ClinVar Miner

List of variants in gene FLVCR1 reported as uncertain significance by Athena Diagnostics Inc

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Total variants: 25
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HGVS dbSNP
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.1085A>G (p.Tyr362Cys) rs199842709
NM_014053.4(FLVCR1):c.1097A>T (p.Glu366Val) rs949984167
NM_014053.4(FLVCR1):c.1158T>G (p.Ile386Met) rs149834738
NM_014053.4(FLVCR1):c.1406C>G (p.Ser469Cys)
NM_014053.4(FLVCR1):c.143C>T (p.Pro48Leu)
NM_014053.4(FLVCR1):c.1619A>G (p.Gln540Arg) rs144226457
NM_014053.4(FLVCR1):c.1624C>T (p.Pro542Ser) rs141575859
NM_014053.4(FLVCR1):c.1642del (p.Ser548fs) rs766024598
NM_014053.4(FLVCR1):c.169C>G (p.Leu57Val)
NM_014053.4(FLVCR1):c.18T>A (p.Asp6Glu)
NM_014053.4(FLVCR1):c.267G>A (p.Glu89=) rs1553261817
NM_014053.4(FLVCR1):c.346C>T (p.Leu116=)
NM_014053.4(FLVCR1):c.364G>A (p.Ala122Thr) rs1553261879
NM_014053.4(FLVCR1):c.391A>G (p.Ile131Val) rs1558104917
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.595C>T (p.Leu199Phe) rs41296694
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.819T>C (p.Asn273=) rs1558107967
NM_014053.4(FLVCR1):c.987T>G (p.Phe329Leu) rs762546149

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