ClinVar Miner

List of variants in gene TCIRG1 reported as benign for not provided

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Gene type:
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Total variants: 46
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HGVS dbSNP gnomAD frequency
NM_006019.4(TCIRG1):c.1245G>C (p.Leu415=) rs2471829 0.97643
NM_006019.4(TCIRG1):c.1166-970A>G rs906713 0.81709
NM_006019.4(TCIRG1):c.417+11A>G rs3808974 0.32688
NM_006019.4(TCIRG1):c.714-19C>A rs10896289 0.18721
NM_006019.4(TCIRG1):c.1020+152G>T rs72926459 0.18098
NM_006019.4(TCIRG1):c.2237-78C>T rs11228127 0.16951
NM_006019.4(TCIRG1):c.166C>T (p.Arg56Trp) rs36027301 0.04199
NM_006019.4(TCIRG1):c.1672G>C (p.Val558Leu) rs35089741 0.00806
NM_006019.4(TCIRG1):c.2476G>A (p.Ala826Thr) rs75596506 0.00755
NM_006019.4(TCIRG1):c.714-11C>T rs370019546 0.00607
NM_006019.4(TCIRG1):c.479G>A (p.Gly160Glu) rs186758849 0.00601
NM_006019.4(TCIRG1):c.1515C>T (p.Thr505=) rs34211419 0.00473
NM_006019.4(TCIRG1):c.247A>G (p.Lys83Glu) rs142855299 0.00448
NM_006019.4(TCIRG1):c.630+14G>A rs201531306 0.00161
NM_006019.4(TCIRG1):c.528C>A (p.Pro176=) rs538805960 0.00135
NM_006019.4(TCIRG1):c.412C>T (p.Pro138Ser) rs35354504 0.00118
NM_006019.4(TCIRG1):c.813C>T (p.Leu271=) rs377108710 0.00099
NM_006019.4(TCIRG1):c.1536C>T (p.Tyr512=) rs138049763 0.00093
NM_006019.4(TCIRG1):c.197-5C>T rs183885218 0.00088
NM_006019.4(TCIRG1):c.476G>A (p.Gly159Glu) rs199632510 0.00046
NM_006019.4(TCIRG1):c.154G>C (p.Val52Leu) rs118141250 0.00038
NM_006019.4(TCIRG1):c.2236+18C>T rs372043757 0.00031
NM_006019.4(TCIRG1):c.1673+13G>A rs372404641 0.00029
NM_006019.4(TCIRG1):c.1165+12G>A rs199554924 0.00026
NM_006019.4(TCIRG1):c.1464-15C>G rs564284005 0.00026
NM_006019.4(TCIRG1):c.2193C>T (p.Thr731=) rs141601593 0.00025
NM_006019.4(TCIRG1):c.714-20G>A rs200087340 0.00024
NM_006019.4(TCIRG1):c.629C>T (p.Thr210Met) rs372826788 0.00015
NM_006019.4(TCIRG1):c.1464-5C>T rs372813575 0.00011
NM_006019.4(TCIRG1):c.307C>T (p.Arg103Cys) rs771198568 0.00006
NM_006019.4(TCIRG1):c.1904C>T (p.Thr635Met) rs763119311 0.00004
NM_006019.4(TCIRG1):c.-5+560dup rs5792431
NM_006019.4(TCIRG1):c.117+83T>C rs7116924
NM_006019.4(TCIRG1):c.1245= (p.Leu415=)
NM_006019.4(TCIRG1):c.1407C>A (p.Thr469=) rs570336313
NM_006019.4(TCIRG1):c.1555-254G>C rs72926470
NM_006019.4(TCIRG1):c.1673+24del
NM_006019.4(TCIRG1):c.1673+24dup rs534065091
NM_006019.4(TCIRG1):c.1887+175A>G rs2075609
NM_006019.4(TCIRG1):c.2013+12del rs2134463264
NM_006019.4(TCIRG1):c.2118+24dup
NM_006019.4(TCIRG1):c.2119-5dup
NM_006019.4(TCIRG1):c.2279TGGGCC[3] (p.760LG[3]) rs199973759
NM_006019.4(TCIRG1):c.384C>T (p.His128=) rs3808973
NM_006019.4(TCIRG1):c.624C>G (p.Pro208=) rs779281265
NM_006019.4(TCIRG1):c.807+13G>C rs773072992

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