Variant #0001044740 (NC_000006.11:g.152419922T>A, NM_000125.3:c.1609T>A (ESR1))
| Chromosome |
6 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.152419922T>A |
| DNA change (hg38) |
- |
| Published as |
- |
| ISCN |
- |
| DB-ID |
ESR1_000002 |
| Variant remarks |
- |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
rs2152506534 |
| Origin |
Unknown |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
MobiDetails |
| Database submission license |
Creative Commons Attribution 4.0 International |
| Created by |
MobiDetails |
| Date created |
2025-05-16 12:02:01 +02:00 (CEST) |
| Date last edited |
N/A |

Variant on transcripts
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