ClinVar Miner

List of variants in gene IL7R reported as uncertain significance by Illumina Laboratory Services, Illumina

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 64
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HGVS dbSNP gnomAD frequency
NM_002185.5(IL7R):c.*1974A>G rs145691961 0.00411
NM_002185.5(IL7R):c.*2413T>G rs192345351 0.00247
NM_002185.5(IL7R):c.*2294C>G rs563733521 0.00132
NM_002185.5(IL7R):c.*2065G>A rs541801251 0.00111
NM_002185.5(IL7R):c.*1702A>C rs147528974 0.00096
NM_002185.5(IL7R):c.*695C>A rs11567768 0.00096
NM_002185.5(IL7R):c.*1545G>C rs1494575 0.00054
NM_002185.5(IL7R):c.*2242C>A rs757519422 0.00050
NM_002185.5(IL7R):c.*2183C>A rs753982280 0.00049
NM_002185.5(IL7R):c.152C>T (p.Ser51Leu) rs138482569 0.00047
NM_002185.5(IL7R):c.*1614T>C rs563820481 0.00046
NM_002185.5(IL7R):c.*807G>A rs886060536 0.00038
NM_002185.5(IL7R):c.214G>C (p.Glu72Gln) rs148001159 0.00038
NM_002185.5(IL7R):c.1316C>G (p.Thr439Ser) rs148931962 0.00031
NM_002185.5(IL7R):c.*2873C>T rs377053917 0.00029
NM_002185.5(IL7R):c.*674A>G rs565860240 0.00024
NM_002185.5(IL7R):c.707G>A (p.Gly236Glu) rs201084372 0.00023
NM_002185.5(IL7R):c.1165G>C (p.Asp389His) rs143596606 0.00021
NM_002185.5(IL7R):c.*2817C>A rs113393512 0.00020
NM_002185.5(IL7R):c.419G>A (p.Arg140Gln) rs200373233 0.00019
NM_002185.5(IL7R):c.602A>G (p.Tyr201Cys) rs145810271 0.00017
NM_002185.5(IL7R):c.760G>A (p.Ala254Thr) rs137868226 0.00012
NM_002185.5(IL7R):c.*304G>A rs896970443 0.00008
NM_002185.5(IL7R):c.*1489G>C rs774913403 0.00007
NM_002185.5(IL7R):c.*35G>A rs758988107 0.00004
NM_002185.5(IL7R):c.*735C>T rs886060535 0.00004
NM_002185.5(IL7R):c.*845G>A rs1157306788 0.00004
NM_002185.5(IL7R):c.379+8G>A rs111370546 0.00004
NM_002185.5(IL7R):c.800+10T>C rs202114203 0.00004
NM_002185.5(IL7R):c.*1855T>C rs953683949 0.00003
NM_002185.5(IL7R):c.*1091G>A rs781372644 0.00002
NM_002185.5(IL7R):c.*2479A>G rs1270525952 0.00002
NM_002185.5(IL7R):c.*663T>A rs763740085 0.00002
NM_002185.5(IL7R):c.111C>T (p.Asp37=) rs763937095 0.00002
NM_002185.5(IL7R):c.695A>G (p.Asn232Ser) rs199714011 0.00002
NM_002185.5(IL7R):c.990G>A (p.Gln330=) rs201093124 0.00002
NM_002185.5(IL7R):c.*1821C>T rs1302897570 0.00001
NM_002185.5(IL7R):c.*2408G>A rs1318974974 0.00001
NM_002185.5(IL7R):c.*539C>T rs886060532 0.00001
NM_002185.5(IL7R):c.*646C>T rs569906853 0.00001
NM_002185.5(IL7R):c.*862C>T rs886060537 0.00001
NM_002185.5(IL7R):c.149G>T (p.Gly50Val) rs202083738 0.00001
NM_002185.5(IL7R):c.418C>T (p.Arg140Trp) rs773491081 0.00001
NM_002185.5(IL7R):c.554G>T (p.Ser185Ile) rs1188286965 0.00001
NM_002185.5(IL7R):c.682A>C (p.Thr228Pro) rs762736419 0.00001
NM_002185.5(IL7R):c.83-2A>T rs886060531 0.00001
NM_002185.5(IL7R):c.*1079C>A rs886060538
NM_002185.5(IL7R):c.*1198G>A rs1760251460
NM_002185.5(IL7R):c.*1548A>T rs886060539
NM_002185.5(IL7R):c.*2068T>G rs1332372176
NM_002185.5(IL7R):c.*2275C>T rs886060541
NM_002185.5(IL7R):c.*266dup rs202167692
NM_002185.5(IL7R):c.*3050G>T rs1760300993
NM_002185.5(IL7R):c.*3112A>G rs1760302344
NM_002185.5(IL7R):c.*554G>A rs886060533
NM_002185.5(IL7R):c.*574G>T rs886060534
NM_002185.5(IL7R):c.*676T>C rs762308822
NM_002185.5(IL7R):c.*86A>C rs202075594
NM_002185.5(IL7R):c.1241C>A (p.Thr414Lys) rs2229232
NM_002185.5(IL7R):c.221+7G>A rs200937717
NM_002185.5(IL7R):c.359A>T (p.Lys120Ile) rs201710684
NM_002185.5(IL7R):c.376A>C (p.Ile126Leu) rs201207454
NM_002185.5(IL7R):c.491T>A (p.Met164Lys) rs771957502
NM_002185.5(IL7R):c.83-2A>G rs886060531

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