NM_152743.4(BRAT1):c.1507C>T (p.Pro503Ser) AND not provided

Clinical significance:Conflicting interpretations of pathogenicity, Likely benign(1);Uncertain significance(1) (Last evaluated: May 28, 2021)

Review status:1 star out of maximum of 4 stars

criteria provided, conflicting interpretations

Based on:
2 submissions [Details]
Record status:
current
Accession:
RCV000710742.6

Allele description [Variation Report for NM_152743.4(BRAT1):c.1507C>T (p.Pro503Ser)]

NM_152743.4(BRAT1):c.1507C>T (p.Pro503Ser)

Gene:
BRAT1:BRCA1 associated ATM activator 1 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
7p22.3
Genomic location:
Preferred name:
NM_152743.4(BRAT1):c.1507C>T (p.Pro503Ser)
HGVS:
  • NC_000007.14:g.2539634G>A
  • NG_032167.1:g.21125C>T
  • NM_001350626.2:c.1507C>T
  • NM_001350627.2:c.982C>T
  • NM_152743.4:c.1507C>TMANE SELECT
  • NP_001337555.1:p.Pro503Ser
  • NP_001337556.1:p.Pro328Ser
  • NP_689956.2:p.Pro503Ser
  • NC_000007.13:g.2579268G>A
  • NM_152743.3:c.1507C>T
  • NR_146879.2:n.1690C>T
Protein change:
P328S
Links:
dbSNP: rs147745609
NCBI 1000 Genomes Browser:
rs147745609
Molecular consequence:
  • NM_001350626.2:c.1507C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001350627.2:c.982C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_152743.4:c.1507C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NR_146879.2:n.1690C>T - non-coding transcript variant - [Sequence Ontology: SO:0001619]

Condition(s)

Identifiers:
MedGen: CN517202

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Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV000841040Athena Diagnostics Inccriteria provided, single submitter
Uncertain significance
(Nov 28, 2017)
germlineclinical testing

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

SCV001805412GeneDxcriteria provided, single submitter
Likely benign
(May 28, 2021)
germlineclinical testing

Citation Link

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineyesnot providednot providednot providednot providednot providedclinical testing
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 Athena Diagnostics Inc, SCV000841040.1

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

From GeneDx, SCV001805412.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testingnot provided
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineyesnot providednot providednot providednot providednot providednot providednot provided

Last Updated: Sep 29, 2021

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