Variant #0000289072 (NC_000006.11:g.31324046C>T, NM_005514.6:c.517G>A (HLA-B))

Chromosome 6
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.31324046C>T
DNA change (hg38) g.31356269C>T
Published as HLA-B(NM_005514.7):c.517G>A (p.A173T)
ISCN -
DB-ID HLA-B_000061
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +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.517G>A r.(?) p.(Ala173Thr)


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