Variant #0000576754 (NC_000023.10:g.54842023G>A, NM_014599.4:c.1729G>A (MAGED2))

Chromosome X
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.54842023G>A
DNA change (hg38) g.54815590G>A
Published as MAGED2(NM_014599.5):c.1729G>A (p.(Ala577Thr)), MAGED2(NM_177433.2):c.1729G>A (p.A577T)
ISCN -
DB-ID MAGED2_000033 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) 0.0004 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MAGED2 NM_014599.4 -?/. - c.1729G>A r.(?) p.(Ala577Thr)


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