Variant #0000618505 (NC_000022.10:g.25603025_25603026dup, NM_004076.3:c.482_483dup (CRYBB3))
Chromosome |
22 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
pathogenic |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.25603025_25603026dup |
DNA change (hg38) |
g.25207058_25207059dup |
Published as |
CRYBB3(NM_004076.4):c.482_483dupAT (p.E162Mfs*?) |
ISCN |
- |
DB-ID |
CRYBB3_000016 |
Variant remarks |
VKGL data sharing initiative Nederland |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
CLASSIFICATION record |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
VKGL-NL_Rotterdam |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Rotterdam |
Date created |
2019-12-04 15:24:38 +01:00 (CET) |
Date last edited |
2020-07-17 11:50:59 +02:00 (CEST) |

Variant on transcripts
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