ClinVar Miner

List of variants in gene LILRB3 studied for not specified

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Total variants: 70
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HGVS dbSNP gnomAD frequency
NM_006864.4(LILRB3):c.1346C>T (p.Ser449Leu) rs202146775 0.00038
NM_006864.4(LILRB3):c.1744A>G (p.Thr582Ala) rs149149343 0.00025
NM_006864.4(LILRB3):c.417T>A (p.Asn139Lys) rs564814709 0.00016
NM_006864.4(LILRB3):c.418A>G (p.Met140Val) rs544847770 0.00016
NM_006864.4(LILRB3):c.1846G>A (p.Gly616Arg) rs771882122 0.00011
NM_006864.4(LILRB3):c.1202G>A (p.Ser401Asn) rs752402706 0.00005
NM_006864.4(LILRB3):c.1192G>A (p.Gly398Ser) rs781128474 0.00004
NM_006864.4(LILRB3):c.1522G>A (p.Val508Ile) rs372186200 0.00004
NM_006864.4(LILRB3):c.1205C>T (p.Ser402Phe) rs754441781 0.00002
NM_006864.4(LILRB3):c.1357G>A (p.Val453Ile) rs572753215 0.00002
NM_006864.4(LILRB3):c.1436A>C (p.Lys479Thr) rs2077760453 0.00001
NM_006864.4(LILRB3):c.1592A>G (p.Gln531Arg) rs758222404 0.00001
NM_006864.4(LILRB3):c.4A>C (p.Thr2Pro) rs1352310433 0.00001
NM_006864.4(LILRB3):c.1020C>A (p.Asn340Lys) rs760034371
NM_006864.4(LILRB3):c.1042= (p.Arg348=)
NM_006864.4(LILRB3):c.1057A>G (p.Thr353Ala)
NM_006864.4(LILRB3):c.1060T>G (p.Phe354Val) rs2078074870
NM_006864.4(LILRB3):c.1070C>A (p.Thr357Asn)
NM_006864.4(LILRB3):c.1112T>A (p.Met371Lys)
NM_006864.4(LILRB3):c.1124A>C (p.His375Pro) rs140601439
NM_006864.4(LILRB3):c.1133A>G (p.Gln378Arg)
NM_006864.4(LILRB3):c.1134G>C (p.Gln378His) rs367643312
NM_006864.4(LILRB3):c.1181A>T (p.Tyr394Phe) rs763319782
NM_006864.4(LILRB3):c.1203C>A (p.Ser401Arg) rs778389068
NM_006864.4(LILRB3):c.1207A>G (p.Asn403Asp) rs757732370
NM_006864.4(LILRB3):c.1207A>T (p.Asn403Tyr) rs757732370
NM_006864.4(LILRB3):c.1208A>T (p.Asn403Ile) rs751953523
NM_006864.4(LILRB3):c.1222T>A (p.Ser408Thr) rs765393514
NM_006864.4(LILRB3):c.1295C>T (p.Pro432Leu)
NM_006864.4(LILRB3):c.1375C>G (p.Leu459Val)
NM_006864.4(LILRB3):c.1375C>T (p.Leu459Phe)
NM_006864.4(LILRB3):c.1394T>A (p.Leu465His) rs61734493
NM_006864.4(LILRB3):c.1450C>T (p.Arg484Cys) rs369201617
NM_006864.4(LILRB3):c.1504T>C (p.Ser502Pro)
NM_006864.4(LILRB3):c.1516G>C (p.Ala506Pro) rs1320961903
NM_006864.4(LILRB3):c.1572C>G (p.Asp524Glu) rs200450535
NM_006864.4(LILRB3):c.1582C>A (p.Leu528Met) rs781393400
NM_006864.4(LILRB3):c.1589G>C (p.Ser530Thr) rs751447602
NM_006864.4(LILRB3):c.1710G>C (p.Lys570Asn)
NM_006864.4(LILRB3):c.1733G>A (p.Arg578Lys)
NM_006864.4(LILRB3):c.1745C>G (p.Thr582Ser) rs199967832
NM_006864.4(LILRB3):c.1790A>G (p.Gln597Arg)
NM_006864.4(LILRB3):c.1803G>T (p.Leu601Phe)
NM_006864.4(LILRB3):c.1814G>C (p.Arg605Pro) rs368764058
NM_006864.4(LILRB3):c.1880C>T (p.Thr627Ile)
NM_006864.4(LILRB3):c.1888A>G (p.Ile630Val) rs2515652014
NM_006864.4(LILRB3):c.188A>G (p.Glu63Gly) rs2515967872
NM_006864.4(LILRB3):c.193A>G (p.Ser65Gly) rs2515967455
NM_006864.4(LILRB3):c.194G>A (p.Ser65Asn)
NM_006864.4(LILRB3):c.202C>T (p.Pro68Ser) rs759487807
NM_006864.4(LILRB3):c.290G>A (p.Arg97His) rs771379356
NM_006864.4(LILRB3):c.330C>A (p.Ser110Arg)
NM_006864.4(LILRB3):c.333C>A (p.Asp111Glu) rs772494497
NM_006864.4(LILRB3):c.334C>G (p.Pro112Ala) rs1357870902
NM_006864.4(LILRB3):c.343C>G (p.Leu115Val) rs56182917
NM_006864.4(LILRB3):c.368A>G (p.Lys123Arg)
NM_006864.4(LILRB3):c.377T>G (p.Leu126Arg) rs767975317
NM_006864.4(LILRB3):c.400G>T (p.Val134Leu) rs745901543
NM_006864.4(LILRB3):c.422C>T (p.Thr141Ile) rs752162678
NM_006864.4(LILRB3):c.478G>A (p.Glu160Lys)
NM_006864.4(LILRB3):c.514C>T (p.Leu172Phe)
NM_006864.4(LILRB3):c.527G>C (p.Gly176Ala) rs771073265
NM_006864.4(LILRB3):c.527G>T (p.Gly176Val) rs771073265
NM_006864.4(LILRB3):c.547G>A (p.Val183Met) rs2515931306
NM_006864.4(LILRB3):c.556G>A (p.Val186Met)
NM_006864.4(LILRB3):c.643G>C (p.Glu215Gln) rs2515922194
NM_006864.4(LILRB3):c.644A>G (p.Glu215Gly) rs2515922095
NM_006864.4(LILRB3):c.884G>C (p.Arg295Thr) rs1183285152
NM_006864.4(LILRB3):c.968A>G (p.Asp323Gly)
NM_006864.4(LILRB3):c.988C>G (p.Gln330Glu) rs1341322280

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