NM_000399.5(EGR2):c.897AGC[3] (p.Ala308_Ala309del) AND Charcot-Marie-Tooth disease, type I

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Sep 30, 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:: RCV003857577.2

Allele description [Variation Report for NM_000399.5(EGR2):c.897AGC[3] (p.Ala308_Ala309del)]

NM_000399.5(EGR2):c.897AGC[3] (p.Ala308_Ala309del)

Gene:

EGR2:early growth response 2 [Gene - OMIM - HGNC]

Variant type:

Microsatellite

Cytogenetic location:

10q21.3

Genomic location:

Preferred name:

NM_000399.5(EGR2):c.897AGC[3] (p.Ala308_Ala309del)

HGVS:

NC_000010.11:g.62813728CTG[3]
NG_008936.2:g.111160AGC[3]
NM_000399.5:c.897AGC[3]MANE SELECT
NM_001136177.3:c.897AGC[3]
NM_001136178.2:c.897AGC[3]
NM_001136179.3:c.747AGC[3]
NM_001321037.2:c.747AGC[3]
NM_001410931.1:c.936AGC[3]
NP_000390.2:p.Ala308_Ala309del
NP_000390.2:p.Ala308_Ala309del
NP_001129649.1:p.Ala308_Ala309del
NP_001129650.1:p.Ala308_Ala309del
NP_001129651.1:p.Ala258_Ala259del
NP_001307966.1:p.Ala258_Ala259del
NP_001397860.1:p.Ala321_Ala322del
LRG_239t1:c.896_898CAG[3]
LRG_239:g.111160AGC[3]
LRG_239p1:p.Ala308_Ala309del
NC_000010.10:g.64573487_64573492del
NC_000010.10:g.64573488CTG[3]
NM_000399.3:c.896_898CAG[3]

Molecular consequence:

NM_000399.5:c.897AGC[3] - inframe_deletion - [Sequence Ontology: SO:0001822]
NM_001136177.3:c.897AGC[3] - inframe_deletion - [Sequence Ontology: SO:0001822]
NM_001136178.2:c.897AGC[3] - inframe_deletion - [Sequence Ontology: SO:0001822]
NM_001136179.3:c.747AGC[3] - inframe_deletion - [Sequence Ontology: SO:0001822]
NM_001321037.2:c.747AGC[3] - inframe_deletion - [Sequence Ontology: SO:0001822]
NM_001410931.1:c.936AGC[3] - inframe_deletion - [Sequence Ontology: SO:0001822]

Condition(s)

Name:: Charcot-Marie-Tooth disease, type I (CMT1)
Synonyms:: Charcot-Marie-Tooth Neuropathy Type 1; Hereditary Motor and Sensory Neuropathy 1; Charcot-Marie-Tooth, Type 1
Identifiers:: MONDO: MONDO:0019011; MedGen: C0751036

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV004662372	Labcorp Genetics (formerly Invitae), Labcorp	criteria provided, single submitter (Invitae Variant Classification Sherloc (09022015))	Uncertain significance (Sep 30, 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

SCV004662372

Labcorp Genetics (formerly Invitae), Labcorp

criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))

Uncertain significance
(Sep 30, 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, SCV004662372.1

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

Description

In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance. Experimental studies and prediction algorithms are not available or were not evaluated, and the functional significance of this variant is currently unknown. This variant has not been reported in the literature in individuals affected with EGR2-related conditions. This variant is not present in population databases (gnomAD no frequency). This variant, c.906_911del, results in the deletion of 2 amino acid(s) of the EGR2 protein (p.Ala308_Ala309del), 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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