NM_206937.2:c.2569G>A

Variant names:

Variant summary

Our verdict is Benign. The variant received -20 ACMG points: 0P and 20B. BP4_StrongBP6_Very_StrongBA1

The NM_206937.2(LIG4):c.2569G>A(p.Ala857Thr) variant causes a missense change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.00556 in 1,614,144 control chromosomes in the GnomAD database, including 460 homozygotes. In-silico tool predicts a benign outcome for this variant. 14/21 in silico tools predict a benign outcome for this variant. Variant has been reported in ClinVar as Benign (★★).

Frequency

Genomes: 𝑓 0.030 ( 237 hom., cov: 32)

Exomes 𝑓: 0.0030 ( 223 hom. )

Consequence

LIG4
NM_206937.2 missense

Scores

Clinical Significance

Benign criteria provided, multiple submitters, no conflicts B:6

Conservation

PhyloP100: 1.66

Publications

17 publications found

Variant links:

Genes affected

LIG4 (HGNC:6601): (DNA ligase 4) The protein encoded by this gene is a DNA ligase that joins single-strand breaks in a double-stranded polydeoxynucleotide in an ATP-dependent reaction. This protein is essential for V(D)J recombination and DNA double-strand break (DSB) repair through nonhomologous end joining (NHEJ). This protein forms a complex with the X-ray repair cross complementing protein 4 (XRCC4), and further interacts with the DNA-dependent protein kinase (DNA-PK). Both XRCC4 and DNA-PK are known to be required for NHEJ. The crystal structure of the complex formed by this protein and XRCC4 has been resolved. Defects in this gene are the cause of LIG4 syndrome. Alternatively spliced transcript variants encoding the same protein have been observed. [provided by RefSeq, Jul 2008]

LIG4 Gene-Disease associations (from GenCC):

DNA ligase IV deficiency
Inheritance: AR Classification: DEFINITIVE, STRONG, SUPPORTIVE Submitted by: ClinGen, Labcorp Genetics (formerly Invitae), Orphanet, G2P
Dubowitz syndrome
Inheritance: AR Classification: SUPPORTIVE Submitted by: Orphanet
Omenn syndrome
Inheritance: AR Classification: SUPPORTIVE Submitted by: Orphanet

LIG4 links:

Genome browser will be placed here

ACMG classification

Classification was made for transcript

Our verdict: Benign. The variant received -20 ACMG points.

BP4

Computational evidence support a benign effect (MetaRNN=0.0017314553).

BP6

Variant 13-108208700-C-T is Benign according to our data. Variant chr13-108208700-C-T is described in CliVar as Benign. Clinvar id is 310973.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr13-108208700-C-T is described in CliVar as Benign. Clinvar id is 310973.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr13-108208700-C-T is described in CliVar as Benign. Clinvar id is 310973.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr13-108208700-C-T is described in CliVar as Benign. Clinvar id is 310973.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr13-108208700-C-T is described in CliVar as Benign. Clinvar id is 310973.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr13-108208700-C-T is described in CliVar as Benign. Clinvar id is 310973.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr13-108208700-C-T is described in CliVar as Benign. Clinvar id is 310973.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr13-108208700-C-T is described in CliVar as Benign. Clinvar id is 310973.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr13-108208700-C-T is described in CliVar as Benign. Clinvar id is 310973.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr13-108208700-C-T is described in CliVar as Benign. Clinvar id is 310973.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr13-108208700-C-T is described in CliVar as Benign. Clinvar id is 310973.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr13-108208700-C-T is described in CliVar as Benign. Clinvar id is 310973.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr13-108208700-C-T is described in CliVar as Benign. Clinvar id is 310973.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr13-108208700-C-T is described in CliVar as Benign. Clinvar id is 310973.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr13-108208700-C-T is described in CliVar as Benign. Clinvar id is 310973.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr13-108208700-C-T is described in CliVar as Benign. Clinvar id is 310973.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr13-108208700-C-T is described in CliVar as Benign. Clinvar id is 310973.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr13-108208700-C-T is described in CliVar as Benign. Clinvar id is 310973.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr13-108208700-C-T is described in CliVar as Benign. Clinvar id is 310973.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr13-108208700-C-T is described in CliVar as Benign. Clinvar id is 310973.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr13-108208700-C-T is described in CliVar as Benign. Clinvar id is 310973.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr13-108208700-C-T is described in CliVar as Benign. Clinvar id is 310973.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr13-108208700-C-T is described in CliVar as Benign. Clinvar id is 310973.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr13-108208700-C-T is described in CliVar as Benign. Clinvar id is 310973.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr13-108208700-C-T is described in CliVar as Benign. Clinvar id is 310973.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr13-108208700-C-T is described in CliVar as Benign. Clinvar id is 310973.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr13-108208700-C-T is described in CliVar as Benign. Clinvar id is 310973.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr13-108208700-C-T is described in CliVar as Benign. Clinvar id is 310973.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr13-108208700-C-T is described in CliVar as Benign. Clinvar id is 310973.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr13-108208700-C-T is described in CliVar as Benign. Clinvar id is 310973.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr13-108208700-C-T is described in CliVar as Benign. Clinvar id is 310973.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr13-108208700-C-T is described in CliVar as Benign. Clinvar id is 310973.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr13-108208700-C-T is described in CliVar as Benign. Clinvar id is 310973.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr13-108208700-C-T is described in CliVar as Benign. Clinvar id is 310973.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr13-108208700-C-T is described in CliVar as Benign. Clinvar id is 310973.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr13-108208700-C-T is described in CliVar as Benign. Clinvar id is 310973.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr13-108208700-C-T is described in CliVar as Benign. Clinvar id is 310973.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr13-108208700-C-T is described in CliVar as Benign. Clinvar id is 310973.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr13-108208700-C-T is described in CliVar as Benign. Clinvar id is 310973.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr13-108208700-C-T is described in CliVar as Benign. Clinvar id is 310973.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars.

BA1

GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.102 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
LIG4	NM_206937.2 link	c.2569G>A	p.Ala857Thr	missense_variant	Exon 3 of 3	ENST00000442234.6	NP_996820.1	P49917A0A024RE06

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
LIG4	ENST00000442234.6 link	c.2569G>A	p.Ala857Thr	missense_variant	Exon 3 of 3	1	NM_206937.2	ENSP00000402030.1		P49917

Frequencies

GnomAD3 genomes

AF:

0.0300

AC:

4562

AN:

152170

Hom.:

234

Cov.:

show subpopulations

Gnomad AFR

AF:

0.104

Gnomad AMI

AF:

0.00

Gnomad AMR

AF:

0.0113

Gnomad ASJ

AF:

0.00

Gnomad EAS

AF:

0.00

Gnomad SAS

AF:

0.000207

Gnomad FIN

AF:

0.00

Gnomad MID

AF:

0.0127

Gnomad NFE

AF:

0.000206

Gnomad OTH

AF:

0.0220

GnomAD2 exomes

AF:

0.00771

AC:

1938

AN:

251442

AF XY:

0.00552

show subpopulations

Gnomad AFR exome

AF:

0.107

Gnomad AMR exome

AF:

0.00468

Gnomad ASJ exome

AF:

0.00

Gnomad EAS exome

AF:

0.00

Gnomad FIN exome

AF:

0.00

Gnomad NFE exome

AF:

0.000158

Gnomad OTH exome

AF:

0.00342

GnomAD4 exome

AF:

0.00300

AC:

4381

AN:

1461854

Hom.:

223

Cov.:

AF XY:

0.00254

AC XY:

1844

AN XY:

727226

show subpopulations

African (AFR)

AF:

0.108

AC:

3615

AN:

33474

American (AMR)

AF:

0.00512

AC:

229

AN:

44724

Ashkenazi Jewish (ASJ)

AF:

0.00

AC:

AN:

26134

East Asian (EAS)

AF:

0.00

AC:

AN:

39694

South Asian (SAS)

AF:

0.000128

AC:

AN:

86256

European-Finnish (FIN)

AF:

0.00

AC:

AN:

53408

Middle Eastern (MID)

AF:

0.00399

AC:

AN:

5768

European-Non Finnish (NFE)

AF:

0.0000890

AC:

AN:

1112002

Other (OTH)

AF:

0.00669

AC:

404

AN:

60394

Allele Balance Distribution

Red line indicates average allele balance

Average allele balance: 0.465

Heterozygous variant carriers

241

483

724

966

1207

0.00

0.20

0.40

0.60

0.80

0.95

Allele balance

Age Distribution

Exome Het

Exome Hom

Variant carriers

110

220

330

440

550

<30

30-35

35-40

40-45

45-50

50-55

55-60

60-65

65-70

70-75

75-80

>80

Age

GnomAD4 genome

AF:

0.0302

AC:

4598

AN:

152290

Hom.:

237

Cov.:

AF XY:

0.0297

AC XY:

2215

AN XY:

74472

show subpopulations

African (AFR)

AF:

0.105

AC:

4362

AN:

41548

American (AMR)

AF:

0.0112

AC:

172

AN:

15294

Ashkenazi Jewish (ASJ)

AF:

0.00

AC:

AN:

3470

East Asian (EAS)

AF:

0.00

AC:

AN:

5190

South Asian (SAS)

AF:

0.000207

AC:

AN:

4830

European-Finnish (FIN)

AF:

0.00

AC:

AN:

10612

Middle Eastern (MID)

AF:

0.0102

AC:

AN:

294

European-Non Finnish (NFE)

AF:

0.000206

AC:

AN:

68024

Other (OTH)

AF:

0.0217

AC:

AN:

2116

Allele Balance Distribution

Red line indicates average allele balance

Average allele balance: 0.504

Heterozygous variant carriers

206

411

617

822

1028

0.00

0.20

0.40

0.60

0.80

0.95

Allele balance

Age Distribution

Genome Het

Genome Hom

Variant carriers

144

192

240

<30

30-35

35-40

40-45

45-50

50-55

55-60

60-65

65-70

70-75

75-80

>80

Age

Alfa

AF:

0.0125

Hom.:

231

Bravo

AF:

0.0342

ESP6500AA

AF:

0.100

AC:

442

ESP6500EA

AF:

0.000465

AC:

ExAC

AF:

0.00957

AC:

1162

Asia WGS

AF:

0.00895

AC:

AN:

3478

EpiCase

AF:

0.000164

EpiControl

AF:

0.000237

ClinVar

Significance: Benign

Submissions summary: Benign:6

Revision: criteria provided, multiple submitters, no conflicts

LINK: link

Submissions by phenotype

DNA ligase IV deficiency

Benign:3

Jul 07, 2023

KCCC/NGS Laboratory, Kuwait Cancer Control Center

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. -

Feb 03, 2025

Labcorp Genetics (formerly Invitae), Labcorp

Significance: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

- -

Mar 03, 2015

GeneDx

Significance:Benign

Review Status:criteria provided, single submitter

Collection Method:clinical testing

- -

Severe combined immunodeficiency due to DCLRE1C deficiency

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

0.070

BayesDel_addAF

Benign

-0.58

BayesDel_noAF

Benign

-0.52

CADD

Benign

(source)

DANN

Uncertain

0.99

DEOGEN2

Benign

0.061

T;T;T;T;.

Eigen

Benign

-0.32

Eigen_PC

Benign

-0.16

FATHMM_MKL

Uncertain

0.85

LIST_S2

Benign

0.83

.;.;.;T;T

MetaRNN

Benign

0.0017

T;T;T;T;T

MetaSVM

Benign

-1.1

MutationAssessor

Uncertain

2.3

M;M;M;M;.

PhyloP100

1.7

PrimateAI

Benign

0.24

PROVEAN

Benign

0.88

N;.;N;N;.

REVEL

Benign

0.13

Sift

Benign

0.13

T;.;T;T;.

Sift4G

Uncertain

0.043

D;D;D;D;D

Polyphen

0.0030

B;B;B;B;.

Vest4

0.055

MVP

0.69

MPC

0.048

ClinPred

0.014

GERP RS

2.9

Varity_R

0.067

gMVP

0.42

Mutation Taster

=100/0

polymorphism (auto)

(source)

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

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Variant summary

Frequency

Consequence

Scores

Clinical Significance

Conservation

Publications

ACMG classification

Transcripts

RefSeq

Ensembl

Frequencies

Age Distribution

Age Distribution

ClinVar

Submissions by phenotype

Computational scores

Splicing

Publications

Other links and lift over