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) Variant not found in online data sets
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MAGEB5 NM_001271752.1 ?/. - c.357_365del r.(?) p.(Arg120_His122del)