ClinVar Miner

List of variants in gene PRKAG2 reported as likely benign for not specified

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Total variants: 77
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HGVS dbSNP gnomAD frequency
NM_016203.4(PRKAG2):c.864+35_864+36insA rs35348247 0.76395
NM_016203.4(PRKAG2):c.59G>T (p.Ser20Ile) rs116605521 0.02188
NM_016203.4(PRKAG2):c.1593G>A (p.Arg531=) rs148197254 0.00374
NM_016203.4(PRKAG2):c.864+32G>T rs200549512 0.00147
NM_016203.4(PRKAG2):c.298G>A (p.Gly100Ser) rs79474211 0.00144
NM_016203.4(PRKAG2):c.1584+7C>T rs111627309 0.00086
NM_016203.4(PRKAG2):c.250C>T (p.Arg84Trp) rs61746358 0.00056
NM_016203.4(PRKAG2):c.1106+9G>C rs200429988 0.00055
NM_016203.4(PRKAG2):c.472G>A (p.Gly158Ser) rs727504512 0.00054
NM_016203.4(PRKAG2):c.1318C>T (p.His440Tyr) rs201878539 0.00051
NM_016203.4(PRKAG2):c.247C>T (p.Pro83Ser) rs148791216 0.00035
NM_016203.4(PRKAG2):c.1585-4G>A rs373649956 0.00023
NM_016203.4(PRKAG2):c.123C>T (p.Ser41=) rs397517263 0.00019
NM_016203.4(PRKAG2):c.1452G>A (p.Glu484=) rs768299371 0.00016
NM_016203.4(PRKAG2):c.240C>A (p.Gly80=) rs142482217 0.00010
NM_016203.4(PRKAG2):c.1644G>A (p.Ser548=) rs376450705 0.00009
NM_016203.4(PRKAG2):c.594G>A (p.Pro198=) rs397517276 0.00009
NM_016203.4(PRKAG2):c.182G>A (p.Arg61Gln) rs564358410 0.00006
NM_016203.4(PRKAG2):c.1679-3C>T rs371543989 0.00005
NM_016203.4(PRKAG2):c.312C>T (p.Thr104=) rs397517268 0.00004
NM_016203.4(PRKAG2):c.981A>G (p.Leu327=) rs764162597 0.00004
NM_016203.4(PRKAG2):c.*2C>T rs199559205 0.00003
NM_016203.4(PRKAG2):c.181C>A (p.Arg61=) rs770100112 0.00003
NM_016203.4(PRKAG2):c.591C>T (p.Pro197=) rs587781126 0.00003
NM_016203.4(PRKAG2):c.864+13C>T rs727505238 0.00003
NM_016203.4(PRKAG2):c.945A>G (p.Val315=) rs759393540 0.00003
NM_016203.4(PRKAG2):c.114G>A (p.Pro38=) rs397517261 0.00002
NM_016203.4(PRKAG2):c.1005+11C>T rs776445450 0.00001
NM_016203.4(PRKAG2):c.1020A>G (p.Glu340=) rs770773856 0.00001
NM_016203.4(PRKAG2):c.1071A>T (p.Thr357=) rs397517260 0.00001
NM_016203.4(PRKAG2):c.1106+17T>C rs769793016 0.00001
NM_016203.4(PRKAG2):c.115-27881G>A rs1057521688 0.00001
NM_016203.4(PRKAG2):c.1234-7C>T rs1456377814 0.00001
NM_016203.4(PRKAG2):c.1440T>C (p.Asn480=) rs397517265 0.00001
NM_016203.4(PRKAG2):c.1479G>A (p.Thr493=) rs367768776 0.00001
NM_016203.4(PRKAG2):c.1620T>C (p.Ser540=) rs1196648905 0.00001
NM_016203.4(PRKAG2):c.186+12T>C rs374155169 0.00001
NM_016203.4(PRKAG2):c.202G>A (p.Gly68Ser) rs730880970 0.00001
NM_016203.4(PRKAG2):c.222A>G (p.Lys74=) rs1265668637 0.00001
NM_016203.4(PRKAG2):c.393C>T (p.Ser131=) rs1057520352 0.00001
NM_016203.4(PRKAG2):c.42T>A (p.Val14=) rs141316327 0.00001
NM_016203.4(PRKAG2):c.466+19T>C rs376621063 0.00001
NM_016203.4(PRKAG2):c.466+7C>A rs397517272 0.00001
NM_016203.4(PRKAG2):c.531G>T (p.Leu177=) rs373000537 0.00001
NM_016203.4(PRKAG2):c.570C>T (p.Arg190=) rs141191531 0.00001
NM_016203.4(PRKAG2):c.582G>A (p.Ser194=) rs756215060 0.00001
NM_016203.4(PRKAG2):c.660G>A (p.Pro220=) rs774279454 0.00001
NM_016203.4(PRKAG2):c.897C>T (p.Asn299=) rs201876556 0.00001
NM_016203.4(PRKAG2):c.946+19A>G rs745525434 0.00001
NM_016203.4(PRKAG2):c.-39C>A rs1554622689
NM_016203.4(PRKAG2):c.102C>G (p.Arg34=) rs1057522970
NM_016203.4(PRKAG2):c.1107-14G>C rs201150309
NM_016203.4(PRKAG2):c.1129T>C (p.Leu377=) rs1057521896
NM_016203.4(PRKAG2):c.1449T>C (p.Ala483=) rs148632949
NM_016203.4(PRKAG2):c.1584+19T>C rs775336252
NM_016203.4(PRKAG2):c.1585-19C>G rs1057523714
NM_016203.4(PRKAG2):c.1679-19A>G rs200262620
NM_016203.4(PRKAG2):c.1679-19A>T rs200262620
NM_016203.4(PRKAG2):c.186+20A>C rs771538031
NM_016203.4(PRKAG2):c.224G>C (p.Gly75Ala) rs199963585
NM_016203.4(PRKAG2):c.375G>A (p.Gly125=) rs748041666
NM_016203.4(PRKAG2):c.387C>A (p.Ser129=) rs138610896
NM_016203.4(PRKAG2):c.471C>T (p.Ser157=) rs141804012
NM_016203.4(PRKAG2):c.516G>A (p.Gln172=) rs1022959045
NM_016203.4(PRKAG2):c.521C>A (p.Thr174Lys) rs148056866
NM_016203.4(PRKAG2):c.591C>A (p.Pro197=) rs587781126
NM_016203.4(PRKAG2):c.618G>T (p.Pro206=) rs145827515
NM_016203.4(PRKAG2):c.649C>T (p.Leu217=) rs1554530565
NM_016203.4(PRKAG2):c.66C>G (p.Gly22=) rs730880971
NM_016203.4(PRKAG2):c.807G>A (p.Lys269=) rs727504618
NM_016203.4(PRKAG2):c.837G>A (p.Lys279=) rs876657566
NM_016203.4(PRKAG2):c.864+10C>G rs1554480836
NM_016203.4(PRKAG2):c.882T>C (p.Phe294=) rs1554465561
NM_016203.4(PRKAG2):c.894C>G (p.Ala298=) rs1057522338
NM_016203.4(PRKAG2):c.912G>A (p.Ala304=) rs145029525
NM_016203.4(PRKAG2):c.946+13G>C rs727505059
NM_016203.4(PRKAG2):c.993T>C (p.Tyr331=) rs397517284

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