ClinVar Miner

List of variants in gene FLCN reported as benign by Quest Diagnostics Nichols Institute San Juan Capistrano

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Gene type:
ClinVar version:
Total variants: 21
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HGVS dbSNP gnomAD frequency
NM_144997.7(FLCN):c.1233G>A (p.Glu411=) rs61750032 0.03557
NM_144997.7(FLCN):c.726A>T (p.Thr242=) rs113938514 0.02907
NM_144997.7(FLCN):c.1333G>A (p.Ala445Thr) rs41419545 0.00217
NM_144997.7(FLCN):c.1414C>G (p.Pro472Ala) rs151312899 0.00080
NM_144997.7(FLCN):c.959G>A (p.Arg320Gln) rs143483053 0.00069
NM_144997.7(FLCN):c.1269C>T (p.His423=) rs41464156 0.00053
NM_144997.7(FLCN):c.735A>C (p.Thr245=) rs150175875 0.00032
NM_144997.7(FLCN):c.268G>T (p.Ala90Ser) rs141140415 0.00026
NM_144997.7(FLCN):c.1326C>T (p.His442=) rs145004158 0.00023
NM_144997.7(FLCN):c.1062+7G>A rs540198776 0.00016
NM_144997.7(FLCN):c.75G>A (p.Leu25=) rs200350612 0.00016
NM_144997.7(FLCN):c.1539-6C>T rs779028759 0.00008
NM_144997.7(FLCN):c.687C>T (p.Phe229=) rs754710935 0.00008
NM_144997.7(FLCN):c.779+9C>T rs373504780 0.00008
NM_144997.7(FLCN):c.792G>A (p.Ala264=) rs140500421 0.00007
NM_144997.7(FLCN):c.1389C>T (p.Tyr463=) rs137852929 0.00005
NM_144997.7(FLCN):c.711C>T (p.Ala237=) rs111258744 0.00004
NM_144997.7(FLCN):c.1464G>A (p.Ala488=) rs747029882 0.00002
NM_144997.7(FLCN):c.279G>A (p.Pro93=) rs138688941 0.00002
NM_144997.7(FLCN):c.83C>G (p.Pro28Arg) rs780588085 0.00002
NM_144997.7(FLCN):c.1227C>T (p.Tyr409=) rs561236067 0.00001

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