ENST00000433582.1:n.56-1759C>A

Variant names:

• chr6-33094896-G-T
• rs2395314
• ENST00000433582.1:n.56-1759C>A

Variant summary

Our verdict is Benign. The variant received -12 ACMG points: 0P and 12B. BP4_Strong BA1

The ENST00000433582.1(HLA-DPA2):​n.56-1759C>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.33 in 152,060 control chromosomes in the GnomAD database, including 9,358 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 0.33 (9358 hom., cov: 32)
• Consequence: HLA-DPA2 ENST00000433582.1 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.0150
• Publications: 19 publications found

Genes affected

HLA-DPA2 (HGNC:4939): (major histocompatibility complex, class II, DP alpha 2 (pseudogene))

ACMG classification

Our verdict: Benign. The variant received -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-1.0).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.548 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: ENST00000433582.1. You can select a different transcript below to see updated ACMG assignments.

RefSeq Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
There are no transcript annotations for this variant.

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	HLA-DPA2	ENST00000433582.1	TSL:6	n.56-1759C>A		intron	N/A

Frequencies

GnomAD3 genomes AF: 0.330 AC: 50070 AN: 151942 Hom.: 9335 Cov.: 32

Gnomad AFR AF: 0.485

Gnomad AMI AF: 0.133

Gnomad AMR AF: 0.256

Gnomad ASJ AF: 0.156

Gnomad EAS AF: 0.564

Gnomad SAS AF: 0.262

Gnomad FIN AF: 0.250

Gnomad MID AF: 0.215

Gnomad NFE AF: 0.263

Gnomad OTH AF: 0.317

We have no GnomAD4 exomes data on this position. Probably position not covered by the project.

GnomAD4 genome AF: 0.330 AC: 50123 AN: 152060 Hom.: 9358 Cov.: 32 AF XY: 0.325 AC XY: 24152 AN XY: 74326

African (AFR) AF: 0.485 AC: 20092 AN: 41462

American (AMR) AF: 0.256 AC: 3911 AN: 15286

Ashkenazi Jewish (ASJ) AF: 0.156 AC: 540 AN: 3472

East Asian (EAS) AF: 0.565 AC: 2919 AN: 5170

South Asian (SAS) AF: 0.260 AC: 1250 AN: 4814

European-Finnish (FIN) AF: 0.250 AC: 2641 AN: 10584

Middle Eastern (MID) AF: 0.214 AC: 63 AN: 294

European-Non Finnish (NFE) AF: 0.263 AC: 17897 AN: 67960

Other (OTH) AF: 0.327 AC: 689 AN: 2108

Alfa AF: 0.285 Hom.: 9858

Bravo AF: 0.334

Asia WGS AF: 0.396 AC: 1376 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-1.0
CADD	Benign	1.7
DANN	Benign	0.54
PhyloP100		-0.015

Splicing

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

Other links and lift over

dbSNP: rs2395314; hg19: chr6-33062673;