ClinVar Miner

List of variants in gene RAG1 reported as uncertain significance for Histiocytic medullary reticulosis

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Total variants: 44
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HGVS dbSNP
NM_000448.2(RAG1):c.*1101G>A rs145963034
NM_000448.2(RAG1):c.*1130A>G rs554469239
NM_000448.2(RAG1):c.*1366A>G rs371127461
NM_000448.2(RAG1):c.*1562A>G rs185464049
NM_000448.2(RAG1):c.*1611G>A rs886048262
NM_000448.2(RAG1):c.*1701T>C rs886048263
NM_000448.2(RAG1):c.*1705A>G rs886048264
NM_000448.2(RAG1):c.*200C>T rs886048256
NM_000448.2(RAG1):c.*2211C>T rs538916870
NM_000448.2(RAG1):c.*2289T>G rs200013770
NM_000448.2(RAG1):c.*2308G>A rs766934756
NM_000448.2(RAG1):c.*238G>A rs4151035
NM_000448.2(RAG1):c.*2442G>A rs886048265
NM_000448.2(RAG1):c.*2599A>C rs375155856
NM_000448.2(RAG1):c.*3058A>G rs746468007
NM_000448.2(RAG1):c.*3122del rs141384582
NM_000448.2(RAG1):c.*3156A>G rs183729240
NM_000448.2(RAG1):c.*344G>A rs886048257
NM_000448.2(RAG1):c.*370G>T rs569692485
NM_000448.2(RAG1):c.*386del rs886048258
NM_000448.2(RAG1):c.*739C>T rs4151039
NM_000448.2(RAG1):c.*766A>G rs886048259
NM_000448.2(RAG1):c.*834dup rs745747958
NM_000448.2(RAG1):c.*856C>A rs886048261
NM_000448.2(RAG1):c.-10C>T rs886048251
NM_000448.2(RAG1):c.-114G>A rs872052
NM_000448.2(RAG1):c.-15+12A>G rs190968516
NM_000448.2(RAG1):c.1077A>G (p.Pro359=) rs886048253
NM_000448.2(RAG1):c.1367C>A (p.Ala456Asp) rs201779957
NM_000448.2(RAG1):c.152A>T (p.Asp51Val) rs147486240
NM_000448.2(RAG1):c.1A>G (p.Met1Val) rs200575481
NM_000448.2(RAG1):c.2110A>G (p.Ile704Val) rs886048254
NM_000448.2(RAG1):c.2426A>G (p.Lys809Arg) rs773703055
NM_000448.2(RAG1):c.2626G>A (p.Glu876Lys) rs145772007
NM_000448.2(RAG1):c.2751G>A (p.Gln917=) rs150721661
NM_000448.2(RAG1):c.2825C>T (p.Thr942Ile) rs762625040
NM_000448.2(RAG1):c.2968G>A (p.Val990Ile) rs886048255
NM_000448.2(RAG1):c.37T>G (p.Ser13Ala) rs760746448
NM_000448.2(RAG1):c.382C>T (p.Pro128Ser) rs886048252
NM_000448.2(RAG1):c.577G>A (p.Glu193Lys) rs34841221
NM_000448.2(RAG1):c.592A>C (p.Arg198=) rs746425890
NM_000448.2(RAG1):c.653G>A (p.Arg218His) rs202178215
NM_000448.2(RAG1):c.739C>T (p.Arg247Cys) rs147203889
NM_000448.2(RAG1):c.799G>A (p.Ala267Thr) rs148393376

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