Variant #0000927614 (NC_000015.9:g.23891887G>T, NM_019066.4:c.1003C>A (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.23891887G>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID MAGEL2_000242
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs1054820321
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2023-05-14 14:06:01 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MAGEL2 NM_019066.4 ?/. - c.1003C>A r.(?) p.(Pro335Thr)


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