Variant #0000053238 (NC_000013.10:g.32900433C>T, NC_000013.10(NM_000059.3):c.516+14C>T (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.32900433C>T |
| DNA change (hg38) |
g.32326296C>T |
| Published as |
c.516+14C>T |
| ISCN |
- |
| DB-ID |
BRCA2_000030 See all 30 reported entries |
| Variant remarks |
mRNA analysis and splicing reporter minigene; predicted neutral |
| Reference |
PubMed: Bonnet 2008 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
In vitro (cloned) |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0.00034 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 |
2019-02-25 21:51:16 +01:00 (CET) |

Variant on transcripts
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