List of variants in gene TNXB reported as not provided

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: 8

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_001365276.2(TNXB):c.1480A>T (p.Thr494Ser)	rs770149701	0.00015
NM_001365276.2(TNXB):c.5491G>A (p.Val1831Met)	rs188124424	0.00013
NM_001365276.2(TNXB):c.6805C>T (p.Gln2269Ter)	rs749742731	0.00002
NM_001365276.2(TNXB):c.1263_1448del (p.Thr428_Gly489del)	rs2127289918
NM_001365276.2(TNXB):c.2531A>G (p.Gln844Arg)	rs1187997184
NM_001365276.2(TNXB):c.496A>C (p.Thr166Pro)	rs2127293388
NM_001365276.2(TNXB):c.5645C>T (p.Pro1882Leu)
NM_001365276.2(TNXB):c.7338G>C (p.Lys2446Asn)	rs2151907242

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.