Variant #0000054948 (NC_000017.10:g.41223249G>A, NM_007294.3:c.4682C>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.41223249G>A
DNA change (hg38) g.43071232G>A
Published as c.4682C>T
ISCN -
DB-ID BRCA1_000333 See all 18 reported entries
Variant remarks splicing reporter minigene; no splicing defect
Reference PubMed: Théry 2011
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.0003 View details
Owner Maaike Vreeswijk
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Maaike Vreeswijk
Date created 2014-02-19 14:08:12 +01:00 (CET)
Date last edited 2019-02-25 21:12:28 +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 ?/. 16 c.4682C>T r.= p.Thr1561Ile -


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