ClinVar Miner

Submissions for variant NM_000492.3(CFTR):c.2280G>A (p.Thr760=) (rs138634146)

Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 4
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV000781288 SCV000919201 likely benign not specified 2019-08-28 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics,ARUP Laboratories RCV000781288 SCV001160049 uncertain significance not specified 2018-10-31 criteria provided, single submitter clinical testing The CFTR c.2280G>A; p.Thr760Thr variant (rs138634146) is reported in the literature in a single individual affected with chronic pancreatitis (Midha 2010). This variant is observed on only 10 chromosomes in the Genome Aggregation Database, indicating it is not a common polymorphism. This is a synonymous variant in a weakly conserved nucleotide, and computational analyses (Alamut v.2.11) predict that this variant does not alter splicing. When this variant was transfected into cultured bronchial epithelial cells (CFBE41o-) derived from a CF patient homozygous for p.Phe508del, expression analyses suggested the p.Thr760Thr variant led to a reduction in CFTR mRNA, although the amount of CFTR protein was within normal parameters for the cell type (Kirchner 2017). Due to limited information, the clinical significance of the p.Thr760Thr variant is uncertain at this time. References: Kirchner S et al. Alteration of protein function by a silent polymorphism linked to tRNA abundance. PLoS Biol. 2017 May 16;15(5):e2000779. Midha S et al. Idiopathic chronic pancreatitis in India: phenotypic characterisation and strong genetic susceptibility due to SPINK1 and CFTR gene mutations. Gut. 2010 Jun;59(6):800-7.
Invitae RCV001411256 SCV001613315 likely benign Cystic fibrosis 2020-07-21 criteria provided, single submitter clinical testing
Nilou-Genome Lab RCV001411256 SCV001822104 likely benign Cystic fibrosis 2021-07-22 criteria provided, single submitter clinical testing

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.