ClinVar Miner

List of variants reported as uncertain significance for autosomal recessive Mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR2 deficiency

Included ClinVar conditions (1):
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ClinVar version:
Total variants: 92
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HGVS dbSNP gnomAD frequency
NM_005534.4(IFNGR2):c.708A>T (p.Glu236Asp) rs121913212 0.00235
NM_005534.4(IFNGR2):c.37C>T (p.Leu13Phe) rs1012938610 0.00124
NM_005534.4(IFNGR2):c.308C>T (p.Ala103Val) rs139212989 0.00026
NM_005534.4(IFNGR2):c.319A>G (p.Met107Val) rs756119057 0.00021
NM_005534.4(IFNGR2):c.53C>T (p.Ala18Val) rs773932279 0.00013
NM_005534.4(IFNGR2):c.940G>A (p.Asp314Asn) rs369529404 0.00012
NM_005534.4(IFNGR2):c.347G>A (p.Arg116Gln) rs760780330 0.00010
NM_005534.4(IFNGR2):c.616A>G (p.Arg206Gly) rs147894635 0.00010
NM_005534.4(IFNGR2):c.524A>G (p.Tyr175Cys) rs368333636 0.00008
NM_005534.4(IFNGR2):c.889G>A (p.Asp297Asn) rs121913219 0.00007
NM_005534.4(IFNGR2):c.8C>G (p.Pro3Arg) rs773084508 0.00007
NM_005534.4(IFNGR2):c.879+5G>A rs375538161 0.00006
NM_005534.4(IFNGR2):c.20_31dup (p.Leu10_Leu11insArgSerLeuLeu) rs1466765626 0.00004
NM_005534.4(IFNGR2):c.451G>A (p.Gly151Arg) rs902362680 0.00004
NM_005534.4(IFNGR2):c.496G>A (p.Ala166Thr) rs552291982 0.00004
NM_005534.4(IFNGR2):c.532C>T (p.His178Tyr) rs769963583 0.00004
NM_005534.4(IFNGR2):c.533A>G (p.His178Arg) rs115346998 0.00004
NM_005534.4(IFNGR2):c.665A>T (p.Asn222Ile) rs201843430 0.00004
NM_005534.4(IFNGR2):c.724T>A (p.Ser242Thr) rs145216430 0.00004
NM_005534.4(IFNGR2):c.764C>T (p.Thr255Ile) rs373582182 0.00004
NM_005534.4(IFNGR2):c.115C>T (p.Arg39Cys) rs572786148 0.00003
NM_005534.4(IFNGR2):c.116G>A (p.Arg39His) rs755959582 0.00003
NM_005534.4(IFNGR2):c.436A>G (p.Ile146Val) rs776581325 0.00003
NM_005534.4(IFNGR2):c.442G>A (p.Val148Met) rs766274599 0.00003
NM_005534.4(IFNGR2):c.484C>T (p.Pro162Ser) rs755628412 0.00003
NM_005534.4(IFNGR2):c.977C>T (p.Pro326Leu) rs202237583 0.00003
NM_005534.4(IFNGR2):c.757G>A (p.Val253Met) rs191792822 0.00002
NM_005534.4(IFNGR2):c.869A>C (p.Gln290Pro) rs143025663 0.00002
NM_005534.4(IFNGR2):c.879+4C>T rs770663375 0.00002
NM_005534.4(IFNGR2):c.232G>A (p.Asp78Asn) rs760048640 0.00001
NM_005534.4(IFNGR2):c.239T>C (p.Met80Thr) rs775577939 0.00001
NM_005534.4(IFNGR2):c.277G>C (p.Glu93Gln) rs1287012312 0.00001
NM_005534.4(IFNGR2):c.56C>T (p.Ala19Val) rs956427420 0.00001
NM_005534.4(IFNGR2):c.589A>T (p.Ile197Phe) rs749339064 0.00001
NM_005534.4(IFNGR2):c.58G>A (p.Ala20Thr) rs1176465152 0.00001
NM_005534.4(IFNGR2):c.610C>T (p.Pro204Ser) rs963619980 0.00001
NM_005534.4(IFNGR2):c.668T>C (p.Ile223Thr) rs764922061 0.00001
NM_005534.4(IFNGR2):c.718G>C (p.Asp240His) rs369753667 0.00001
NM_005534.4(IFNGR2):c.91C>T (p.Pro31Ser) rs750951592 0.00001
NM_005534.4(IFNGR2):c.946G>A (p.Val316Ile) rs766433285 0.00001
NM_005534.4(IFNGR2):c.949T>C (p.Trp317Arg) rs755201347 0.00001
NM_005534.4(IFNGR2):c.94G>A (p.Ala32Thr) rs772248868 0.00001
NM_005534.4(IFNGR2):c.971C>T (p.Ser324Leu) rs749163514 0.00001
NC_000021.8:g.(?_34638751)_(34809289_?)dup
NC_000021.8:g.(?_34799171)_(34809289_?)dup
NM_005534.4(IFNGR2):c.1006A>G (p.Thr336Ala) rs202122427
NM_005534.4(IFNGR2):c.1007C>G (p.Thr336Arg) rs763384272
NM_005534.4(IFNGR2):c.1007C>T (p.Thr336Met) rs763384272
NM_005534.4(IFNGR2):c.1013G>C (p.Ter338Ser)
NM_005534.4(IFNGR2):c.127G>A (p.Ala43Thr)
NM_005534.4(IFNGR2):c.166A>G (p.Asn56Asp) rs2123339315
NM_005534.4(IFNGR2):c.188A>G (p.Tyr63Cys)
NM_005534.4(IFNGR2):c.19T>C (p.Trp7Arg)
NM_005534.4(IFNGR2):c.19_36dup (p.Leu12_Leu13insTrpSerLeuLeuLeuLeu)
NM_005534.4(IFNGR2):c.227C>T (p.Thr76Met) rs1208240776
NM_005534.4(IFNGR2):c.24GCT[6] (p.Leu13dup) rs753866192
NM_005534.4(IFNGR2):c.295G>A (p.Ala99Thr)
NM_005534.4(IFNGR2):c.298A>G (p.Ser100Gly) rs2123349022
NM_005534.4(IFNGR2):c.361G>C (p.Ala121Pro) rs776967196
NM_005534.4(IFNGR2):c.374C>A (p.Ala125Asp)
NM_005534.4(IFNGR2):c.406C>T (p.Arg136Trp) rs1320302979
NM_005534.4(IFNGR2):c.407G>A (p.Arg136Gln) rs979344163
NM_005534.4(IFNGR2):c.437T>A (p.Ile146Asn) rs188848981
NM_005534.4(IFNGR2):c.437T>C (p.Ile146Thr)
NM_005534.4(IFNGR2):c.454G>C (p.Glu152Gln) rs936531276
NM_005534.4(IFNGR2):c.463C>G (p.Leu155Val) rs1211518898
NM_005534.4(IFNGR2):c.48CGC[1] (p.Ala19_Ala22del) rs765468464
NM_005534.4(IFNGR2):c.48CGC[2] (p.Ala20_Ala22del) rs765468464
NM_005534.4(IFNGR2):c.48CGC[3] (p.Ala21_Ala22del) rs765468464
NM_005534.4(IFNGR2):c.48CGC[6] (p.Ala22dup) rs765468464
NM_005534.4(IFNGR2):c.48CGC[7] (p.Ala22_Pro23insAlaAla)
NM_005534.4(IFNGR2):c.509C>T (p.Thr170Met)
NM_005534.4(IFNGR2):c.514T>A (p.Phe172Ile) rs375419913
NM_005534.4(IFNGR2):c.514T>G (p.Phe172Val)
NM_005534.4(IFNGR2):c.553A>C (p.Ile185Leu)
NM_005534.4(IFNGR2):c.568G>C (p.Gly190Arg)
NM_005534.4(IFNGR2):c.569G>A (p.Gly190Asp)
NM_005534.4(IFNGR2):c.65C>T (p.Ala22Val) rs1555878402
NM_005534.4(IFNGR2):c.705C>T (p.Tyr235=)
NM_005534.4(IFNGR2):c.706G>A (p.Glu236Lys)
NM_005534.4(IFNGR2):c.761G>A (p.Gly254Glu)
NM_005534.4(IFNGR2):c.761G>T (p.Gly254Val)
NM_005534.4(IFNGR2):c.788C>T (p.Ala263Val) rs2083902202
NM_005534.4(IFNGR2):c.791G>A (p.Gly264Glu) rs2083902242
NM_005534.4(IFNGR2):c.802T>C (p.Phe268Leu) rs2123370275
NM_005534.4(IFNGR2):c.80T>C (p.Leu27Pro) rs2123339140
NM_005534.4(IFNGR2):c.824G>T (p.Gly275Val)
NM_005534.4(IFNGR2):c.83C>T (p.Ser28Phe) rs2083743038
NM_005534.4(IFNGR2):c.914C>T (p.Ala305Val) rs893539360
NM_005534.4(IFNGR2):c.934C>T (p.Pro312Ser) rs2123384586
NM_005534.4(IFNGR2):c.958G>C (p.Val320Leu)
NM_005534.4(IFNGR2):c.990AGA[1] (p.Glu331del) rs760530034

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