ClinVar Miner

Submissions for variant NM_001378454.1(ALMS1):c.7013C>A (p.Thr2338Lys) (rs373004988)

Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000439314 SCV000535804 uncertain significance not provided 2017-01-06 criteria provided, single submitter clinical testing A variant of uncertain significance has been identified in the ALMS1 gene. The T2339K variant has not been published as a pathogenic variant or been reported as a benign variant to our knowledge. This variant was not observed with any significant frequency in both the Exome Aggregation Consortium and in approximately 6,00 individuals of European and African American ancestry in the NHLBI Exome Sequencing Project, indicating it is not a common benign variant in these populations. The T2339K variant is a semi-conservative amino acid substitution, which may impact secondary protein structure as these residues differ in some properties. This substitution occurs at a position that is conserved in mammals. Furthermore, in silico analysis predicts this variant is probably damaging to the protein structure/function.Therefore, based on the currently available information, it is unclear whether this variant is pathogenic or benign. This result cannot be interpreted for diagnosis or used for family member screening at this time. As Alstrom syndrome due to pathogenic variants in the ALMS1 gene is an autosomal recessive disease, it is expected that an affected individual would harbor variants in both alleles of the ALMS1 gene (in trans). No second variant was identified by this sequencing or deletion/duplication analysis. The possibility that this patient harbors a second ALMS1 variant that is undetectable by this test cannot be excluded.
Counsyl RCV000667850 SCV000792360 uncertain significance Alstrom syndrome 2017-06-14 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.