Variant #0000806600 (NC_000015.9:g.23892386_23892415del, NM_019066.4:c.509_538del (MAGEL2))

Chromosome 15
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.23892386_23892415del
DNA change (hg38) -
Published as MAGEL2(NM_019066.4):c.509_538del (p.(Ala170_Met179del)), MAGEL2(NM_019066.5):c.509_538delCCCATCCTCCTCCTCCGGGGACCCCGATGG (p.A170_M179del)
ISCN -
DB-ID MAGEL2_000120 See all 3 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) Retrieve
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2021-09-17 14:40:49 +02:00 (CEST)
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.509_538del r.(?) p.(Ala170_Met179del)


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