NM_001377265.1(MAPT):c.1857A>G (p.Ala619=) AND MAPT-Related Spectrum Disorders

Clinical significance:Benign (Last evaluated: Jan 13, 2018)
Review status:1 star out of maximum of 4 stars
criteria provided, single submitter

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Based on:: 1 submission [Details]
Record status:: current
Accession:: RCV000295833.3

Allele description [Variation Report for NM_001377265.1(MAPT):c.1857A>G (p.Ala619=)]

NM_001377265.1(MAPT):c.1857A>G (p.Ala619=)

Gene:

MAPT:microtubule associated protein tau [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

17q21.31

Genomic location:

Preferred name:

NM_001377265.1(MAPT):c.1857A>G (p.Ala619=)

HGVS:

NC_000017.11:g.45996523A>G
NG_007398.1:g.107103A>G
NG_007398.2:g.107061A>G
NM_001123066.4:c.1686A>G
NM_001123067.4:c.594A>G
NM_001203251.2:c.594A>G
NM_001203252.2:c.681A>G
NM_001377265.1:c.1857A>GMANE SELECT
NM_001377266.1:c.1659A>G
NM_001377267.1:c.594A>G
NM_001377268.1:c.507A>G
NM_005910.6:c.681A>G
NM_016834.5:c.507A>G
NM_016835.5:c.1632A>G
NM_016841.5:c.507A>G
NP_001116538.2:p.Ala562=
NP_001116538.2:p.Ala562=
NP_001116539.1:p.Ala198=
NP_001190180.1:p.Ala198=
NP_001190181.1:p.Ala227=
NP_001364194.1:p.Ala619=
NP_001364195.1:p.Ala553=
NP_001364196.1:p.Ala198=
NP_001364197.1:p.Ala169=
NP_005901.2:p.Ala227=
NP_005901.2:p.Ala227=
NP_058518.1:p.Ala169=
NP_058519.3:p.Ala544=
NP_058525.1:p.Ala169=
LRG_660t1:c.1632A>G
LRG_660t2:c.1857A>G
LRG_660:g.107061A>G
LRG_660p1:p.Ala544=
LRG_660p2:p.Ala619=
NC_000017.10:g.44073889A>G
NM_001123066.3:c.1686A>G
NM_005910.5:c.681A>G
NR_165166.1:n.605A>G
p.Ala227Ala

Links:

dbSNP: rs1052553

NCBI 1000 Genomes Browser:

rs1052553

Molecular consequence:

NR_165166.1:n.605A>G - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NM_001123066.4:c.1686A>G - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001123067.4:c.594A>G - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001203251.2:c.594A>G - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001203252.2:c.681A>G - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001377265.1:c.1857A>G - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001377266.1:c.1659A>G - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001377267.1:c.594A>G - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001377268.1:c.507A>G - synonymous variant - [Sequence Ontology: SO:0001819]
NM_005910.6:c.681A>G - synonymous variant - [Sequence Ontology: SO:0001819]
NM_016834.5:c.507A>G - synonymous variant - [Sequence Ontology: SO:0001819]
NM_016835.5:c.1632A>G - synonymous variant - [Sequence Ontology: SO:0001819]
NM_016841.5:c.507A>G - synonymous variant - [Sequence Ontology: SO:0001819]

Condition(s)

Name:: MAPT-Related Spectrum Disorders
Identifiers:: MedGen: CN239327

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV000403484	Illumina Laboratory Services,Illumina	criteria provided, single submitter ICSL Variant Classification Criteria 13 December 2019	Benign (Jan 13, 2018)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV000403484

Illumina Laboratory Services,Illumina

criteria provided, single submitter

ICSL Variant Classification Criteria 13 December 2019

Benign
(Jan 13, 2018)

germline

clinical testing

Citation Link

Summary from all submissions

Help

Ethnicity	Origin	Affected	Individuals	Families	Chromosomes tested	Number Tested	Family history	Method
not provided	germline	unknown	not provided	not provided	not provided	not provided	not provided	clinical testing

Details of each submission

From Illumina Laboratory Services,Illumina, SCV000403484.3

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	not provided	not provided	not provided	clinical testing	not provided

Description

This variant was observed in the ICSL laboratory as part of a predisposition screen in an ostensibly healthy population. It had not been previously curated by ICSL or reported in the Human Gene Mutation Database (HGMD: prior to June 1st, 2018), and was therefore a candidate for classification through an automated scoring system. Utilizing variant allele frequency, disease prevalence and penetrance estimates, and inheritance mode, an automated score was calculated to assess if this variant is too frequent to cause the disease. Based on the score and internal cut-off values, a variant classified as benign is not then subjected to further curation. The score for this variant resulted in a classification of benign for this disease.

#	Sample				Method		Observation
#	Origin	Affected	Number tested	Tissue	Purpose	Method	Individuals	Allele frequency	Families	Co-occurrences
1	germline	unknown	not provided	not provided	not provided		not provided	not provided	not provided	not provided

Last Updated: Aug 23, 2022

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