Menu
GeneBe

rs7750458

Variant summary

Our verdict is Benign. Variant got -12 ACMG points: 0P and 12B. BP4_StrongBA1

The NM_002121.6(HLA-DPB1):c.100+1780G>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.0974 in 152,202 control chromosomes in the GnomAD database, including 790 homozygotes. In-silico tool predicts a benign outcome for this variant. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar.

Frequency

Genomes: 𝑓 0.097 ( 790 hom., cov: 31)

Consequence

HLA-DPB1
NM_002121.6 intron

Scores

2

Clinical Significance

Not reported in ClinVar

Conservation

PhyloP100: 0.280
Variant links:
Genes affected
HLA-DPB1 (HGNC:4940): (major histocompatibility complex, class II, DP beta 1) HLA-DPB belongs to the HLA class II beta chain paralogues. This class II molecule is a heterodimer consisting of an alpha (DPA) and a beta chain (DPB), both anchored in the membrane. It plays a central role in the immune system by presenting peptides derived from extracellular proteins. Class II molecules are expressed in antigen presenting cells (APC: B lymphocytes, dendritic cells, macrophages). The beta chain is approximately 26-28 kDa and its gene contains 6 exons. Exon one encodes the leader peptide, exons 2 and 3 encode the two extracellular domains, exon 4 encodes the transmembrane domain and exon 5 encodes the cytoplasmic tail. Within the DP molecule both the alpha chain and the beta chain contain the polymorphisms specifying the peptide binding specificities, resulting in up to 4 different molecules. [provided by RefSeq, Jul 2008]
HLA-DPA1 (HGNC:4938): (major histocompatibility complex, class II, DP alpha 1) HLA-DPA1 belongs to the HLA class II alpha chain paralogues. This class II molecule is a heterodimer consisting of an alpha (DPA) and a beta (DPB) chain, both anchored in the membrane. It plays a central role in the immune system by presenting peptides derived from extracellular proteins. Class II molecules are expressed in antigen presenting cells (APC: B lymphocytes, dendritic cells, macrophages). The alpha chain is approximately 33-35 kDa and its gene contains 5 exons. Exon one encodes the leader peptide, exons 2 and 3 encode the two extracellular domains, exon 4 encodes the transmembrane domain and the cytoplasmic tail. Within the DP molecule both the alpha chain and the beta chain contain the polymorphisms specifying the peptide binding specificities, resulting in up to 4 different molecules. [provided by RefSeq, Jul 2008]

Genome browser will be placed here

ACMG classification

Classification made for transcript

Verdict is Benign. Variant got -12 ACMG points.

BP4
Computational evidence support a benign effect (BayesDel_noAF=-0.89).
BA1
GnomAd4 highest subpopulation (SAS) allele frequency at 95% confidence interval = 0.14 is higher than 0.05.

Transcripts

RefSeq

Gene Transcript HGVSc HGVSp Effect #exon/exons MANE UniProt
HLA-DPB1NM_002121.6 linkuse as main transcriptc.100+1780G>A intron_variant ENST00000418931.7
HLA-DPA1NM_001242525.2 linkuse as main transcriptc.-24+2759C>T intron_variant
HLA-DPA1NM_001242524.2 linkuse as main transcriptc.-100+2759C>T intron_variant

Ensembl

Gene Transcript HGVSc HGVSp Effect #exon/exons TSL MANE Appris UniProt
HLA-DPB1ENST00000418931.7 linkuse as main transcriptc.100+1780G>A intron_variant NM_002121.6 P1

Frequencies

GnomAD3 genomes
AF:
0.0974
AC:
14820
AN:
152084
Hom.:
790
Cov.:
31
show subpopulations
Gnomad AFR
AF:
0.122
Gnomad AMI
AF:
0.0746
Gnomad AMR
AF:
0.136
Gnomad ASJ
AF:
0.171
Gnomad EAS
AF:
0.0880
Gnomad SAS
AF:
0.150
Gnomad FIN
AF:
0.0284
Gnomad MID
AF:
0.184
Gnomad NFE
AF:
0.0765
Gnomad OTH
AF:
0.125
We have no GnomAD4 exomes data on this position. Probably position not covered by the project.
GnomAD4 genome
AF:
0.0974
AC:
14827
AN:
152202
Hom.:
790
Cov.:
31
AF XY:
0.0976
AC XY:
7262
AN XY:
74440
show subpopulations
Gnomad4 AFR
AF:
0.122
Gnomad4 AMR
AF:
0.136
Gnomad4 ASJ
AF:
0.171
Gnomad4 EAS
AF:
0.0880
Gnomad4 SAS
AF:
0.149
Gnomad4 FIN
AF:
0.0284
Gnomad4 NFE
AF:
0.0765
Gnomad4 OTH
AF:
0.125
Alfa
AF:
0.0858
Hom.:
305
Bravo
AF:
0.105
Asia WGS
AF:
0.124
AC:
432
AN:
3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name
Calibrated prediction
Score
Prediction
BayesDel_noAF
Benign
-0.89
Cadd
Benign
4.8
Dann
Benign
0.49

Splicing

Name
Calibrated prediction
Score
Prediction
SpliceAI score (max)
0.0
Details are displayed if max score is > 0.2

Find out detailed SpliceAI scores and Pangolin per-transcript scores at spliceailookup.broadinstitute.org

Publications

LitVar

Below is the list of publications found by LitVar. It may be empty.

Other links and lift over

dbSNP: rs7750458; hg19: chr6-33045698; API