List of variants in gene TAP2 reported as benign by Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine

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: 11

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_001290043.2(TAP2):c.1636-10T>C	rs241436	0.42321
NM_001290043.2(TAP2):c.2059T>C (p.Ter687Gln)	rs241448	0.26784
NM_001290043.2(TAP2):c.1993A>G (p.Thr665Ala)	rs241447	0.25756
NM_001290043.2(TAP2):c.*30G>T	rs241449	0.25754
NM_001290043.2(TAP2):c.1812A>G (p.Gly604=)	rs241441	0.25585
NM_001290043.2(TAP2):c.1932+9C>T	rs241442	0.25438
NM_001290043.2(TAP2):c.1135G>A (p.Val379Ile)	rs1800454	0.14502
NM_018833.3(TAP2):c.1939C>T (p.Leu647Phe)	rs16870908	0.10895
NM_001290043.2(TAP2):c.1308C>T (p.Asn436=)	rs1042116	0.08275
NM_001290043.2(TAP2):c.1800A>C (p.Val600=)	rs2229527	0.06729
NM_018833.3(TAP2):c.1933-5dup	rs61021012

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.