Variant #0000054896 (NC_000017.10:g.41234470A>G, NM_007294.3:c.4308T>C (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.41234470A>G |
| DNA change (hg38) |
g.43082453A>G |
| Published as |
S1436S |
| ISCN |
- |
| DB-ID |
BRCA1_000309 See all 1437 reported entries |
| Variant remarks |
- |
| Reference |
PubMed: McKean-Cowdin 2005 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
In vitro (cloned) |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0.34927 View details |
| Owner |
Peter Devilee |
| Database submission license |
Creative Commons Attribution 4.0 International |
| Created by |
Maaike Vreeswijk |
| Date created |
2009-10-03 16:25:00 +02:00 (CEST) |
| Date last edited |
2019-02-07 08:31:26 +01:00 (CET) |

Variant on transcripts
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