ClinVar Miner

List of variants in gene NR3C2 reported as uncertain significance for not provided

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Total variants: 56
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HGVS dbSNP gnomAD frequency
NM_000901.5(NR3C2):c.*804G>T rs72648707 0.00209
NM_000901.5(NR3C2):c.*1206G>C rs557553789 0.00025
NM_000901.5(NR3C2):c.1757+6T>C rs184268528 0.00009
NM_000901.5(NR3C2):c.739A>T (p.Arg247Trp) rs149902988 0.00001
GRCh37/hg19 4q31.23(chr4:149002223-149039656)x1
NM_000901.5(NR3C2):c.1000T>C (p.Cys334Arg)
NM_000901.5(NR3C2):c.104A>C (p.Glu35Ala)
NM_000901.5(NR3C2):c.1067G>A (p.Arg356Gln)
NM_000901.5(NR3C2):c.112G>A (p.Asp38Asn)
NM_000901.5(NR3C2):c.1150A>C (p.Ile384Leu)
NM_000901.5(NR3C2):c.1183G>T (p.Val395Phe) rs764140077
NM_000901.5(NR3C2):c.1207G>T (p.Asp403Tyr) rs2126652388
NM_000901.5(NR3C2):c.1225T>G (p.Ser409Ala)
NM_000901.5(NR3C2):c.1245C>G (p.Ser415Arg)
NM_000901.5(NR3C2):c.1462G>A (p.Gly488Arg)
NM_000901.5(NR3C2):c.1546G>A (p.Val516Met)
NM_000901.5(NR3C2):c.1615G>T (p.Ala539Ser)
NM_000901.5(NR3C2):c.1748A>G (p.Asn583Ser)
NM_000901.5(NR3C2):c.1750G>A (p.Val584Ile)
NM_000901.5(NR3C2):c.1862G>A (p.Gly621Asp)
NM_000901.5(NR3C2):c.1952G>A (p.Arg651Gln) rs2149802718
NM_000901.5(NR3C2):c.1975A>G (p.Arg659Gly)
NM_000901.5(NR3C2):c.2018G>A (p.Arg673Gln) rs1420676853
NM_000901.5(NR3C2):c.2056G>A (p.Glu686Lys)
NM_000901.5(NR3C2):c.2085ACCCCC[4] (p.Pro701_Gln702insProPro)
NM_000901.5(NR3C2):c.2090C>T (p.Pro697Leu) rs1196633933
NM_000901.5(NR3C2):c.2092C>T (p.Pro698Ser)
NM_000901.5(NR3C2):c.2102C>G (p.Pro701Arg) rs754694314
NM_000901.5(NR3C2):c.2198C>T (p.Ala733Val)
NM_000901.5(NR3C2):c.2309A>G (p.Asn770Ser)
NM_000901.5(NR3C2):c.2331G>A (p.Met777Ile)
NM_000901.5(NR3C2):c.2348G>T (p.Trp783Leu) rs2149767325
NM_000901.5(NR3C2):c.2425C>G (p.Leu809Val)
NM_000901.5(NR3C2):c.2455T>G (p.Tyr819Asp)
NM_000901.5(NR3C2):c.2491C>A (p.Pro831Thr)
NM_000901.5(NR3C2):c.2510+4_2510+7del
NM_000901.5(NR3C2):c.2534T>G (p.Met845Arg)
NM_000901.5(NR3C2):c.2730T>G (p.Cys910Trp)
NM_000901.5(NR3C2):c.2842G>A (p.Glu948Lys)
NM_000901.5(NR3C2):c.2843_2844del (p.Glu948fs)
NM_000901.5(NR3C2):c.2860G>A (p.Val954Ile)
NM_000901.5(NR3C2):c.2933C>T (p.Pro978Leu)
NM_000901.5(NR3C2):c.335T>C (p.Val112Ala)
NM_000901.5(NR3C2):c.367A>G (p.Asn123Asp)
NM_000901.5(NR3C2):c.448C>T (p.Arg150Cys)
NM_000901.5(NR3C2):c.455C>T (p.Ser152Phe)
NM_000901.5(NR3C2):c.458C>T (p.Thr153Ile)
NM_000901.5(NR3C2):c.496T>C (p.Ser166Pro) rs2126655915
NM_000901.5(NR3C2):c.553A>G (p.Ile185Val)
NM_000901.5(NR3C2):c.577T>C (p.Ser193Pro)
NM_000901.5(NR3C2):c.596A>G (p.Asn199Ser)
NM_000901.5(NR3C2):c.596A>T (p.Asn199Ile)
NM_000901.5(NR3C2):c.731G>A (p.Arg244Gln)
NM_000901.5(NR3C2):c.758A>G (p.His253Arg)
NM_000901.5(NR3C2):c.898C>G (p.Pro300Ala)
NM_000901.5(NR3C2):c.928_939del (p.Val310_Pro313del)

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