Variant #0000333526 (NC_000023.10:g.26157163G>A, MAGEB18(NM_173699.3):c.61G>A)

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.26157163G>A
DNA change (hg38) g.26139046G>A
Published as MAGEB18(NM_173699.3):c.61G>A (p.(Glu21Lys))
ISCN -
DB-ID MAGEB18_000001
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) 6.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MAGEB18 NM_173699.3 ?/. - c.61G>A r.(?) p.(Glu21Lys)