ClinVar Miner

Submissions for variant NM_015335.4(MED13L):c.5162C>T (p.Ser1721Phe) (rs755513948)

Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000793090 SCV000932429 uncertain significance Transposition of the great arteries, dextro-looped 1 2019-07-09 criteria provided, single submitter clinical testing This sequence change replaces serine with phenylalanine at codon 1721 of the MED13L protein (p.Ser1721Phe). The serine residue is moderately conserved and there is a large physicochemical difference between serine and phenylalanine. This variant is present in population databases (rs755513948, ExAC 0.005%). This variant has been observed in one or more individuals who were not affected with MED13L-related disease (Invitae). Algorithms developed to predict the effect of missense changes on protein structure and function are either unavailable or do not agree on the potential impact of this missense change (SIFT: Tolerated; PolyPhen-2: Probably Damaging; Align-GVGD: Class C0). In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance.

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.