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 International |
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) |

Variant on transcripts
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