NM_000251.3(MSH2):c.788_789del (p.Asn263fs) AND not provided

Germline classification:: Pathogenic (1 submission)
Last evaluated:: May 1, 2021
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:: RCV001531919.20

Allele description [Variation Report for NM_000251.3(MSH2):c.788_789del (p.Asn263fs)]

NM_000251.3(MSH2):c.788_789del (p.Asn263fs)

Gene:

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

Variant type:

Deletion

Cytogenetic location:

2p21

Genomic location:

Preferred name:

NM_000251.3(MSH2):c.788_789del (p.Asn263fs)

HGVS:

NC_000002.12:g.47412556_47412557del
NG_007110.2:g.14433_14434del
NM_000251.3:c.788_789delMANE SELECT
NM_001258281.1:c.590_591del
NP_000242.1:p.Asn263fs
NP_001245210.1:p.Asn197fs
LRG_218:g.14433_14434del
NC_000002.11:g.47639695_47639696del
NM_000251.1:c.788_789del

Protein change:

N197fs

Links:

dbSNP: rs63751614

NCBI 1000 Genomes Browser:

rs63751614

Molecular consequence:

NM_000251.3:c.788_789del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001258281.1:c.590_591del - frameshift variant - [Sequence Ontology: SO:0001589]

Observations:

Condition(s)

Synonyms:: none provided
Identifiers:: MedGen: C3661900

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV001747250	CeGaT Center for Human Genetics Tuebingen	criteria provided, single submitter (CeGaT Center For Human Genetics Tuebingen Variant Classification Criteria Version 2)	Pathogenic (May 1, 2021)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV001747250

CeGaT Center for Human Genetics Tuebingen

criteria provided, single submitter

(CeGaT Center For Human Genetics Tuebingen Variant Classification Criteria Version 2)

Pathogenic
(May 1, 2021)

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	1	not provided	not provided	not provided	not provided	clinical testing

Details of each submission

From CeGaT Center for Human Genetics Tuebingen, SCV001747250.20

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

#	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		1	not provided	not provided	not provided

Last Updated: Oct 20, 2024

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