Variant #0000299416 (NC_000011.9:g.75277757C>G, NM_001207014.1:c.363C>G (SERPINH1))
| Chromosome |
11 |
| Allele |
Unknown |
| Affects function (as reported) |
Does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.75277757C>G |
| DNA change (hg38) |
g.75566712C>G |
| Published as |
SERPINH1(NM_001207014.3):c.363C>G (p.S121=), SERPINH1(NM_001235.5):c.363C>G (p.S121=) |
| ISCN |
- |
| DB-ID |
SERPINH1_000003 See all 3 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) |
0.34597 View details |
| Owner |
VKGL-NL_VUmc |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_VUmc |
| Date created |
2018-01-15 20:58:59 +01:00 (CET) |
| Date last edited |
2023-01-11 15:44:22 +01:00 (CET) |

Variant on transcripts
|