Variant #0000055640 (NC_000017.10:g.41199693G>C, NM_007294.3:c.5434C>G (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.41199693G>C
DNA change (hg38) g.43047676G>C
Published as P1812A
ISCN -
DB-ID BRCA1_000478 See all 12 reported entries
Variant remarks mRNA analysis; affects RNA splicing
Reference PubMed: Gaildrat 2010
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0 View details
Owner Maaike Vreeswijk
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Maaike Vreeswijk
Date created 2010-11-09 15:40:14 +01:00 (CET)
Date last edited 2019-02-25 21:12:28 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
BRCA1 NM_007294.3 +/. 23 c.5434C>G r.5407_5467del p.Gly1803Glnfs*11 -


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