ClinVar Miner

List of variants in gene RNF224 studied for not specified

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Total variants: 32
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HGVS dbSNP gnomAD frequency
NM_001190228.2(RNF224):c.37G>A (p.Gly13Arg) rs772970963 0.00021
NM_001190228.2(RNF224):c.463G>A (p.Glu155Lys) rs761579574 0.00013
NM_001190228.2(RNF224):c.116G>A (p.Arg39His) rs1030069211 0.00011
NM_001190228.2(RNF224):c.182A>G (p.Glu61Gly) rs909883292 0.00009
NM_001190228.2(RNF224):c.212G>A (p.Arg71His) rs941378560 0.00009
NM_001190228.2(RNF224):c.86C>T (p.Ser29Leu) rs868258879 0.00007
NM_001190228.2(RNF224):c.176C>T (p.Ala59Val) rs1460486716 0.00006
NM_001190228.2(RNF224):c.235G>A (p.Gly79Arg) rs775478295 0.00006
NM_001190228.2(RNF224):c.187C>T (p.Arg63Cys) rs1252343966 0.00003
NM_001190228.2(RNF224):c.211C>T (p.Arg71Cys) rs1307794161 0.00002
NM_001190228.2(RNF224):c.259G>A (p.Asp87Asn) rs969252437 0.00002
NM_001190228.2(RNF224):c.28C>T (p.Pro10Ser) rs984428759 0.00002
NM_001190228.2(RNF224):c.155T>C (p.Val52Ala) rs1404019756 0.00001
NM_001190228.2(RNF224):c.55G>A (p.Glu19Lys) rs925341803 0.00001
NM_001190228.2(RNF224):c.89C>T (p.Ala30Val) rs535732266 0.00001
NM_001190228.2(RNF224):c.92A>G (p.Tyr31Cys) rs1435881449 0.00001
NM_001190228.2(RNF224):c.135C>A (p.His45Gln)
NM_001190228.2(RNF224):c.161G>A (p.Arg54Gln)
NM_001190228.2(RNF224):c.182A>T (p.Glu61Val) rs909883292
NM_001190228.2(RNF224):c.219C>G (p.Ser73Arg)
NM_001190228.2(RNF224):c.22G>C (p.Gly8Arg)
NM_001190228.2(RNF224):c.233G>T (p.Arg78Leu) rs780826115
NM_001190228.2(RNF224):c.248T>C (p.Met83Thr)
NM_001190228.2(RNF224):c.25C>T (p.Pro9Ser)
NM_001190228.2(RNF224):c.293G>C (p.Arg98Pro) rs749663328
NM_001190228.2(RNF224):c.361G>C (p.Ala121Pro)
NM_001190228.2(RNF224):c.365G>A (p.Gly122Glu) rs930241762
NM_001190228.2(RNF224):c.41G>A (p.Gly14Glu)
NM_001190228.2(RNF224):c.428G>A (p.Cys143Tyr)
NM_001190228.2(RNF224):c.446C>T (p.Pro149Leu) rs1231580921
NM_001190228.2(RNF224):c.466G>C (p.Val156Leu) rs767347083
NM_001190228.2(RNF224):c.94G>T (p.Asp32Tyr)

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