Variant #0000054599 (NC_000017.10:g.41245466G>A, NM_007294.3:c.2082C>T (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.41245466G>A
DNA change (hg38) g.43093449G>A
Published as 2201C/T (S694S)
ISCN -
DB-ID BRCA1_000183 See all 1489 reported entries
Variant remarks -
Reference PubMed: Shattuck-Eidens 1997
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.35333 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 16:24:59 +02:00 (CEST)
Date last edited 2019-02-08 16:32:34 +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 ?/. 11 c.2082C>T r.(?) p.Ser694Ser -


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