ClinVar Miner

List of variants in gene IFRD1 reported as uncertain significance for not specified

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Total variants: 40
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HGVS dbSNP gnomAD frequency
NM_001550.4(IFRD1):c.1232C>T (p.Thr411Met) rs144614382 0.00040
NM_001550.4(IFRD1):c.938C>T (p.Thr313Met) rs373824184 0.00017
NM_001550.4(IFRD1):c.1256G>A (p.Arg419His) rs778656390 0.00007
NM_001550.4(IFRD1):c.1058C>T (p.Thr353Ile) rs188279852 0.00005
NM_001550.4(IFRD1):c.1211C>T (p.Pro404Leu) rs770267292 0.00005
NM_001550.4(IFRD1):c.976C>A (p.His326Asn) rs199704602 0.00005
NM_001550.4(IFRD1):c.73G>A (p.Ala25Thr) rs373600693 0.00004
NM_001550.4(IFRD1):c.967G>A (p.Gly323Arg) rs1030765204 0.00004
NM_001550.4(IFRD1):c.1207C>T (p.Pro403Ser) rs1307825162 0.00003
NM_001550.4(IFRD1):c.1333G>A (p.Ala445Thr) rs1230781853 0.00002
NM_001550.4(IFRD1):c.142A>G (p.Ile48Val) rs372855145 0.00002
NM_001550.4(IFRD1):c.1247A>G (p.Lys416Arg) rs369365976 0.00001
NM_001550.4(IFRD1):c.191C>G (p.Ala64Gly) rs375707852 0.00001
NM_001550.4(IFRD1):c.428G>A (p.Arg143His) rs1024269408 0.00001
NM_001550.4(IFRD1):c.730T>A (p.Ser244Thr) rs1287818660 0.00001
NM_001550.4(IFRD1):c.7A>C (p.Lys3Gln) rs1185179802 0.00001
NM_001550.4(IFRD1):c.947T>C (p.Leu316Pro) rs1366826223 0.00001
NM_001550.4(IFRD1):c.1055C>G (p.Pro352Arg) rs1795768421
NM_001550.4(IFRD1):c.1151G>A (p.Gly384Glu)
NM_001550.4(IFRD1):c.1214T>C (p.Val405Ala) rs1416982894
NM_001550.4(IFRD1):c.1231A>G (p.Thr411Ala)
NM_001550.4(IFRD1):c.136G>A (p.Ala46Thr)
NM_001550.4(IFRD1):c.314G>A (p.Gly105Asp)
NM_001550.4(IFRD1):c.371T>C (p.Met124Thr) rs1795308377
NM_001550.4(IFRD1):c.394C>T (p.Arg132Cys)
NM_001550.4(IFRD1):c.52G>T (p.Gly18Cys)
NM_001550.4(IFRD1):c.616A>G (p.Thr206Ala)
NM_001550.4(IFRD1):c.652A>G (p.Ile218Val) rs774923155
NM_001550.4(IFRD1):c.722A>C (p.His241Pro) rs1354426179
NM_001550.4(IFRD1):c.731C>A (p.Ser244Tyr) rs1346940033
NM_001550.4(IFRD1):c.827C>T (p.Ser276Phe)
NM_001550.4(IFRD1):c.833A>G (p.Asp278Gly)
NM_001550.4(IFRD1):c.885A>T (p.Glu295Asp) rs2486537559
NM_001550.4(IFRD1):c.898A>C (p.Ile300Leu)
NM_001550.4(IFRD1):c.901G>A (p.Glu301Lys) rs2486537601
NM_001550.4(IFRD1):c.91G>A (p.Ala31Thr)
NM_001550.4(IFRD1):c.931T>A (p.Ser311Thr) rs2486552005
NM_001550.4(IFRD1):c.932C>A (p.Ser311Tyr)
NM_001550.4(IFRD1):c.956T>C (p.Leu319Ser) rs2486552138
NM_001550.4(IFRD1):c.979C>T (p.Arg327Trp)

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