List of variants in gene FLNA reported as not provided

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 17

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HGVS	dbSNP	gnomAD frequency
NM_001110556.2(FLNA):c.2449C>T (p.Pro817Ser)	rs200053635	0.00029
NM_001110556.2(FLNA):c.2123G>A (p.Arg708Gln)	rs371707134	0.00009
NM_001110556.2(FLNA):c.5407G>A (p.Glu1803Lys)	rs368750879	0.00003
NM_001110556.2(FLNA):c.1200G>T (p.Lys400Asn)	rs781879374	0.00001
NM_001110556.2(FLNA):c.1267C>T (p.Pro423Ser)	rs863223643
NM_001110556.2(FLNA):c.1571G>A (p.Gly524Glu)	rs1557178957
NM_001110556.2(FLNA):c.1910C>A (p.Pro637Gln)	rs267606815
NM_001110556.2(FLNA):c.1923C>T (p.Gly641=)	rs80338841
NM_001110556.2(FLNA):c.2228A>C (p.His743Pro)	rs2148115732
NM_001110556.2(FLNA):c.3552C>A (p.Asp1184Glu)	rs80338837
NM_001110556.2(FLNA):c.3562G>A (p.Ala1188Thr)	rs28935472
NM_001110556.2(FLNA):c.3596C>T (p.Ser1199Leu)	rs28935473
NM_001110556.2(FLNA):c.477G>C (p.Glu159Asp)	rs2067775793
NM_001110556.2(FLNA):c.5217G>A (p.Thr1739=)	rs387907371
NM_001110556.2(FLNA):c.67_68del (p.Thr23fs)	rs80338840
NM_001110556.2(FLNA):c.7165G>A (p.Ala2389Thr)	rs2067608494
NM_001110556.2(FLNA):c.862G>A (p.Gly288Arg)	rs267606816

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