Variant #0000055799 (NC_000017.10:g.41223275T>C, NC_000017.10(NM_007294.3):c.4676-20A>G (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.41223275T>C |
DNA change (hg38) |
g.43071258T>C |
Published as |
4795-20A>G |
ISCN |
- |
DB-ID |
BRCA1_000564 See all 2 reported entries |
Variant remarks |
Splicing reporter minigene; predicted neutral, Out-of-frame deletion of 1 bp of exon 19 |
Reference |
PubMed: Steffensen 2014 |
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 |
2014-02-19 14:51:59 +01:00 (CET) |
Date last edited |
2019-02-25 21:12:28 +01:00 (CET) |

Variant on transcripts
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