Variant #0000191111 (NC_000013.10:g.32891305T>C, NC_000013.10(NM_000059.3):c.67+641T>C (BRCA2))

Chromosome 13
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.32891305T>C
DNA change (hg38) g.32317168T>C
Published as -
ISCN -
DB-ID BRCA2_003961
Variant remarks Class 1 not pathogenic based on frequency >1% in an outbred sampleset. Frequency 0.09441 (Asian), 0.01626 (African), 0.04749 (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 Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by ENIGMA consortium
Date created 2015-12-01 12:00:00 +01:00 (CET)
Date last edited 2019-02-07 08:37:59 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
BRCA2 NM_000059.3 -/- 2i c.67+641T>C r.(?) p.(=) -


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