Variant #0000169130 (NC_000017.10:g.41247892T>C, NM_007294.3:c.641A>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.41247892T>C
DNA change (hg38) g.43095875T>C
Published as -
ISCN -
DB-ID BRCA1_001629 See all 44 reported entries
Variant remarks minigene splice expression cloning ex10 and ex8-ex12 in several cell lines
Reference PubMed: de la Hoya 2016, Journal: de la Hoya 2016
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 Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2017-04-23 15:28:01 +02:00 (CEST)
Date last edited 2019-02-07 08:31:26 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
BRCA1 NM_007294.3 +/. 10 c.641A>G r.[=, 594_670del] p.[=, Val199fs] -


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