ClinVar Miner

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

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Gene type:
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Total variants: 32
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HGVS dbSNP gnomAD frequency
NM_014053.4(FLVCR1):c.1624C>T (p.Pro542Ser) rs141575859 0.00117
NM_014053.4(FLVCR1):c.1158T>G (p.Ile386Met) rs149834738 0.00032
NM_014053.4(FLVCR1):c.595C>T (p.Leu199Phe) rs41296694 0.00026
NM_014053.4(FLVCR1):c.1619A>G (p.Gln540Arg) rs144226457 0.00011
NM_014053.4(FLVCR1):c.554G>C (p.Cys185Ser) rs747064078 0.00010
NM_014053.4(FLVCR1):c.1642del (p.Ser548fs) rs766024598 0.00009
NM_014053.4(FLVCR1):c.1022A>G (p.Tyr341Cys) rs200151282 0.00006
NM_014053.4(FLVCR1):c.944C>G (p.Pro315Arg) rs572881055 0.00006
NM_014053.4(FLVCR1):c.1365C>T (p.Tyr455=) rs779980010 0.00004
NM_014053.4(FLVCR1):c.346C>T (p.Leu116=) rs150645228 0.00003
NM_014053.4(FLVCR1):c.49C>G (p.Pro17Ala) rs543847452 0.00003
NM_014053.4(FLVCR1):c.987T>G (p.Phe329Leu) rs762546149 0.00003
NM_014053.4(FLVCR1):c.-7C>T rs1323079807 0.00001
NM_014053.4(FLVCR1):c.1085A>G (p.Tyr362Cys) rs199842709 0.00001
NM_014053.4(FLVCR1):c.1506T>G (p.Phe502Leu) rs369869680 0.00001
NM_014053.4(FLVCR1):c.18T>A (p.Asp6Glu) rs1029247819 0.00001
NM_014053.4(FLVCR1):c.488C>T (p.Pro163Leu) rs369434267 0.00001
NM_014053.4(FLVCR1):c.785A>G (p.Asn262Ser) rs547679833 0.00001
NM_014053.4(FLVCR1):c.1015A>T (p.Ile339Phe) rs1558113016
NM_014053.4(FLVCR1):c.1097A>T (p.Glu366Val) rs949984167
NM_014053.4(FLVCR1):c.1281C>A (p.Ile427=)
NM_014053.4(FLVCR1):c.1406C>G (p.Ser469Cys) rs1203409620
NM_014053.4(FLVCR1):c.1459G>C (p.Asp487His)
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.555C>T (p.Cys185=)
NM_014053.4(FLVCR1):c.573G>A (p.Lys191=)
NM_014053.4(FLVCR1):c.585GCA[2] (p.Gln197del)
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.839G>A (p.Gly280Glu)
NM_014053.4(FLVCR1):c.853G>T (p.Ala285Ser)

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