ClinVar Miner

List of variants in gene FLCN reported as likely benign by Illumina Laboratory Services, Illumina

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Gene type:
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Total variants: 14
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HGVS dbSNP gnomAD frequency
NM_144997.7(FLCN):c.-176G>A rs117215381 0.00772
NM_144997.7(FLCN):c.1538+14T>G rs112111994 0.00721
NM_144997.7(FLCN):c.*911G>A rs571893996 0.00356
NM_144997.7(FLCN):c.-480G>C rs564584154 0.00265
NM_144997.7(FLCN):c.*526T>C rs574547835 0.00235
NM_144997.7(FLCN):c.1333G>A (p.Ala445Thr) rs41419545 0.00217
NM_144997.7(FLCN):c.959G>A (p.Arg320Gln) rs143483053 0.00071
NM_144997.7(FLCN):c.1269C>T (p.His423=) rs41464156 0.00053
NM_144997.7(FLCN):c.715C>T (p.Arg239Cys) rs78683075 0.00024
NM_144997.7(FLCN):c.1332C>T (p.Ala444=) rs141283741 0.00015
NM_144997.7(FLCN):c.-430C>T rs553452028 0.00001
NM_144997.7(FLCN):c.135G>A (p.Ala45=) rs759930161 0.00001
NM_144997.7(FLCN):c.-141G>T rs541105214
NM_144997.7(FLCN):c.75G>A (p.Leu25=) rs200350612

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