NM_000179.3(MSH6):c.2187C>A (p.Ala729=) AND Hereditary cancer-predisposing syndrome

Clinical significance:Likely benign (Last evaluated: Apr 27, 2016)

Review status:2 stars out of maximum of 4 stars

criteria provided, multiple submitters, no conflicts

Based on:
2 submissions [Details]
Record status:
current
Accession:
RCV000563596.2

Allele description [Variation Report for NM_000179.3(MSH6):c.2187C>A (p.Ala729=)]

NM_000179.3(MSH6):c.2187C>A (p.Ala729=)

Gene:
MSH6:mutS homolog 6 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
2p16.3
Genomic location:
Preferred name:
NM_000179.3(MSH6):c.2187C>A (p.Ala729=)
Other names:
p.A729A:GCC>GCA
HGVS:
  • NC_000002.12:g.47800170C>A
  • NG_007111.1:g.22024C>A
  • NM_000179.2:c.2187C>A
  • NM_000179.3:c.2187C>AMANE SELECT
  • NM_001281492.2:c.1797C>A
  • NM_001281493.2:c.1281C>A
  • NM_001281494.2:c.1281C>A
  • NP_000170.1:p.Ala729=
  • NP_000170.1:p.Ala729=
  • NP_001268421.1:p.Ala599=
  • NP_001268422.1:p.Ala427=
  • NP_001268423.1:p.Ala427=
  • LRG_219t1:c.2187C>A
  • LRG_219:g.22024C>A
  • LRG_219p1:p.Ala729=
  • NC_000002.11:g.48027309C>A
Links:
dbSNP: rs375610656
NCBI 1000 Genomes Browser:
rs375610656
Molecular consequence:
  • NM_000179.2:c.2187C>A - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_000179.3:c.2187C>A - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001281492.2:c.1797C>A - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001281493.2:c.1281C>A - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001281494.2:c.1281C>A - synonymous variant - [Sequence Ontology: SO:0001819]
Observations:
1

Condition(s)

Name:
Hereditary cancer-predisposing syndrome
Synonyms:
Neoplastic Syndromes, Hereditary; Tumor predisposition; Cancer predisposition; See all synonyms [MedGen]
Identifiers:
MONDO: MONDO:0015356; MedGen: C0027672

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Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV000669978Ambry Geneticscriteria provided, single submitter
Likely benign
(Apr 27, 2016)
germlineclinical testing

Citation Link,

SCV000685263Color Health, Inccriteria provided, single submitter
Likely benign
(Sep 30, 2015)
germlineclinical testing

PubMed (1)
[See all records that cite this PMID]

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineunknown1not providednot provided1not providedclinical testing

Citations

PubMed

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.

Richards S, Aziz N, Bale S, Bick D, Das S, Gastier-Foster J, Grody WW, Hegde M, Lyon E, Spector E, Voelkerding K, Rehm HL; ACMG Laboratory Quality Assurance Committee..

Genet Med. 2015 May;17(5):405-24. doi: 10.1038/gim.2015.30. Epub 2015 Mar 5.

PubMed [citation]
PMID:
25741868
PMCID:
PMC4544753

Details of each submission

From Ambry Genetics, SCV000669978.3

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not provided1not providednot providedclinical testingnot provided

Description

Synonymous alterations with insufficient evidence to classify as benign

#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineunknown1not providednot provided1not providednot providednot provided

From Color Health, Inc, SCV000685263.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testing PubMed (1)
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineunknownnot providednot providednot providednot providednot providednot providednot provided

Last Updated: Oct 30, 2021

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