List of variants in gene TBX4 reported by NIHR Bioresource Rare Diseases, University of Cambridge

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: 8

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_001321120.2(TBX4):c.1001_1004dup (p.His335fs)	rs1603255336
NM_001321120.2(TBX4):c.1011_1012delinsTT (p.Lys338Ter)	rs1603255339
NM_001321120.2(TBX4):c.1115dup (p.Pro373fs)	rs754897911
NM_001321120.2(TBX4):c.1163_1170del (p.Thr388fs)	rs1603256095
NM_001321120.2(TBX4):c.121G>T (p.Gly41Ter)	rs1397811125
NM_001321120.2(TBX4):c.40_49del (p.Phe14fs)	rs1603248167
NM_001321120.2(TBX4):c.885dup (p.Thr296fs)	rs1603255267
NM_001321120.2(TBX4):c.972del (p.Thr326fs)	rs1603255327

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.