ClinVar Miner

List of variants in gene NF1 reported as likely benign by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 54
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001042492.3(NF1):c.2033C>T (p.Pro678Leu) rs17881753 0.00058
NM_001042492.3(NF1):c.7461A>G (p.Thr2487=) rs149924365 0.00052
NM_001042492.3(NF1):c.4851A>G (p.Gln1617=) rs150309802 0.00032
NM_001042492.3(NF1):c.5906A>T (p.Gln1969Leu) rs143502927 0.00029
NM_001042492.3(NF1):c.5883G>A (p.Lys1961=) rs144808600 0.00026
NM_001042492.3(NF1):c.6172A>G (p.Ile2058Val) rs201712827 0.00017
NM_001042492.3(NF1):c.107C>G (p.Thr36Ser) rs199966218 0.00015
NM_001042492.3(NF1):c.2133C>T (p.Arg711=) rs148085908 0.00014
NM_001042492.3(NF1):c.1599C>G (p.Val533=) rs369458366 0.00013
NM_001042492.3(NF1):c.2838C>T (p.Asp946=) rs147188807 0.00013
NM_001042492.3(NF1):c.7026G>A (p.Leu2342=) rs371581213 0.00013
NM_001042492.3(NF1):c.1005T>C (p.Asn335=) rs777369021 0.00011
NM_001042492.3(NF1):c.5757G>A (p.Glu1919=) rs141077224 0.00009
NM_001042492.3(NF1):c.6171A>T (p.Ile2057=) rs140733963 0.00008
NM_001042492.3(NF1):c.3636C>A (p.Val1212=) rs145126193 0.00007
NM_001042492.3(NF1):c.4803T>C (p.Ala1601=) rs148662566 0.00007
NM_001042492.3(NF1):c.8395G>A (p.Val2799Ile) rs377393842 0.00006
NM_001042492.3(NF1):c.5523A>G (p.Gln1841=) rs151046636 0.00005
NM_001042492.3(NF1):c.3690G>T (p.Val1230=) rs183296277 0.00004
NM_001042492.3(NF1):c.5793T>C (p.Ile1931=) rs779114598 0.00004
NM_001042492.3(NF1):c.6664A>G (p.Thr2222Ala) rs745945481 0.00004
NM_001042492.3(NF1):c.4362C>T (p.Leu1454=) rs864622298 0.00003
NM_001042492.3(NF1):c.696A>G (p.Thr232=) rs368691517 0.00003
NM_001042492.3(NF1):c.8223G>C (p.Thr2741=) rs777755159 0.00003
NM_001042492.3(NF1):c.8394C>T (p.Asn2798=) rs376136174 0.00003
NM_001042492.3(NF1):c.8484C>T (p.Gly2828=) rs143289497 0.00003
NM_001042492.3(NF1):c.2224G>T (p.Ala742Ser) rs587781896 0.00002
NM_001042492.3(NF1):c.2294G>A (p.Arg765His) rs199474777 0.00002
NM_001042492.3(NF1):c.4434T>C (p.Phe1478=) rs1310523976 0.00002
NM_001042492.3(NF1):c.5574A>G (p.Ala1858=) rs760561904 0.00002
NM_001042492.3(NF1):c.8139G>A (p.Arg2713=) rs139527415 0.00002
NM_001042492.3(NF1):c.2361A>G (p.Ala787=) rs371589922 0.00001
NM_001042492.3(NF1):c.2490C>T (p.Asp830=) rs786201629 0.00001
NM_001042492.3(NF1):c.3111T>C (p.Phe1037=) rs200240170 0.00001
NM_001042492.3(NF1):c.3303G>A (p.Gln1101=) rs876659944 0.00001
NM_001042492.3(NF1):c.3395G>A (p.Arg1132His) rs778920556 0.00001
NM_001042492.3(NF1):c.354C>T (p.Cys118=) rs768777585 0.00001
NM_001042492.3(NF1):c.4421C>T (p.Ala1474Val) rs587781553 0.00001
NM_001042492.3(NF1):c.4431-17A>T rs754657048 0.00001
NM_001042492.3(NF1):c.6546C>T (p.Tyr2182=) rs876659768 0.00001
NM_001042492.3(NF1):c.6552C>T (p.Asp2184=) rs376808264 0.00001
NM_001042492.3(NF1):c.7086A>C (p.Ala2362=) rs1241296625 0.00001
NM_001042492.3(NF1):c.7479A>G (p.Pro2493=) rs144957306 0.00001
NM_001042492.3(NF1):c.7870-19C>T rs542314717 0.00001
NM_001042492.3(NF1):c.1332T>C (p.Gly444=) rs1597688871
NM_001042492.3(NF1):c.1764T>C (p.His588=) rs1229784876
NM_001042492.3(NF1):c.2028C>G (p.Thr676=) rs878853873
NM_001042492.3(NF1):c.2661A>G (p.Ala887=) rs1555614292
NM_001042492.3(NF1):c.2739A>C (p.Ile913=)
NM_001042492.3(NF1):c.6072A>G (p.Gly2024=) rs2151553361
NM_001042492.3(NF1):c.7458-18A>G rs371362605
NM_001042492.3(NF1):c.753C>T (p.Asp251=) rs1567826636
NM_001042492.3(NF1):c.7830T>G (p.Leu2610=) rs1555536705
NM_001042492.3(NF1):c.8286C>T (p.Tyr2762=) rs1597870245

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.