Variant #0000371841 (NC_000014.8:g.35182668C>T, NM_138638.4:c.103G>A (CFL2))
| Chromosome |
14 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
NA |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.35182668C>T |
| DNA change (hg38) |
g.34713462C>T |
| Published as |
- |
| ISCN |
- |
| DB-ID |
CFL2_000001 See all 3 reported entries |
| Variant remarks |
pcDNA-DEST cloned; C2C12 normal expression, bacterial expression reduced stability and/or solubility, probable protein misfolding |
| Reference |
PubMed: Agrawal 2007, OMIM:var0001 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
In vitro (cloned) |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Alan Beggs |
| Database submission license |
No license selected |
| Created by |
Alan Beggs |
| Date created |
2009-10-17 20:05:27 +02:00 (CEST) |
| Date last edited |
2020-07-14 21:50:58 +02:00 (CEST) |

Variant on transcripts
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