ClinVar Miner

List of variants in gene FLCN reported as benign by Invitae

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Gene type:
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Total variants: 22
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NM_144997.7(FLCN):c.1062+6C>T rs8065832
NM_144997.7(FLCN):c.1149C>T (p.Leu383=) rs150752548
NM_144997.7(FLCN):c.1177-21G>A rs150687840
NM_144997.7(FLCN):c.1233G>A (p.Glu411=) rs61750032
NM_144997.7(FLCN):c.1269C>T (p.His423=) rs41464156
NM_144997.7(FLCN):c.1281C>G (p.Pro427=) rs372207262
NM_144997.7(FLCN):c.1332C>T (p.Ala444=) rs141283741
NM_144997.7(FLCN):c.1333G>A (p.Ala445Thr) rs41419545
NM_144997.7(FLCN):c.1414C>G (p.Pro472Ala) rs151312899
NM_144997.7(FLCN):c.1463C>T (p.Ala488Val) rs200660337
NM_144997.7(FLCN):c.1464G>A (p.Ala488=) rs747029882
NM_144997.7(FLCN):c.1523A>G (p.Lys508Arg) rs199643834
NM_144997.7(FLCN):c.1538+10A>C rs12451312
NM_144997.7(FLCN):c.1692C>T (p.His564=) rs201810397
NM_144997.7(FLCN):c.450T>C (p.Phe150=) rs200672897
NM_144997.7(FLCN):c.726A>T (p.Thr242=) rs113938514
NM_144997.7(FLCN):c.735A>C (p.Thr245=) rs150175875
NM_144997.7(FLCN):c.75G>A (p.Leu25=) rs200350612
NM_144997.7(FLCN):c.779+9C>T rs373504780
NM_144997.7(FLCN):c.871+36G>A rs3744124
NM_144997.7(FLCN):c.871+47G>A rs142934950
NM_144997.7(FLCN):c.959G>A (p.Arg320Gln) rs143483053

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