Variant #0000190796 (NC_000017.10:g.41256086_41256097del, NC_000017.10(NM_007294.3):c.441+52_441+63del (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.41256086_41256097del
DNA change (hg38) g.43104069_43104080del
Published as -
ISCN -
DB-ID BRCA1_001952 See all 6 reported entries
Variant remarks Class 1 not pathogenic based on frequency >1% in an outbred sampleset. Frequency 0.3559 (European), 0.3321 (African), 0.4006 (Admixed American/Latino), 0.3899 (East Asian), 0.5204 (South Asian), 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 15:42:55 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
BRCA1 NM_007294.3 -/- 7i c.441+52_441+63del r.(?) p.(=) -


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.