Variant #0000981116 (NC_000015.9:g.23892577G>C, NM_019066.4:c.313C>G (MAGEL2))

Chromosome 15
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.23892577G>C
DNA change (hg38) -
Published as MAGEL2(NM_019066.4):c.313C>G (p.P105A), MAGEL2(NM_019066.5):c.313C>G (p.(Pro105Ala))
ISCN -
DB-ID MAGEL2_000150 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) 1.0E-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
Date created 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MAGEL2 NM_019066.4 ?/. - c.313C>G r.(?) p.(Pro105Ala)


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