NM_000251.3(MSH2):c.95C>T (p.Thr32Ile) AND Hereditary cancer-predisposing syndrome

Germline classification:: Likely benign (1 submission)
Last evaluated:: Jun 7, 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:: RCV002385287.2

Allele description [Variation Report for NM_000251.3(MSH2):c.95C>T (p.Thr32Ile)]

NM_000251.3(MSH2):c.95C>T (p.Thr32Ile)

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.95C>T (p.Thr32Ile)

HGVS:

NC_000002.12:g.47403286C>T
NG_007110.2:g.5163C>T
NG_095167.1:g.490C>T
NM_000251.3:c.95C>TMANE SELECT
NM_001258281.1:c.-30-74C>T
NM_001406631.1:c.95C>T
NM_001406632.1:c.95C>T
NM_001406633.1:c.95C>T
NM_001406634.1:c.95C>T
NM_001406635.1:c.95C>T
NM_001406636.1:c.95C>T
NM_001406637.1:c.95C>T
NM_001406638.1:c.95C>T
NM_001406639.1:c.95C>T
NM_001406640.1:c.95C>T
NM_001406641.1:c.95C>T
NM_001406642.1:c.95C>T
NM_001406643.1:c.95C>T
NM_001406644.1:c.95C>T
NM_001406645.1:c.95C>T
NM_001406646.1:c.95C>T
NM_001406647.1:c.95C>T
NM_001406648.1:c.95C>T
NM_001406649.1:c.95C>T
NM_001406650.1:c.95C>T
NM_001406651.1:c.95C>T
NM_001406652.1:c.95C>T
NM_001406653.1:c.95C>T
NM_001406654.1:c.-246C>T
NM_001406655.1:c.95C>T
NM_001406656.1:c.-901C>T
NM_001406657.1:c.95C>T
NM_001406658.1:c.-1224C>T
NM_001406659.1:c.-1374C>T
NM_001406660.1:c.-1571C>T
NM_001406661.1:c.-1526C>T
NM_001406662.1:c.-1443C>T
NM_001406666.1:c.95C>T
NM_001406669.1:c.-1374C>T
NM_001406672.1:c.95C>T
NM_001406674.1:c.95C>T
NP_000242.1:p.Thr32Ile
NP_000242.1:p.Thr32Ile
NP_001393560.1:p.Thr32Ile
NP_001393561.1:p.Thr32Ile
NP_001393562.1:p.Thr32Ile
NP_001393563.1:p.Thr32Ile
NP_001393564.1:p.Thr32Ile
NP_001393565.1:p.Thr32Ile
NP_001393566.1:p.Thr32Ile
NP_001393567.1:p.Thr32Ile
NP_001393568.1:p.Thr32Ile
NP_001393569.1:p.Thr32Ile
NP_001393570.1:p.Thr32Ile
NP_001393571.1:p.Thr32Ile
NP_001393572.1:p.Thr32Ile
NP_001393573.1:p.Thr32Ile
NP_001393574.1:p.Thr32Ile
NP_001393575.1:p.Thr32Ile
NP_001393576.1:p.Thr32Ile
NP_001393577.1:p.Thr32Ile
NP_001393578.1:p.Thr32Ile
NP_001393579.1:p.Thr32Ile
NP_001393580.1:p.Thr32Ile
NP_001393581.1:p.Thr32Ile
NP_001393582.1:p.Thr32Ile
NP_001393584.1:p.Thr32Ile
NP_001393586.1:p.Thr32Ile
NP_001393595.1:p.Thr32Ile
NP_001393601.1:p.Thr32Ile
NP_001393603.1:p.Thr32Ile
LRG_218t1:c.95C>T
LRG_218:g.5163C>T
LRG_218p1:p.Thr32Ile
NC_000002.11:g.47630425C>T
NM_000251.1:c.95C>T
NM_000251.2:c.95C>T
NR_176230.1:n.131C>T
NR_176231.1:n.131C>T
NR_176232.1:n.131C>T
NR_176233.1:n.131C>T
NR_176234.1:n.131C>T
NR_176235.1:n.131C>T
NR_176236.1:n.131C>T
NR_176237.1:n.131C>T
NR_176238.1:n.131C>T
NR_176239.1:n.131C>T
NR_176240.1:n.131C>T
NR_176241.1:n.131C>T
NR_176242.1:n.131C>T
NR_176243.1:n.131C>T
NR_176244.1:n.131C>T
NR_176245.1:n.131C>T
NR_176246.1:n.131C>T
NR_176247.1:n.131C>T
NR_176248.1:n.131C>T
NR_176249.1:n.131C>T
NR_176250.1:n.131C>T

Protein change:

T32I

Molecular consequence:

NM_001258281.1:c.-30-74C>T - intron variant - [Sequence Ontology: SO:0001627]
NM_000251.3:c.95C>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001406631.1:c.95C>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001406632.1:c.95C>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001406633.1:c.95C>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001406634.1:c.95C>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001406635.1:c.95C>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001406636.1:c.95C>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001406637.1:c.95C>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001406638.1:c.95C>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001406639.1:c.95C>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001406640.1:c.95C>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001406641.1:c.95C>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001406642.1:c.95C>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001406643.1:c.95C>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001406644.1:c.95C>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001406645.1:c.95C>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001406646.1:c.95C>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001406647.1:c.95C>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001406648.1:c.95C>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001406649.1:c.95C>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001406650.1:c.95C>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001406651.1:c.95C>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001406652.1:c.95C>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001406653.1:c.95C>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001406655.1:c.95C>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001406657.1:c.95C>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001406666.1:c.95C>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001406672.1:c.95C>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001406674.1:c.95C>T - 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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PREDICTED: Rattus norvegicus CD59b molecule (Cd59b), transcript variant X1, mRNA
PREDICTED: Rattus norvegicus CD59b molecule (Cd59b), transcript variant X1, mRNA
gi|2678927432|ref|XM_039104370.2|

Nucleotide

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV002694800	Ambry Genetics	criteria provided, single submitter (Ambry Variant Classification Scheme 2023)	Likely benign (Jun 7, 2022)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV002694800

Ambry Genetics

criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)

Likely benign
(Jun 7, 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, SCV002694800.2

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

Description

This alteration is classified as likely benign based on a combination of the following: seen in unaffected individuals, population frequency, intact protein function, lack of segregation with disease, co-occurrence, RNA analysis, in silico models, amino acid conservation, lack of disease association in case-control studies, and/or the mechanism of disease or impacted region is inconsistent with a known cause of pathogenicity.

#	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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Relating variation to medicine