ClinVar Miner

List of variants in gene ICOS reported as uncertain significance for Common variable immunodeficiency 1

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Gene type:
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Total variants: 45
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HGVS dbSNP
NM_012092.3(ICOS):c.*1004C>G rs866710563
NM_012092.3(ICOS):c.*1093C>T rs886055499
NM_012092.3(ICOS):c.*1094C>T rs144036725
NM_012092.3(ICOS):c.*1293T>C rs528769953
NM_012092.3(ICOS):c.*1854G>A rs140979765
NM_012092.3(ICOS):c.*77C>T rs769887283
NM_012092.3(ICOS):c.*931A>G rs886055497
NM_012092.3(ICOS):c.*977T>G rs886055498
NM_012092.3(ICOS):c.*995C>T rs190590580
NM_012092.3(ICOS):c.184C>T (p.Leu62Phe) rs886055496
NM_012092.3(ICOS):c.401A>C (p.Gln134Pro) rs367905290
NM_012092.3(ICOS):c.451G>C (p.Val151Leu) rs76778263
NM_012092.3(ICOS):c.501+6C>G rs4264550
NM_012092.3(ICOS):c.502A>C (p.Lys168Gln)
NM_012092.3(ICOS):c.58+9T>G rs140049646
NM_012092.3(ICOS):c.586+2T>A rs1559036416
NM_012092.3(ICOS):c.589G>A (p.Val197Met)
NM_012092.3(ICOS):c.591G>A (p.Val197=) rs55655222
NM_012092.3(ICOS):c.597A>G (p.Leu199=) rs145698501
NM_012092.4(ICOS):c.*1025A>T
NM_012092.4(ICOS):c.*1137C>T
NM_012092.4(ICOS):c.*1172G>A
NM_012092.4(ICOS):c.*1269A>C
NM_012092.4(ICOS):c.*1300C>T
NM_012092.4(ICOS):c.*1416G>T
NM_012092.4(ICOS):c.*1457A>G
NM_012092.4(ICOS):c.*1869A>C
NM_012092.4(ICOS):c.*1901A>G
NM_012092.4(ICOS):c.*1948G>T
NM_012092.4(ICOS):c.*399G>A
NM_012092.4(ICOS):c.*474G>T
NM_012092.4(ICOS):c.*512T>C
NM_012092.4(ICOS):c.*594C>T
NM_012092.4(ICOS):c.*73T>C
NM_012092.4(ICOS):c.*939A>G
NM_012092.4(ICOS):c.-24G>T
NM_012092.4(ICOS):c.106G>A (p.Gly36Arg)
NM_012092.4(ICOS):c.229A>G (p.Ile77Val)
NM_012092.4(ICOS):c.375A>G (p.Gly125=)
NM_012092.4(ICOS):c.42C>A (p.Arg14=)
NM_012092.4(ICOS):c.495A>C (p.Thr165=)
NM_012092.4(ICOS):c.510A>G (p.Ser170=)
NM_012092.4(ICOS):c.523G>A (p.Asp175Asn)
NM_012092.4(ICOS):c.586+3A>G
NM_012092.4(ICOS):c.77C>A (p.Ala26Asp)

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