ClinVar Miner

List of variants in gene FLVCR1 reported as uncertain significance for not provided

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Total variants: 83
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HGVS dbSNP
NC_000001.11:g.(?_212894986)_(212895290_?)dup
NM_014053.4(FLVCR1):c.-7C>T rs1323079807
NM_014053.4(FLVCR1):c.1015A>T (p.Ile339Phe) rs1558113016
NM_014053.4(FLVCR1):c.1022A>G (p.Tyr341Cys)
NM_014053.4(FLVCR1):c.1074G>T (p.Met358Ile)
NM_014053.4(FLVCR1):c.1085A>G (p.Tyr362Cys) rs199842709
NM_014053.4(FLVCR1):c.1093G>A (p.Gly365Arg)
NM_014053.4(FLVCR1):c.1096G>C (p.Glu366Gln)
NM_014053.4(FLVCR1):c.1097A>T (p.Glu366Val) rs949984167
NM_014053.4(FLVCR1):c.1097AAG[1] (p.Glu367del)
NM_014053.4(FLVCR1):c.112C>G (p.Leu38Val)
NM_014053.4(FLVCR1):c.1158T>G (p.Ile386Met) rs149834738
NM_014053.4(FLVCR1):c.1200G>T (p.Gln400His)
NM_014053.4(FLVCR1):c.1235G>C (p.Gly412Ala) rs775587493
NM_014053.4(FLVCR1):c.1271A>G (p.Tyr424Cys)
NM_014053.4(FLVCR1):c.1282G>A (p.Val428Met)
NM_014053.4(FLVCR1):c.133G>A (p.Gly45Ser) rs532977695
NM_014053.4(FLVCR1):c.1406C>G (p.Ser469Cys)
NM_014053.4(FLVCR1):c.1409C>T (p.Ala470Val)
NM_014053.4(FLVCR1):c.1413G>A (p.Gln471=)
NM_014053.4(FLVCR1):c.1424T>C (p.Ile475Thr)
NM_014053.4(FLVCR1):c.143C>T (p.Pro48Leu)
NM_014053.4(FLVCR1):c.1457C>T (p.Ser486Leu)
NM_014053.4(FLVCR1):c.1474G>T (p.Ala492Ser)
NM_014053.4(FLVCR1):c.1482C>A (p.Asn494Lys)
NM_014053.4(FLVCR1):c.1503G>A (p.Met501Ile)
NM_014053.4(FLVCR1):c.1546C>T (p.Arg516Ter) rs538343832
NM_014053.4(FLVCR1):c.1559T>C (p.Ile520Thr)
NM_014053.4(FLVCR1):c.1567G>A (p.Gly523Arg)
NM_014053.4(FLVCR1):c.1572dup (p.Thr525fs)
NM_014053.4(FLVCR1):c.1619A>G (p.Gln540Arg) rs144226457
NM_014053.4(FLVCR1):c.1619_1631delinsGACCCAAAAAT (p.Gln540fs) rs886044676
NM_014053.4(FLVCR1):c.1624C>T (p.Pro542Ser) rs141575859
NM_014053.4(FLVCR1):c.1642del (p.Ser548fs) rs766024598
NM_014053.4(FLVCR1):c.1657T>G (p.Ser553Ala) rs149887215
NM_014053.4(FLVCR1):c.169C>G (p.Leu57Val)
NM_014053.4(FLVCR1):c.178G>T (p.Ala60Ser)
NM_014053.4(FLVCR1):c.178_179delinsAT (p.Ala60Ile)
NM_014053.4(FLVCR1):c.18T>A (p.Asp6Glu)
NM_014053.4(FLVCR1):c.202C>G (p.Gln68Glu)
NM_014053.4(FLVCR1):c.254G>C (p.Gly85Ala)
NM_014053.4(FLVCR1):c.25G>A (p.Gly9Arg)
NM_014053.4(FLVCR1):c.26G>A (p.Gly9Glu)
NM_014053.4(FLVCR1):c.307C>T (p.Leu103Phe)
NM_014053.4(FLVCR1):c.30G>A (p.Ala10=) rs1572001189
NM_014053.4(FLVCR1):c.322T>G (p.Phe108Val)
NM_014053.4(FLVCR1):c.346C>T (p.Leu116=)
NM_014053.4(FLVCR1):c.362A>G (p.Asn121Ser)
NM_014053.4(FLVCR1):c.369T>A (p.Phe123Leu)
NM_014053.4(FLVCR1):c.391A>G (p.Ile131Val) rs1558104917
NM_014053.4(FLVCR1):c.398A>C (p.Asn133Thr)
NM_014053.4(FLVCR1):c.40C>T (p.Pro14Ser)
NM_014053.4(FLVCR1):c.476C>G (p.Pro159Arg)
NM_014053.4(FLVCR1):c.488C>T (p.Pro163Leu) rs369434267
NM_014053.4(FLVCR1):c.49C>G (p.Pro17Ala) rs543847452
NM_014053.4(FLVCR1):c.501G>A (p.Leu167=) rs886043715
NM_014053.4(FLVCR1):c.551A>C (p.Asn184Thr)
NM_014053.4(FLVCR1):c.554G>C (p.Cys185Ser)
NM_014053.4(FLVCR1):c.563C>T (p.Ala188Val)
NM_014053.4(FLVCR1):c.593A>G (p.His198Arg)
NM_014053.4(FLVCR1):c.595C>T (p.Leu199Phe) rs41296694
NM_014053.4(FLVCR1):c.642G>C (p.Gln214His)
NM_014053.4(FLVCR1):c.692C>A (p.Pro231His)
NM_014053.4(FLVCR1):c.700G>T (p.Val234Leu)
NM_014053.4(FLVCR1):c.71C>T (p.Pro24Leu) rs562153726
NM_014053.4(FLVCR1):c.785A>G (p.Asn262Ser) rs547679833
NM_014053.4(FLVCR1):c.799A>G (p.Thr267Ala) rs1558107949
NM_014053.4(FLVCR1):c.7C>T (p.Arg3Trp) rs998058913
NM_014053.4(FLVCR1):c.819T>C (p.Asn273=) rs1558107967
NM_014053.4(FLVCR1):c.820A>G (p.Ile274Val)
NM_014053.4(FLVCR1):c.82G>A (p.Gly28Ser)
NM_014053.4(FLVCR1):c.832T>C (p.Phe278Leu)
NM_014053.4(FLVCR1):c.847G>C (p.Ala283Pro) rs777525949
NM_014053.4(FLVCR1):c.877G>A (p.Ala293Thr)
NM_014053.4(FLVCR1):c.889A>G (p.Lys297Glu)
NM_014053.4(FLVCR1):c.901C>T (p.Arg301Trp)
NM_014053.4(FLVCR1):c.908C>T (p.Pro303Leu)
NM_014053.4(FLVCR1):c.937G>A (p.Asp313Asn) rs139175550
NM_014053.4(FLVCR1):c.944C>G (p.Pro315Arg)
NM_014053.4(FLVCR1):c.944C>T (p.Pro315Leu)
NM_014053.4(FLVCR1):c.974T>G (p.Ile325Arg)
NM_014053.4(FLVCR1):c.987T>G (p.Phe329Leu) rs762546149
NM_014053.4(FLVCR1):c.991A>C (p.Asn331His)

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