Variant #0000054696 (NC_000017.10:g.41244936G>A, NM_007294.3:c.2612C>T (BRCA1))

Chromosome 17
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.41244936G>A
DNA change (hg38) g.43092919G>A
Published as P871L
ISCN -
DB-ID BRCA1_000213 See all 1549 reported entries
Variant remarks Multifactorial likelihood-ratio model; predicted neutral
Reference PubMed: Tavtigian 2005
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.40316 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 16:25:00 +02:00 (CEST)
Date last edited 2020-07-13 15:11:01 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
BRCA1 NM_007294.3 -/. 11 c.2612C>T r.(?) p.Pro871Leu -


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