ClinVar Miner

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

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Total variants: 78
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HGVS dbSNP gnomAD frequency
NM_016203.4(PRKAG2):c.1437+47A>G rs73156279 0.02725
NM_016203.4(PRKAG2):c.59G>T (p.Ser20Ile) rs116605521 0.02188
NM_016203.4(PRKAG2):c.1678+86T>C rs75273149 0.01378
NM_016203.3(PRKAG2):c.-520C>T rs73160072 0.01266
NM_016203.4(PRKAG2):c.1399+130A>G rs73475418 0.00949
NM_016203.4(PRKAG2):c.1052-244C>T rs114431229 0.00939
NM_016203.4(PRKAG2):c.114+152C>G rs181719939 0.00627
NM_016203.4(PRKAG2):c.207G>A (p.Pro69=) rs144384573 0.00538
NM_016203.4(PRKAG2):c.947-293A>G rs75279516 0.00503
NM_016203.4(PRKAG2):c.1006-280A>C rs113540490 0.00502
NM_016203.4(PRKAG2):c.1005+301C>T rs112367952 0.00501
NM_016203.4(PRKAG2):c.186+241G>A rs151014818 0.00480
NM_016203.4(PRKAG2):c.186+49G>A rs76585974 0.00466
NM_016203.4(PRKAG2):c.1678+277A>C rs149111981 0.00434
NM_016203.4(PRKAG2):c.1437+292C>T rs137867804 0.00413
NM_016203.4(PRKAG2):c.1593G>A (p.Arg531=) rs148197254 0.00374
NM_016203.4(PRKAG2):c.1296G>A (p.Thr432=) rs114079815 0.00280
NM_016203.4(PRKAG2):c.111T>A (p.Ile37=) rs144426409 0.00259
NM_016203.4(PRKAG2):c.1704G>A (p.Thr568=) rs138167675 0.00150
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.946+3A>G rs376173303 0.00041
NM_016203.4(PRKAG2):c.251G>A (p.Arg84Gln) rs201953758 0.00036
NM_016203.4(PRKAG2):c.247C>T (p.Pro83Ser) rs148791216 0.00035
NM_016203.4(PRKAG2):c.325T>G (p.Ser109Ala) rs139579816 0.00025
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.240C>A (p.Gly80=) rs142482217 0.00010
NM_016203.4(PRKAG2):c.1644G>A (p.Ser548=) rs376450705 0.00009
NM_016203.4(PRKAG2):c.429G>A (p.Ser143=) rs757727533 0.00008
NM_016203.4(PRKAG2):c.*6G>A rs181109799 0.00006
NM_016203.4(PRKAG2):c.130G>A (p.Ala44Thr) rs144857453 0.00006
NM_016203.4(PRKAG2):c.466+45211G>A rs149506922 0.00006
NM_016203.4(PRKAG2):c.147C>T (p.Asp49=) rs761196275 0.00005
NM_016203.4(PRKAG2):c.1659C>T (p.Ala553=) rs374476363 0.00005
NM_016203.4(PRKAG2):c.1335C>T (p.Ile445=) rs781153622 0.00004
NM_016203.4(PRKAG2):c.312C>T (p.Thr104=) rs397517268 0.00004
NM_016203.4(PRKAG2):c.489G>A (p.Pro163=) rs556852534 0.00004
NM_016203.4(PRKAG2):c.981A>G (p.Leu327=) rs764162597 0.00004
NM_016203.4(PRKAG2):c.-16A>G rs200468798 0.00003
NM_016203.4(PRKAG2):c.1584+8G>A rs762649633 0.00003
NM_016203.4(PRKAG2):c.342G>A (p.Pro114=) rs147365679 0.00003
NM_016203.4(PRKAG2):c.1051+3A>G rs376499470 0.00002
NM_016203.4(PRKAG2):c.138G>A (p.Pro46=) rs767613486 0.00002
NM_016203.4(PRKAG2):c.432C>T (p.Pro144=) rs764742900 0.00002
NM_016203.4(PRKAG2):c.1254T>C (p.Pro418=) rs753059650 0.00001
NM_016203.4(PRKAG2):c.186+10C>G rs759913875 0.00001
NM_016203.4(PRKAG2):c.186+12T>C rs374155169 0.00001
NM_016203.4(PRKAG2):c.331C>A (p.Gln111Lys) rs778331706 0.00001
NM_016203.4(PRKAG2):c.393C>T (p.Ser131=) rs1057520352 0.00001
NM_016203.4(PRKAG2):c.466+45251C>T rs1399276796 0.00001
NM_016203.4(PRKAG2):c.531G>T (p.Leu177=) rs373000537 0.00001
NM_016203.4(PRKAG2):c.585T>A (p.Ser195=) rs781522393 0.00001
NM_016203.4(PRKAG2):c.897C>T (p.Asn299=) rs201876556 0.00001
NM_016203.4(PRKAG2):c.-287C>G rs75059373
NM_016203.4(PRKAG2):c.1005+8G>C rs1245068890
NM_016203.4(PRKAG2):c.1106+10dup rs374874465
NM_016203.4(PRKAG2):c.115-28211_115-28200del rs544464975
NM_016203.4(PRKAG2):c.1234-8C>G rs2150996653
NM_016203.4(PRKAG2):c.1584+20C>G rs1450315040
NM_016203.4(PRKAG2):c.1679-19A>G rs200262620
NM_016203.4(PRKAG2):c.1679-246dup rs199780905
NM_016203.4(PRKAG2):c.248C>T (p.Pro83Leu) rs757900380
NM_016203.4(PRKAG2):c.303T>C (p.Ser101=) rs774628602
NM_016203.4(PRKAG2):c.466+45239T>G
NM_016203.4(PRKAG2):c.467-113_467-76dup rs1554531144
NM_016203.4(PRKAG2):c.471C>T (p.Ser157=) rs141804012
NM_016203.4(PRKAG2):c.591C>G (p.Pro197=) rs587781126
NM_016203.4(PRKAG2):c.606G>A (p.Gln202=)
NM_016203.4(PRKAG2):c.810T>C (p.Cys270=) rs61752000
NM_016203.4(PRKAG2):c.865-66dup rs1208767401
NM_016203.4(PRKAG2):c.912G>A (p.Ala304=) rs145029525
NM_016203.4(PRKAG2):c.912G>T (p.Ala304=) rs145029525
NM_016203.4(PRKAG2):c.993T>C (p.Tyr331=) rs397517284

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