Variant #0000887146 (NC_000006.11:g.31324604del, NM_005514.6:c.204del (HLA-B))

Chromosome 6
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.31324604del
DNA change (hg38) -
Published as HLA-B(NM_005514.8):c.204delA (p.E69Rfs*8)
ISCN -
DB-ID HLA-B_000068
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) 0.1492 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2022-11-01 13:01:21 +01:00 (CET)
Date last edited 2024-02-26 20:06:56 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Haplotype     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HLA-B NM_005514.6 -?/. - - c.204del r.(?) p.(Glu69Argfs*8)


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