Variant #0000055682 (NC_000017.10:g.41197778A>G, NM_007294.3:c.5509T>C (BRCA1))

Chromosome 17
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.41197778A>G
DNA change (hg38) g.43045761A>G
Published as W1837R
ISCN -
DB-ID BRCA1_000489 See all 31 reported entries
Variant remarks Transcription activation in yeast (GAL4-fusions); as variant control
Reference PubMed: Phelan 2005
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Peter Devilee
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Maaike Vreeswijk
Date created 2009-10-03 16:25:02 +02:00 (CEST)
Date last edited 2020-07-13 14:14:55 +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 ?/. 24 c.5509T>C r.(?) p.Trp1837Arg -


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