rs1057190

chr12-43754456-T-Cchr12-43754456-T-G

Variant summary

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

The NM_031292.5(PUS7L):c.790A>G(p.Lys264Glu) variant causes a missense change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.132 in 1,613,506 control chromosomes in the GnomAD database, including 20,851 homozygotes. In-silico tool predicts a benign outcome for this variant. 14/20 in silico tools predict a benign outcome for this variant. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar. Another nucleotide change resulting in same amino acid change has been previously reported as Likely benignin UniProt.

• Frequency:
  • Genomes: 𝑓 0.23 (6452 hom., cov: 33)
  • Exomes 𝑓: 0.12 (14399 hom.)
• Consequence: PUS7L NM_031292.5 missense
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 2.67

Genes affected

PUS7L (HGNC:25276): (pseudouridine synthase 7 like) Predicted to enable pseudouridine synthase activity. Predicted to be involved in pseudouridine synthesis. Predicted to be active 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 (MetaRNN=6.487023E-5).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.508 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
PUS7L	NM_031292.5	c.790A>G	p.Lys264Glu	missense_variant	2/9	ENST00000344862.10

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
PUS7L	ENST00000344862.10	c.790A>G	p.Lys264Glu	missense_variant	2/9	1	NM_031292.5	P1

Frequencies

GnomAD3 genomes AF: 0.231 AC: 35045 AN: 152020 Hom.: 6425 Cov.: 33

Gnomad AFR AF: 0.513

Gnomad AMI AF: 0.0923

Gnomad AMR AF: 0.175

Gnomad ASJ AF: 0.186

Gnomad EAS AF: 0.159

Gnomad SAS AF: 0.142

Gnomad FIN AF: 0.0955

Gnomad MID AF: 0.199

Gnomad NFE AF: 0.109

Gnomad OTH AF: 0.223

GnomAD3 exomes AF: 0.153 AC: 38353 AN: 251256 Hom.: 4261 AF XY: 0.144 AC XY: 19527 AN XY: 135822

Gnomad AFR exome AF: 0.525

Gnomad AMR exome AF: 0.148

Gnomad ASJ exome AF: 0.191

Gnomad EAS exome AF: 0.174

Gnomad SAS exome AF: 0.139

Gnomad FIN exome AF: 0.0971

Gnomad NFE exome AF: 0.109

Gnomad OTH exome AF: 0.140

GnomAD4 exome AF: 0.122 AC: 178538 AN: 1461368 Hom.: 14399 Cov.: 33 AF XY: 0.121 AC XY: 88133 AN XY: 726984

Gnomad4 AFR exome AF: 0.526

Gnomad4 AMR exome AF: 0.153

Gnomad4 ASJ exome AF: 0.193

Gnomad4 EAS exome AF: 0.145

Gnomad4 SAS exome AF: 0.134

Gnomad4 FIN exome AF: 0.101

Gnomad4 NFE exome AF: 0.105

Gnomad4 OTH exome AF: 0.149

GnomAD4 genome AF: 0.231 AC: 35110 AN: 152138 Hom.: 6452 Cov.: 33 AF XY: 0.227 AC XY: 16871 AN XY: 74412

Gnomad4 AFR AF: 0.513

Gnomad4 AMR AF: 0.174

Gnomad4 ASJ AF: 0.186

Gnomad4 EAS AF: 0.159

Gnomad4 SAS AF: 0.141

Gnomad4 FIN AF: 0.0955

Gnomad4 NFE AF: 0.109

Gnomad4 OTH AF: 0.220

Alfa AF: 0.137 Hom.: 4428

Bravo AF: 0.249

TwinsUK AF: 0.0968 AC: 359

ALSPAC AF: 0.106 AC: 408

ESP6500AA AF: 0.513 AC: 2262

ESP6500EA AF: 0.115 AC: 990

ExAC AF: 0.158 AC: 19219

Asia WGS AF: 0.185 AC: 642 AN: 3478

EpiCase AF: 0.113

EpiControl AF: 0.112

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
AlphaMissense	Benign	0.053
BayesDel_addAF	Benign	-0.76	T
BayesDel_noAF	Benign	-0.71
Cadd	Benign	11
Dann	Benign	0.51
DEOGEN2	Benign	0.000031	T;T;T
Eigen	Benign	-1.1
Eigen_PC	Benign	-0.87
FATHMM_MKL	Benign	0.0031	N
MetaRNN	Benign	0.000065	T;T;T
MetaSVM	Benign	-0.95	T
MutationAssessor	Benign	-2.2	N;N;N
MutationTaster	Benign	1.0	P;P;P;P
PrimateAI	Benign	0.37	T
PROVEAN	Benign	0.41	N;N;N
REVEL	Benign	0.097
Sift	Benign	1.0	T;T;T
Sift4G	Benign	1.0	T;T;T
Polyphen		0.0	B;B;B
Vest4		0.013
MPC		0.039
ClinPred		0.0069	T
GERP RS		5.3
Varity_R		0.072
gMVP		0.15

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

Other links and lift over

dbSNP: rs1057190; hg19: chr12-44148259; COSMIC: COSV61262008; COSMIC: COSV61262008;