Variant #0000190981 (NC_000017.10:g.41268215_41268216dup, NC_000017.10(NM_007294.3):c.81-414_81-413dup (BRCA1))

Chromosome 17
Allele Parent #1
Affects function (as reported) Does not affect function
Affects function (by curator) Does not affect function
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.41268215_41268216dup
DNA change (hg38) g.43116198_43116199dup
Published as -
ISCN -
DB-ID BRCA1_004520
Variant remarks Class 1 not pathogenic based on frequency >1% in an outbred sampleset. Frequency 0.0268 (European), 0.0115 (Admixed American/Latino), derived from 1000 genomes (2013-05-02).
Reference ENIGMA classification criteria
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner ENIGMA consortium
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by ENIGMA consortium
Date created 2016-09-28 12:00:00 +02:00 (CEST)
Date last edited 2020-07-13 15:50:06 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
BRCA1 NM_007294.3 -/- 2i c.81-414_81-413dup r.(?) p.(=) -


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