rs6729124

chr2-218519768-C-T

Variant summary

Our verdict is Benign. Variant got -12 ACMG points: 0P and 12B. BP4_Strong BA1

The NM_020935.3(USP37):c.864-9628G>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.0401 in 151,600 control chromosomes in the GnomAD database, including 160 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 0.040 (160 hom., cov: 30)
• Consequence: USP37 NM_020935.3 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.281

Genes affected

USP37 (HGNC:20063): (ubiquitin specific peptidase 37) Enables cysteine-type endopeptidase activity; protein kinase binding activity; and thiol-dependent deubiquitinase. Involved in G1/S transition of mitotic cell cycle; protein deubiquitination; and regulation of DNA replication. Located in nucleus. [provided by Alliance of Genome Resources, Apr 2022]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.91).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.109 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
USP37	NM_020935.3	c.864-9628G>A		intron_variant		ENST00000258399.8

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
USP37	ENST00000258399.8	c.864-9628G>A		intron_variant		1	NM_020935.3	P1

Frequencies

GnomAD3 genomes AF: 0.0401 AC: 6077 AN: 151482 Hom.: 159 Cov.: 30

Gnomad AFR AF: 0.0521

Gnomad AMI AF: 0.0221

Gnomad AMR AF: 0.0225

Gnomad ASJ AF: 0.0318

Gnomad EAS AF: 0.117

Gnomad SAS AF: 0.0442

Gnomad FIN AF: 0.0272

Gnomad MID AF: 0.0380

Gnomad NFE AF: 0.0334

Gnomad OTH AF: 0.0381

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

GnomAD4 genome AF: 0.0401 AC: 6080 AN: 151600 Hom.: 160 Cov.: 30 AF XY: 0.0394 AC XY: 2916 AN XY: 74060

Gnomad4 AFR AF: 0.0520

Gnomad4 AMR AF: 0.0226

Gnomad4 ASJ AF: 0.0318

Gnomad4 EAS AF: 0.117

Gnomad4 SAS AF: 0.0442

Gnomad4 FIN AF: 0.0272

Gnomad4 NFE AF: 0.0334

Gnomad4 OTH AF: 0.0377

Alfa AF: 0.0365 Hom.: 8

Bravo AF: 0.0409

Asia WGS AF: 0.0690 AC: 238 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.91
Cadd	Benign	2.3
Dann	Benign	0.57

Splicing

Name	Calibrated prediction	Score	Prediction
SpliceAI score (max)		0.010		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

Other links and lift over

dbSNP: rs6729124; hg19: chr2-219384491;