Variant #0000054092 (NC_000013.10:g.32900251C>T, NM_000059.3:c.439C>T (BRCA2))
| Chromosome |
13 |
| Allele |
Unknown |
| 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.32900251C>T |
| DNA change (hg38) |
g.32326114C>T |
| Published as |
- |
| ISCN |
- |
| DB-ID |
BRCA2_000487 See all 7 reported entries |
| Variant remarks |
ESEfinder/ESRsearch. RT-PCR /hybrid minigenes; ESE disruption/ESS creation, exon 5 skipping |
| Reference |
PubMed: Sanz 2010 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
In vitro (cloned) |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Eladio A Velasco |
| Database submission license |
Creative Commons Attribution 4.0 International |
| Created by |
Maaike Vreeswijk |
| Date created |
2010-07-01 15:17:03 +02:00 (CEST) |
| Date last edited |
2019-02-25 21:51:16 +01:00 (CET) |

Variant on transcripts
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