Variant #0000054673 (NC_000017.10:g.41245027G>A, NM_007294.3:c.2521C>T (BRCA1))

Chromosome 17
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.41245027G>A
DNA change (hg38) g.43093010G>A
Published as R841W
ISCN -
DB-ID BRCA1_000207 See all 52 reported entries
Variant remarks Bayesian statistics; predicted deleterious
Reference PubMed: Petersen 1998
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.0017 View details
Owner Peter Devilee
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Maaike Vreeswijk
Date created 2009-10-03 16:24:59 +02:00 (CEST)
Date last edited 2020-07-13 15:14:01 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
BRCA1 NM_007294.3 +/. 11 c.2521C>T r.(?) p.Arg841Trp -


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