rs4813945

Variant names:

• chr20-1156012-G-A
• rs4813945
• NM_006814.5:c.552-7118G>A

Your query was ambiguous. Multiple possible variants found:

• chr20-1156012-G-A
• chr20-1156012-G-C
• chr20-1156012-G-T

Variant summary

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

The NM_006814.5(PSMF1):​c.552-7118G>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.439 in 152,022 control chromosomes in the GnomAD database, including 15,194 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 0.44 (15194 hom., cov: 32)
• Consequence: PSMF1 NM_006814.5 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.497
• Publications: 2 publications found

Genes affected

PSMF1 (HGNC:9571): (proteasome inhibitor subunit 1) The 26S proteasome is a multicatalytic proteinase complex with a highly ordered structure composed of 2 complexes, a 20S core and a 19S regulator. The 20S core is composed of 4 rings of 28 non-identical subunits; 2 rings are composed of 7 alpha subunits and 2 rings are composed of 7 beta subunits. The 19S regulator is composed of a base, which contains 6 ATPase subunits and 2 non-ATPase subunits, and a lid, which contains up to 10 non-ATPase subunits. Proteasomes are distributed throughout eukaryotic cells at a high concentration and cleave peptides in an ATP/ubiquitin-dependent process in a non-lysosomal pathway. An essential function of a modified proteasome, the immunoproteasome, is the processing of class I MHC peptides. This gene encodes a protein that inhibits the activation of the proteasome by the 11S and 19S regulators. Alternative transcript variants have been identified for this gene. [provided by RefSeq, Jul 2008]

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.93).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.686 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
PSMF1	NM_006814.5	c.552-7118G>A		intron_variant	Intron 4 of 6	ENST00000335877.11	NP_006805.2

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
PSMF1	ENST00000335877.11	c.552-7118G>A		intron_variant	Intron 4 of 6	1	NM_006814.5	ENSP00000338039.6

Frequencies

GnomAD3 genomes AF: 0.439 AC: 66716 AN: 151904 Hom.: 15169 Cov.: 32

Gnomad AFR AF: 0.519

Gnomad AMI AF: 0.268

Gnomad AMR AF: 0.417

Gnomad ASJ AF: 0.424

Gnomad EAS AF: 0.705

Gnomad SAS AF: 0.463

Gnomad FIN AF: 0.392

Gnomad MID AF: 0.481

Gnomad NFE AF: 0.384

Gnomad OTH AF: 0.442

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

GnomAD4 genome AF: 0.439 AC: 66784 AN: 152022 Hom.: 15194 Cov.: 32 AF XY: 0.442 AC XY: 32840 AN XY: 74292

African (AFR) AF: 0.520 AC: 21533 AN: 41448

American (AMR) AF: 0.417 AC: 6382 AN: 15294

Ashkenazi Jewish (ASJ) AF: 0.424 AC: 1471 AN: 3466

East Asian (EAS) AF: 0.705 AC: 3647 AN: 5174

South Asian (SAS) AF: 0.461 AC: 2227 AN: 4826

European-Finnish (FIN) AF: 0.392 AC: 4139 AN: 10552

Middle Eastern (MID) AF: 0.483 AC: 142 AN: 294

European-Non Finnish (NFE) AF: 0.384 AC: 26071 AN: 67952

Other (OTH) AF: 0.441 AC: 929 AN: 2108

Alfa AF: 0.275 Hom.: 691

Bravo AF: 0.442

Asia WGS AF: 0.546 AC: 1898 AN: 3476

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.93
CADD	Benign	5.2
DANN	Benign	0.76
PhyloP100		0.50
Mutation Taster		=100/0	polymorphism (auto)

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

Other links and lift over

dbSNP: rs4813945; hg19: chr20-1136656;