Variant #0000409880 (NC_000017.10:g.41277541C>T, NM_007294.3:c.-273G>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.41277541C>T |
| DNA change (hg38) |
g.43125524C>T |
| Published as |
- |
| ISCN |
- |
| DB-ID |
BRCA1_004586 See all 3 reported entries |
| Variant remarks |
expression cloning luciferase assay no effect |
| Reference |
PubMed: Burke 2018, Journal: Burke 2018 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
In vitro (cloned) |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Lez J Burke |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2018-10-27 18:08:29 +02:00 (CEST) |
| Date last edited |
2019-02-07 08:31:26 +01:00 (CET) |

Variant on transcripts
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