NM_007299.4(BRCA1):c.212+21G>A AND not specified

Clinical significance:Likely benign (Last evaluated: Nov 7, 2016)

Review status:1 star out of maximum of 4 stars

criteria provided, single submitter

Based on:
1 submission [Details]
Record status:
current
Accession:
RCV000506766.1

Allele description [Variation Report for NM_007299.4(BRCA1):c.212+21G>A]

NM_007299.4(BRCA1):c.212+21G>A

Gene:
BRCA1:BRCA1 DNA repair associated [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
17q21.31
Genomic location:
Preferred name:
NM_007299.4(BRCA1):c.212+21G>A
Other names:
IVS5+21G>A
HGVS:
  • NC_000017.11:g.43106435C>T
  • NG_005905.2:g.111549G>A
  • NM_007294.3:c.212+21G>A
  • NM_007297.4:c.71+21G>A
  • NM_007298.3:c.212+21G>A
  • NM_007299.4:c.212+21G>A
  • NM_007300.4:c.212+21G>A
  • LRG_292t1:c.212+21G>A
  • LRG_292:g.111549G>A
  • NC_000017.10:g.41258452C>T
  • NM_007299.3:c.212+21G>A
  • U14680.1:n.331+21G>A
Links:
Breast Cancer Information Core (BIC) (BRCA1): 331+21&base_change=G to A; dbSNP: rs80358147
NCBI 1000 Genomes Browser:
rs80358147
Molecular consequence:
  • NM_007294.3:c.212+21G>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_007297.4:c.71+21G>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_007298.3:c.212+21G>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_007299.4:c.212+21G>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_007300.4:c.212+21G>A - intron variant - [Sequence Ontology: SO:0001627]

Condition(s)

Synonyms:
AllHighlyPenetrant
Identifiers:
MedGen: CN169374

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Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV000602697ARUP Laboratories, Molecular Genetics and Genomics,ARUP Laboratoriescriteria provided, single submitter
Likely benign
(Nov 7, 2016)
germlineclinical testing

Citation Link

Summary from all submissions

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

Details of each submission

From ARUP Laboratories, Molecular Genetics and Genomics,ARUP Laboratories, SCV000602697.1

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

Last Updated: Apr 1, 2021

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