Variant #0000977193 (NC_000006.11:g.32552138G>C, NM_002124.3:c.118C>G (HLA-DRB1))

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.32552138G>C
DNA change (hg38) -
Published as HLA-DRB1(NM_002124.4):c.118C>G (p.(Pro40Ala))
ISCN -
DB-ID HLA-DRB1_000070
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) 0.00615 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     
HLA-DRB1 NM_002124.3 -?/. - c.118C>G r.(?) p.(Pro40Ala)


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