U.S. flag

An official website of the United States government

NM_000059.4(BRCA2):c.6423T>G (p.Gly2141=) AND not provided

Clinical significance:Uncertain significance (Last evaluated: Aug 10, 2019)

Review status:1 star out of maximum of 4 stars

criteria provided, single submitter

Help
Based on:
1 submission [Details]
Record status:
current
Accession:
RCV000985565.3

Allele description [Variation Report for NM_000059.4(BRCA2):c.6423T>G (p.Gly2141=)]

NM_000059.4(BRCA2):c.6423T>G (p.Gly2141=)

Gene:
BRCA2:BRCA2 DNA repair associated [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
13q13.1
Genomic location:
Preferred name:
NM_000059.4(BRCA2):c.6423T>G (p.Gly2141=)
HGVS:
  • NC_000013.11:g.32340778T>G
  • NG_012772.3:g.30299T>G
  • NM_000059.4:c.6423T>GMANE SELECT
  • NP_000050.2:p.Gly2141=
  • NP_000050.3:p.Gly2141=
  • LRG_293t1:c.6423T>G
  • LRG_293:g.30299T>G
  • LRG_293p1:p.Gly2141=
  • NC_000013.10:g.32914915T>G
  • NM_000059.3:c.6423T>G
Links:
dbSNP: rs780721021
NCBI 1000 Genomes Browser:
rs780721021
Molecular consequence:
  • NM_000059.4:c.6423T>G - synonymous variant - [Sequence Ontology: SO:0001819]

Condition(s)

Synonyms:
none provided
Identifiers:
MedGen: CN517202

Recent activity

Clear Turn Off Turn On

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...

Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV001133863Quest Diagnostics Nichols Institute San Juan Capistranocriteria provided, single submitter
Uncertain significance
(Aug 10, 2019) 		germlineclinical testing

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

Summary from all submissions

Help
EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineunknownnot providednot providednot providednot providednot providedclinical testing

Citations

PubMed

A Standardized DNA Variant Scoring System for Pathogenicity Assessments in Mendelian Disorders.

Karbassi I, Maston GA, Love A, DiVincenzo C, Braastad CD, Elzinga CD, Bright AR, Previte D, Zhang K, Rowland CM, McCarthy M, Lapierre JL, Dubois F, Medeiros KA, Batish SD, Jones J, Liaquat K, Hoffman CA, Jaremko M, Wang Z, Sun W, Buller-Burckle A, et al.

Hum Mutat. 2016 Jan;37(1):127-34. doi: 10.1002/humu.22918. Epub 2015 Oct 29.

PubMed [citation]
PMID:
26467025
PMCID:
PMC4737317

Details of each submission

From Quest Diagnostics Nichols Institute San Juan Capistrano, SCV001133863.2

#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: Nov 29, 2022