Variant #0000724989 (NC_000015.9:g.23892102_23892111del, NM_019066.4:c.785_794del (MAGEL2))

Chromosome 15
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.23892102_23892111del
DNA change (hg38) -
Published as MAGEL2(NM_019066.5):c.785_794delCGCCTCCAGC (p.P262Qfs*3)
ISCN -
DB-ID MAGEL2_000188
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_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MAGEL2 NM_019066.4 +?/. - c.785_794del r.(?) p.(Pro262Glnfs*3)


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