NM_152296.5(ATP1A3):c.886TTC[1] (p.Phe297del) AND Dystonia 12

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Jun 5, 2017
Review status:: 1 star out of maximum of 4 stars
criteria provided, single submitter

Somatic classification of clinical impact:: None
Review status:: (0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided

Somatic classification of oncogenicity:: None
Review status:: (0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided

Record status:: current
Accession:: RCV000534182.7

Allele description [Variation Report for NM_152296.5(ATP1A3):c.886TTC[1] (p.Phe297del)]

NM_152296.5(ATP1A3):c.886TTC[1] (p.Phe297del)

Gene:

ATP1A3:ATPase Na+/K+ transporting subunit alpha 3 [Gene - OMIM - HGNC]

Variant type:

Microsatellite

Cytogenetic location:

19q13.2

Genomic location:

Preferred name:

NM_152296.5(ATP1A3):c.886TTC[1] (p.Phe297del)

HGVS:

NC_000019.10:g.41985021AAG[1]
NG_008015.1:g.14206TTC[1]
NM_001256213.2:c.919TTC[1]
NM_001256214.2:c.925TTC[1]
NM_152296.5:c.886TTC[1]MANE SELECT
NP_001243142.1:p.Phe308del
NP_001243143.1:p.Phe310del
NP_689509.1:p.Phe297del
LRG_1186t1:c.886TTC[1]
LRG_1186:g.14206TTC[1]
LRG_1186p1:p.Phe297del
NC_000019.9:g.42489172_42489174del
NC_000019.9:g.42489173AAG[1]
NM_152296.4:c.889_891delTTC

Protein change:

F297del

Links:

dbSNP: rs1555864827

NCBI 1000 Genomes Browser:

rs1555864827

Molecular consequence:

NM_001256213.2:c.919TTC[1] - inframe_deletion - [Sequence Ontology: SO:0001822]
NM_001256214.2:c.925TTC[1] - inframe_deletion - [Sequence Ontology: SO:0001822]
NM_152296.5:c.886TTC[1] - inframe_deletion - [Sequence Ontology: SO:0001822]

Condition(s)

Name:: Dystonia 12 (DYT12)
Synonyms:: DYT-ATP1A3; Rapid-Onset Dystonia-Parkinsonism
Identifiers:: MONDO: MONDO:0007496; MedGen: C1868681; Orphanet: 71517; OMIM: 128235

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV000645418	Labcorp Genetics (formerly Invitae), Labcorp	criteria provided, single submitter (Invitae Variant Classification Sherloc (09022015))	Uncertain significance (Jun 5, 2017)	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

SCV000645418

Labcorp Genetics (formerly Invitae), Labcorp

criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))

Uncertain significance
(Jun 5, 2017)

germline

clinical testing

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

Help

Summary from all submissions

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. doi: 10.1038/s41436-019-0624-9.

PubMed [citation]

PMID:: 28492532
PMCID:: PMC5632818

Details of each submission

From Labcorp Genetics (formerly Invitae), Labcorp, SCV000645418.4

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

Description

Experimental studies and prediction algorithms are not available for this variant, and the functional significance of the deleted amino acid is currently unknown. In summary, this variant has uncertain impact on ATP1A3 function. The available evidence is currently insufficient to determine its role in disease. Therefore, it has been classified as a Variant of Uncertain Significance. This variant has not been reported in the literature in individuals with an ATP1A3-related disease. This variant is not present in population databases (ExAC no frequency). This variant, c.889_891delTTC, results in the deletion of 1 amino acid(s) of the ATP1A3 protein (p.Phe297del), but otherwise preserves the integrity of the reading frame.

#	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: Sep 29, 2024

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