Overview

Clinical Phenotype: Alzheimer's Disease
Position: (GRCh38/hg38):Chr11:121588033 G>A
Position: (GRCh37/hg19):Chr11:121458742 G>A
dbSNP ID: rs536340053
Coding/Non-Coding: Coding
DNA Change: Substitution
Expected Protein Consequence: Silent
Codon Change: ACG to ACA
Reference Isoform: SORL1 Isoform 1 (2214 aa)
Genomic Region: Exon 28

Findings

In a Dutch sample of 640 Alzheimer’s cases and 1268 controls, a 75-year-old AD subject was found to be a heterozygous carrier of this synonymous variant. No additional carriers were found in a pan-European cohort of 1255 cases and 1938 controls from the European Early Onset Dementia Consortium (Holstege et al., 2017).

The T1276T variant is classified as benign by the criteria of Holstege et al. (Holstege et al., 2017).

Comments

No Available Comments

Make a Comment

To make a comment you must login or register.

References

Paper Citations

1. Holstege H, van der Lee SJ, Hulsman M, Wong TH, van Rooij JG, Weiss M, Louwersheimer E, Wolters FJ, Amin N, Uitterlinden AG, Hofman A, Ikram MA, van Swieten JC, Meijers-Heijboer H, van der Flier WM, Reinders MJ, van Duijn CM, Scheltens P. Characterization of pathogenic SORL1 genetic variants for association with Alzheimer's disease: a clinical interpretation strategy. Eur J Hum Genet. 2017 Aug;25(8):973-981. Epub 2017 May 24 PubMed.

Further Reading

No Available Further Reading