Variant #0000053228 (NC_000013.10:g.32893369G>C, NM_000059.3:c.223G>C (BRCA2))
Chromosome |
13 |
Allele |
Unknown |
Affects function (as reported) |
Effect unknown |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
NA |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.32893369G>C |
DNA change (hg38) |
g.32319232G>C |
Published as |
c.223G>C |
ISCN |
- |
DB-ID |
BRCA2_000020 See all 29 reported entries |
Variant remarks |
splicing reporter minigene/patient RNA analysis; no splicing defect |
Reference |
PubMed: Théry 2011 |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
In vitro (cloned) |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
0.00025 View details |
Owner |
Maaike Vreeswijk |
Database submission license |
Creative Commons Attribution 4.0 International |
Created by |
Maaike Vreeswijk |
Date created |
2014-02-19 14:34:22 +01:00 (CET) |
Date last edited |
2019-02-25 21:51:16 +01:00 (CET) |

Variant on transcripts
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