NM_016203.4(PRKAG2):c.1006-9dup AND PRKAG2-related disorder

Germline classification:: Likely benign (1 submission)
Last evaluated:: Mar 15, 2021
Review status:: (0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided

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:: RCV004538400.2

Allele description [Variation Report for NM_016203.4(PRKAG2):c.1006-9dup]

NM_016203.4(PRKAG2):c.1006-9dup

Gene:

PRKAG2:protein kinase AMP-activated non-catalytic subunit gamma 2 [Gene - OMIM - HGNC]

Variant type:

Duplication

Cytogenetic location:

7q36.1

Genomic location:

Preferred name:

NM_016203.4(PRKAG2):c.1006-9dup

HGVS:

NC_000007.14:g.151572718dup
NC_000007.14:g.151572724dup
NG_007486.2:g.309514dup
NM_001040633.2:c.874-9dup
NM_001304527.2:c.631-9dup
NM_001304531.2:c.283-9dup
NM_001363698.2:c.634-9dup
NM_016203.3:c.1006-9dupT
NM_016203.4:c.1006-9dupMANE SELECT
NM_024429.2:c.283-9dup
LRG_430t1:c.1006-9dup
LRG_430:g.309514dup
NC_000007.13:g.151269803_151269804insA
NC_000007.13:g.151269810dup
NG_007486.1:g.309513dup
NM_016203.4:c.1006-9dup

Links:

dbSNP: rs775574266

NCBI 1000 Genomes Browser:

rs775574266

Molecular consequence:

NM_001040633.2:c.874-9dup - intron variant - [Sequence Ontology: SO:0001627]
NM_001304527.2:c.631-9dup - intron variant - [Sequence Ontology: SO:0001627]
NM_001304531.2:c.283-9dup - intron variant - [Sequence Ontology: SO:0001627]
NM_001363698.2:c.634-9dup - intron variant - [Sequence Ontology: SO:0001627]
NM_016203.4:c.1006-9dup - intron variant - [Sequence Ontology: SO:0001627]
NM_024429.2:c.283-9dup - intron variant - [Sequence Ontology: SO:0001627]

Condition(s)

Name:: PRKAG2-related disorder
Synonyms:: PRKAG2-Related Disorders; PRKAG2-related condition
Identifiers:

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV004714944	PreventionGenetics, part of Exact Sciences	no assertion criteria provided	Likely benign (Mar 15, 2021)	germline	clinical testing

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV004714944

PreventionGenetics, part of Exact Sciences

no assertion criteria provided

Likely benign
(Mar 15, 2021)

germline

clinical testing

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

Details of each submission

From PreventionGenetics, part of Exact Sciences, SCV004714944.2

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

Description

This variant is classified as likely benign based on ACMG/AMP sequence variant interpretation guidelines (Richards et al. 2015 PMID: 25741868, with internal and published modifications).

#	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: Feb 25, 2025

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