Variant #0000190172 (NC_000017.10:g.41245159C>A, NM_007294.3:c.2389G>T (BRCA1))

Chromosome 17
Allele Parent #1
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Classification method -
Clinical classification pathogenic (dominant)
DNA change (genomic) (Relative to hg19 / GRCh37) g.41245159C>A
DNA change (hg38) g.43093142C>A
Published as -
ISCN -
DB-ID BRCA1_002957 See all 6 reported entries
Variant remarks Variant allele predicted to encode truncated non-functional protein
Reference ENIGMA classification criteria
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner ENIGMA consortium
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by ENIGMA consortium
Date created 2016-04-22 12:00:00 +02:00 (CEST)
Date last edited 2020-02-20 16:15:54 +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.2389G>T r.(?) p.(Glu797*) -


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