Mutations

MAPT P512H

Overview

Pathogenicity: Alzheimer's Disease : Benign
Clinical Phenotype: Alzheimer's Disease
Position: (GRCh38/hg38):Chr17:45993951 C>A
Position: (GRCh37/hg19):Chr17:44071317 C>A
dbSNP ID: rs192236920
Coding/Non-Coding: Coding
DNA Change: Substitution
Expected RNA Consequence: Substitution
Expected Protein Consequence: Missense
Codon Change: CCC to CAC
Reference Isoform: Tau Isoform PNS Tau (758 aa)
Genomic Region: Exon 8

Findings

This variant was detected in a Caucasian from Italy who met clinical criteria for probable Alzheimer’s disease (Piccoli et al., 2016). Further clinical details were not reported. This rare variant is thought to be benign. It is found at low frequency in the ExAC database.

Note that this variant is excluded from the six major tau isoforms expressed in the human brain, including Tau-F, the isoform most commonly used as a reference. Exon 8 is included in longer tau isoforms PNS-Tau and Tau-G. The amino acid numbering of this variant (512) is thus according to the amino acid position in these longer isoforms.

Neuropathology

Not applicable.

Biological Effect

In silico this variant has been predicted probably damaging by PolyPhen and tolerated by SIFT.

Last Updated: 31 Dec 2016

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References

Paper Citations

  1. . Novel PSEN1 mutations (H214N and R220P) associated with familial Alzheimer's disease identified by targeted exome sequencing. Neurobiol Aging. 2016 Apr;40:192.e7-11. Epub 2016 Feb 28 PubMed.

External Citations

  1. ExAC database.

Further Reading

No Available Further Reading

Protein Diagram

Primary Papers

  1. . Novel PSEN1 mutations (H214N and R220P) associated with familial Alzheimer's disease identified by targeted exome sequencing. Neurobiol Aging. 2016 Apr;40:192.e7-11. Epub 2016 Feb 28 PubMed.

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