List of variants in gene BRCA2 reported as likely pathogenic for central nervous system neoplasm

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: 14

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_000059.4(BRCA2):c.7878G>C (p.Trp2626Cys)	rs80359013	0.00001
NM_000059.4(BRCA2):c.8350C>T (p.Arg2784Trp)	rs80359075	0.00001
NM_000059.4(BRCA2):c.-39-1_-39del	rs758732038
NM_000059.4(BRCA2):c.15del (p.Glu7fs)	rs1064795072
NM_000059.4(BRCA2):c.1889del (p.Thr630fs)	rs80359315
NM_000059.4(BRCA2):c.2279del (p.Leu760fs)	rs886038071
NM_000059.4(BRCA2):c.3222dup (p.Ser1075Ter)
NM_000059.4(BRCA2):c.3722_3723insA (p.Phe1241fs)
NM_000059.4(BRCA2):c.4851dup (p.Asp1618Ter)
NM_000059.4(BRCA2):c.574_575del (p.Met192fs)	rs80359533
NM_000059.4(BRCA2):c.6787delinsTT (p.Val2263fs)
NM_000059.4(BRCA2):c.8165C>T (p.Thr2722Ile)	rs80359062
NM_000059.4(BRCA2):c.9010_9013del (p.Lys3004fs)
NM_000059.4(BRCA2):c.9599C>G (p.Ser3200Ter)	rs80359230

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.