ClinVar Miner

Submissions for variant NM_032444.4(SLX4):c.5410C>T (p.His1804Tyr)

gnomAD frequency: 0.00001  dbSNP: rs772332386
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
Labcorp Genetics (formerly Invitae), Labcorp RCV001923487 SCV002188172 uncertain significance Fanconi anemia 2023-07-07 criteria provided, single submitter clinical testing 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. An algorithm developed to predict the effect of missense changes on protein structure and function (PolyPhen-2) suggests that this variant is likely to be disruptive. ClinVar contains an entry for this variant (Variation ID: 1417020). This variant has not been reported in the literature in individuals affected with SLX4-related conditions. This variant is present in population databases (rs772332386, gnomAD 0.009%). This sequence change replaces histidine, which is basic and polar, with tyrosine, which is neutral and polar, at codon 1804 of the SLX4 protein (p.His1804Tyr).
Fulgent Genetics, Fulgent Genetics RCV002484515 SCV002785127 uncertain significance Fanconi anemia complementation group P 2024-05-25 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.