Variant #0000054624 (NC_000017.10:g.41245237A>G, NM_007294.3:c.2311T>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.41245237A>G |
DNA change (hg38) |
g.43093220A>G |
Published as |
L771L |
ISCN |
- |
DB-ID |
BRCA1_000194 See all 1478 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) |
0.34819 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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