Variant #0000094338 (NC_000023.10:g.68049516_68049525delinsTTGGGCGCCC, NM_004429.4:c.-104_-95delinsTTGGGCGCCC (EFNB1))
| Chromosome |
X |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
NA |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.68049516_68049525delinsTTGGGCGCCC |
| DNA change (hg38) |
g.68829673_68829682delinsTTGGGCGCCC |
| Published as |
c.[-104A>T;-95T>C] |
| ISCN |
- |
| DB-ID |
EFNB1_000046 |
| Variant remarks |
luciferase assay shows raised protein translation (1.6) |
| Reference |
PubMed: Twigg 2013, Journal: Twigg 2013 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
In vitro (cloned) |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Johan den Dunnen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2016-04-08 19:03:59 +02:00 (CEST) |
| Date last edited |
2020-07-14 21:50:58 +02:00 (CEST) |

Variant on transcripts
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