Variant #0000727870 (NC_000021.8:g.11021220dup, NC_000021.8(NM_182482.2):c.*1176-5dup (BAGE2))

Chromosome 21
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.11021220dup
DNA change (hg38) -
Published as BAGE2(NM_182482.2):c.*1176-5dupT, BAGE3(NM_182481.1):c.*1176-5dupT, BAGE4(NM_181704.1):c.*1309-5dupT
ISCN -
DB-ID BAGE2_000001
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BAGE2 NM_182482.2 -?/. - c.*1176-5dup r.spl? p.?


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