Variant #0000565175 (NC_000018.9:g.57122133dup, NM_133459.3:c.604dup (CCBE1))
Chromosome |
18 |
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.57122133dup |
DNA change (hg38) |
g.59454901dup |
Published as |
CCBE1(NM_133459.4):c.604dupT (p.C202Lfs*27) |
ISCN |
- |
DB-ID |
CCBE1_000034 |
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_VUmc |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_VUmc |
Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
Date last edited |
2020-07-14 19:13:54 +02:00 (CEST) |

Variant on transcripts
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