ClinVar Miner

List of variants in gene NF2 reported as likely benign for Hereditary cancer-predisposing syndrome

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 19
Download table as spreadsheet
HGVS dbSNP
NM_000268.3(NF2):c.1128G>C (p.Arg376=) rs757322524
NM_000268.3(NF2):c.1206C>T (p.Ala402=) rs137953976
NM_000268.3(NF2):c.1248G>A (p.Ala416=) rs759993776
NM_000268.3(NF2):c.1311A>G (p.Ala437=) rs144628209
NM_000268.3(NF2):c.1360C>T (p.Leu454=) rs1274431013
NM_000268.3(NF2):c.1386C>T (p.Arg462=) rs138354622
NM_000268.3(NF2):c.1395G>A (p.Glu465=) rs1556001388
NM_000268.3(NF2):c.1416C>T (p.Leu472=) rs148776784
NM_000268.3(NF2):c.1451T>C (p.Met484Thr) rs141538143
NM_000268.3(NF2):c.1500C>T (p.Leu500=) rs758182356
NM_000268.3(NF2):c.1749G>A (p.Gln583=) rs201911915
NM_000268.3(NF2):c.246G>A (p.Leu82=) rs371270318
NM_000268.3(NF2):c.435C>T (p.Ala145=) rs955424447
NM_000268.3(NF2):c.48G>A (p.Arg16=) rs774973059
NM_000268.3(NF2):c.504G>A (p.Leu168=) rs182990439
NM_000268.3(NF2):c.783C>T (p.Ile261=) rs765223726
NM_000268.3(NF2):c.816T>A (p.Thr272=) rs1555997539
NM_000268.3(NF2):c.879T>C (p.Asn293=) rs151198477
NM_000268.3(NF2):c.912T>C (p.His304=) rs200272173

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.