ClinVar Miner

List of variants reported as likely pathogenic for Lymphoma

Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 10
Download table as spreadsheet
NM_000546.5(TP53):c.743G>A (p.Arg248Gln) rs11540652
NM_001172567.2(MYD88):c.779T>C (p.Leu260Pro) rs387907272
NM_003482.3(KMT2D):c.10622_10623CT[1] (p.Leu3542fs)
NM_003482.3(KMT2D):c.11897_11911del (p.Phe3966_Gln3971delinsTer)
NM_004456.4(EZH2):c.1936T>A (p.Tyr646Asn) rs267601395
NM_004456.4(EZH2):c.1936T>C (p.Tyr646His) rs267601395
NM_004456.4(EZH2):c.1937A>C (p.Tyr646Ser) rs267601394
NM_004456.4(EZH2):c.1937A>T (p.Tyr646Phe) rs267601394
NM_004456.4(EZH2):c.2045C>G (p.Ala682Gly) rs1057519833
NM_015559.3(SETBP1):c.1703G>T (p.Ser568Ile)

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.