Variant #0000054292 (NC_000017.10:g.41258474T>C, NM_007294.3:c.211A>G (BRCA1))
| Chromosome |
17 |
| 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.41258474T>C |
| DNA change (hg38) |
g.43106457T>C |
| Published as |
R71G |
| ISCN |
- |
| DB-ID |
BRCA1_000059 See all 49 reported entries |
| Variant remarks |
cDNA analysis; predicted deleterious, increased in-frame skipping of exon 5 and out-of-frame skipping of the last 22 nucleotides of exon 5 |
| Reference |
PubMed: Vega 2001 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
In vitro (cloned) |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0 View details |
| Owner |
Peter Devilee |
| Database submission license |
Creative Commons Attribution 4.0 International |
| Created by |
Maaike Vreeswijk |
| Date created |
2009-10-03 16:24:59 +02:00 (CEST) |
| Date last edited |
2019-02-25 21:12:28 +01:00 (CET) |

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