Variant #0000302048 (NC_000011.9:g.57365723T>C, NM_000062.2:c.-21T>C (SERPING1))
| Chromosome |
11 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably does not affect function |
| Affects function (by curator) |
Probably does not affect function |
| Classification method |
ACMG |
| Clinical classification |
likely benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.57365723T>C |
| DNA change (hg38) |
g.57598250T>C |
| Published as |
SERPING1(NM_000062.2):c.-21T>C |
| ISCN |
- |
| DB-ID |
SERPING1_000001 See all 3 reported entries |
| Variant remarks |
VKGL data sharing initiative Nederland |
| Reference |
Journal: Duponchel 2006 Journal: Ponard 2019 |
| ClinVar ID |
ClinVar-SCV000372547.3 |
| dbSNP ID |
rs28362944 |
| Origin |
CLASSIFICATION record |
| Segregation |
no |
| Frequency |
0.029081 (GnomAD_exome); 0.030270 (TOPMed) |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0.02893 View details |
| Owner |
VKGL-NL_Utrecht |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Utrecht |
| Date created |
2018-01-15 20:58:59 +01:00 (CET) |
| Date last edited |
2023-07-07 10:10:56 +02:00 (CEST) |

Variant on transcripts
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