ClinVar Miner

List of variants in gene combination CYP19A1, MIR4713HG, PIRC66 reported as uncertain significance for not provided

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Total variants: 25
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HGVS dbSNP gnomAD frequency
NM_000103.4(CYP19A1):c.*125T>C rs781742620 0.00024
NM_000103.4(CYP19A1):c.721T>A (p.Tyr241Asn) rs143562020 0.00017
NM_000103.4(CYP19A1):c.953T>C (p.Met318Thr) rs143839949 0.00015
NM_000103.4(CYP19A1):c.*747G>A rs866111735 0.00005
NM_000103.4(CYP19A1):c.791G>A (p.Arg264His) rs2304462 0.00003
NM_000103.4(CYP19A1):c.1113C>T (p.Asp371=) rs774007712 0.00002
NM_000103.4(CYP19A1):c.187G>A (p.Gly63Ser) rs750143398 0.00002
NM_000103.4(CYP19A1):c.254T>G (p.Met85Arg) rs779820447 0.00002
NM_000103.4(CYP19A1):c.1289T>C (p.Phe430Ser) rs2030919916 0.00001
NM_000103.4(CYP19A1):c.1433C>T (p.Ser478Phe) rs571532730 0.00001
NM_000103.4(CYP19A1):c.233A>G (p.Asn78Ser) rs1422135097 0.00001
NM_000103.4(CYP19A1):c.466G>A (p.Gly156Ser) rs757460733 0.00001
NM_000103.4(CYP19A1):c.916G>A (p.Ala306Thr) rs747006734 0.00001
NM_000103.4(CYP19A1):c.948C>G (p.Phe316Leu) rs1391027657 0.00001
NM_000103.4(CYP19A1):c.1154G>A (p.Gly385Asp) rs988300125
NM_000103.4(CYP19A1):c.1160C>T (p.Pro387Leu)
NM_000103.4(CYP19A1):c.1499G>A (p.Cys500Tyr)
NM_000103.4(CYP19A1):c.253A>G (p.Met85Val) rs989424694
NM_000103.4(CYP19A1):c.376G>A (p.Gly126Ser) rs745845217
NM_000103.4(CYP19A1):c.448A>G (p.Lys150Glu) rs750596718
NM_000103.4(CYP19A1):c.640G>A (p.Val214Met)
NM_000103.4(CYP19A1):c.73A>G (p.Thr25Ala) rs983210603
NM_000103.4(CYP19A1):c.80_81insTGCTGCCTCCATGCC (p.Pro27_Val28insAlaAlaSerMetPro) rs1430135631
NM_000103.4(CYP19A1):c.820G>A (p.Glu274Lys) rs764710550
NM_000103.4(CYP19A1):c.911T>G (p.Leu304Arg) rs1244426810

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