List of variants in gene FLNA reported as uncertain significance by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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: 36

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HGVS	dbSNP	gnomAD frequency
NM_001110556.2(FLNA):c.2813C>T (p.Thr938Met)	rs782180774	0.00014
NM_001110556.2(FLNA):c.4304-25_4304-17del	rs782740969	0.00008
NM_001110556.2(FLNA):c.7172G>A (p.Arg2391His)	rs727503930	0.00007
NM_001110556.2(FLNA):c.901C>T (p.Arg301Trp)	rs192609440	0.00007
NM_001110556.2(FLNA):c.6230A>G (p.Tyr2077Cys)	rs781860863	0.00006
NM_001110556.2(FLNA):c.7067G>A (p.Ser2356Asn)	rs782739586	0.00005
NM_001110556.2(FLNA):c.1964G>A (p.Arg655His)	rs782563602	0.00004
NM_001110556.2(FLNA):c.3368C>G (p.Ser1123Cys)	rs782361719	0.00003
NM_001110556.2(FLNA):c.4106C>T (p.Thr1369Ile)	rs376774130	0.00003
NM_001110556.2(FLNA):c.4517C>T (p.Thr1506Ile)	rs797045579	0.00003
NM_001110556.2(FLNA):c.5059A>G (p.Thr1687Ala)	rs782469665	0.00003
NM_001110556.2(FLNA):c.5219C>T (p.Ala1740Val)	rs782714867	0.00003
NM_001110556.2(FLNA):c.5951C>T (p.Thr1984Met)	rs782639698	0.00003
NM_001110556.2(FLNA):c.6481G>A (p.Asp2161Asn)	rs782477734	0.00003
NM_001110556.2(FLNA):c.1462C>T (p.Arg488Trp)	rs782434042	0.00002
NM_001110556.2(FLNA):c.3515G>A (p.Arg1172Gln)	rs782694926	0.00002
NM_001110556.2(FLNA):c.4420G>A (p.Asp1474Asn)	rs782129236	0.00002
NM_001110556.2(FLNA):c.6002G>A (p.Arg2001Gln)	rs1483960506	0.00002
NM_001110556.2(FLNA):c.1372G>A (p.Val458Ile)	rs782791907	0.00001
NM_001110556.2(FLNA):c.1555G>A (p.Val519Met)	rs938952718	0.00001
NM_001110556.2(FLNA):c.3323G>A (p.Cys1108Tyr)	rs371677498	0.00001
NM_001110556.2(FLNA):c.3460G>A (p.Val1154Met)	rs1557177750	0.00001
NM_001110556.2(FLNA):c.4997T>C (p.Ile1666Thr)	rs863223639	0.00001
NM_001110556.2(FLNA):c.6983C>T (p.Pro2328Leu)	rs782310851	0.00001
NM_001110556.2(FLNA):c.7000C>T (p.Arg2334Cys)	rs782689584	0.00001
NM_001110556.2(FLNA):c.7013C>G (p.Ser2338Cys)	rs781878646	0.00001
NM_001110556.2(FLNA):c.2092G>T (p.Asp698Tyr)	rs2067738279
NM_001110556.2(FLNA):c.2614G>T (p.Ala872Ser)
NM_001110556.2(FLNA):c.2788G>A (p.Asp930Asn)
NM_001110556.2(FLNA):c.3223C>T (p.Pro1075Ser)	rs1336237133
NM_001110556.2(FLNA):c.373+811C>T
NM_001110556.2(FLNA):c.4243A>G (p.Ile1415Val)	rs2067686132
NM_001110556.2(FLNA):c.494A>G (p.Lys165Arg)	rs1569551874
NM_001110556.2(FLNA):c.5075_5092dup (p.Asp1692_Asp1697dup)	rs781960834
NM_001110556.2(FLNA):c.677G>A (p.Arg226Gln)	rs2067772868
NM_001110556.2(FLNA):c.830C>T (p.Pro277Leu)	rs1557179540

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