Variant #0000054120 (NC_000013.10:g.32893302_32893303insN[?], NM_000059.3:c.156_157insN[?] (BRCA2))
Chromosome |
13 |
Allele |
Paternal (confirmed) |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
NA |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.32893302_32893303insN[?] |
DNA change (hg38) |
- |
Published as |
- |
ISCN |
- |
DB-ID |
BRCA2_000518 See all 9 reported entries |
Variant remarks |
- |
Reference |
PubMed: Teugels 2009 |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
In vitro (cloned) |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Erik Teugels |
Database submission license |
Creative Commons Attribution 4.0 International |
Created by |
Maaike Vreeswijk |
Date created |
2013-01-24 18:11:01 +01:00 (CET) |
Date last edited |
2021-12-15 21:27:20 +01:00 (CET) |

Variant on transcripts
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