NM_001377265.1(MAPT):c.1986G>A (p.Pro662=) AND Frontotemporal dementia

Clinical significance:Benign (Last evaluated: Dec 18, 2021)
Review status:1 star out of maximum of 4 stars
criteria provided, single submitter

Help

Based on:: 1 submission [Details]
Record status:: current
Accession:: RCV000554260.6

Allele description [Variation Report for NM_001377265.1(MAPT):c.1986G>A (p.Pro662=)]

NM_001377265.1(MAPT):c.1986G>A (p.Pro662=)

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.1986G>A (p.Pro662=)

HGVS:

NC_000017.11:g.45996652G>A
NG_007398.1:g.107232G>A
NG_007398.2:g.107190G>A
NM_001123066.4:c.1815G>A
NM_001123067.4:c.723G>A
NM_001203251.2:c.723G>A
NM_001203252.2:c.810G>A
NM_001377265.1:c.1986G>AMANE SELECT
NM_001377266.1:c.1788G>A
NM_001377267.1:c.723G>A
NM_001377268.1:c.636G>A
NM_005910.6:c.810G>A
NM_016834.5:c.636G>A
NM_016835.5:c.1761G>A
NM_016841.5:c.636G>A
NP_001116538.2:p.Pro605=
NP_001116538.2:p.Pro605=
NP_001116539.1:p.Pro241=
NP_001190180.1:p.Pro241=
NP_001190181.1:p.Pro270=
NP_001364194.1:p.Pro662=
NP_001364195.1:p.Pro596=
NP_001364196.1:p.Pro241=
NP_001364197.1:p.Pro212=
NP_005901.2:p.Pro270=
NP_005901.2:p.Pro270=
NP_058518.1:p.Pro212=
NP_058519.3:p.Pro587=
NP_058525.1:p.Pro212=
LRG_660t1:c.1761G>A
LRG_660t2:c.1986G>A
LRG_660:g.107190G>A
LRG_660p1:p.Pro587=
LRG_660p2:p.Pro662=
NC_000017.10:g.44074018G>A
NM_001123066.3:c.1815G>A
NM_005910.5:c.810G>A
NR_165166.1:n.734G>A
p.Pro270Pro

Links:

dbSNP: rs11568305

NCBI 1000 Genomes Browser:

rs11568305

Molecular consequence:

NR_165166.1:n.734G>A - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NM_001123066.4:c.1815G>A - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001123067.4:c.723G>A - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001203251.2:c.723G>A - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001203252.2:c.810G>A - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001377265.1:c.1986G>A - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001377266.1:c.1788G>A - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001377267.1:c.723G>A - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001377268.1:c.636G>A - synonymous variant - [Sequence Ontology: SO:0001819]
NM_005910.6:c.810G>A - synonymous variant - [Sequence Ontology: SO:0001819]
NM_016834.5:c.636G>A - synonymous variant - [Sequence Ontology: SO:0001819]
NM_016835.5:c.1761G>A - synonymous variant - [Sequence Ontology: SO:0001819]
NM_016841.5:c.636G>A - synonymous variant - [Sequence Ontology: SO:0001819]

Condition(s)

Name:: Frontotemporal dementia (FTD)
Synonyms:: FRONTOTEMPORAL LOBE DEMENTIA; WILHELMSEN-LYNCH DISEASE; Dementia, frontotemporal, with parkinsonism; See all synonyms [MedGen]
Identifiers:: MONDO: MONDO:0017276; MedGen: C0338451; Orphanet: 282; OMIM: 600274; Human Phenotype Ontology: HP:0002145

Recent activity

Clear Turn Off Turn On

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

Help

Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV000632353	Invitae	criteria provided, single submitter Invitae Variant Classification Sherloc (09022015)	Benign (Dec 18, 2021)	germline	clinical testing	PubMed (1) [See all records that cite this PMID]

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV000632353

Invitae

criteria provided, single submitter

Invitae Variant Classification Sherloc (09022015)

Benign
(Dec 18, 2021)

germline

clinical testing

PubMed (1)
[See all records that cite this PMID]

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

Citations

PubMed

Sherloc: a comprehensive refinement of the ACMG-AMP variant classification criteria.

Nykamp K, Anderson M, Powers M, Garcia J, Herrera B, Ho YY, Kobayashi Y, Patil N, Thusberg J, Westbrook M; Invitae Clinical Genomics Group., Topper S.

Genet Med. 2017 Oct;19(10):1105-1117. doi: 10.1038/gim.2017.37. Epub 2017 May 11. Erratum in: Genet Med. 2020 Jan;22(1):240-242.

PubMed [citation]

PMID:: 28492532
PMCID:: PMC5632818

Details of each submission

From Invitae, SCV000632353.4

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

#	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

ClinVar

Relating variation to medicine