ClinVar Miner

List of variants in gene RAG1 reported as uncertain significance for not provided

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Total variants: 16
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HGVS dbSNP gnomAD frequency
NM_000448.3(RAG1):c.725A>G (p.Gln242Arg) rs76897604 0.00164
NM_000448.3(RAG1):c.1A>G (p.Met1Val) rs200575481 0.00007
NM_000448.3(RAG1):c.850C>T (p.Pro284Ser) rs768862261 0.00005
NM_000448.3(RAG1):c.335G>A (p.Arg112His) rs749223640 0.00003
NM_000448.3(RAG1):c.314C>T (p.Ala105Val) rs916855592 0.00002
NM_000448.3(RAG1):c.1467G>C (p.Arg489Ser) rs1270133689 0.00001
NM_000448.3(RAG1):c.416G>T (p.Gly139Val) rs140648865 0.00001
NM_000448.3(RAG1):c.1618G>A (p.Gly540Arg) rs1590703267
NM_000448.3(RAG1):c.1875T>G (p.Phe625Leu) rs749669514
NM_000448.3(RAG1):c.1988C>A (p.Ala663Glu) rs2133296713
NM_000448.3(RAG1):c.1993G>A (p.Glu665Lys) rs1590703553
NM_000448.3(RAG1):c.2161C>G (p.Leu721Val) rs1590703677
NM_000448.3(RAG1):c.2564A>G (p.Asn855Ser) rs199474690
NM_000448.3(RAG1):c.2815T>C (p.Phe939Leu)
NM_000448.3(RAG1):c.2966A>G (p.Asp989Gly)
NM_000448.3(RAG1):c.506C>G (p.Ser169Trp) rs4151027

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