Variant #0000054200 (NC_000017.10:g.41267802A>T, NC_000017.10(NM_007294.3):c.81-6T>A (BRCA1))
| Chromosome |
17 |
| 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.41267802A>T |
| DNA change (hg38) |
g.43115785A>T |
| Published as |
IVS2-6T>A |
| ISCN |
- |
| DB-ID |
BRCA1_000022 See all 3 reported entries |
| Variant remarks |
cDNA analysis; as variant control |
| Reference |
PubMed: Vreeswijk 2008 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
In vitro (cloned) |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Peter Devilee |
| Database submission license |
Creative Commons Attribution 4.0 International |
| Created by |
Maaike Vreeswijk |
| Date created |
2009-10-03 16:24:58 +02:00 (CEST) |
| Date last edited |
2020-07-20 17:28:07 +02:00 (CEST) |

Variant on transcripts
|
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
|