NM_000251.3(MSH2):c.89C>T (p.Pro30Leu) AND not provided

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Mar 1, 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:: RCV001762369.3

Allele description [Variation Report for NM_000251.3(MSH2):c.89C>T (p.Pro30Leu)]

NM_000251.3(MSH2):c.89C>T (p.Pro30Leu)

Gene:

MSH2:mutS homolog 2 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

2p21

Genomic location:

Preferred name:

NM_000251.3(MSH2):c.89C>T (p.Pro30Leu)

HGVS:

NC_000002.12:g.47403280C>T
NG_007110.2:g.5157C>T
NM_000251.3:c.89C>TMANE SELECT
NM_001258281.1:c.-30-80C>T
NP_000242.1:p.Pro30Leu
NP_000242.1:p.Pro30Leu
LRG_218t1:c.89C>T
LRG_218:g.5157C>T
LRG_218p1:p.Pro30Leu
NC_000002.11:g.47630419C>T
NM_000251.1:c.89C>T
NM_000251.2:c.89C>T
p.P30L

Protein change:

P30L

Links:

dbSNP: rs757892928

NCBI 1000 Genomes Browser:

rs757892928

Molecular consequence:

NM_001258281.1:c.-30-80C>T - intron variant - [Sequence Ontology: SO:0001627]
NM_000251.3:c.89C>T - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Synonyms:: none provided; RECLASSIFIED - ADRA2C POLYMORPHISM; RECLASSIFIED - ADRB1 POLYMORPHISM
Identifiers:: MedGen: C3661900

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV001991148	GeneDx	criteria provided, single submitter (GeneDx Variant Classification Process June 2021)	Uncertain significance (Mar 1, 2023)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV001991148

GeneDx

criteria provided, single submitter

(GeneDx Variant Classification Process June 2021)

Uncertain significance
(Mar 1, 2023)

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	yes	not provided	not provided	not provided	not provided	not provided	clinical testing

Details of each submission

From GeneDx, SCV001991148.4

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

Description

Not observed at significant frequency in large population cohorts (gnomAD); In silico analysis supports that this missense variant has a deleterious effect on protein structure/function; Published functional studies suggest neutral mismatch repair function (Jia et al., 2020); Observed in zero breast cancer cases and one control individual (Dorling et al., 2021); This variant is associated with the following publications: (PMID: 18822302, 21120944, 31391288, 33357406, 33471991)

#	Sample				Method		Observation
#	Origin	Affected	Number tested	Tissue	Purpose	Method	Individuals	Allele frequency	Families	Co-occurrences
1	germline	yes	not provided	not provided	not provided		not provided	not provided	not provided	not provided

Last Updated: Dec 22, 2024

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