ClinVar Miner

List of variants in gene combination ADCY10, DCAF6 reported as uncertain significance for not provided

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Total variants: 54
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HGVS dbSNP gnomAD frequency
NM_018417.6(ADCY10):c.20A>C (p.Glu7Ala) rs56142912 0.00054
NM_018417.6(ADCY10):c.239G>A (p.Ser80Asn) rs375317807 0.00011
NM_018417.6(ADCY10):c.147A>C (p.Ser49=) rs376787544 0.00010
NM_018417.6(ADCY10):c.758G>A (p.Cys253Tyr) rs145461869 0.00009
NM_018417.6(ADCY10):c.229T>C (p.Tyr77His) rs148603197 0.00004
NM_018417.6(ADCY10):c.349A>G (p.Thr117Ala) rs529970359 0.00004
NM_018417.6(ADCY10):c.461T>A (p.Met154Lys) rs771448841 0.00002
NM_018417.6(ADCY10):c.1025G>T (p.Cys342Phe) rs199965059 0.00001
NM_018417.6(ADCY10):c.1139+6T>G rs777564091 0.00001
NM_018417.6(ADCY10):c.1354G>A (p.Gly452Ser) rs747117539 0.00001
NM_018417.6(ADCY10):c.1401G>C (p.Glu467Asp) rs761630756 0.00001
NM_018417.6(ADCY10):c.1595T>C (p.Leu532Pro) rs200416907 0.00001
NM_018417.6(ADCY10):c.224T>C (p.Leu75Pro) rs1250431989 0.00001
NM_018417.6(ADCY10):c.1090G>A (p.Glu364Lys)
NM_018417.6(ADCY10):c.1153G>A (p.Gly385Ser)
NM_018417.6(ADCY10):c.1185C>A (p.Ile395=) rs757261904
NM_018417.6(ADCY10):c.1196C>T (p.Thr399Ile)
NM_018417.6(ADCY10):c.1202G>A (p.Arg401Lys)
NM_018417.6(ADCY10):c.1216+15C>T
NM_018417.6(ADCY10):c.1307A>G (p.Asn436Ser)
NM_018417.6(ADCY10):c.1355G>T (p.Gly452Val)
NM_018417.6(ADCY10):c.1358T>C (p.Val453Ala)
NM_018417.6(ADCY10):c.1373C>G (p.Pro458Arg)
NM_018417.6(ADCY10):c.1376T>C (p.Leu459Ser)
NM_018417.6(ADCY10):c.1378T>C (p.Tyr460His)
NM_018417.6(ADCY10):c.1385A>G (p.Tyr462Cys)
NM_018417.6(ADCY10):c.1397C>T (p.Thr466Ile)
NM_018417.6(ADCY10):c.1415G>A (p.Gly472Asp) rs756991569
NM_018417.6(ADCY10):c.1415G>T (p.Gly472Val)
NM_018417.6(ADCY10):c.1451A>G (p.Tyr484Cys)
NM_018417.6(ADCY10):c.1490T>A (p.Met497Lys)
NM_018417.6(ADCY10):c.1559A>G (p.Tyr520Cys)
NM_018417.6(ADCY10):c.1580T>C (p.Met527Thr)
NM_018417.6(ADCY10):c.184A>G (p.Met62Val)
NM_018417.6(ADCY10):c.253+4A>G rs949024270
NM_018417.6(ADCY10):c.28G>C (p.Asp10His)
NM_018417.6(ADCY10):c.292+6G>A
NM_018417.6(ADCY10):c.307G>T (p.Ala103Ser) rs1669443980
NM_018417.6(ADCY10):c.331C>G (p.Gln111Glu)
NM_018417.6(ADCY10):c.369C>G (p.Ser123Arg)
NM_018417.6(ADCY10):c.489C>G (p.Ser163Arg) rs1669248047
NM_018417.6(ADCY10):c.497T>A (p.Leu166Gln)
NM_018417.6(ADCY10):c.595C>T (p.Arg199Trp)
NM_018417.6(ADCY10):c.661C>A (p.Pro221Thr)
NM_018417.6(ADCY10):c.667A>C (p.Asn223His)
NM_018417.6(ADCY10):c.709A>T (p.Met237Leu)
NM_018417.6(ADCY10):c.710T>C (p.Met237Thr)
NM_018417.6(ADCY10):c.828G>A (p.Gln276=)
NM_018417.6(ADCY10):c.82C>G (p.His28Asp)
NM_018417.6(ADCY10):c.849G>C (p.Gln283His)
NM_018417.6(ADCY10):c.878C>G (p.Thr293Arg) rs373886057
NM_018417.6(ADCY10):c.87C>A (p.Phe29Leu)
NM_018417.6(ADCY10):c.889G>A (p.Val297Met)
NM_018417.6(ADCY10):c.983T>C (p.Phe328Ser)

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