rs1041981

Variant names:

Variant summary

Our verdict is Benign. Variant got -13 ACMG points: 0P and 13B. BP4_StrongBP6BA1

The ENST00000454783.5(LTA):c.179C>A(p.Thr60Asn) variant causes a missense change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.354 in 1,611,200 control chromosomes in the GnomAD database, including 103,451 homozygotes. In-silico tool predicts a benign outcome for this variant. 13/20 in silico tools predict a benign outcome for this variant. Variant has been reported in ClinVar as Benign,risk factor (no stars). Another variant affecting the same amino acid position, but resulting in a different missense (i.e. T60A) has been classified as Uncertain significance.

Frequency

Genomes: 𝑓 0.38 ( 11465 hom., cov: 28)

Exomes 𝑓: 0.35 ( 91986 hom. )

Consequence

LTA
ENST00000454783.5 missense

Scores

Clinical Significance

Benign; risk factor no assertion criteria provided B:1O:1

Conservation

PhyloP100: 0.741

Variant links:

Genes affected

LTA (HGNC:6709): (lymphotoxin alpha) The encoded protein, a member of the tumor necrosis factor family, is a cytokine produced by lymphocytes. The protein is highly inducible, secreted, and forms heterotrimers with lymphotoxin-beta which anchor lymphotoxin-alpha to the cell surface. This protein also mediates a large variety of inflammatory, immunostimulatory, and antiviral responses, is involved in the formation of secondary lymphoid organs during development and plays a role in apoptosis. Genetic variations in this gene are associated with susceptibility to leprosy type 4, myocardial infarction, non-Hodgkin's lymphoma, and psoriatic arthritis. Alternatively spliced transcript variants have been observed for this gene. [provided by RefSeq, Jul 2012]

LTA links:

Genome browser will be placed here

ACMG classification

Classification made for transcript

Verdict is Benign. Variant got -13 ACMG points.

BP4

Computational evidence support a benign effect (MetaRNN=4.4083595E-4).

BP6

Variant 6-31573007-C-A is Benign according to our data. Variant chr6-31573007-C-A is described in ClinVar as [Benign, risk_factor]. Clinvar id is 14379.Status of the report is no_assertion_criteria_provided, 0 stars.

BA1

GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.496 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
LTA	NM_000595.4 link	c.179C>A	p.Thr60Asn	missense_variant	Exon 3 of 4	ENST00000418386.3	NP_000586.2	P01374Q5STV3
LTA	NM_001159740.2 link	c.179C>A	p.Thr60Asn	missense_variant	Exon 3 of 4		NP_001153212.1	P01374Q5STV3
LTA	XM_047418773.1 link	c.179C>A	p.Thr60Asn	missense_variant	Exon 5 of 6		XP_047274729.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	UniProt
LTA	ENST00000418386.3 link	c.179C>A	p.Thr60Asn	missense_variant	Exon 3 of 4	1	NM_000595.4	ENSP00000413450.2	P01374
LTA	ENST00000454783.5 link	c.179C>A	p.Thr60Asn	missense_variant	Exon 3 of 4	2		ENSP00000403495.1	P01374
LTA	ENST00000471842.1 link	n.427C>A		non_coding_transcript_exon_variant	Exon 2 of 3	2
LTA	ENST00000489638.5 link	n.307C>A		non_coding_transcript_exon_variant	Exon 2 of 3	5

Frequencies

GnomAD3 genomes

AF:

0.381

AC:

57634

AN:

151122

Hom.:

11454

Cov.:

show subpopulations

Gnomad AFR

AF:

0.502

Gnomad AMI

AF:

0.366

Gnomad AMR

AF:

0.346

Gnomad ASJ

AF:

0.241

Gnomad EAS

AF:

0.471

Gnomad SAS

AF:

0.277

Gnomad FIN

AF:

0.298

Gnomad MID

AF:

0.341

Gnomad NFE

AF:

0.339

Gnomad OTH

AF:

0.350

GnomAD3 exomes

AF:

0.347

AC:

85595

AN:

246840

Hom.:

15475

AF XY:

0.339

AC XY:

45608

AN XY:

134378

show subpopulations

Gnomad AFR exome

AF:

0.501

Gnomad AMR exome

AF:

0.338

Gnomad ASJ exome

AF:

0.241

Gnomad EAS exome

AF:

0.498

Gnomad SAS exome

AF:

0.288

Gnomad FIN exome

AF:

0.300

Gnomad NFE exome

AF:

0.338

Gnomad OTH exome

AF:

0.331

GnomAD4 exome

AF:

0.351

AC:

512722

AN:

1459960

Hom.:

91986

Cov.:

AF XY:

0.348

AC XY:

252459

AN XY:

726340

show subpopulations

Gnomad4 AFR exome

AF:

0.508

Gnomad4 AMR exome

AF:

0.336

Gnomad4 ASJ exome

AF:

0.250

Gnomad4 EAS exome

AF:

0.434

Gnomad4 SAS exome

AF:

0.284

Gnomad4 FIN exome

AF:

0.313

Gnomad4 NFE exome

AF:

0.353

Gnomad4 OTH exome

AF:

0.352

GnomAD4 genome

AF:

0.381

AC:

57687

AN:

151240

Hom.:

11465

Cov.:

AF XY:

0.377

AC XY:

27836

AN XY:

73858

show subpopulations

Gnomad4 AFR

AF:

0.502

Gnomad4 AMR

AF:

0.346

Gnomad4 ASJ

AF:

0.241

Gnomad4 EAS

AF:

0.471

Gnomad4 SAS

AF:

0.277

Gnomad4 FIN

AF:

0.298

Gnomad4 NFE

AF:

0.339

Gnomad4 OTH

AF:

0.348

Alfa

AF:

0.337

Hom.:

19942

Bravo

AF:

0.391

TwinsUK

AF:

0.375

AC:

1391

ALSPAC

AF:

0.379

AC:

1459

ESP6500AA

AF:

0.511

AC:

1543

ESP6500EA

AF:

0.331

AC:

1793

ExAC

AF:

0.347

AC:

41204

Asia WGS

AF:

0.329

AC:

1145

AN:

3478

EpiCase

AF:

0.318

EpiControl

AF:

0.322

ClinVar

Significance: Benign; risk factor

Submissions summary: Benign:1Other:1

Revision: no assertion criteria provided

LINK: link

Submissions by phenotype

LTA-related disorder

Benign:1

Oct 16, 2019

PreventionGenetics, part of Exact Sciences

Significance: Benign

Review Status: no assertion criteria provided

Collection Method: clinical testing

This variant is classified as benign based on ACMG/AMP sequence variant interpretation guidelines (Richards et al. 2015 PMID: 25741868, with internal and published modifications). -

Myocardial infarction, susceptibility to

Other:1

Sep 01, 2004

OMIM

Significance: risk factor

Review Status: no assertion criteria provided

Collection Method: literature only

- -

Computational scores

Source: dbNSFP v4.3

Name

Calibrated prediction

Score

Prediction

AlphaMissense

Benign

0.060

BayesDel_addAF

Benign

-0.74

BayesDel_noAF

Benign

-0.69

CADD

Benign

DANN

Benign

0.95

DEOGEN2

Benign

0.17

T;T

Eigen

Benign

-0.34

Eigen_PC

Benign

-0.26

FATHMM_MKL

Benign

0.42

MetaRNN

Benign

0.00044

T;T

MetaSVM

Benign

-1.0

MutationAssessor

Uncertain

2.0

M;M

PrimateAI

Benign

0.34

PROVEAN

Benign

-0.010

N;N

REVEL

Benign

0.025

Sift

Benign

0.39

T;T

Sift4G

Uncertain

0.045

D;D

Polyphen

0.0050

B;B

Vest4

0.047

MPC

1.1

ClinPred

0.0010

GERP RS

3.1

Varity_R

0.030

gMVP

0.30

Splicing

Name

Calibrated prediction

Score

Prediction

SpliceAI score (max)

0.020

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