Variant #0000054229 (NC_000017.10:g.41267746C>A, NM_007294.3:c.131G>T (BRCA1))

Chromosome 17
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.41267746C>A
DNA change (hg38) g.43115729C>A
Published as C44F
ISCN -
DB-ID BRCA1_000036 See all 20 reported entries
Variant remarks Homology directed recombination; impact on protein function
Reference PubMed: Ransburgh 2010
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Maaike Vreeswijk
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Maaike Vreeswijk
Date created 2011-01-27 15:55:48 +01:00 (CET)
Date last edited 2020-07-13 15:49:04 +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 +?/. 3 c.131G>T r.(?) p.Cys44Phe -


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