List of variants reported as benign for Immunodeficiency due to CD25 deficiency

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Total variants: 28

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HGVS	dbSNP	gnomAD frequency
NM_000417.3(IL2RA):c.368-18A>G	rs942200	0.89589
NM_000417.3(IL2RA):c.*1267G>A	rs1570538	0.41620
NM_000417.3(IL2RA):c.*1461T>C	rs12244380	0.40826
NM_000417.3(IL2RA):c.367+12A>T	rs12358961	0.31345
NM_000417.3(IL2RA):c.367+7G>C	rs11256369	0.20897
NM_000417.3(IL2RA):c.*1702C>T	rs12722606	0.15795
NM_000417.3(IL2RA):c.*969G>A	rs12722602	0.10647
NC_000010.11:g.6010681A>C	rs12722609	0.10644
NM_000417.3(IL2RA):c.*1672A>T	rs12722605	0.10588
NM_000417.3(IL2RA):c.656-17T>G	rs28360490	0.08627
NM_000417.3(IL2RA):c.84G>A (p.Pro28=)	rs2228150	0.08221
NM_000417.3(IL2RA):c.516C>T (p.His172=)	rs2228149	0.05507
NM_000417.3(IL2RA):c.*1994G>T	rs12722608	0.05371
NM_000417.3(IL2RA):c.*677G>A	rs12719919	0.04736
NM_000417.3(IL2RA):c.*1880C>G	rs12722607	0.04629
NM_000417.3(IL2RA):c.*1549C>T	rs12722604	0.04214
NM_000417.3(IL2RA):c.*70G>A	rs12722600	0.01848
NM_000417.3(IL2RA):c.753C>T (p.Ile251=)	rs12722698	0.01702
NM_000417.3(IL2RA):c.*1024G>A	rs12722718	0.00760
NM_000417.3(IL2RA):c.*55T>C	rs12722713	0.00719
NM_000417.3(IL2RA):c.65-20A>G	rs12722687	0.00558
NM_000417.3(IL2RA):c.272C>T (p.Thr91Met)	rs72650666	0.00183
NM_000417.3(IL2RA):c.*2108T>G	rs74895246	0.00171
NM_000417.3(IL2RA):c.*1008G>A	rs34164172	0.00170
NM_000417.3(IL2RA):c.711A>G (p.Thr237=)	rs11256354	0.00053
NM_000417.3(IL2RA):c.368-16T>C	rs191340172	0.00027
NM_000417.3(IL2RA):c.457G>A (p.Val153Ile)	rs201188114	0.00009
NM_000417.3(IL2RA):c.64+15308T>A	rs12722508

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