NM_015340.4:c.1053T>C

Variant names:

• chr3-45485726-T-C
• rs7610357
• NM_015340.4:c.1053T>C

Variant summary

Our verdict is Benign. Variant got -21 ACMG points: 0P and 21B. BP4_Strong BP6_Very_Strong BP7 BA1

The NM_015340.4(LARS2):​c.1053T>C​(p.Leu351Leu) variant causes a synonymous change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.922 in 1,610,528 control chromosomes in the GnomAD database, including 695,764 homozygotes. In-silico tool predicts a benign outcome for this variant. Variant has been reported in ClinVar as Benign (★★).

• Frequency:
  • Genomes: 𝑓 0.80 (52820 hom., cov: 32)
  • Exomes 𝑓: 0.94 (642944 hom.)
• Consequence: LARS2 NM_015340.4 synonymous
• Clinical Significance: Benign criteria provided, multiple submitters, no conflicts B:8
• Conservation: PhyloP100: -0.0250

Genes affected

LARS2 (HGNC:17095): (leucyl-tRNA synthetase 2, mitochondrial) This gene encodes a class 1 aminoacyl-tRNA synthetase, mitochondrial leucyl-tRNA synthetase. Each of the twenty aminoacyl-tRNA synthetases catalyzes the aminoacylation of a specific tRNA or tRNA isoaccepting family with the cognate amino acid. [provided by RefSeq, Jul 2008]

LARS2-AS1 (HGNC:40796): (LARS2 antisense RNA 1)

ACMG classification

Verdict is Benign. Variant got -21 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.52).
• BP6: Variant 3-45485726-T-C is Benign according to our data. Variant chr3-45485726-T-C is described in ClinVar as [Benign]. Clinvar id is 226691.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars.
• BP7: Synonymous conserved (PhyloP=-0.025 with no splicing effect.
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.953 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
LARS2	NM_015340.4	c.1053T>C	p.Leu351Leu	synonymous_variant	Exon 11 of 22	ENST00000645846.2	NP_056155.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
LARS2	ENST00000645846.2	c.1053T>C	p.Leu351Leu	synonymous_variant	Exon 11 of 22		NM_015340.4	ENSP00000495093.1

Frequencies

GnomAD3 genomes AF: 0.800 AC: 121588 AN: 152062 Hom.: 52803 Cov.: 32

Gnomad AFR AF: 0.422

Gnomad AMI AF: 0.986

Gnomad AMR AF: 0.905

Gnomad ASJ AF: 0.889

Gnomad EAS AF: 0.976

Gnomad SAS AF: 0.921

Gnomad FIN AF: 0.976

Gnomad MID AF: 0.861

Gnomad NFE AF: 0.948

Gnomad OTH AF: 0.826

GnomAD3 exomes AF: 0.912 AC: 227498 AN: 249454 Hom.: 106020 AF XY: 0.921 AC XY: 124302 AN XY: 134990

Gnomad AFR exome AF: 0.413

Gnomad AMR exome AF: 0.946

Gnomad ASJ exome AF: 0.885

Gnomad EAS exome AF: 0.978

Gnomad SAS exome AF: 0.930

Gnomad FIN exome AF: 0.973

Gnomad NFE exome AF: 0.948

Gnomad OTH exome AF: 0.919

GnomAD4 exome AF: 0.935 AC: 1363611 AN: 1458348 Hom.: 642944 Cov.: 34 AF XY: 0.936 AC XY: 679546 AN XY: 725746

Gnomad4 AFR exome AF: 0.402

Gnomad4 AMR exome AF: 0.940

Gnomad4 ASJ exome AF: 0.882

Gnomad4 EAS exome AF: 0.977

Gnomad4 SAS exome AF: 0.929

Gnomad4 FIN exome AF: 0.971

Gnomad4 NFE exome AF: 0.951

Gnomad4 OTH exome AF: 0.908

GnomAD4 genome AF: 0.799 AC: 121638 AN: 152180 Hom.: 52820 Cov.: 32 AF XY: 0.806 AC XY: 59943 AN XY: 74412

Gnomad4 AFR AF: 0.422

Gnomad4 AMR AF: 0.905

Gnomad4 ASJ AF: 0.889

Gnomad4 EAS AF: 0.976

Gnomad4 SAS AF: 0.921

Gnomad4 FIN AF: 0.976

Gnomad4 NFE AF: 0.948

Gnomad4 OTH AF: 0.827

Alfa AF: 0.877 Hom.: 32107

Bravo AF: 0.775

Asia WGS AF: 0.915 AC: 3182 AN: 3478

ClinVar

Significance: Benign

Submissions summary: Benign:8

Revision: criteria provided, multiple submitters, no conflicts

Submissions by phenotype

not specified Benign:3

-

PreventionGenetics, part of Exact Sciences

Significance: Benign

Review Status: criteria provided, single submitter

Collection Method: clinical testing

- -

Dec 02, 2015

GeneDx

Significance: Benign

Review Status: criteria provided, single submitter

Collection Method: clinical testing

This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease. -

Nov 24, 2014

Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine

Significance: Benign

Review Status: criteria provided, single submitter

Collection Method: clinical testing

Leu351Leu in exon 11 of LARS2: This variant is not expected to have clinical sig nificance because it does not alter an amino acid residue and is not located wit hin the splice consensus sequence. It has been identified in 44.0% (1937/4406) o f African American chromosomes from a broad population by the NHLBI Exome Sequen cing Project (http://evs.gs.washington.edu/EVS; dbSNP rs7610357). -

not provided Benign:3

Feb 16, 2016

Mayo Clinic Laboratories, Mayo Clinic

Significance: Benign

Review Status: no assertion criteria provided

Collection Method: clinical testing

- -

Feb 03, 2025

Labcorp Genetics (formerly Invitae), Labcorp

Significance: Benign

Review Status: criteria provided, single submitter

Collection Method: clinical testing

- -

-

Breakthrough Genomics, Breakthrough Genomics

Significance: Benign

Review Status: criteria provided, single submitter

Collection Method: not provided

- -

Perrault syndrome 4 Benign:1

Aug 19, 2021

Genome-Nilou Lab

Significance: Benign

Review Status: criteria provided, single submitter

Collection Method: clinical testing

- -

Hydrops-lactic acidosis-sideroblastic anemia-multisystemic failure syndrome Benign:1

Aug 19, 2021

Genome-Nilou Lab

Significance: Benign

Review Status: criteria provided, single submitter

Collection Method: clinical testing

- -

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.52
CADD	Benign	9.5
DANN	Benign	0.77
RBP_binding_hub_radar		0.0
RBP_regulation_power_radar		1.7

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: rs7610357; hg19: chr3-45527218;