Variant #0000575428 (NC_000023.10:g.26235775_26235783del, MAGEB5(NM_001271752.1):c.357_365del)
Chromosome |
X |
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.26235775_26235783del |
DNA change (hg38) |
g.26217658_26217666del |
Published as |
MAGEB5(NM_001271752.1):c.357_365del (p.(Arg120_His122del)) |
ISCN |
- |
DB-ID |
MAGEB5_000004 |
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_Leiden |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Leiden |

Variant on transcripts
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