NM_005800.5:c.1592T>C

Variant names:

• chr13-30657669-T-C
• rs7984952
• NM_005800.5:c.1592T>C

Variant summary

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

The NM_005800.5(USPL1):​c.1592T>C​(p.Leu531Ser) variant causes a missense change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.419 in 1,613,916 control chromosomes in the GnomAD database, including 149,975 homozygotes. In-silico tool predicts a benign outcome for this variant. 15/21 in silico tools predict a benign outcome for this variant. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar.

• Frequency:
  • Genomes: 𝑓 0.50 (21740 hom., cov: 32)
  • Exomes 𝑓: 0.41 (128235 hom.)
• Consequence: USPL1 NM_005800.5 missense
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.508
• Publications: 47 publications found

Genes affected

USPL1 (HGNC:20294): (ubiquitin specific peptidase like 1) Enables SUMO binding activity and SUMO-specific isopeptidase activity. Involved in several processes, including Cajal body organization; protein desumoylation; and snRNA transcription. Located in Cajal body. [provided by Alliance of Genome Resources, Apr 2022]

ACMG classification

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

• BP4: Computational evidence support a benign effect (MetaRNN=1.2610923E-6).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.775 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_005800.5. You can select a different transcript below to see updated ACMG assignments.

RefSeq Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	USPL1	NM_005800.5	MANE Select	c.1592T>C	p.Leu531Ser	missense	Exon 9 of 9	NP_005791.3
	USPL1	NM_001321532.2		c.1049T>C	p.Leu350Ser	missense	Exon 8 of 8	NP_001308461.1
	USPL1	NM_001321533.2		c.605T>C	p.Leu202Ser	missense	Exon 7 of 7	NP_001308462.1

Ensembl Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	USPL1	ENST00000255304.9	TSL:1 MANE Select	c.1592T>C	p.Leu531Ser	missense	Exon 9 of 9	ENSP00000255304.4
	USPL1	ENST00000614860.1	TSL:1	c.605T>C	p.Leu202Ser	missense	Exon 7 of 7	ENSP00000480656.1

Frequencies

GnomAD3 genomes AF: 0.501 AC: 76073 AN: 151956 Hom.: 21693 Cov.: 32

Gnomad AFR AF: 0.781

Gnomad AMI AF: 0.409

Gnomad AMR AF: 0.438

Gnomad ASJ AF: 0.418

Gnomad EAS AF: 0.164

Gnomad SAS AF: 0.467

Gnomad FIN AF: 0.301

Gnomad MID AF: 0.642

Gnomad NFE AF: 0.408

Gnomad OTH AF: 0.498

GnomAD2 exomes AF: 0.411 AC: 103217 AN: 251312 AF XY: 0.414

Gnomad AFR exome AF: 0.787

Gnomad AMR exome AF: 0.346

Gnomad ASJ exome AF: 0.432

Gnomad EAS exome AF: 0.166

Gnomad FIN exome AF: 0.309

Gnomad NFE exome AF: 0.412

Gnomad OTH exome AF: 0.440

GnomAD4 exome AF: 0.410 AC: 599837 AN: 1461842 Hom.: 128235 Cov.: 59 AF XY: 0.413 AC XY: 300157 AN XY: 727230

African (AFR) AF: 0.798 AC: 26728 AN: 33478

American (AMR) AF: 0.360 AC: 16096 AN: 44722

Ashkenazi Jewish (ASJ) AF: 0.425 AC: 11097 AN: 26134

East Asian (EAS) AF: 0.170 AC: 6745 AN: 39694

South Asian (SAS) AF: 0.483 AC: 41670 AN: 86256

European-Finnish (FIN) AF: 0.306 AC: 16325 AN: 53416

Middle Eastern (MID) AF: 0.569 AC: 3283 AN: 5768

European-Non Finnish (NFE) AF: 0.406 AC: 451672 AN: 1111980

Other (OTH) AF: 0.434 AC: 26221 AN: 60394

GnomAD4 genome AF: 0.501 AC: 76167 AN: 152074 Hom.: 21740 Cov.: 32 AF XY: 0.493 AC XY: 36622 AN XY: 74334

African (AFR) AF: 0.782 AC: 32438 AN: 41488

American (AMR) AF: 0.438 AC: 6692 AN: 15290

Ashkenazi Jewish (ASJ) AF: 0.418 AC: 1451 AN: 3470

East Asian (EAS) AF: 0.164 AC: 852 AN: 5180

South Asian (SAS) AF: 0.467 AC: 2245 AN: 4810

European-Finnish (FIN) AF: 0.301 AC: 3183 AN: 10568

Middle Eastern (MID) AF: 0.650 AC: 191 AN: 294

European-Non Finnish (NFE) AF: 0.408 AC: 27697 AN: 67954

Other (OTH) AF: 0.496 AC: 1045 AN: 2108

Alfa AF: 0.450 Hom.: 57087

Bravo AF: 0.523

TwinsUK AF: 0.420 AC: 1556

ALSPAC AF: 0.416 AC: 1605

ESP6500AA AF: 0.774 AC: 3409

ESP6500EA AF: 0.411 AC: 3537

ExAC AF: 0.420 AC: 50951

Asia WGS AF: 0.370 AC: 1286 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
AlphaMissense	Benign	0.051
BayesDel_addAF	Benign	-0.84	T
BayesDel_noAF	Benign	-0.84
CADD	Benign	12
DANN	Benign	0.95
DEOGEN2	Benign	0.00055	T
Eigen	Benign	-1.2
Eigen_PC	Benign	-1.1
FATHMM_MKL	Benign	0.0050	N
LIST_S2	Benign	0.13	T
MetaRNN	Benign	0.0000013	T
MetaSVM	Benign	-1.0	T
MutationAssessor	Benign	-0.69	N
PhyloP100		0.51
PrimateAI	Benign	0.25	T
PROVEAN	Benign	1.7	N
REVEL	Benign	0.054
Sift	Benign	0.64	T
Sift4G	Benign	0.29	T
Polyphen		0.0	B
Vest4		0.018
MPC		0.061
ClinPred		0.0038	T
GERP RS		3.5
Varity_R		0.016
gMVP		0.18
Mutation Taster		=99/1	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: rs7984952; hg19: chr13-31231806; COSMIC: COSV54998611;