Variant #0000191012 (NC_000017.10:g.41273422C>T, BRCA1(NM_007294.3):c.80+2612G>A)

Chromosome 17
Allele Parent #1
Affects function (as reported) Does not affect function
Affects function (by curator) Does not affect function
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.41273422C>T
DNA change (hg38) g.43121405C>T
Published as -
ISCN -
DB-ID BRCA1_004550
Variant remarks Class 1 not pathogenic based on frequency >1% in an outbred sampleset. Frequency 0.01187 (European), derived from 1000 genomes (2012-04-30).
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 No license selected
Created by ENIGMA consortium
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
BRCA1 NM_007294.3 -/- 2i c.80+2612G>A r.(?) p.(=) -