ClinVar Miner

List of variants in gene PRKAG3 reported as uncertain significance for not specified

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Total variants: 52
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HGVS dbSNP gnomAD frequency
NM_017431.4(PRKAG3):c.1036C>T (p.Arg346Cys) rs200343848 0.00017
NM_017431.4(PRKAG3):c.10G>A (p.Gly4Arg) rs775874370 0.00011
NM_017431.4(PRKAG3):c.14T>A (p.Leu5Gln) rs145686425 0.00011
NM_017431.4(PRKAG3):c.667G>A (p.Gly223Ser) rs144281244 0.00008
NM_017431.4(PRKAG3):c.755G>A (p.Arg252His) rs199795628 0.00008
NM_017431.4(PRKAG3):c.1177G>A (p.Val393Met) rs375349598 0.00006
NM_017431.4(PRKAG3):c.1345C>T (p.Arg449Trp) rs773973238 0.00006
NM_017431.4(PRKAG3):c.509T>G (p.Leu170Arg) rs762040545 0.00006
NM_017431.4(PRKAG3):c.22G>A (p.Ala8Thr) rs760249619 0.00004
NM_017431.4(PRKAG3):c.488C>T (p.Pro163Leu) rs200455339 0.00004
NM_017431.4(PRKAG3):c.148C>T (p.Arg50Cys) rs551266755 0.00003
NM_017431.4(PRKAG3):c.25C>A (p.Leu9Met) rs535544559 0.00003
NM_017431.4(PRKAG3):c.529C>T (p.Arg177Trp) rs759108860 0.00003
NM_017431.4(PRKAG3):c.298G>C (p.Ala100Pro) rs779691724 0.00002
NM_017431.4(PRKAG3):c.465G>C (p.Glu155Asp) rs746853657 0.00002
NM_017431.4(PRKAG3):c.602C>G (p.Ser201Cys) rs948666411 0.00002
NM_017431.4(PRKAG3):c.110G>C (p.Trp37Ser) rs1944010385 0.00001
NM_017431.4(PRKAG3):c.1192C>T (p.Arg398Cys) rs765464278 0.00001
NM_017431.4(PRKAG3):c.1214C>T (p.Ala405Val) rs950043181 0.00001
NM_017431.4(PRKAG3):c.1333G>A (p.Asp445Asn) rs750886488 0.00001
NM_017431.4(PRKAG3):c.278T>A (p.Phe93Tyr) rs778304244 0.00001
NM_017431.4(PRKAG3):c.566A>G (p.Gln189Arg) rs372351300 0.00001
NM_017431.4(PRKAG3):c.619G>T (p.Asp207Tyr) rs768675439 0.00001
NM_017431.4(PRKAG3):c.938C>T (p.Pro313Leu) rs751962538 0.00001
NM_017431.4(PRKAG3):c.977G>A (p.Arg326His) rs1272818509 0.00001
NM_017431.4(PRKAG3):c.1024T>G (p.Ser342Ala) rs2470243843
NM_017431.4(PRKAG3):c.1037G>A (p.Arg346His)
NM_017431.4(PRKAG3):c.1103T>A (p.Ile368Asn)
NM_017431.4(PRKAG3):c.1126G>A (p.Val376Met) rs2470243703
NM_017431.4(PRKAG3):c.1162G>A (p.Glu388Lys) rs1943940908
NM_017431.4(PRKAG3):c.1193G>A (p.Arg398His)
NM_017431.4(PRKAG3):c.11G>C (p.Gly4Ala)
NM_017431.4(PRKAG3):c.1234C>T (p.His412Tyr)
NM_017431.4(PRKAG3):c.176G>A (p.Arg59Lys) rs746256172
NM_017431.4(PRKAG3):c.305C>A (p.Ala102Asp)
NM_017431.4(PRKAG3):c.320T>A (p.Val107Glu) rs1944000597
NM_017431.4(PRKAG3):c.32G>C (p.Arg11Thr) rs768697010
NM_017431.4(PRKAG3):c.347G>T (p.Cys116Phe)
NM_017431.4(PRKAG3):c.383C>G (p.Ser128Cys)
NM_017431.4(PRKAG3):c.386G>C (p.Ser129Thr)
NM_017431.4(PRKAG3):c.523G>A (p.Glu175Lys)
NM_017431.4(PRKAG3):c.541G>C (p.Ala181Pro)
NM_017431.4(PRKAG3):c.568G>A (p.Glu190Lys)
NM_017431.4(PRKAG3):c.644C>T (p.Ala215Val) rs767253674
NM_017431.4(PRKAG3):c.720G>A (p.Met240Ile) rs2470245641
NM_017431.4(PRKAG3):c.740T>C (p.Ile247Thr)
NM_017431.4(PRKAG3):c.78G>A (p.Met26Ile)
NM_017431.4(PRKAG3):c.836G>A (p.Gly279Asp)
NM_017431.4(PRKAG3):c.836G>C (p.Gly279Ala)
NM_017431.4(PRKAG3):c.871G>T (p.Asp291Tyr) rs1417320602
NM_017431.4(PRKAG3):c.878T>C (p.Leu293Pro)
NM_017431.4(PRKAG3):c.976C>T (p.Arg326Cys)

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