Variant #0000055768 (NC_000017.10:g.41258495A>G, NM_007294.3:c.190T>C (BRCA1))
| Chromosome |
17 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
NA |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.41258495A>G |
| DNA change (hg38) |
g.43106478A>G |
| Published as |
C64R |
| ISCN |
- |
| DB-ID |
BRCA1_000532 See all 24 reported entries |
| Variant remarks |
RNA analysis; normal RNA splicing |
| Reference |
PubMed: Willems 2009 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
In vitro (cloned) |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Maaike Vreeswijk |
| Database submission license |
Creative Commons Attribution 4.0 International |
| Created by |
Maaike Vreeswijk |
| Date created |
2013-02-12 10:04:35 +01:00 (CET) |
| Date last edited |
2019-02-25 21:12:28 +01:00 (CET) |

Variant on transcripts
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