ClinVar Miner

List of variants reported as uncertain significance for Immunodeficiency 67 by Labcorp Genetics (formerly Invitae), Labcorp

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Total variants: 95
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HGVS dbSNP gnomAD frequency
NM_016123.4(IRAK4):c.346G>A (p.Glu116Lys) rs62642475 0.00067
NM_016123.4(IRAK4):c.529A>G (p.Thr177Ala) rs141209982 0.00044
NM_016123.4(IRAK4):c.58A>T (p.Arg20Trp) rs143625818 0.00021
NM_016123.4(IRAK4):c.691G>A (p.Asp231Asn) rs111935971 0.00016
NM_016123.4(IRAK4):c.206A>C (p.Glu69Ala) rs202134282 0.00006
NM_016123.4(IRAK4):c.613G>A (p.Val205Ile) rs370225662 0.00006
NM_016123.4(IRAK4):c.1063A>C (p.Met355Leu) rs142376871 0.00005
NM_016123.4(IRAK4):c.1229T>C (p.Ile410Thr) rs146538989 0.00005
NM_016123.4(IRAK4):c.652-3del rs768745789 0.00005
NM_016123.4(IRAK4):c.35G>A (p.Arg12His) rs370524518 0.00004
NM_016123.4(IRAK4):c.427C>A (p.Gln143Lys) rs773476797 0.00004
NM_016123.4(IRAK4):c.749G>A (p.Gly250Asp) rs769470855 0.00004
NM_016123.4(IRAK4):c.1371G>A (p.Met457Ile) rs766606181 0.00003
NM_016123.4(IRAK4):c.1124T>C (p.Val375Ala) rs779773825 0.00002
NM_016123.4(IRAK4):c.1334C>A (p.Pro445Gln) rs752108446 0.00002
NM_016123.4(IRAK4):c.7A>C (p.Lys3Gln) rs752890848 0.00002
NM_016123.4(IRAK4):c.831+5G>T rs758539498 0.00002
NM_016123.4(IRAK4):c.1000C>T (p.Arg334Trp) rs774525787 0.00001
NM_016123.4(IRAK4):c.103T>A (p.Leu35Ile) rs1423382149 0.00001
NM_016123.4(IRAK4):c.1082G>A (p.Arg361His) rs764106350 0.00001
NM_016123.4(IRAK4):c.1109T>C (p.Ile370Thr) rs372448559 0.00001
NM_016123.4(IRAK4):c.1125+5G>A rs1234743900 0.00001
NM_016123.4(IRAK4):c.1148G>A (p.Gly383Glu) rs755772831 0.00001
NM_016123.4(IRAK4):c.1188+6T>C rs372909606 0.00001
NM_016123.4(IRAK4):c.1240A>G (p.Ile414Val) rs758846627 0.00001
NM_016123.4(IRAK4):c.1291T>G (p.Ser431Ala) rs769754150 0.00001
NM_016123.4(IRAK4):c.1347G>A (p.Lys449=) rs2040738109 0.00001
NM_016123.4(IRAK4):c.1369A>T (p.Met457Leu) rs1565689685 0.00001
NM_016123.4(IRAK4):c.161G>A (p.Arg54Lys) rs1345805635 0.00001
NM_016123.4(IRAK4):c.266T>C (p.Ile89Thr) rs758974509 0.00001
NM_016123.4(IRAK4):c.290C>T (p.Ala97Val) rs764597369 0.00001
NM_016123.4(IRAK4):c.34C>T (p.Arg12Cys) rs377584435 0.00001
NM_016123.4(IRAK4):c.376C>T (p.Pro126Ser) rs1379851408 0.00001
NM_016123.4(IRAK4):c.406A>G (p.Thr136Ala) rs769345767 0.00001
NM_016123.4(IRAK4):c.424G>C (p.Glu142Gln) rs762213099 0.00001
NM_016123.4(IRAK4):c.467A>G (p.Lys156Arg) rs780919244 0.00001
NM_016123.4(IRAK4):c.522G>T (p.Lys174Asn) rs771324378 0.00001
NM_016123.4(IRAK4):c.598G>C (p.Val200Leu) rs377074100 0.00001
NM_016123.4(IRAK4):c.631G>T (p.Ala211Ser) rs1445249498 0.00001
NM_016123.4(IRAK4):c.77T>C (p.Ile26Thr) rs138116867 0.00001
NM_016123.4(IRAK4):c.783A>G (p.Val261=) rs1465941653 0.00001
NM_016123.4(IRAK4):c.811C>A (p.Leu271Ile) rs1001238686 0.00001
NM_016123.4(IRAK4):c.832G>A (p.Asp278Asn) rs757311009 0.00001
NM_016123.4(IRAK4):c.850T>C (p.Ser284Pro) rs778616067 0.00001
NM_016123.4(IRAK4):c.889A>G (p.Asn297Asp) rs556565376 0.00001
NM_016123.4(IRAK4):c.938A>C (p.Lys313Thr) rs1555169543 0.00001
NM_016123.4(IRAK4):c.93A>T (p.Gly31=) rs1367304662 0.00001
NC_000012.11:g.(?_44171413)_(44180518_?)del
NC_000012.11:g.(?_44180182)_(44180518_?)del
NM_016123.4(IRAK4):c.1019C>T (p.Ala340Val) rs2138046830
NM_016123.4(IRAK4):c.1115G>A (p.Ser372Asn) rs2138047917
NM_016123.4(IRAK4):c.1126-9T>A rs1226593914
NM_016123.4(IRAK4):c.113C>G (p.Ala38Gly) rs1402262535
NM_016123.4(IRAK4):c.1188G>A (p.Leu396=) rs2138059924
NM_016123.4(IRAK4):c.1195A>G (p.Ile399Val)
NM_016123.4(IRAK4):c.1317A>C (p.Glu439Asp)
NM_016123.4(IRAK4):c.1327A>G (p.Lys443Glu)
NM_016123.4(IRAK4):c.1329G>C (p.Lys443Asn)
NM_016123.4(IRAK4):c.1340T>A (p.Ile447Asn)
NM_016123.4(IRAK4):c.225CAC[1] (p.Thr77del)
NM_016123.4(IRAK4):c.229A>G (p.Thr77Ala) rs1555167569
NM_016123.4(IRAK4):c.232A>G (p.Asn78Asp)
NM_016123.4(IRAK4):c.255_260dup (p.Asp86_Leu87dup) rs1450996169
NM_016123.4(IRAK4):c.284C>T (p.Ala95Val) rs1940738214
NM_016123.4(IRAK4):c.316C>T (p.Pro106Ser)
NM_016123.4(IRAK4):c.32T>G (p.Val11Gly) rs1940363408
NM_016123.4(IRAK4):c.331A>G (p.Thr111Ala)
NM_016123.4(IRAK4):c.335T>C (p.Leu112Pro) rs1940836736
NM_016123.4(IRAK4):c.343A>G (p.Lys115Glu)
NM_016123.4(IRAK4):c.354A>G (p.Ile118Met) rs1940838592
NM_016123.4(IRAK4):c.38G>A (p.Cys13Tyr) rs1163230363
NM_016123.4(IRAK4):c.392A>T (p.Asp131Val) rs757025762
NM_016123.4(IRAK4):c.431G>C (p.Ser144Thr) rs147079926
NM_016123.4(IRAK4):c.447C>G (p.Asp149Glu)
NM_016123.4(IRAK4):c.447CTC[1] (p.Ser152del) rs556809469
NM_016123.4(IRAK4):c.44A>G (p.Asn15Ser)
NM_016123.4(IRAK4):c.488C>T (p.Thr163Ile)
NM_016123.4(IRAK4):c.537C>G (p.Asn179Lys)
NM_016123.4(IRAK4):c.562G>C (p.Gly188Arg) rs1677335963
NM_016123.4(IRAK4):c.610T>G (p.Tyr204Asp) rs1940932293
NM_016123.4(IRAK4):c.655G>T (p.Val219Phe) rs1941030825
NM_016123.4(IRAK4):c.667A>G (p.Thr223Ala)
NM_016123.4(IRAK4):c.737T>A (p.Val246Glu)
NM_016123.4(IRAK4):c.739G>C (p.Glu247Gln)
NM_016123.4(IRAK4):c.760G>T (p.Asp254Tyr)
NM_016123.4(IRAK4):c.76A>G (p.Ile26Val)
NM_016123.4(IRAK4):c.784T>C (p.Tyr262His) rs2137999821
NM_016123.4(IRAK4):c.795G>A (p.Met265Ile)
NM_016123.4(IRAK4):c.797C>T (p.Pro266Leu)
NM_016123.4(IRAK4):c.833A>T (p.Asp278Val) rs780005506
NM_016123.4(IRAK4):c.869A>G (p.Lys290Arg) rs1941465718
NM_016123.4(IRAK4):c.899A>G (p.Asn300Ser)
NM_016123.4(IRAK4):c.91G>A (p.Gly31Arg) rs2137901159
NM_016123.4(IRAK4):c.949A>G (p.Ile317Val)
NM_016123.4(IRAK4):c.951C>G (p.Ile317Met)

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