ClinVar Miner

List of variants in gene RCOR2 reported as uncertain significance for not specified

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Total variants: 50
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HGVS dbSNP gnomAD frequency
NM_173587.4(RCOR2):c.1517A>C (p.Gln506Pro) rs750159142 0.00053
NM_173587.4(RCOR2):c.1352C>T (p.Pro451Leu) rs774946706 0.00005
NM_173587.4(RCOR2):c.38G>C (p.Gly13Ala) rs1479842879 0.00004
NM_173587.4(RCOR2):c.242A>G (p.Asn81Ser) rs981994837 0.00003
NM_173587.4(RCOR2):c.625C>G (p.Arg209Gly) rs762273099 0.00003
NM_173587.4(RCOR2):c.626G>A (p.Arg209Gln) rs199984646 0.00003
NM_173587.4(RCOR2):c.40A>T (p.Ile14Phe) rs372768915 0.00002
NM_173587.4(RCOR2):c.1385C>A (p.Thr462Asn) rs1277791369 0.00001
NM_173587.4(RCOR2):c.437C>G (p.Ala146Gly) rs767244177 0.00001
NM_173587.4(RCOR2):c.703C>T (p.Arg235Cys) rs758917942 0.00001
NM_173587.4(RCOR2):c.1025A>G (p.Gln342Arg)
NM_173587.4(RCOR2):c.1121G>A (p.Arg374Gln)
NM_173587.4(RCOR2):c.1153G>A (p.Glu385Lys) rs2539359938
NM_173587.4(RCOR2):c.1223C>A (p.Pro408Gln)
NM_173587.4(RCOR2):c.1226T>G (p.Leu409Trp)
NM_173587.4(RCOR2):c.1232C>T (p.Ala411Val) rs2539359826
NM_173587.4(RCOR2):c.1285G>A (p.Val429Met)
NM_173587.4(RCOR2):c.1291C>G (p.Arg431Gly) rs1179884901
NM_173587.4(RCOR2):c.1292G>A (p.Arg431Gln) rs548233693
NM_173587.4(RCOR2):c.130A>C (p.Ser44Arg) rs1034054539
NM_173587.4(RCOR2):c.1460C>T (p.Pro487Leu) rs565254520
NM_173587.4(RCOR2):c.1492C>T (p.Arg498Cys)
NM_173587.4(RCOR2):c.1493G>A (p.Arg498His)
NM_173587.4(RCOR2):c.1502C>T (p.Ala501Val) rs2539358724
NM_173587.4(RCOR2):c.1504C>G (p.Arg502Gly) rs913201485
NM_173587.4(RCOR2):c.1552C>T (p.Pro518Ser)
NM_173587.4(RCOR2):c.1556C>T (p.Pro519Leu)
NM_173587.4(RCOR2):c.1561C>T (p.Pro521Ser)
NM_173587.4(RCOR2):c.191C>T (p.Pro64Leu) rs1941839518
NM_173587.4(RCOR2):c.22C>G (p.Pro8Ala) rs772745604
NM_173587.4(RCOR2):c.284T>C (p.Met95Thr)
NM_173587.4(RCOR2):c.443G>A (p.Gly148Asp)
NM_173587.4(RCOR2):c.449A>G (p.His150Arg)
NM_173587.4(RCOR2):c.513A>C (p.Lys171Asn) rs377722799
NM_173587.4(RCOR2):c.541A>G (p.Ser181Gly) rs2539363910
NM_173587.4(RCOR2):c.557T>C (p.Met186Thr)
NM_173587.4(RCOR2):c.634G>C (p.Val212Leu)
NM_173587.4(RCOR2):c.647A>T (p.Glu216Val)
NM_173587.4(RCOR2):c.652G>C (p.Asp218His) rs371327834
NM_173587.4(RCOR2):c.683C>T (p.Pro228Leu)
NM_173587.4(RCOR2):c.71C>A (p.Pro24His)
NM_173587.4(RCOR2):c.742T>C (p.Tyr248His) rs1276485780
NM_173587.4(RCOR2):c.766C>T (p.Arg256Trp)
NM_173587.4(RCOR2):c.785G>A (p.Gly262Asp)
NM_173587.4(RCOR2):c.811A>G (p.Thr271Ala)
NM_173587.4(RCOR2):c.812C>A (p.Thr271Lys)
NM_173587.4(RCOR2):c.842A>G (p.Asn281Ser)
NM_173587.4(RCOR2):c.88C>T (p.His30Tyr) rs754458985
NM_173587.4(RCOR2):c.899G>A (p.Ser300Asn) rs1476311673
NM_173587.4(RCOR2):c.911C>T (p.Thr304Met)

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