Variant #0000021774 (NC_000017.10:g.41247941T>G, NC_000017.10(NM_007294.3):c.594-2A>C (BRCA1))

Chromosome 17
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.41247941T>G
DNA change (hg38) g.43095924T>G
Published as -
ISCN -
DB-ID BRCA1_000099 See all 51 reported entries
Variant remarks Classified by NLB-labs
Reference M Vreeswijk
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation yes
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 3.0E-5 View details
Owner Maaike Vreeswijk
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2013-11-09 17:42:07 +01:00 (CET)
Date last edited 2020-07-13 15:38:35 +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 +/+ 9i c.594-2A>C r.spl p.? -


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