NM_005591.4(MRE11):c.1800G>T (p.Glu600Asp) AND Ataxia-telangiectasia-like disorder 1

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Jun 17, 2019
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:: RCV003133268.3

Allele description [Variation Report for NM_005591.4(MRE11):c.1800G>T (p.Glu600Asp)]

NM_005591.4(MRE11):c.1800G>T (p.Glu600Asp)

Gene:

MRE11:MRE11 homolog, double strand break repair nuclease [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

11q21

Genomic location:

Preferred name:

NM_005591.4(MRE11):c.1800G>T (p.Glu600Asp)

HGVS:

NC_000011.10:g.94445877C>A
NG_007261.1:g.52998G>T
NM_001330347.2:c.1797G>T
NM_005590.4:c.1783+1342G>T
NM_005591.4:c.1800G>TMANE SELECT
NP_001317276.1:p.Glu599Asp
NP_005582.1:p.Glu600Asp
NP_005582.1:p.Glu600Asp
LRG_85t1:c.1800G>T
LRG_85:g.52998G>T
LRG_85p1:p.Glu600Asp
NC_000011.9:g.94179043C>A
NM_005591.3:c.1800G>T

Protein change:

E599D

Links:

dbSNP: rs1028566396

NCBI 1000 Genomes Browser:

rs1028566396

Molecular consequence:

NM_005590.4:c.1783+1342G>T - intron variant - [Sequence Ontology: SO:0001627]
NM_001330347.2:c.1797G>T - missense variant - [Sequence Ontology: SO:0001583]
NM_005591.4:c.1800G>T - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:: Ataxia-telangiectasia-like disorder 1 (ATLD1)
Identifiers:: MONDO: MONDO:0024557; MedGen: C4012790; Orphanet: 251347; OMIM: 604391

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV003808922	Revvity Omics, Revvity	criteria provided, single submitter (ACMG Guidelines, 2015)	Uncertain significance (Jun 17, 2019)	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

SCV003808922

Revvity Omics, Revvity

criteria provided, single submitter

(ACMG Guidelines, 2015)

Uncertain significance
(Jun 17, 2019)

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 Revvity Omics, Revvity, SCV003808922.2

#	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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