ClinVar Miner

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

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Gene type:
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Total variants: 65
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HGVS dbSNP gnomAD frequency
NM_001128148.3(TFRC):c.687+9A>G rs480760 0.89339
NM_001128148.3(TFRC):c.1468+25G>T rs507131 0.79828
NM_001128148.3(TFRC):c.-23-305T>C rs41300431 0.48353
NM_001128148.3(TFRC):c.1468+39A>G rs2239641 0.48268
NM_001128148.3(TFRC):c.37-135T>C rs9877119 0.48208
NM_001128148.3(TFRC):c.687+320C>G rs3761717 0.48179
NM_001128148.3(TFRC):c.434+254G>A rs9859260 0.48176
NM_001128148.3(TFRC):c.1040+148T>A rs9858727 0.48156
NM_001128148.3(TFRC):c.1469-190G>C rs9846149 0.48114
NM_001128148.3(TFRC):c.434+198G>T rs9859401 0.48080
NM_001128148.3(TFRC):c.585-153G>A rs9990392 0.47410
NM_001128148.3(TFRC):c.585-231A>G rs34221479 0.47312
NM_001128148.3(TFRC):c.238+92A>T rs5021790 0.43720
NM_001128148.3(TFRC):c.424G>A (p.Gly142Ser) rs3817672 0.42627
NM_001128148.3(TFRC):c.1900-280C>T rs557527 0.31551
NM_001128148.3(TFRC):c.1677+158C>T rs3933 0.31549
NM_001128148.3(TFRC):c.1678-5T>C rs366268 0.31431
NM_001128148.3(TFRC):c.2041-100G>A rs41298097 0.31418
NM_001128148.3(TFRC):c.1678-12G>A rs419059 0.31409
NM_001128148.3(TFRC):c.1678-4G>A rs419068 0.31401
NM_001128148.3(TFRC):c.801+277C>A rs4927866 0.18744
NM_001128148.3(TFRC):c.-23-28C>T rs41300435 0.18732
NM_001128148.3(TFRC):c.1468+77G>A rs526860 0.18728
NM_001128148.3(TFRC):c.1198+13C>A rs41295873 0.09058
NM_001128148.3(TFRC):c.239-29A>T rs3736651 0.08129
NM_001128148.3(TFRC):c.1319-105T>C rs926149 0.08027
NM_001128148.3(TFRC):c.1198+166del rs201413498 0.07470
NM_001128148.3(TFRC):c.2124G>A (p.Thr708=) rs1805051 0.07465
NM_001128148.3(TFRC):c.1199-207T>C rs2272622 0.03327
NM_001128148.3(TFRC):c.1596-92G>A rs13088791 0.03326
NM_001128148.3(TFRC):c.1469-188A>G rs13071789 0.03321
NM_001128148.3(TFRC):c.1678-15C>T rs41297537 0.03316
NM_001128148.3(TFRC):c.1258G>A (p.Gly420Ser) rs41295879 0.00907
NM_001128148.3(TFRC):c.1503G>A (p.Leu501=) rs114157544 0.00545
NM_001128148.3(TFRC):c.312C>T (p.Thr104=) rs41301359 0.00525
NM_001128148.3(TFRC):c.810T>C (p.Asn270=) rs35181492 0.00490
NM_001128148.3(TFRC):c.802-12G>T rs41295845 0.00483
NM_001128148.3(TFRC):c.1485G>A (p.Lys495=) rs111276121 0.00230
NM_001128148.3(TFRC):c.901-12T>G rs183412409 0.00212
NM_001128148.3(TFRC):c.1596-11T>C rs548927299 0.00138
NM_001128148.3(TFRC):c.1674C>T (p.Cys558=) rs151279600 0.00133
NM_001128148.3(TFRC):c.162C>T (p.Ala54=) rs41300443 0.00065
NM_001128148.3(TFRC):c.634C>G (p.Leu212Val) rs41301381 0.00062
NM_001128148.3(TFRC):c.663G>A (p.Ala221=) rs142709816 0.00044
NM_001128148.3(TFRC):c.135A>G (p.Glu45=) rs552921034 0.00035
NM_001128148.3(TFRC):c.1548G>A (p.Pro516=) rs145738445 0.00027
NM_001128148.3(TFRC):c.1053A>G (p.Gly351=) rs532098606 0.00026
NM_001128148.3(TFRC):c.239-8C>G rs145157774 0.00011
NM_001128148.3(TFRC):c.1198+17_1198+18insA rs375392784 0.00005
NM_001128148.3(TFRC):c.1198+17C>G rs770408812
NM_001128148.3(TFRC):c.1198+180del rs55922619
NM_001128148.3(TFRC):c.1198+22_1198+25del rs55639089
NM_001128148.3(TFRC):c.1198+23_1198+25del rs55639089
NM_001128148.3(TFRC):c.1199-318G>A rs34830025
NM_001128148.3(TFRC):c.1319-212T>A rs499591
NM_001128148.3(TFRC):c.1323G>A (p.Gly441=)
NM_001128148.3(TFRC):c.1404+17C>A rs2239640
NM_001128148.3(TFRC):c.1900-248G>A rs41298063
NM_001128148.3(TFRC):c.2040+290dup rs202084265
NM_001128148.3(TFRC):c.2041-109del rs529214594
NM_001128148.3(TFRC):c.2041-111_2041-109del rs529214594
NM_001128148.3(TFRC):c.2041-113_2041-109del rs529214594
NM_001128148.3(TFRC):c.238+280del rs34596231
NM_001128148.3(TFRC):c.238+93dup rs56119775
NM_001128148.3(TFRC):c.396G>A (p.Ser132=) rs150889988

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