Variant #0000190882 (NC_000017.10:g.41258504A>C, NM_007294.3:c.181T>G (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.41258504A>C
DNA change (hg38) g.43106487A>C
Published as -
ISCN -
DB-ID BRCA1_000050 See all 134 reported entries
Variant remarks IARC class based on posterior probability from multifactorial likelihood analysis, thresholds for class as per Plon 2008 (PMID:18951446). Class 5 based on posterior probability = 1
Reference ENIGMA classification criteria, Details in BRCA database Tavtigian lab, PubMed: Lindor 2012
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 3.0E-5 View details
Owner ENIGMA consortium
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by ENIGMA consortium
Date created 2015-10-08 12:00:00 +02:00 (CEST)
Date last edited 2020-03-29 13:34:55 +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 +/+ 5 c.181T>G r.(?) p.(Cys61Gly) -


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