NM_005591.4(MRE11):c.1130G>C (p.Ser377Thr) AND Hereditary cancer-predisposing syndrome

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Sep 16, 2022
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:: RCV002463305.2

Allele description [Variation Report for NM_005591.4(MRE11):c.1130G>C (p.Ser377Thr)]

NM_005591.4(MRE11):c.1130G>C (p.Ser377Thr)

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.1130G>C (p.Ser377Thr)

HGVS:

NC_000011.10:g.94464208C>G
NG_007261.1:g.34667G>C
NM_001330347.2:c.1130G>C
NM_005590.4:c.1130G>C
NM_005591.4:c.1130G>CMANE SELECT
NP_001317276.1:p.Ser377Thr
NP_005581.2:p.Ser377Thr
NP_005582.1:p.Ser377Thr
NP_005582.1:p.Ser377Thr
LRG_85t1:c.1130G>C
LRG_85:g.34667G>C
LRG_85p1:p.Ser377Thr
NC_000011.9:g.94197374C>G
NM_005591.3:c.1130G>C

Protein change:

S377T

Molecular consequence:

NM_001330347.2:c.1130G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_005590.4:c.1130G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_005591.4:c.1130G>C - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:: Hereditary cancer-predisposing syndrome
Synonyms:: Neoplastic Syndromes, Hereditary; Tumor predisposition; Cancer predisposition; See all synonyms [MedGen]
Identifiers:: MONDO: MONDO:0015356; MeSH: D009386; MedGen: C0027672

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV002755536	Ambry Genetics	criteria provided, single submitter (Ambry Variant Classification Scheme 2023)	Uncertain significance (Sep 16, 2022)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV002755536

Ambry Genetics

criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)

Uncertain significance
(Sep 16, 2022)

germline

clinical testing

Citation Link

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 Ambry Genetics, SCV002755536.2

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

Description

The p.S377T variant (also known as c.1130G>C), located in coding exon 10 of the MRE11A gene, results from a G to C substitution at nucleotide position 1130. The serine at codon 377 is replaced by threonine, an amino acid with similar properties. This amino acid position is poorly conserved in available vertebrate species. In addition, this alteration is predicted to be tolerated by in silico analysis. Since supporting evidence is limited at this time, the clinical significance of this alteration remains unclear.

#	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: May 1, 2024

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