NM_203486.3:c.425T>A

Variant names:

Variant summary

Our verdict is Benign. Variant got -20 ACMG points: 0P and 20B. BP4_StrongBP6_Very_StrongBA1

The NM_203486.3(DLL3):c.425T>A(p.Leu142Gln) variant causes a missense change. The variant allele was found at a frequency of 0.0767 in 1,421,728 control chromosomes in the GnomAD database, including 4,802 homozygotes. In-silico tool predicts a benign outcome for this variant. Variant has been reported in ClinVar as Likely benign (★★).

Frequency

Genomes: 𝑓 0.065 ( 398 hom., cov: 32)

Exomes 𝑓: 0.078 ( 4404 hom. )

Consequence

DLL3
NM_203486.3 missense

Scores

Clinical Significance

Benign/Likely benign criteria provided, multiple submitters, no conflicts B:9

Conservation

PhyloP100: 4.82

Variant links:

Genes affected

DLL3 (HGNC:2909): (delta like canonical Notch ligand 3) This gene encodes a member of the delta protein ligand family. This family functions as Notch ligands that are characterized by a DSL domain, EGF repeats, and a transmembrane domain. Mutations in this gene cause autosomal recessive spondylocostal dysostosis 1. Two transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Jul 2008]

DLL3 links:

Genome browser will be placed here

ACMG classification

Classification made for transcript

Verdict is Benign. Variant got -20 ACMG points.

BP4

Computational evidence support a benign effect (MetaRNN=0.0025883317).

BP6

Variant 19-39502830-T-A is Benign according to our data. Variant chr19-39502830-T-A is described in ClinVar as [Likely_benign]. Clinvar id is 41377.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr19-39502830-T-A is described in Lovd as [Likely_benign].

BA1

GnomAd4 highest subpopulation (NFE) allele frequency at 95% confidence interval = 0.0783 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
DLL3	NM_203486.3 link	c.425T>A	p.Leu142Gln	missense_variant	Exon 4 of 9	ENST00000356433.10	NP_982353.1	Q9NYJ7-2
DLL3	NM_016941.4 link	c.425T>A	p.Leu142Gln	missense_variant	Exon 4 of 8		NP_058637.1	Q9NYJ7-1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	UniProt
DLL3	ENST00000356433.10 link	c.425T>A	p.Leu142Gln	missense_variant	Exon 4 of 9	2	NM_203486.3	ENSP00000348810.4	Q9NYJ7-2
DLL3	ENST00000205143.4 link	c.425T>A	p.Leu142Gln	missense_variant	Exon 4 of 8	1		ENSP00000205143.3	Q9NYJ7-1
DLL3	ENST00000600437.1 link	n.505T>A		non_coding_transcript_exon_variant	Exon 4 of 6	1
DLL3	ENST00000596614.5 link	c.409+2158T>A		intron_variant	Intron 3 of 3	2		ENSP00000471688.1	M0R177

Frequencies

GnomAD3 genomes

AF:

0.0649

AC:

9859

AN:

152010

Hom.:

398

Cov.:

show subpopulations

Gnomad AFR

AF:

0.0675

Gnomad AMI

AF:

0.103

Gnomad AMR

AF:

0.0478

Gnomad ASJ

AF:

0.0199

Gnomad EAS

AF:

0.000582

Gnomad SAS

AF:

0.0128

Gnomad FIN

AF:

0.0512

Gnomad MID

AF:

0.0127

Gnomad NFE

AF:

0.0801

Gnomad OTH

AF:

0.0550

GnomAD3 exomes

AF:

0.0579

AC:

3980

AN:

68696

Hom.:

156

AF XY:

0.0557

AC XY:

2276

AN XY:

40880

show subpopulations

Gnomad AFR exome

AF:

0.0814

Gnomad AMR exome

AF:

0.0545

Gnomad ASJ exome

AF:

0.0209

Gnomad EAS exome

AF:

0.000928

Gnomad SAS exome

AF:

0.0113

Gnomad FIN exome

AF:

0.0521

Gnomad NFE exome

AF:

0.0825

Gnomad OTH exome

AF:

0.0480

GnomAD4 exome

AF:

0.0782

AC:

99239

AN:

1269604

Hom.:

4404

Cov.:

AF XY:

0.0756

AC XY:

47260

AN XY:

625458

show subpopulations

Gnomad4 AFR exome

AF:

0.0632

Gnomad4 AMR exome

AF:

0.0464

Gnomad4 ASJ exome

AF:

0.0198

Gnomad4 EAS exome

AF:

0.000241

Gnomad4 SAS exome

AF:

0.0118

Gnomad4 FIN exome

AF:

0.0539

Gnomad4 NFE exome

AF:

0.0881

Gnomad4 OTH exome

AF:

0.0653

GnomAD4 genome

AF:

0.0648

AC:

9857

AN:

152124

Hom.:

398

Cov.:

AF XY:

0.0614

AC XY:

4569

AN XY:

74382

show subpopulations

Gnomad4 AFR

AF:

0.0673

Gnomad4 AMR

AF:

0.0477

Gnomad4 ASJ

AF:

0.0199

Gnomad4 EAS

AF:

0.000583

Gnomad4 SAS

AF:

0.0128

Gnomad4 FIN

AF:

0.0512

Gnomad4 NFE

AF:

0.0801

Gnomad4 OTH

AF:

0.0544

Alfa

AF:

0.0703

Hom.:

Bravo

AF:

0.0670

TwinsUK

AF:

0.0955

AC:

354

ALSPAC

AF:

0.0939

AC:

362

ESP6500AA

AF:

0.0526

AC:

134

ESP6500EA

AF:

0.0611

AC:

328

ExAC

AF:

0.0434

AC:

4668

Asia WGS

AF:

0.0110

AC:

AN:

3478

ClinVar

Significance: Benign/Likely benign

Submissions summary: Benign:9

Revision: criteria provided, multiple submitters, no conflicts

LINK: link

Submissions by phenotype

not specified

Benign:3

PreventionGenetics, part of Exact Sciences

Significance: Benign

Review Status: criteria provided, single submitter

Collection Method: clinical testing

- -

Mar 03, 2016

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. -

Oct 03, 2016

Eurofins Ntd Llc (ga)

Significance: Benign

Review Status: criteria provided, single submitter

Collection Method: clinical testing

- -

Spondylocostal dysostosis 1, autosomal recessive

Benign:3

Oct 23, 2024

ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

Significance: Benign

Review Status: criteria provided, single submitter

Collection Method: clinical testing

- -

Jan 13, 2018

Illumina Laboratory Services, Illumina

Significance: Benign

Review Status: criteria provided, single submitter

Collection Method: clinical testing

This variant was observed in the ICSL laboratory as part of a predisposition screen in an ostensibly healthy population. It had not been previously curated by ICSL or reported in the Human Gene Mutation Database (HGMD: prior to June 1st, 2018), and was therefore a candidate for classification through an automated scoring system. Utilizing variant allele frequency, disease prevalence and penetrance estimates, and inheritance mode, an automated score was calculated to assess if this variant is too frequent to cause the disease. Based on the score and internal cut-off values, a variant classified as benign is not then subjected to further curation. The score for this variant resulted in a classification of benign for this disease. -

Oct 25, 2021

Fulgent Genetics, Fulgent Genetics

Significance: Likely benign

Review Status: criteria provided, single submitter

Collection Method: clinical testing

- -

not provided

Benign:2

Breakthrough Genomics, Breakthrough Genomics

Significance: Benign

Review Status: criteria provided, single submitter

Collection Method: not provided

- -

Feb 03, 2025

Labcorp Genetics (formerly Invitae), Labcorp

Significance: Benign

Review Status: criteria provided, single submitter

Collection Method: clinical testing

- -

Syndactyly

Benign:1

Jan 13, 2018

Illumina Laboratory Services, Illumina

Significance: Benign

Review Status: criteria provided, single submitter

Collection Method: clinical testing

Computational scores

Source: dbNSFP v4.3

Name

Calibrated prediction

Score

Prediction

AlphaMissense

Benign

0.29

BayesDel_addAF

Benign

-0.28

BayesDel_noAF

Benign

-0.10

CADD

Uncertain

DANN

Uncertain

0.98

DEOGEN2

Uncertain

0.77

.;D

Eigen

Benign

-0.13

Eigen_PC

Benign

-0.23

FATHMM_MKL

Uncertain

0.94

LIST_S2

Benign

0.73

T;T

MetaRNN

Benign

0.0026

T;T

MetaSVM

Uncertain

-0.28

MutationAssessor

Pathogenic

3.1

M;M

PrimateAI

Uncertain

0.71

PROVEAN

Uncertain

-4.0

D;D

REVEL

Uncertain

0.34

Sift

Uncertain

0.0010

D;D

Sift4G

Uncertain

0.020

D;D

Polyphen

0.95

.;P

Vest4

0.68

MPC

1.6

ClinPred

0.023

GERP RS

2.4

Varity_R

0.64

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

Below is the list of publications found by LitVar. It may be empty.

Variant summary

Frequency

Consequence

Scores

Clinical Significance

Conservation

ACMG classification

Transcripts

RefSeq

Ensembl

Frequencies

ClinVar

Submissions by phenotype

Computational scores

Splicing

Publications

LitVar

Other links and lift over