Variant #0000615187 (NC_000015.9:g.23891934_23891954del, NM_019066.4:c.960_980del (MAGEL2))

Chromosome 15
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.23891934_23891954del
DNA change (hg38) g.23646787_23646807del
Published as MAGEL2(NM_019066.4):c.960_980del (p.(Pro321_Ala327del)), MAGEL2(NM_019066.4):c.960_980delCCCACCTGCACAGCCGATGGC (p.P321_A327del), MAGEL2(NM_019066....)
ISCN -
DB-ID MAGEL2_000054 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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-04 15:24:38 +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.960_980del r.(?) p.(Pro321_Ala327del)


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