ClinVar Miner

List of variants in gene RNF13 reported as likely benign for not provided

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Gene type:
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Total variants: 109
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HGVS dbSNP gnomAD frequency
NM_183381.3(RNF13):c.492T>C (p.Tyr164=) rs148516101 0.00564
NM_183381.3(RNF13):c.655C>T (p.Arg219Cys) rs143447610 0.00164
NM_183381.3(RNF13):c.1089C>T (p.Val363=) rs371997640 0.00034
NM_183381.3(RNF13):c.479A>G (p.Asp160Gly) rs144710366 0.00028
NM_183381.3(RNF13):c.700+7A>G rs193248526 0.00024
NM_183381.3(RNF13):c.363T>A (p.Val121=) rs138875909 0.00021
NM_183381.3(RNF13):c.216A>G (p.Lys72=) rs766434167 0.00006
NM_183381.3(RNF13):c.701-15A>G rs773728380 0.00006
NM_183381.3(RNF13):c.980C>T (p.Ser327Leu) rs200489974 0.00006
NM_183381.3(RNF13):c.987C>G (p.Ser329=) rs768209626 0.00006
NM_183381.3(RNF13):c.608T>C (p.Ile203Thr) rs140042189 0.00005
NM_183381.3(RNF13):c.1102C>A (p.Gln368Lys) rs149058915 0.00004
NM_183381.3(RNF13):c.196-15C>T rs1157616435 0.00004
NM_183381.3(RNF13):c.282C>T (p.Ile94=) rs142620410 0.00004
NM_183381.3(RNF13):c.900A>G (p.Gln300=) rs149934250 0.00004
NM_183381.3(RNF13):c.378T>C (p.Ser126=) rs199955067 0.00002
NM_183381.3(RNF13):c.409+8C>T rs1469161562 0.00002
NM_183381.3(RNF13):c.1045A>G (p.Thr349Ala) rs972002974 0.00001
NM_183381.3(RNF13):c.1059T>C (p.Asp353=) rs199606748 0.00001
NM_183381.3(RNF13):c.1090G>A (p.Val364Met) rs865931642 0.00001
NM_183381.3(RNF13):c.393C>T (p.Ser131=) rs772769215 0.00001
NM_183381.3(RNF13):c.548A>G (p.Tyr183Cys) rs1250628602 0.00001
NM_183381.3(RNF13):c.552A>G (p.Leu184=) rs768700103 0.00001
NM_183381.3(RNF13):c.690A>C (p.Lys230Asn) rs769789166 0.00001
NM_183381.3(RNF13):c.701-17A>G rs369953256 0.00001
NM_183381.3(RNF13):c.760A>C (p.Arg254=) rs1802142 0.00001
NM_183381.3(RNF13):c.981G>A (p.Ser327=) rs759934563 0.00001
NM_183381.3(RNF13):c.1009G>C (p.Glu337Gln)
NM_183381.3(RNF13):c.1032C>T (p.Asp344=)
NM_183381.3(RNF13):c.1073T>C (p.Ile358Thr) rs769543244
NM_183381.3(RNF13):c.1086T>C (p.Asp362=)
NM_183381.3(RNF13):c.1089_1091del (p.Val365del) rs368558129
NM_183381.3(RNF13):c.1113T>C (p.Gly371=)
NM_183381.3(RNF13):c.1128C>T (p.Asn376=)
NM_183381.3(RNF13):c.114+18T>C rs2108375702
NM_183381.3(RNF13):c.114+9A>G
NM_183381.3(RNF13):c.15A>G (p.Ile5Met)
NM_183381.3(RNF13):c.16G>C (p.Gly6Arg)
NM_183381.3(RNF13):c.267A>G (p.Ser89=) rs2108442188
NM_183381.3(RNF13):c.273C>T (p.Gly91=)
NM_183381.3(RNF13):c.283G>C (p.Val95Leu) rs146907927
NM_183381.3(RNF13):c.306T>C (p.Cys102=) rs2108442274
NM_183381.3(RNF13):c.321+8T>A
NM_183381.3(RNF13):c.322-4G>C
NM_183381.3(RNF13):c.322-6T>G
NM_183381.3(RNF13):c.333A>G (p.Ala111=)
NM_183381.3(RNF13):c.354A>G (p.Ala118=)
NM_183381.3(RNF13):c.354A>T (p.Ala118=)
NM_183381.3(RNF13):c.387C>A (p.Leu129=)
NM_183381.3(RNF13):c.39A>T (p.Thr13=)
NM_183381.3(RNF13):c.405C>T (p.Asn135=)
NM_183381.3(RNF13):c.409+17C>T
NM_183381.3(RNF13):c.410-18C>G
NM_183381.3(RNF13):c.410-4A>G
NM_183381.3(RNF13):c.410-6A>G
NM_183381.3(RNF13):c.410-7T>A rs377225073
NM_183381.3(RNF13):c.410-7T>C
NM_183381.3(RNF13):c.434T>C (p.Ile145Thr)
NM_183381.3(RNF13):c.438A>G (p.Pro146=) rs774129363
NM_183381.3(RNF13):c.453T>C (p.Gly151=)
NM_183381.3(RNF13):c.453T>G (p.Gly151=)
NM_183381.3(RNF13):c.471T>C (p.Ser157=)
NM_183381.3(RNF13):c.489A>G (p.Thr163=)
NM_183381.3(RNF13):c.489A>T (p.Thr163=)
NM_183381.3(RNF13):c.500+7A>C
NM_183381.3(RNF13):c.510T>C (p.Leu170=)
NM_183381.3(RNF13):c.516A>G (p.Leu172=) rs2108518514
NM_183381.3(RNF13):c.528T>C (p.Phe176=)
NM_183381.3(RNF13):c.591G>A (p.Leu197=)
NM_183381.3(RNF13):c.601T>C (p.Phe201Leu)
NM_183381.3(RNF13):c.606+21_606+30del
NM_183381.3(RNF13):c.606+7A>C
NM_183381.3(RNF13):c.607-13C>G
NM_183381.3(RNF13):c.680C>G (p.Pro227Arg)
NM_183381.3(RNF13):c.696G>A (p.Lys232=)
NM_183381.3(RNF13):c.700+17T>C rs532033282
NM_183381.3(RNF13):c.700+6dup
NM_183381.3(RNF13):c.701-10_701-9del rs745453756
NM_183381.3(RNF13):c.714T>C (p.Asp238=)
NM_183381.3(RNF13):c.735T>C (p.Asp245=)
NM_183381.3(RNF13):c.738G>A (p.Glu246=)
NM_183381.3(RNF13):c.747T>C (p.Asp249=)
NM_183381.3(RNF13):c.757C>T (p.Leu253Phe)
NM_183381.3(RNF13):c.765C>A (p.Ile255=) rs2108620542
NM_183381.3(RNF13):c.781+14C>T
NM_183381.3(RNF13):c.781+15G>A rs370881979
NM_183381.3(RNF13):c.781+15G>C
NM_183381.3(RNF13):c.781+19T>C
NM_183381.3(RNF13):c.781+7G>A
NM_183381.3(RNF13):c.782-14T>C
NM_183381.3(RNF13):c.782-21_782-20del
NM_183381.3(RNF13):c.782-8T>C rs2108621940
NM_183381.3(RNF13):c.782-8T>G rs2108621940
NM_183381.3(RNF13):c.795G>A (p.Lys265=)
NM_183381.3(RNF13):c.807T>C (p.Pro269=)
NM_183381.3(RNF13):c.821C>T (p.Thr274Ile)
NM_183381.3(RNF13):c.845A>T (p.Lys282Met)
NM_183381.3(RNF13):c.858T>C (p.Val286=)
NM_183381.3(RNF13):c.870C>A (p.Gly290=) rs1211424606
NM_183381.3(RNF13):c.870C>T (p.Gly290=)
NM_183381.3(RNF13):c.90G>A (p.Leu30=)
NM_183381.3(RNF13):c.90G>C (p.Leu30=)
NM_183381.3(RNF13):c.927C>A (p.Thr309=)
NM_183381.3(RNF13):c.934C>T (p.Leu312=)
NM_183381.3(RNF13):c.960C>G (p.Ala320=)
NM_183381.3(RNF13):c.978A>G (p.Leu326=)
NM_183381.3(RNF13):c.990C>G (p.Arg330=)
NM_183381.3(RNF13):c.993A>C (p.Ser331=) rs1722344220
NM_183381.3(RNF13):c.99A>G (p.Glu33=)

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