Variant #0000371833 (NC_000014.8:g.35184050dup, NM_138638.4:c.-297dup (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.35184050dup |
DNA change (hg38) |
g.34714844dup |
Published as |
- |
ISCN |
- |
DB-ID |
CFL2_000003 |
Variant remarks |
- |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
rs17523478 |
Origin |
Germline |
Segregation |
- |
Frequency |
0.16-0.21 |
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 |
2020-07-05 14:04:11 +02:00 (CEST) |

Variant on transcripts
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