Variant #0000052237 (NC_000017.10:g.41267762A>C, NM_007294.3:c.115T>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.41267762A>C
DNA change (hg38) g.43115745A>C
Published as C39G
ISCN -
DB-ID BRCA1_000523 See all 3 reported entries
Variant remarks LOH/Evolutionary conservation; predicted deleterious
Reference PubMed: Hansen 2009
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Thomas Hansen
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Maaike Vreeswijk
Date created 2011-09-14 14:30:38 +02:00 (CEST)
Date last edited 2020-07-13 15:49:19 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
BRCA1 NM_007294.3 +/. 3 c.115T>G r.(?) p.Cys39Gly -


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