ClinVar Miner

List of variants in gene FBLN7 reported as uncertain significance for not specified

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Gene type:
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Total variants: 50
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HGVS dbSNP gnomAD frequency
NM_153214.3(FBLN7):c.907G>A (p.Glu303Lys) rs370895871 0.00013
NM_153214.3(FBLN7):c.1090G>A (p.Gly364Ser) rs143675954 0.00007
NM_153214.3(FBLN7):c.229C>T (p.Leu77Phe) rs746771939 0.00007
NM_153214.3(FBLN7):c.1220C>T (p.Thr407Met) rs766235578 0.00005
NM_153214.3(FBLN7):c.35T>C (p.Leu12Pro) rs199704935 0.00004
NM_153214.3(FBLN7):c.836C>T (p.Pro279Leu) rs560016257 0.00004
NM_153214.3(FBLN7):c.543G>C (p.Glu181Asp) rs1342297236 0.00003
NM_153214.3(FBLN7):c.743C>T (p.Pro248Leu) rs373897520 0.00003
NM_153214.3(FBLN7):c.793G>A (p.Gly265Arg) rs147173660 0.00003
NM_153214.3(FBLN7):c.959G>A (p.Arg320Gln) rs757234528 0.00002
NM_153214.3(FBLN7):c.1106A>G (p.Asn369Ser) rs768361747 0.00001
NM_153214.3(FBLN7):c.161G>A (p.Gly54Asp) rs1326767381 0.00001
NM_153214.3(FBLN7):c.508C>T (p.Arg170Cys) rs149363704 0.00001
NM_153214.3(FBLN7):c.590C>A (p.Ala197Glu) rs756399788 0.00001
NM_153214.3(FBLN7):c.862A>G (p.Ile288Val) rs759147714 0.00001
NM_153214.3(FBLN7):c.872G>A (p.Gly291Asp) rs374024290 0.00001
NM_153214.3(FBLN7):c.107C>T (p.Ala36Val) rs1681624852
NM_153214.3(FBLN7):c.1139G>C (p.Ser380Thr) rs1380238635
NM_153214.3(FBLN7):c.1157T>C (p.Met386Thr)
NM_153214.3(FBLN7):c.1244C>T (p.Ser415Leu)
NM_153214.3(FBLN7):c.1283C>T (p.Ser428Phe)
NM_153214.3(FBLN7):c.17C>T (p.Pro6Leu)
NM_153214.3(FBLN7):c.221C>A (p.Pro74Gln) rs758061934
NM_153214.3(FBLN7):c.221C>T (p.Pro74Leu)
NM_153214.3(FBLN7):c.23C>T (p.Ala8Val)
NM_153214.3(FBLN7):c.262G>A (p.Ala88Thr)
NM_153214.3(FBLN7):c.289T>C (p.Tyr97His)
NM_153214.3(FBLN7):c.322A>C (p.Asn108His)
NM_153214.3(FBLN7):c.341T>A (p.Val114Asp) rs1573800425
NM_153214.3(FBLN7):c.371A>G (p.Asn124Ser)
NM_153214.3(FBLN7):c.452G>A (p.Cys151Tyr)
NM_153214.3(FBLN7):c.538C>G (p.Pro180Ala) rs2466823639
NM_153214.3(FBLN7):c.575G>T (p.Arg192Leu) rs1259787119
NM_153214.3(FBLN7):c.623A>G (p.Glu208Gly)
NM_153214.3(FBLN7):c.652G>C (p.Gly218Arg)
NM_153214.3(FBLN7):c.653G>C (p.Gly218Ala)
NM_153214.3(FBLN7):c.710C>T (p.Pro237Leu)
NM_153214.3(FBLN7):c.724C>T (p.His242Tyr)
NM_153214.3(FBLN7):c.725A>G (p.His242Arg) rs2466829016
NM_153214.3(FBLN7):c.761C>T (p.Thr254Ile) rs760028458
NM_153214.3(FBLN7):c.859T>C (p.Cys287Arg)
NM_153214.3(FBLN7):c.890T>C (p.Val297Ala) rs2466838876
NM_153214.3(FBLN7):c.8C>T (p.Pro3Leu) rs759455796
NM_153214.3(FBLN7):c.913A>C (p.Ser305Arg) rs1683216817
NM_153214.3(FBLN7):c.920A>G (p.Asn307Ser)
NM_153214.3(FBLN7):c.962A>G (p.Asn321Ser)
NM_153214.3(FBLN7):c.97C>T (p.Leu33Phe)
NM_153214.3(FBLN7):c.980G>A (p.Ser327Asn)
NM_153214.3(FBLN7):c.991C>T (p.Arg331Cys)
NM_153214.3(FBLN7):c.995A>G (p.His332Arg)

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