List of variants in gene BAP1 reported as likely benign by Illumina Laboratory Services, Illumina

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: 13

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_004656.4(BAP1):c.*444C>T	rs123598	0.03611
NM_004656.4(BAP1):c.2057-4G>T	rs149499021	0.00433
NM_004656.4(BAP1):c.1838C>T (p.Thr613Met)	rs35448940	0.00377
NM_004656.4(BAP1):c.783G>A (p.Gln261=)	rs35003777	0.00377
NM_004656.4(BAP1):c.1729+8T>C	rs150945583	0.00364
NM_004656.4(BAP1):c.1002A>G (p.Leu334=)	rs28997577	0.00310
NM_004656.4(BAP1):c.*441G>T	rs146324979	0.00166
NM_004656.4(BAP1):c.1407C>T (p.Ser469=)	rs150524807	0.00015
NM_004656.4(BAP1):c.931+10G>C	rs199560386	0.00006
NM_004656.4(BAP1):c.1497C>T (p.Ile499=)	rs777417522	0.00004
NM_004656.4(BAP1):c.1791C>T (p.Ser597=)	rs751730111	0.00001
NM_004656.4(BAP1):c.341G>A (p.Arg114His)	rs773494626	0.00001
NM_004656.4(BAP1):c.821A>C (p.His274Pro)	rs565400314

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.