NM_172201.2(KCNE2):c.80G>A (p.Arg27His) AND Long QT syndrome 6

Germline classification:: Likely benign (1 submission)
Last evaluated:: Oct 3, 2023
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:: RCV001088249.8

Allele description [Variation Report for NM_172201.2(KCNE2):c.80G>A (p.Arg27His)]

NM_172201.2(KCNE2):c.80G>A (p.Arg27His)

Genes:

KCNE2:potassium voltage-gated channel subfamily E regulatory subunit 2 [Gene - OMIM - HGNC]
LOC105372791:uncharacterized LOC105372791 [Gene]

Variant type:

single nucleotide variant

Cytogenetic location:

21q22.11

Genomic location:

Preferred name:

NM_172201.2(KCNE2):c.80G>A (p.Arg27His)

HGVS:

NC_000021.9:g.34370558G>A
NG_008804.1:g.11535G>A
NM_172201.2:c.80G>AMANE SELECT
NP_751951.1:p.Arg27His
NP_751951.1:p.Arg27His
LRG_291t1:c.80G>A
LRG_291:g.11535G>A
LRG_291p1:p.Arg27His
NC_000021.8:g.35742857G>A
NM_172201.1:c.80G>A
Q9Y6J6:p.Arg27His

Protein change:

R27H

Links:

UniProtKB: Q9Y6J6#VAR_074923; dbSNP: rs148968498

NCBI 1000 Genomes Browser:

rs148968498

Molecular consequence:

NM_172201.2:c.80G>A - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:: Long QT syndrome 6 (LQT6)
Identifiers:: MONDO: MONDO:0013370; MedGen: C3150953; Orphanet: 101016; Orphanet: 768; OMIM: 613693

Recent activity

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ATP synthase CF1 alpha subunit (chloroplast) [Aegilops umbellulata]
ATP synthase CF1 alpha subunit (chloroplast) [Aegilops umbellulata]
gi|2743175203|gb|XBS33100.1|

Protein
photosystem II protein D1 (chloroplast) [Aegilops umbellulata]
photosystem II protein D1 (chloroplast) [Aegilops umbellulata]
gi|2743175215|gb|XBS33112.1|

Protein
Journalism, Dental
Journalism, Dental
Content, management, editing, policies, and printing of dental periodicals such as journals, newsletters, tabloids, and bulletins.<br/>Year introduced: 1991(1964)

MeSH
FIGO Grade 2 Endometrial Mucinous Adenocarcinoma
FIGO Grade 2 Endometrial Mucinous Adenocarcinoma

MedGen

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV000677002	Labcorp Genetics (formerly Invitae), Labcorp	criteria provided, single submitter (Invitae Variant Classification Sherloc (09022015))	Likely benign (Oct 3, 2023)	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

SCV000677002

Labcorp Genetics (formerly Invitae), Labcorp

criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))

Likely benign
(Oct 3, 2023)

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, SCV000677002.8

#	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: Sep 29, 2024

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