Variant #0000055787 (NC_000017.10:g.41276163_41276164dup, NC_000017.10(NM_007294.3):c.-19-22_-19-21dup (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.41276163_41276164dup |
| DNA change (hg38) |
g.43124146_43124147dup |
| Published as |
101-21insAT |
| ISCN |
- |
| DB-ID |
BRCA1_000552 See all 6 reported entries |
| Variant remarks |
Splicing reporter minigene; predicted neutral, Use of cryptic splice site in exon 3 |
| 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 |
2020-07-13 15:54:57 +02:00 (CEST) |

Variant on transcripts
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