Variant #0000618957 (NC_000023.10:g.119694356_119694364del, NM_003588.3:c.194_202del (CUL4B))
Chromosome |
X |
Allele |
Unknown |
Affects function (as reported) |
Does not affect function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
benign |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.119694356_119694364del |
DNA change (hg38) |
g.120560501_120560509del |
Published as |
CUL4B(NM_001079872.1):c.140_148del (p.(Ser47_Ser49del)), CUL4B(NM_003588.3):c.194_202delGCAGCAGTA (p.S65_S67del) |
ISCN |
- |
DB-ID |
CUL4B_000071 See all 2 reported entries |
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 |
N/A |

Variant on transcripts
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