Variant #0000054128 (NC_000013.10:g.32900744C>T, NM_000059.3:c.625C>T (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.32900744C>T |
| DNA change (hg38) |
g.32326607C>T |
| Published as |
c.625C>T |
| ISCN |
- |
| DB-ID |
BRCA2_000528 |
| Variant remarks |
splicing reporter minigene; no splicing defect |
| Reference |
PubMed: Gaildrat 2012 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
In vitro (cloned) |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| 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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