ClinVar Miner

List of variants in gene PRKG1 studied for not specified

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Total variants: 50
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HGVS dbSNP gnomAD frequency
NM_006258.4(PRKG1):c.479-9C>T rs45615337 0.08494
NM_006258.4(PRKG1):c.1008T>C (p.Phe336=) rs56047641 0.05131
NM_006258.4(PRKG1):c.845A>G (p.Asn282Ser) rs34997494 0.03846
NM_006258.4(PRKG1):c.888T>C (p.Leu296=) rs113994747 0.02057
NM_006258.4(PRKG1):c.408G>A (p.Pro136=) rs55806342 0.01754
NM_006258.4(PRKG1):c.1080T>C (p.Tyr360=) rs141218982 0.00519
NM_006258.4(PRKG1):c.426C>T (p.Asp142=) rs55754654 0.00439
NM_006258.4(PRKG1):c.-31C>T rs41274080 0.00211
NM_006258.4(PRKG1):c.906A>C (p.Gly302=) rs145917628 0.00185
NM_006258.4(PRKG1):c.1299C>T (p.Ser433=) rs145035655 0.00127
NM_006258.4(PRKG1):c.1525C>T (p.His509Tyr) rs139646798 0.00109
NM_006258.4(PRKG1):c.1071A>G (p.Lys357=) rs75650199 0.00097
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.675C>T (p.Thr225=) rs142166726 0.00050
NM_006258.4(PRKG1):c.1466A>T (p.Tyr489Phe) rs149710600 0.00027
NM_006258.4(PRKG1):c.840+14G>T rs146372571 0.00025
NM_006258.4(PRKG1):c.1002-9G>A rs200218082 0.00022
NM_006258.4(PRKG1):c.1017G>A (p.Leu339=) rs187636159 0.00012
NM_006258.4(PRKG1):c.1026G>A (p.Gly342=) rs374834674 0.00011
NM_006258.4(PRKG1):c.1662C>T (p.Ala554=) rs374202731 0.00011
NM_006258.4(PRKG1):c.1928G>A (p.Arg643Lys) rs770812712 0.00006
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.299C>G (p.Pro100Arg) rs763629518 0.00002
NM_006258.4(PRKG1):c.478+5G>A rs763059343 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.1663G>A (p.Asp555Asn) rs773713867 0.00001
NM_006258.4(PRKG1):c.2053G>C (p.Asp685His) rs1398800687 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.763-8C>T rs777859336 0.00001
NM_006258.4(PRKG1):c.1076+19_1076+20insTGGCCTT rs146504019
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.514T>C (p.Leu172=)
NM_006258.4(PRKG1):c.546G>A (p.Gly182=) rs73336216
NM_006258.4(PRKG1):c.642A>G (p.Thr214=) rs370640208
NM_006258.4(PRKG1):c.763-15G>T rs1904010

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