Variant #0000528516 (NC_000006.11:g.32497962_32497963insGC, NM_002125.3:c.39_40insGC (HLA-DRB5))

Chromosome 6
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.32497962_32497963insGC
DNA change (hg38) g.32530185_32530186insGC
Published as HLA-DRB5(NM_002125.4):c.39_40insGC (p.K14Afs*3)
ISCN -
DB-ID HLA-DRB5_000028
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) 0.11473 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-19 09:42:14 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HLA-DRB5 NM_002125.3 -/. - c.39_40insGC r.(?) p.(Lys14AlafsTer3)


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