ClinVar Miner

List of variants in gene RAG2 studied for not specified

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Total variants: 23
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HGVS dbSNP gnomAD frequency
NM_000536.4(RAG2):c.878A>G (p.Glu293Gly) rs16929093 0.03307
NM_000536.4(RAG2):c.741G>A (p.Val247=) rs34092949 0.01778
NM_000536.4(RAG2):c.1158C>A (p.Phe386Leu) rs34629171 0.01070
NM_000536.4(RAG2):c.1504A>G (p.Met502Val) rs145614809 0.00150
NM_000536.4(RAG2):c.*52T>A rs546979744 0.00076
NM_000536.4(RAG2):c.35T>C (p.Ile12Thr) rs146584017 0.00062
NM_000536.4(RAG2):c.477C>T (p.Arg159=) rs141659100 0.00037
NM_000536.4(RAG2):c.644C>T (p.Thr215Ile) rs35691292 0.00032
NM_000536.4(RAG2):c.1006A>G (p.Lys336Glu) rs1490516072 0.00001
NM_000536.4(RAG2):c.1309G>A (p.Glu437Lys) rs193922573 0.00001
NM_000536.4(RAG2):c.1396C>T (p.Leu466Phe) rs1590713653 0.00001
NM_000536.4(RAG2):c.419A>G (p.His140Arg) rs1335036396 0.00001
NM_000536.4(RAG2):c.518A>G (p.Asn173Ser) rs766735610 0.00001
NM_000536.4(RAG2):c.95G>A (p.Gly32Glu) rs1224542443 0.00001
NM_000536.4(RAG2):c.1037A>G (p.Tyr346Cys) rs752759155
NM_000536.4(RAG2):c.1295C>T (p.Pro432Leu) rs753677011
NM_000536.4(RAG2):c.1375A>G (p.Met459Val) rs1204766339
NM_000536.4(RAG2):c.1442A>T (p.His481Leu)
NM_000536.4(RAG2):c.303T>A (p.Asn101Lys) rs2133315445
NM_000536.4(RAG2):c.353A>G (p.Lys118Arg) rs1851094033
NM_000536.4(RAG2):c.501A>C (p.Arg167Ser) rs1159686210
NM_000536.4(RAG2):c.614C>G (p.Ser205Cys)
NM_000536.4(RAG2):c.911C>T (p.Thr304Ile) rs1851070974

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