Variant #0000054591 (NC_000017.10:g.41245471C>T, NM_007294.3:c.2077G>A (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.41245471C>T
DNA change (hg38) g.43093454C>T
Published as D693N
ISCN -
DB-ID BRCA1_000182 See all 403 reported entries
Variant remarks evolutionary conservation analysis; predicted neutral
Reference PubMed: Greenman 1998
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.05871 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 2020-07-13 15:23:40 +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.2077G>A r.(?) p.Asp693Asn -


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