Variant #0000708489 (NC_000011.9:g.57365113C>A, NM_000062.2:c.-105C>A (SERPING1))
| Chromosome |
11 |
| Allele |
Unknown |
| Affects function (as reported) |
Effect unknown |
| Affects function (by curator) |
Effect unknown |
| Classification method |
ACMG |
| Clinical classification |
VUS |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.57365113C>A |
| DNA change (hg38) |
g.57597640C>A |
| Published as |
- |
| ISCN |
- |
| DB-ID |
SERPING1_000815 |
| Variant remarks |
- |
| Reference |
- |
| ClinVar ID |
ClinVar-000305010 |
| dbSNP ID |
rs886048397 |
| Origin |
CLASSIFICATION record |
| Segregation |
- |
| Frequency |
0.00006 (TOPMed) |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Christian Drouet |
| Database submission license |
Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International |
| Created by |
Christian Drouet |
| Date created |
2020-12-04 15:55:23 +01:00 (CET) |
| Date last edited |
2025-03-21 17:41:40 +01:00 (CET) |

Variant on transcripts
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