List of variants in gene NF1 reported as benign by Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine

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: 33

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HGVS	dbSNP	gnomAD frequency
NM_001042492.3(NF1):c.702G>A (p.Leu234=)	rs1801052	0.56607
NM_001042492.3(NF1):c.5609+19T>A	rs2285894	0.49901
NM_001042492.3(NF1):c.2034G>A (p.Pro678=)	rs2285892	0.42930
NM_001042492.3(NF1):c.2544G>A (p.Gly848=)	rs17883704	0.02535
NM_001042492.3(NF1):c.4882T>C (p.Leu1628=)	rs10512435	0.02270
NM_001042492.3(NF1):c.4929G>A (p.Val1643=)	rs17880521	0.01527
NM_001042492.3(NF1):c.168C>T (p.Ser56=)	rs17881168	0.01374
NM_001042492.3(NF1):c.7755C>T (p.Ser2585=)	rs17881980	0.01075
NM_001042492.3(NF1):c.1845+13A>T	rs17885739	0.01016
NM_001042492.3(NF1):c.2022C>T (p.Ser674=)	rs2230851	0.00908
NM_001042492.3(NF1):c.7322-17C>T	rs17884859	0.00744
NM_001042492.3(NF1):c.6393C>T (p.His2131=)	rs17881788	0.00655
NM_001042492.3(NF1):c.2985G>C (p.Leu995=)	rs17881467	0.00426
NM_001042492.3(NF1):c.528T>A (p.Asp176Glu)	rs112306990	0.00398
NM_001042492.3(NF1):c.3498C>T (p.Gly1166=)	rs2066733	0.00392
NM_001042492.3(NF1):c.4577+12C>T	rs17878332	0.00352
NM_001042492.3(NF1):c.5235G>A (p.Lys1745=)	rs17887014	0.00305
NM_001042492.3(NF1):c.4269A>G (p.Glu1423=)	rs17886566	0.00238
NM_001042492.3(NF1):c.1994C>T (p.Ser665Phe)	rs145891889	0.00220
NM_001042492.3(NF1):c.5035A>G (p.Ile1679Val)	rs147327414	0.00195
NM_001042492.3(NF1):c.2553C>T (p.Cys851=)	rs2230852	0.00190
NM_001042492.3(NF1):c.846G>A (p.Gln282=)	rs138840528	0.00149
NM_001042492.3(NF1):c.1810T>C (p.Leu604=)	rs142712751	0.00123
NM_001042492.3(NF1):c.3270A>C (p.Gly1090=)	rs150015024	0.00079
NM_001042492.3(NF1):c.7595C>T (p.Ala2532Val)	rs148154172	0.00066
NM_001042492.3(NF1):c.7461A>G (p.Thr2487=)	rs149924365	0.00052
NM_001042492.3(NF1):c.8151G>A (p.Pro2717=)	rs2285895	0.00050
NM_001042492.3(NF1):c.1976G>A (p.Arg659Gln)	rs151138158	0.00029
NM_001042492.3(NF1):c.6929C>T (p.Pro2310Leu)	rs148736217	0.00015
NM_001042492.3(NF1):c.7368A>G (p.Lys2456=)	rs201287021	0.00014
NM_001042492.3(NF1):c.*4T>C	rs201044568	0.00003
NM_001042492.3(NF1):c.6147+8C>G	rs182709912
NM_001042492.3(NF1):c.7190-33TTGT[5]	rs149197458

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