Variant #0000170190 (NC_000001.10:g.26140389C>T, NM_020451.2:c.1405C>T (SEPN1))
| Chromosome |
1 |
| Allele |
Unknown |
| Affects function (as reported) |
Effect unknown |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
NA |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.26140389C>T |
| DNA change (hg38) |
g.25813898C>T |
| Published as |
- |
| ISCN |
- |
| DB-ID |
SEPN1_000026 See all 11 reported entries |
| Variant remarks |
cloned in pUGA2SECIS; Sec in vitro insertion efficiency unaffected |
| Reference |
PubMed: Maiti 2009 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
In vitro (cloned) |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
1.0E-5 View details |
| Owner |
Johan den Dunnen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2009-02-21 17:28:23 +01:00 (CET) |
| Date last edited |
2020-07-14 21:50:58 +02:00 (CEST) |

Variant on transcripts
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