ClinVar Miner

List of variants in gene NF1 reported as benign by Integrated Genetics/Laboratory Corporation of America

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 51
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HGVS dbSNP
NM_000267.3(NF1):c.1933A>G (p.Met645Val) rs146051850
NM_000267.3(NF1):c.2541T>C (p.Leu847=) rs147433258
NM_000267.3(NF1):c.2851-16T>C rs17880825
NM_000267.3(NF1):c.3198-4T>C rs587782218
NM_000267.3(NF1):c.340C>T (p.Leu114=) rs7207410
NM_000267.3(NF1):c.3468C>T (p.Asn1156=) rs147955381
NM_000267.3(NF1):c.3496+19T>C rs9890283
NM_000267.3(NF1):c.369C>G (p.Thr123=) rs146691765
NM_000267.3(NF1):c.4686A>G (p.Glu1562=) rs144091165
NM_000267.3(NF1):c.4986C>T (p.Asn1662=) rs140994965
NM_000267.3(NF1):c.5097G>T (p.Glu1699Asp) rs773378630
NM_000267.3(NF1):c.7127-33TTGT[5] rs149197458
NM_000267.3(NF1):c.7347T>C (p.Asn2449=) rs17881903
NM_000267.3(NF1):c.7491C>G (p.Ala2497=) rs141897690
NM_000267.3(NF1):c.7908-19G>T rs17887156
NM_000267.3(NF1):c.8050+20G>A rs55747230
NM_001042492.3(NF1):c.168C>T (p.Ser56=) rs17881168
NM_001042492.3(NF1):c.1810T>C (p.Leu604=) rs142712751
NM_001042492.3(NF1):c.1994C>T (p.Ser665Phe) rs145891889
NM_001042492.3(NF1):c.2022C>T (p.Ser674=) rs2230851
NM_001042492.3(NF1):c.2034G>A (p.Pro678=) rs2285892
NM_001042492.3(NF1):c.2544G>A (p.Gly848=) rs17883704
NM_001042492.3(NF1):c.2553C>T (p.Cys851=) rs2230852
NM_001042492.3(NF1):c.2985G>C (p.Leu995=) rs17881467
NM_001042492.3(NF1):c.3270A>C (p.Gly1090=) rs150015024
NM_001042492.3(NF1):c.3498C>T (p.Gly1166=) rs2066733
NM_001042492.3(NF1):c.3867C>T (p.Phe1289=) rs138186428
NM_001042492.3(NF1):c.4269A>G (p.Glu1423=) rs17886566
NM_001042492.3(NF1):c.4882T>C (p.Leu1628=) rs10512435
NM_001042492.3(NF1):c.4929G>A (p.Val1643=) rs17880521
NM_001042492.3(NF1):c.5035A>G (p.Ile1679Val) rs147327414
NM_001042492.3(NF1):c.5235G>A (p.Lys1745=) rs17887014
NM_001042492.3(NF1):c.528T>A (p.Asp176Glu) rs112306990
NM_001042492.3(NF1):c.5609+19T>A rs2285894
NM_001042492.3(NF1):c.61-14del rs376172637
NM_001042492.3(NF1):c.61-14dup
NM_001042492.3(NF1):c.61-4del rs551568608
NM_001042492.3(NF1):c.6147+8C>G rs182709912
NM_001042492.3(NF1):c.6148-17dup rs33925668
NM_001042492.3(NF1):c.6148-18_6148-17dup
NM_001042492.3(NF1):c.6393C>T (p.His2131=) rs17881788
NM_001042492.3(NF1):c.6922-14_6922-13del rs146785663
NM_001042492.3(NF1):c.702G>A (p.Leu234=) rs1801052
NM_001042492.3(NF1):c.7190-33TTGT[3] rs149197458
NM_001042492.3(NF1):c.7322-17C>T rs17884859
NM_001042492.3(NF1):c.7531G>C (p.Val2511Leu) rs2230850
NM_001042492.3(NF1):c.7584A>G (p.Gln2528=) rs55865524
NM_001042492.3(NF1):c.7755C>T (p.Ser2585=) rs17881980
NM_001042492.3(NF1):c.7971-8del rs564545012
NM_001042492.3(NF1):c.8151G>A (p.Pro2717=) rs2285895
NM_001042492.3(NF1):c.846G>A (p.Gln282=) rs138840528

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