Variant #0000409881 (NC_000017.10:g.41277532A>C, BRCA1(NM_007294.3):c.-264T>G)
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.41277532A>C |
DNA change (hg38) |
g.43125515A>C |
Published as |
- |
ISCN |
- |
DB-ID |
BRCA1_005301 See all 2 reported entries |
Variant remarks |
expression cloning luciferase assay no effect |
Reference |
PubMed: Burke 2018, Journal: Burke 2018 |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
In vitro (cloned) |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Lez J Burke |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
Johan den Dunnen |
Date created |
2018-10-27 18:08:29 +02:00 (CEST) |
Date last edited |
2019-02-07 08:31:26 +01:00 (CET) |

Variant on transcripts
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