Variant #0000053500 (NC_000013.10:g.32918675T>A, NC_000013.10(NM_000059.3):c.6842-20T>A (BRCA2))
Chromosome |
13 |
Allele |
Unknown |
Affects function (as reported) |
Does not affect function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
NA |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.32918675T>A |
DNA change (hg38) |
g.32344538T>A |
Published as |
IVS11-20T/A |
ISCN |
- |
DB-ID |
BRCA2_000169 See all 26 reported entries |
Variant remarks |
Multifactorial likelihood-ratio model; predicted neutral |
Reference |
PubMed: Easton 2007 |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
In vitro (cloned) |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
0.00024 View details |
Owner |
Peter Devilee |
Database submission license |
Creative Commons Attribution 4.0 International |
Created by |
Maaike Vreeswijk |
Date created |
2009-10-03 17:15:53 +02:00 (CEST) |
Date last edited |
2020-07-03 15:46:08 +02:00 (CEST) |

Variant on transcripts
|