NM_000525.4(KCNJ11):c.637G>A (p.Ala213Thr) AND KCNJ11-related disorder

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Mar 2, 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:: RCV004539024.2

Allele description [Variation Report for NM_000525.4(KCNJ11):c.637G>A (p.Ala213Thr)]

NM_000525.4(KCNJ11):c.637G>A (p.Ala213Thr)

Gene:

KCNJ11:potassium inwardly rectifying channel subfamily J member 11 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

11p15.1

Genomic location:

Preferred name:

NM_000525.4(KCNJ11):c.637G>A (p.Ala213Thr)

HGVS:

NC_000011.10:g.17387455C>T
NG_012446.1:g.6205G>A
NG_122014.1:g.368C>T
NM_000525.4:c.637G>AMANE SELECT
NM_001166290.2:c.376G>A
NM_001377296.1:c.376G>A
NM_001377297.1:c.376G>A
NP_000516.3:p.Ala213Thr
NP_001159762.1:p.Ala126Thr
NP_001364225.1:p.Ala126Thr
NP_001364226.1:p.Ala126Thr
NC_000011.9:g.17409002C>T
NM_000525.3:c.637G>A

Protein change:

A126T

Molecular consequence:

NM_000525.4:c.637G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001166290.2:c.376G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001377296.1:c.376G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001377297.1:c.376G>A - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:: KCNJ11-related disorder
Synonyms:: KCNJ11-Related Disorders; KCNJ11-related condition
Identifiers:

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
SCV004110031	PreventionGenetics, part of Exact Sciences	criteria provided, single submitter (ACMG Guidelines, 2015)	Uncertain significance (Mar 2, 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

SCV004110031

PreventionGenetics, part of Exact Sciences

criteria provided, single submitter

(ACMG Guidelines, 2015)

Uncertain significance
(Mar 2, 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

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.

Richards S, Aziz N, Bale S, Bick D, Das S, Gastier-Foster J, Grody WW, Hegde M, Lyon E, Spector E, Voelkerding K, Rehm HL; ACMG Laboratory Quality Assurance Committee..

Genet Med. 2015 May;17(5):405-24. doi: 10.1038/gim.2015.30. Epub 2015 Mar 5.

PubMed [citation]

PMID:: 25741868
PMCID:: PMC4544753

Details of each submission

From PreventionGenetics, part of Exact Sciences, SCV004110031.1

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

Description

The KCNJ11 c.637G>A variant is predicted to result in the amino acid substitution p.Ala213Thr. This variant was reported in an individual with focal congenital hyperinsulinism, although no additional functional or genetic evidence that could help establish pathogenicity was reported (Bellanné-Chantelot et al. 2010. PubMed ID: 20685672). This variant is reported in 0.0050% of alleles in individuals of East Asian descent in gnomAD (http://gnomad.broadinstitute.org/variant/11-17409002-C-T). At this time, the clinical significance of this variant is uncertain due to the absence of conclusive functional and genetic evidence.

#	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: Oct 26, 2024

ClinVar

Relating variation to medicine