Variant #0000054384 (NC_000017.10:g.41247941T>G, NC_000017.10(NM_007294.3):c.594-2A>C (BRCA1))

Chromosome 17
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.41247941T>G
DNA change (hg38) g.43095924T>G
Published as 713-2A>C
ISCN -
DB-ID BRCA1_000099 See all 51 reported entries
Variant remarks Splicing reporter minigene; predicted neutral
Reference PubMed: Steffensen 2014
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 3.0E-5 View details
Owner Maaike Vreeswijk
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Maaike Vreeswijk
Date created 2014-02-19 14:51:59 +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 -?/. 9i c.594-2A>C r.= ? -


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