Variant #0000055352 (NC_000017.10:g.41209139A>C, NM_007294.3:c.5207T>G (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.41209139A>C |
| DNA change (hg38) |
g.43057122A>C |
| Published as |
V1736G |
| ISCN |
- |
| DB-ID |
BRCA1_000421 See all 3 reported entries |
| Variant remarks |
transcription activation/PS/BA/BS; strong functional effect |
| Reference |
PubMed: Lee 2010 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
In vitro (cloned) |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Thomas Hansen |
| Database submission license |
Creative Commons Attribution 4.0 International |
| Created by |
Maaike Vreeswijk |
| Date created |
2011-09-14 12:27:00 +02:00 (CEST) |
| Date last edited |
2020-07-13 14:26:00 +02:00 (CEST) |

Variant on transcripts
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