Variant #0000193391 (NC_000013.10:g.32953453G>A, NC_000013.10(NM_000059.3):c.8755-1G>A (BRCA2))
Chromosome |
13 |
Allele |
Parent #1 |
Affects function (as reported) |
Effect unknown |
Affects function (by curator) |
Effect unknown |
Classification method |
- |
Clinical classification |
VUS |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.32953453G>A |
DNA change (hg38) |
g.32379316G>A |
Published as |
- |
ISCN |
- |
DB-ID |
BRCA2_001084 See all 18 reported entries |
Variant remarks |
Insufficient evidence to determine clinical significance. Variant allele produces r.8755_8953del, r.8755_9004del AND full-length transcripts. |
Reference |
ENIGMA classification criteria, PubMed: Colombo 2013 |
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 |
2016-04-15 12:00:00 +02:00 (CEST) |
Date last edited |
2020-07-03 16:09:47 +02:00 (CEST) |

Variant on transcripts
|