NM_000251.3(MSH2):c.198C>G (p.Tyr66Ter) AND Hereditary nonpolyposis colorectal neoplasms

Germline classification:: Pathogenic (1 submission)
Last evaluated:: Apr 12, 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:: RCV002550598.3

Allele description [Variation Report for NM_000251.3(MSH2):c.198C>G (p.Tyr66Ter)]

NM_000251.3(MSH2):c.198C>G (p.Tyr66Ter)

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.198C>G (p.Tyr66Ter)

HGVS:

NC_000002.12:g.47403389C>G
NG_007110.2:g.5266C>G
NG_095167.1:g.593C>G
NM_000251.3:c.198C>GMANE SELECT
NM_001258281.1:c.-1C>G
NM_001406631.1:c.198C>G
NM_001406632.1:c.198C>G
NM_001406633.1:c.198C>G
NM_001406634.1:c.198C>G
NM_001406635.1:c.198C>G
NM_001406636.1:c.198C>G
NM_001406637.1:c.198C>G
NM_001406638.1:c.198C>G
NM_001406639.1:c.198C>G
NM_001406640.1:c.198C>G
NM_001406641.1:c.198C>G
NM_001406642.1:c.198C>G
NM_001406643.1:c.198C>G
NM_001406644.1:c.198C>G
NM_001406645.1:c.198C>G
NM_001406646.1:c.198C>G
NM_001406647.1:c.198C>G
NM_001406648.1:c.198C>G
NM_001406649.1:c.198C>G
NM_001406650.1:c.198C>G
NM_001406651.1:c.198C>G
NM_001406652.1:c.198C>G
NM_001406653.1:c.198C>G
NM_001406654.1:c.-143C>G
NM_001406655.1:c.198C>G
NM_001406656.1:c.-798C>G
NM_001406657.1:c.198C>G
NM_001406658.1:c.-1121C>G
NM_001406659.1:c.-1271C>G
NM_001406660.1:c.-1468C>G
NM_001406661.1:c.-1423C>G
NM_001406662.1:c.-1340C>G
NM_001406666.1:c.198C>G
NM_001406669.1:c.-1271C>G
NM_001406672.1:c.198C>G
NM_001406674.1:c.198C>G
NP_000242.1:p.Tyr66Ter
NP_000242.1:p.Tyr66Ter
NP_001393560.1:p.Tyr66Ter
NP_001393561.1:p.Tyr66Ter
NP_001393562.1:p.Tyr66Ter
NP_001393563.1:p.Tyr66Ter
NP_001393564.1:p.Tyr66Ter
NP_001393565.1:p.Tyr66Ter
NP_001393566.1:p.Tyr66Ter
NP_001393567.1:p.Tyr66Ter
NP_001393568.1:p.Tyr66Ter
NP_001393569.1:p.Tyr66Ter
NP_001393570.1:p.Tyr66Ter
NP_001393571.1:p.Tyr66Ter
NP_001393572.1:p.Tyr66Ter
NP_001393573.1:p.Tyr66Ter
NP_001393574.1:p.Tyr66Ter
NP_001393575.1:p.Tyr66Ter
NP_001393576.1:p.Tyr66Ter
NP_001393577.1:p.Tyr66Ter
NP_001393578.1:p.Tyr66Ter
NP_001393579.1:p.Tyr66Ter
NP_001393580.1:p.Tyr66Ter
NP_001393581.1:p.Tyr66Ter
NP_001393582.1:p.Tyr66Ter
NP_001393584.1:p.Tyr66Ter
NP_001393586.1:p.Tyr66Ter
NP_001393595.1:p.Tyr66Ter
NP_001393601.1:p.Tyr66Ter
NP_001393603.1:p.Tyr66Ter
LRG_218t1:c.198C>G
LRG_218:g.5266C>G
LRG_218p1:p.Tyr66Ter
NC_000002.11:g.47630528C>G
NM_000251.1:c.198C>G
NM_000251.2:c.198C>G
NR_176230.1:n.234C>G
NR_176231.1:n.234C>G
NR_176232.1:n.234C>G
NR_176233.1:n.234C>G
NR_176234.1:n.234C>G
NR_176235.1:n.234C>G
NR_176236.1:n.234C>G
NR_176237.1:n.234C>G
NR_176238.1:n.234C>G
NR_176239.1:n.234C>G
NR_176240.1:n.234C>G
NR_176241.1:n.234C>G
NR_176242.1:n.234C>G
NR_176243.1:n.234C>G
NR_176244.1:n.234C>G
NR_176245.1:n.234C>G
NR_176246.1:n.234C>G
NR_176247.1:n.234C>G
NR_176248.1:n.234C>G
NR_176249.1:n.234C>G
NR_176250.1:n.234C>G

Protein change:

Y66*

Links:

dbSNP: rs730881784

NCBI 1000 Genomes Browser:

rs730881784

Molecular consequence:

NM_001258281.1:c.-1C>G - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
NM_001406654.1:c.-143C>G - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
NM_001406656.1:c.-798C>G - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
NM_001406658.1:c.-1121C>G - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
NM_001406659.1:c.-1271C>G - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
NM_001406660.1:c.-1468C>G - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
NM_001406661.1:c.-1423C>G - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
NM_001406662.1:c.-1340C>G - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
NM_001406669.1:c.-1271C>G - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
NR_176230.1:n.234C>G - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NR_176231.1:n.234C>G - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NR_176232.1:n.234C>G - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NR_176233.1:n.234C>G - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NR_176234.1:n.234C>G - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NR_176235.1:n.234C>G - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NR_176236.1:n.234C>G - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NR_176237.1:n.234C>G - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NR_176238.1:n.234C>G - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NR_176239.1:n.234C>G - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NR_176240.1:n.234C>G - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NR_176241.1:n.234C>G - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NR_176242.1:n.234C>G - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NR_176243.1:n.234C>G - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NR_176244.1:n.234C>G - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NR_176245.1:n.234C>G - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NR_176246.1:n.234C>G - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NR_176247.1:n.234C>G - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NR_176248.1:n.234C>G - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NR_176249.1:n.234C>G - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NR_176250.1:n.234C>G - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NM_000251.3:c.198C>G - nonsense - [Sequence Ontology: SO:0001587]
NM_001406631.1:c.198C>G - nonsense - [Sequence Ontology: SO:0001587]
NM_001406632.1:c.198C>G - nonsense - [Sequence Ontology: SO:0001587]
NM_001406633.1:c.198C>G - nonsense - [Sequence Ontology: SO:0001587]
NM_001406634.1:c.198C>G - nonsense - [Sequence Ontology: SO:0001587]
NM_001406635.1:c.198C>G - nonsense - [Sequence Ontology: SO:0001587]
NM_001406636.1:c.198C>G - nonsense - [Sequence Ontology: SO:0001587]
NM_001406637.1:c.198C>G - nonsense - [Sequence Ontology: SO:0001587]
NM_001406638.1:c.198C>G - nonsense - [Sequence Ontology: SO:0001587]
NM_001406639.1:c.198C>G - nonsense - [Sequence Ontology: SO:0001587]
NM_001406640.1:c.198C>G - nonsense - [Sequence Ontology: SO:0001587]
NM_001406641.1:c.198C>G - nonsense - [Sequence Ontology: SO:0001587]
NM_001406642.1:c.198C>G - nonsense - [Sequence Ontology: SO:0001587]
NM_001406643.1:c.198C>G - nonsense - [Sequence Ontology: SO:0001587]
NM_001406644.1:c.198C>G - nonsense - [Sequence Ontology: SO:0001587]
NM_001406645.1:c.198C>G - nonsense - [Sequence Ontology: SO:0001587]
NM_001406646.1:c.198C>G - nonsense - [Sequence Ontology: SO:0001587]
NM_001406647.1:c.198C>G - nonsense - [Sequence Ontology: SO:0001587]
NM_001406648.1:c.198C>G - nonsense - [Sequence Ontology: SO:0001587]
NM_001406649.1:c.198C>G - nonsense - [Sequence Ontology: SO:0001587]
NM_001406650.1:c.198C>G - nonsense - [Sequence Ontology: SO:0001587]
NM_001406651.1:c.198C>G - nonsense - [Sequence Ontology: SO:0001587]
NM_001406652.1:c.198C>G - nonsense - [Sequence Ontology: SO:0001587]
NM_001406653.1:c.198C>G - nonsense - [Sequence Ontology: SO:0001587]
NM_001406655.1:c.198C>G - nonsense - [Sequence Ontology: SO:0001587]
NM_001406657.1:c.198C>G - nonsense - [Sequence Ontology: SO:0001587]
NM_001406666.1:c.198C>G - nonsense - [Sequence Ontology: SO:0001587]
NM_001406672.1:c.198C>G - nonsense - [Sequence Ontology: SO:0001587]
NM_001406674.1:c.198C>G - nonsense - [Sequence Ontology: SO:0001587]

Condition(s)

Name:: Hereditary nonpolyposis colorectal neoplasms
Identifiers:: MeSH: D003123; MedGen: C0009405

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV003524756	Labcorp Genetics (formerly Invitae), Labcorp	criteria provided, single submitter (Invitae Variant Classification Sherloc (09022015))	Pathogenic (Apr 12, 2022)	germline	clinical testing	PubMed (4) [See all records that cite these PMIDs] 15849733, 24362816, 21642682, 28492532

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV003524756

Labcorp Genetics (formerly Invitae), Labcorp

criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))

Pathogenic
(Apr 12, 2022)

germline

clinical testing

PubMed (4)
[See all records that cite these PMIDs]

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

Spectrum and frequencies of mutations in MSH2 and MLH1 identified in 1,721 German families suspected of hereditary nonpolyposis colorectal cancer.

Mangold E, Pagenstecher C, Friedl W, Mathiak M, Buettner R, Engel C, Loeffler M, Holinski-Feder E, Müller-Koch Y, Keller G, Schackert HK, Krüger S, Goecke T, Moeslein G, Kloor M, Gebert J, Kunstmann E, Schulmann K, Rüschoff J, Propping P.

Int J Cancer. 2005 Sep 20;116(5):692-702.

PubMed [citation]

PMID:: 15849733

Application of a 5-tiered scheme for standardized classification of 2,360 unique mismatch repair gene variants in the InSiGHT locus-specific database.

Thompson BA, Spurdle AB, Plazzer JP, Greenblatt MS, Akagi K, Al-Mulla F, Bapat B, Bernstein I, Capellá G, den Dunnen JT, du Sart D, Fabre A, Farrell MP, Farrington SM, Frayling IM, Frebourg T, Goldgar DE, Heinen CD, Holinski-Feder E, Kohonen-Corish M, Robinson KL, Leung SY, et al.

Nat Genet. 2014 Feb;46(2):107-115. doi: 10.1038/ng.2854. Epub 2013 Dec 22.

PubMed [citation]

PMID:: 24362816
PMCID:: PMC4294709

See all PubMed Citations (4)

Details of each submission

From Labcorp Genetics (formerly Invitae), Labcorp, SCV003524756.2

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	not provided	not provided	not provided	clinical testing	PubMed (4)

Description

This sequence change creates a premature translational stop signal (p.Tyr66*) in the MSH2 gene. It is expected to result in an absent or disrupted protein product. Loss-of-function variants in MSH2 are known to be pathogenic (PMID: 15849733, 24362816). This variant is not present in population databases (gnomAD no frequency). This premature translational stop signal has been observed in individual(s) with Lynch syndrome (PMID: 21642682). ClinVar contains an entry for this variant (Variation ID: 801677). For these reasons, this variant has been classified as Pathogenic.

#	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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