ClinVar Miner

List of variants in gene ADCY10 reported as uncertain significance for not provided

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Gene type:
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Total variants: 130
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HGVS dbSNP gnomAD frequency
NM_018417.6(ADCY10):c.2042C>T (p.Ala681Val) rs75116612 0.00160
NM_018417.6(ADCY10):c.3592G>A (p.Gly1198Arg) rs41270739 0.00088
NM_018417.6(ADCY10):c.4558G>A (p.Val1520Ile) rs144839993 0.00046
NM_018417.6(ADCY10):c.4424A>G (p.Gln1475Arg) rs199702241 0.00030
NM_018417.6(ADCY10):c.2740C>T (p.Arg914Cys) rs144433453 0.00028
NM_018417.6(ADCY10):c.3619C>T (p.Arg1207Trp) rs147104989 0.00024
NM_018417.6(ADCY10):c.4547T>C (p.Leu1516Pro) rs186485513 0.00013
NM_018417.6(ADCY10):c.2278A>C (p.Lys760Gln) rs200458596 0.00006
NM_018417.6(ADCY10):c.3746T>C (p.Phe1249Ser) rs368942743 0.00006
NM_018417.6(ADCY10):c.4232T>A (p.Ile1411Asn) rs375622466 0.00006
NM_018417.6(ADCY10):c.2111A>G (p.Asp704Gly) rs202048906 0.00005
NM_018417.6(ADCY10):c.4816G>A (p.Val1606Met) rs201892899 0.00005
NM_018417.6(ADCY10):c.2005A>G (p.Ile669Val) rs764189405 0.00004
NM_018417.6(ADCY10):c.2026G>A (p.Val676Ile) rs576877531 0.00004
NM_018417.6(ADCY10):c.4317T>A (p.Phe1439Leu) rs200807095 0.00004
NM_018417.6(ADCY10):c.4504C>G (p.Gln1502Glu) rs200833497 0.00004
NM_018417.6(ADCY10):c.2056G>A (p.Val686Ile) rs373573088 0.00003
NM_018417.6(ADCY10):c.3667T>C (p.Tyr1223His) rs151050988 0.00003
NM_018417.6(ADCY10):c.3082G>A (p.Glu1028Lys) rs745937549 0.00002
NM_018417.6(ADCY10):c.3307A>C (p.Met1103Leu) rs755931495 0.00002
NM_018417.6(ADCY10):c.1897A>C (p.Ile633Leu) rs1665903568 0.00001
NM_018417.6(ADCY10):c.2102A>G (p.Gln701Arg) rs1243130529 0.00001
NM_018417.6(ADCY10):c.3422G>C (p.Cys1141Ser) rs1186181573 0.00001
NM_018417.6(ADCY10):c.4573G>A (p.Gly1525Arg) rs1662155517 0.00001
NM_018417.6(ADCY10):c.4763G>C (p.Arg1588Thr) rs755426228 0.00001
NC_000001.10:g.(?_167798485)_(167802420_?)dup
NC_000001.10:g.(?_167817579)_(167817747_?)dup
NC_000001.10:g.(?_167863071)_(167865949_?)dup
NM_018417.6(ADCY10):c.1625C>T (p.Ala542Val)
NM_018417.6(ADCY10):c.1664A>G (p.Tyr555Cys)
NM_018417.6(ADCY10):c.1780T>C (p.Cys594Arg)
NM_018417.6(ADCY10):c.1787T>C (p.Leu596Pro)
NM_018417.6(ADCY10):c.1793A>G (p.Asp598Gly)
NM_018417.6(ADCY10):c.1795A>G (p.Ile599Val)
NM_018417.6(ADCY10):c.1823G>A (p.Arg608Gln)
NM_018417.6(ADCY10):c.1839G>A (p.Met613Ile)
NM_018417.6(ADCY10):c.1850A>G (p.Lys617Arg)
NM_018417.6(ADCY10):c.1878T>A (p.Phe626Leu)
NM_018417.6(ADCY10):c.1896+5G>C
NM_018417.6(ADCY10):c.1915A>C (p.Ile639Leu)
NM_018417.6(ADCY10):c.1932T>A (p.Asp644Glu)
NM_018417.6(ADCY10):c.1934A>G (p.Glu645Gly)
NM_018417.6(ADCY10):c.1937C>G (p.Ala646Gly)
NM_018417.6(ADCY10):c.1970T>G (p.Met657Arg)
NM_018417.6(ADCY10):c.1996A>G (p.Ile666Val)
NM_018417.6(ADCY10):c.2141A>G (p.Asn714Ser)
NM_018417.6(ADCY10):c.2235_2237del (p.Glu745_His746delinsAsp)
NM_018417.6(ADCY10):c.2241T>A (p.His747Gln)
NM_018417.6(ADCY10):c.2251G>A (p.Val751Ile)
NM_018417.6(ADCY10):c.2255T>C (p.Phe752Ser)
NM_018417.6(ADCY10):c.2348C>G (p.Thr783Ser)
NM_018417.6(ADCY10):c.2353C>A (p.His785Asn)
NM_018417.6(ADCY10):c.2372AAG[1] (p.Glu792del)
NM_018417.6(ADCY10):c.2397_2398inv (p.Val800Ile)
NM_018417.6(ADCY10):c.2402G>C (p.Arg801Thr)
NM_018417.6(ADCY10):c.2404C>A (p.Leu802Met)
NM_018417.6(ADCY10):c.2464A>T (p.Met822Leu)
NM_018417.6(ADCY10):c.2474C>G (p.Ser825Cys) rs1558179811
NM_018417.6(ADCY10):c.2507T>C (p.Ile836Thr)
NM_018417.6(ADCY10):c.2516C>T (p.Thr839Ile)
NM_018417.6(ADCY10):c.2525C>G (p.Thr842Ser)
NM_018417.6(ADCY10):c.2548C>A (p.Pro850Thr)
NM_018417.6(ADCY10):c.2585C>G (p.Ala862Gly)
NM_018417.6(ADCY10):c.2620C>T (p.Arg874Trp)
NM_018417.6(ADCY10):c.2662C>T (p.Pro888Ser)
NM_018417.6(ADCY10):c.2723G>A (p.Gly908Asp)
NM_018417.6(ADCY10):c.2741G>A (p.Arg914His)
NM_018417.6(ADCY10):c.2863C>A (p.Arg955Ser)
NM_018417.6(ADCY10):c.2864G>A (p.Arg955His)
NM_018417.6(ADCY10):c.2872G>T (p.Glu958Ter) rs376243653
NM_018417.6(ADCY10):c.2893G>T (p.Asp965Tyr)
NM_018417.6(ADCY10):c.2897A>G (p.His966Arg)
NM_018417.6(ADCY10):c.2903G>C (p.Arg968Pro) rs140892164
NM_018417.6(ADCY10):c.2938G>A (p.Val980Met)
NM_018417.6(ADCY10):c.2948G>A (p.Arg983Gln)
NM_018417.6(ADCY10):c.2956G>A (p.Ala986Thr)
NM_018417.6(ADCY10):c.2971G>T (p.Ala991Ser)
NM_018417.6(ADCY10):c.3078-3C>T
NM_018417.6(ADCY10):c.3079C>T (p.Pro1027Ser)
NM_018417.6(ADCY10):c.3085G>A (p.Glu1029Lys)
NM_018417.6(ADCY10):c.3140C>T (p.Thr1047Ile)
NM_018417.6(ADCY10):c.3148G>A (p.Glu1050Lys)
NM_018417.6(ADCY10):c.3311C>T (p.Ala1104Val)
NM_018417.6(ADCY10):c.3326A>G (p.Asn1109Ser)
NM_018417.6(ADCY10):c.3349A>T (p.Thr1117Ser)
NM_018417.6(ADCY10):c.3503A>G (p.Asn1168Ser)
NM_018417.6(ADCY10):c.3565C>T (p.Arg1189Trp)
NM_018417.6(ADCY10):c.3593+6G>A
NM_018417.6(ADCY10):c.3626C>T (p.Thr1209Ile)
NM_018417.6(ADCY10):c.3649C>T (p.Arg1217Cys)
NM_018417.6(ADCY10):c.3650G>A (p.Arg1217His)
NM_018417.6(ADCY10):c.3782ACC[2] (p.His1263del) rs751558916
NM_018417.6(ADCY10):c.3799T>G (p.Tyr1267Asp)
NM_018417.6(ADCY10):c.3812G>T (p.Trp1271Leu)
NM_018417.6(ADCY10):c.3829A>G (p.Met1277Val)
NM_018417.6(ADCY10):c.3833C>A (p.Ala1278Asp)
NM_018417.6(ADCY10):c.3856C>T (p.Pro1286Ser)
NM_018417.6(ADCY10):c.3860T>G (p.Leu1287Arg)
NM_018417.6(ADCY10):c.3864A>C (p.Lys1288Asn)
NM_018417.6(ADCY10):c.3947T>C (p.Ile1316Thr)
NM_018417.6(ADCY10):c.3962G>A (p.Arg1321Gln)
NM_018417.6(ADCY10):c.4055A>G (p.Tyr1352Cys)
NM_018417.6(ADCY10):c.4078G>A (p.Gly1360Arg)
NM_018417.6(ADCY10):c.4081C>T (p.Arg1361Trp)
NM_018417.6(ADCY10):c.4082G>A (p.Arg1361Gln) rs766688731
NM_018417.6(ADCY10):c.4136A>G (p.Tyr1379Cys)
NM_018417.6(ADCY10):c.4171T>G (p.Phe1391Val) rs1662951098
NM_018417.6(ADCY10):c.4175T>C (p.Val1392Ala)
NM_018417.6(ADCY10):c.4227C>A (p.Asn1409Lys)
NM_018417.6(ADCY10):c.4259T>C (p.Leu1420Pro)
NM_018417.6(ADCY10):c.4270T>A (p.Ser1424Thr)
NM_018417.6(ADCY10):c.4287G>C (p.Trp1429Cys)
NM_018417.6(ADCY10):c.4292C>G (p.Ala1431Gly)
NM_018417.6(ADCY10):c.4361C>T (p.Thr1454Ile)
NM_018417.6(ADCY10):c.4378T>C (p.Tyr1460His) rs2101843895
NM_018417.6(ADCY10):c.4399A>G (p.Met1467Val)
NM_018417.6(ADCY10):c.4430A>G (p.Gln1477Arg)
NM_018417.6(ADCY10):c.4441C>G (p.Gln1481Glu)
NM_018417.6(ADCY10):c.4483-12_4484del
NM_018417.6(ADCY10):c.4531C>A (p.Pro1511Thr)
NM_018417.6(ADCY10):c.4615C>T (p.Arg1539Trp)
NM_018417.6(ADCY10):c.4625A>G (p.Glu1542Gly) rs1662151205
NM_018417.6(ADCY10):c.4628C>T (p.Thr1543Ile)
NM_018417.6(ADCY10):c.4647G>T (p.Glu1549Asp)
NM_018417.6(ADCY10):c.4669A>T (p.Lys1557Ter)
NM_018417.6(ADCY10):c.4715T>C (p.Leu1572Pro)
NM_018417.6(ADCY10):c.4751T>C (p.Ile1584Thr)
NM_018417.6(ADCY10):c.4754T>C (p.Val1585Ala)
NM_018417.6(ADCY10):c.4817T>G (p.Val1606Gly)
NM_018417.6(ADCY10):c.4822A>G (p.Asn1608Asp)

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