List of variants in gene TBX22 reported by OMIM

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 11

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_001109878.2(TBX22):c.459-5T>A	rs200060292	0.00020
NM_001109878.2(TBX22):c.1252del (p.Val418fs)	rs1602414282
NM_001109878.2(TBX22):c.166G>T (p.Glu56Ter)	rs104894945
NM_001109878.2(TBX22):c.352G>T (p.Gly118Cys)	rs104894944
NM_001109878.2(TBX22):c.584_586dup (p.Ser195_Phe196insCys)	rs1602410858
NM_001109878.2(TBX22):c.633+1G>A	rs1602410916
NM_001109878.2(TBX22):c.641T>C (p.Leu214Pro)	rs104894946
NM_001109878.2(TBX22):c.667del (p.Arg223fs)
NM_001109878.2(TBX22):c.779C>T (p.Thr260Met)	rs104894943
NM_001109878.2(TBX22):c.790A>T (p.Asn264Tyr)	rs28935177
NM_001109878.2(TBX22):c.863+1G>C	rs1602411954

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.