Variant #0000371837 (NC_000014.8:g.35181265G>A, NM_138638.4:c.*806C>T (CFL2))
| Chromosome |
14 |
| 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.35181265G>A |
| DNA change (hg38) |
g.34712059G>A |
| Published as |
- |
| ISCN |
- |
| DB-ID |
CFL2_000006 |
| Variant remarks |
- |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
rs1059318 |
| Origin |
Germline |
| Segregation |
- |
| Frequency |
0.23 |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Ivo F.A.C. Fokkema |
| Database submission license |
Creative Commons Attribution-ShareAlike 4.0 International |
| Created by |
Ivo F.A.C. Fokkema |
| Date created |
2009-10-17 20:05:27 +02:00 (CEST) |
| Date last edited |
2012-11-02 20:40:42 +01:00 (CET) |

Variant on transcripts
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