Overview

Clinical Phenotype: Alzheimer's Disease
Position: (GRCh38/hg38):Chr11:121514175 C>T
Position: (GRCh37/hg19):Chr11:121384884 C>T
dbSNP ID: rs142899731
Coding/Non-Coding: Coding
DNA Change: Substitution
Expected Protein Consequence: Silent
Codon Change: TCC to TCT
Reference Isoform: SORL1 Isoform 1 (2214 aa)
Genomic Region: Exon 8

Findings

In a Dutch sample of 640 Alzheimer’s cases and 1268 controls, a 57-year-old AD patient was found to be a heterozygous carrier of this variant. The variant was not seen in a cohort of 1255 early onset AD patients and 1938 age-matched controls from the European Early Onset Dementia Consortium (Holstege et al., 2017).

This synonymous variant is classified as likely benign by the criteria of Holstege et al. (Holstege et al., 2017).

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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