List of variants reported as benign for Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-positive

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Total variants: 28

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HGVS	dbSNP	gnomAD frequency
NM_000448.3(RAG1):c.*3184G>A	rs1056403	0.48229
NM_000448.3(RAG1):c.746A>G (p.His249Arg)	rs3740955	0.48211
NM_000536.4(RAG2):c.*328A>G	rs10836573	0.48132
NM_000448.3(RAG1):c.2459A>G (p.Lys820Arg)	rs2227973	0.12928
NM_138787.4(IFTAP):c.-24+3619A>G	rs73455545	0.10925
NM_000448.3(RAG1):c.*2246T>C	rs4151045	0.07666
NM_000448.3(RAG1):c.2880A>G (p.Ala960=)	rs1980131	0.07643
NM_000448.3(RAG1):c.-65A>G	rs872053	0.07575
NM_000536.4(RAG2):c.878A>G (p.Glu293Gly)	rs16929093	0.03307
NM_000536.4(RAG2):c.*183C>A	rs12280564	0.03300
NM_000536.4(RAG2):c.*144G>T	rs12280515	0.03006
NM_000448.3(RAG1):c.*2530G>T	rs4151047	0.02426
NM_000448.3(RAG1):c.906C>A (p.Asp302Glu)	rs4151030	0.02153
NM_000536.4(RAG2):c.741G>A (p.Val247=)	rs34092949	0.01926
NM_000448.3(RAG1):c.303G>A (p.Ala101=)	rs4151025	0.01561
NM_000448.3(RAG1):c.*589G>A	rs4151038	0.01403
NM_000448.3(RAG1):c.*398G>A	rs4151036	0.01396
NM_000448.3(RAG1):c.2638G>A (p.Glu880Lys)	rs4151033	0.01395
NM_000448.3(RAG1):c.*1978C>T	rs4151044	0.01228
NM_000536.4(RAG2):c.1158C>A (p.Phe386Leu)	rs34629171	0.01070
NM_000448.3(RAG1):c.725A>G (p.Gln242Arg)	rs76897604	0.00164
NM_000448.3(RAG1):c.*1366A>G	rs371127461	0.00130
NM_000448.3(RAG1):c.*2599A>C	rs375155856	0.00130
NM_000448.3(RAG1):c.*2654A>G	rs369536926	0.00130
NM_000448.3(RAG1):c.577G>A (p.Glu193Lys)	rs34841221	0.00130
NM_000536.4(RAG2):c.644C>T (p.Thr215Ile)	rs35691292	0.00032
NM_000448.3(RAG1):c.*1178G>A	rs149724031	0.00013
NM_000448.3(RAG1):c.*1083C>T	rs4151040

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