Variant #0000046106 (NC_000017.10:g.41226488C>A, NM_007294.3:c.4535G>T (BRCA1))
| Chromosome |
17 |
| Allele |
Parent #1 |
| Affects function (as reported) |
Does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.41226488C>A |
| DNA change (hg38) |
g.43074471C>A |
| Published as |
4654G>T |
| ISCN |
- |
| DB-ID |
BRCA1_000324 See all 56 reported entries |
| Variant remarks |
- |
| Reference |
UMD BRCA1 database |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
Germline |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0.00232 View details |
| Owner |
UMD |
| Database submission license |
Creative Commons Attribution 4.0 International |
| Created by |
Julia Lopez |
| Date created |
2014-10-20 13:31:25 +02:00 (CEST) |
| Date last edited |
2017-04-22 20:41:19 +02:00 (CEST) |

Variant on transcripts
Screenings
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