Variant #0000054597 (NC_000017.10:g.41245466G>A, NM_007294.3:c.2082C>T (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.41245466G>A |
| DNA change (hg38) |
g.43093449G>A |
| Published as |
S694S |
| ISCN |
- |
| DB-ID |
BRCA1_000183 See all 1489 reported entries |
| Variant remarks |
- |
| Reference |
PubMed: Augello 2006 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
In vitro (cloned) |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0.35333 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 |
2019-02-08 16:32:34 +01:00 (CET) |

Variant on transcripts
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