Overview

Variant ID 25919
Entrez Gene ID 57824
Gene HMHB1 (GeneCards)
Location hg19 5:143303537-143303537
hg38 5:143923972-143923972
Disease Asymptomatic
Method Single cell Sequencing Cell cloning
Mutation(HGVS format) NC_000005.9:g.143303537 T>A (Genome Assembly: GRCh37)

Other information

Exon or Intron NA
Position in protein NA
Amino acid changes in protein NA > NA
Position in cDNA NA
Changes in cDNA NA > NA
mRNA accession NA
mRNA length NA
Reference length 180915260

Annotations and predictions

MAF in gnomAD genome (version 2.0.1) 0
EIGEN score 0.4737
CADD Raw score (version 1.3) 1.309035 (Deleterious)
FATHMM raw prediction score 0.18201 (Tolerated)
Deleterious probability by DeFine 0.5176 (Deleterious)
Entrez Gene ID 57824 (NCBI Gene)
Official Gene Symbol HMHB1 (GeneCards)
Number of variants in HMHB1 in this database 7 (view all the variants)
Full name histocompatibility minor HB-1
Band 5q31.3
Other IDs Vega: OTTHUMG00000163173
OMIM: 609961
HGNC: HGNC:29677
Ensembl: ENSG00000158497
Other names HB-1, HB-1Y, HLA-HB1
Summary This gene encodes one of the minor histocompatibility antigens, which play an important role in the induction of cytotoxic T lymphocyte (CTL) reactivity against leukemia after human histocompatibility leukocyte antigen (HLA)-identical allogeneic bone marrow transplantation (BMT). This gene is only expressed in B cell acute lymphoblastic leukemia cells and Epstein-Barr virus-transformed B cells. The translation of this mRNA initiates at a non-AUG (CUG) codon. [provided by RefSeq, Jul 2008]

Individual #1

Individual ID 29217587.02 (view all the variants in this individual)
Pubmed ID 29217587
Whose mosaic mutation Normal  
Phenotype 1  
Disease Asymptomatic
OMIM ID