Variant #0000054229 (NC_000017.10:g.41267746C>A, NM_007294.3:c.131G>T (BRCA1))
Chromosome |
17 |
Allele |
Unknown |
Affects function (as reported) |
Probably affects function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
NA |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.41267746C>A |
DNA change (hg38) |
g.43115729C>A |
Published as |
C44F |
ISCN |
- |
DB-ID |
BRCA1_000036 See all 20 reported entries |
Variant remarks |
Homology directed recombination; impact on protein function |
Reference |
PubMed: Ransburgh 2010 |
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 |
2011-01-27 15:55:48 +01:00 (CET) |
Date last edited |
2020-07-13 15:49:04 +02:00 (CEST) |

Variant on transcripts
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