ClinVar Miner

List of variants in gene FLNC reported as benign by Athena Diagnostics Inc

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Gene type:
ClinVar version:
Total variants: 22
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NM_001458.4(FLNC):c.1032C>T (p.Val344=) rs2291562
NM_001458.4(FLNC):c.1425C>T (p.Asn475=) rs143610360
NM_001458.4(FLNC):c.1458C>A (p.Pro486=) rs2291563
NM_001458.4(FLNC):c.147C>T (p.His49=) rs3734972
NM_001458.4(FLNC):c.2382G>A (p.Ala794=) rs536456072
NM_001458.4(FLNC):c.3297A>G (p.Val1099=) rs3734973
NM_001458.4(FLNC):c.3624G>A (p.Ala1208=) rs35281128
NM_001458.4(FLNC):c.3838C>T (p.Leu1280=) rs34180031
NM_001458.4(FLNC):c.3973C>T (p.Leu1325=) rs34373805
NM_001458.4(FLNC):c.4056C>T (p.Arg1352=) rs75770585
NM_001458.4(FLNC):c.4140C>T (p.Thr1380=) rs183668401
NM_001458.4(FLNC):c.4302C>T (p.Arg1434=) rs114697352
NM_001458.4(FLNC):c.4425G>A (p.Ala1475=)
NM_001458.4(FLNC):c.4431G>A (p.Leu1477=) rs2291568
NM_001458.4(FLNC):c.4700G>A (p.Arg1567Gln) rs2291569
NM_001458.4(FLNC):c.5427G>C (p.Thr1809=)
NM_001458.4(FLNC):c.5644A>G (p.Ile1882Val) rs184018403
NM_001458.4(FLNC):c.5763T>C (p.Thr1921=) rs3816884
NM_001458.4(FLNC):c.6120C>T (p.Asp2040=) rs116974302
NM_001458.4(FLNC):c.720T>C (p.Ile240=) rs2291560
NM_001458.4(FLNC):c.7221C>T (p.Asp2407=) rs3816885
NM_001458.4(FLNC):c.795T>C (p.Gly265=) rs2291561

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