Variant #0000889989 (NC_000011.9:g.57365748C>T, NM_000062.2:c.5C>T (SERPING1))
Chromosome |
11 |
Allele |
Unknown |
Affects function (as reported) |
Effect unknown |
Affects function (by curator) |
Probably does not affect function |
Classification method |
- |
Clinical classification |
VUS |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.57365748C>T |
DNA change (hg38) |
- |
Published as |
SERPING1(NM_000062.2):c.5C>T (p.A2V), SERPING1(NM_000062.3):c.5C>T (p.A2V) |
ISCN |
- |
DB-ID |
SERPING1_000002 See all 6 reported entries |
Variant remarks |
VKGL data sharing initiative Nederland |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
CLASSIFICATION record |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
0.00128 View details |
Owner |
VKGL-NL_VUmc |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_VUmc |
Date created |
2022-11-01 13:01:21 +01:00 (CET) |
Date last edited |
2023-12-08 11:02:19 +01:00 (CET) |

Variant on transcripts
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