4(PRKG1):c.2013C>T (p.Asn671=) rs373962932 0.00002
NM_006258.4(PRKG1):c.1001+12G>A rs1057524395 0.00001
NM_006258.4(PRKG1):c.1173+4G>A rs886039153 0.00001
NM_006258.4(PRKG1):c.27C>T (p.Tyr9=) rs777472224 0.00001
NM_006258.4(PRKG1):c.585C>T (p.Thr195=) rs139104275 0.00001
NM_006258.4(PRKG1):c.591G>A (p.Lys197=) rs1275290492 0.00001
NM_006258.4(PRKG1):c.114G>C (p.Leu38=) rs913151254
NM_006258.4(PRKG1):c.1174-15C>T rs41280442
NM_006258.4(PRKG1):c.153G>C (p.Ser51=) rs1400601775
NM_006258.4(PRKG1):c.1896-11del rs756748643
NM_006258.4(PRKG1):c.1963-19del rs145115489
NM_006258.4(PRKG1):c.1963-19dup rs145115489
NM_006258.4(PRKG1):c.1963-5dup rs1377958548
NM_006258.4(PRKG1):c.2037C>T (p.Asn679=) rs1322320716
NM_006258.4(PRKG1):c.642A>G (p.Thr214=) rs370640208

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