NM_000251.2(MSH2):c.421A>G (p.Met141Val) AND Hereditary cancer-predisposing syndrome

This record was updated by the submitter. Please see the current version.

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Oct 10, 2014
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:: RCV000115531.5

Allele description

NM_000251.2(MSH2):c.421A>G (p.Met141Val)

Gene:

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

Variant type:

single nucleotide variant

Cytogenetic location:

2p21

Genomic location:

Preferred name:

NM_000251.2(MSH2):c.421A>G (p.Met141Val)

HGVS:

NC_000002.12:g.47410148A>G
NG_007110.2:g.12025A>G
NM_000251.2:c.421A>G
NP_000242.1:p.Met141Val
LRG_218t1:c.421A>G
LRG_218:g.12025A>G
LRG_218p1:p.Met141Val
NC_000002.11:g.47637287A>G
NM_000251.1:c.421A>G
p.M141V
p.M141V:ATG>GTG

Protein change:

M141V

Links:

dbSNP: rs193922374

GMAF:

0.0002(G), 193922374

NCBI 1000 Genomes Browser:

rs193922374

Molecular consequence:

NM_000251.2:c.421A>G - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:: Hereditary cancer-predisposing syndrome
Synonyms:: Neoplastic Syndromes, Hereditary; Tumor predisposition; Cancer predisposition
Identifiers:: MedGen: C0027672

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV000186070	Ambry Genetics,	criteria provided, single submitter (Ambry Autosomal Dominant and X-Linked criteria (9/4/14))	Uncertain significance (Oct 10, 2014)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV000186070

Ambry Genetics,

criteria provided, single submitter

(Ambry Autosomal Dominant and X-Linked criteria (9/4/14))

Uncertain significance
(Oct 10, 2014)

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,, SCV000186070.2

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

Last Updated: Aug 29, 2016

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