Variant #0000054096 (NC_000013.10:g.32950929G>A, NC_000013.10(NM_000059.3):c.8754+1G>A (BRCA2))
Chromosome |
13 |
Allele |
Unknown |
Affects function (as reported) |
Probably affects function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
NA |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.32950929G>A |
DNA change (hg38) |
g.32376792G>A |
Published as |
- |
ISCN |
- |
DB-ID |
BRCA2_000491 See all 8 reported entries |
Variant remarks |
Aberant splicing; predicted deleterious |
Reference |
PubMed: Hansen 2008 |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
In vitro (cloned) |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Thomas Hansen |
Database submission license |
Creative Commons Attribution 4.0 International |
Created by |
Maaike Vreeswijk |
Date created |
2011-09-14 14:38:31 +02:00 (CEST) |
Date last edited |
2019-02-25 21:51:16 +01:00 (CET) |

Variant on transcripts
|
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
|