Variant #0000656915 (NC_000011.9:g.75277974C>A, NM_001207014.1:c.580C>A (SERPINH1))
| Chromosome |
11 |
| Allele |
Unknown |
| Affects function (as reported) |
Effect unknown |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
VUS |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.75277974C>A |
| DNA change (hg38) |
g.75566929C>A |
| Published as |
SERPINH1(NM_001207014.1):c.580C>A (p.(Arg194Ser)) |
| ISCN |
- |
| DB-ID |
SERPINH1_000114 |
| 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) |
0.00075 View details |
| Owner |
VKGL-NL_Leiden |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Leiden |
| Date created |
2020-03-23 16:13:27 +01:00 (CET) |
| Date last edited |
2021-05-12 09:50:17 +02:00 (CEST) |

Variant on transcripts
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