ClinVar Miner

List of variants in gene RRM2B reported by Fulgent Genetics, Fulgent Genetics

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Gene type:
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Total variants: 20
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HGVS dbSNP gnomAD frequency
NM_015713.5(RRM2B):c.48+273G>T rs149523343 0.00928
NM_015713.5(RRM2B):c.48+265C>G rs550765773 0.00178
NM_015713.5(RRM2B):c.48+48C>T rs201028777 0.00142
NM_015713.5(RRM2B):c.685-20A>T rs142382577 0.00104
NM_015713.5(RRM2B):c.551-18C>T rs72554100 0.00062
NM_015713.5(RRM2B):c.790-8C>A rs376542259 0.00014
NM_015713.5(RRM2B):c.48+156G>A rs773501860 0.00005
NM_015713.5(RRM2B):c.613A>G (p.Ile205Val) rs144088421 0.00004
NM_015713.5(RRM2B):c.671T>G (p.Ile224Ser) rs515726196 0.00003
NM_015713.5(RRM2B):c.755G>A (p.Arg252Lys) rs754931572 0.00003
NM_015713.5(RRM2B):c.119G>A (p.Arg40His) rs765953819 0.00001
NM_015713.5(RRM2B):c.253_255del (p.Glu85del) rs515726184 0.00001
NM_015713.5(RRM2B):c.322-7T>C rs570137520 0.00001
NM_015713.5(RRM2B):c.470A>G (p.Asn157Ser) rs751231428 0.00001
NM_015713.5(RRM2B):c.*74del rs886062569
NM_015713.5(RRM2B):c.143A>G (p.Gln48Arg) rs747846279
NM_015713.5(RRM2B):c.258G>T (p.Lys86Asn) rs536874925
NM_015713.5(RRM2B):c.455+1G>A rs2132555188
NM_015713.5(RRM2B):c.48+188del rs758091261
NM_015713.5(RRM2B):c.534T>C (p.Asp178=) rs1810881397

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