rs371334679

Variant names:

• chr16-11553684-C-A
• rs371334679
• NM_001136472.2:c.226G>T

Your query was ambiguous. Multiple possible variants found:

• chr16-11553684-C-A
• chr16-11553684-C-G
• chr16-11553684-C-T

Variant summary

Our verdict is Uncertain significance. Variant got 4 ACMG points: 4P and 0B. PM1 PM2

The NM_001136472.2(LITAF):​c.226G>T​(p.Val76Leu) variant causes a missense change. The variant was absent in control chromosomes in GnomAD project. Variant has been reported in ClinVar as Uncertain significance (★).

• Frequency: Genomes: not found (cov: 32)
• Consequence: LITAF NM_001136472.2 missense
• Clinical Significance: Uncertain significance criteria provided, single submitter U:1
• Conservation: PhyloP100: 5.69

Genes affected

LITAF (HGNC:16841): (lipopolysaccharide induced TNF factor) Lipopolysaccharide is a potent stimulator of monocytes and macrophages, causing secretion of tumor necrosis factor-alpha (TNF-alpha) and other inflammatory mediators. This gene encodes lipopolysaccharide-induced TNF-alpha factor, which is a DNA-binding protein and can mediate the TNF-alpha expression by direct binding to the promoter region of the TNF-alpha gene. The transcription of this gene is induced by tumor suppressor p53 and has been implicated in the p53-induced apoptotic pathway. Mutations in this gene cause Charcot-Marie-Tooth disease type 1C (CMT1C) and may be involved in the carcinogenesis of extramammary Paget's disease (EMPD). Multiple alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Dec 2014]

ACMG classification

Verdict is Uncertain_significance. Variant got 4 ACMG points.

• PM1: In a domain LITAF (size 84) in uniprot entity LITAF_HUMAN there are 9 pathogenic changes around while only 0 benign (100%) in NM_001136472.2
• PM2: Very rare variant in population databases, with high coverage

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
LITAF	NM_001136472.2	c.226G>T	p.Val76Leu	missense_variant	Exon 3 of 4	ENST00000622633.5	NP_001129944.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
LITAF	ENST00000622633.5	c.226G>T	p.Val76Leu	missense_variant	Exon 3 of 4	1	NM_001136472.2	ENSP00000483114.1

Frequencies

GnomAD3 genomes Cov.: 32

GnomAD4 exome Cov.: 32

GnomAD4 genome Cov.: 32

ClinVar

Significance: Uncertain significance

Submissions summary: Uncertain:1

Revision: criteria provided, single submitter

Submissions by phenotype

Charcot-Marie-Tooth disease type 1C Uncertain:1

Aug 10, 2022

Labcorp Genetics (formerly Invitae), Labcorp

Significance: Uncertain significance

Review Status: criteria provided, single submitter

Collection Method: clinical testing

In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance. Algorithms developed to predict the effect of missense changes on protein structure and function are either unavailable or do not agree on the potential impact of this missense change (SIFT: "Deleterious"; PolyPhen-2: "Benign"; Align-GVGD: "Class C0"). ClinVar contains an entry for this variant (Variation ID: 532703). This variant has not been reported in the literature in individuals affected with LITAF-related conditions. This variant is not present in population databases (gnomAD no frequency). This sequence change replaces valine, which is neutral and non-polar, with leucine, which is neutral and non-polar, at codon 76 of the LITAF protein (p.Val76Leu). -

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
AlphaMissense	Uncertain	0.51
BayesDel_addAF	Pathogenic	0.20	D
BayesDel_noAF	Uncertain	0.060
CADD	Benign	23
DANN	Uncertain	0.99
DEOGEN2	Uncertain	0.43	T;T;.;T;.;T;T;T;T;.;.;.;.
Eigen	Benign	0.082
Eigen_PC	Benign	0.085
FATHMM_MKL	Uncertain	0.89	D
LIST_S2	Benign	0.82	.;T;.;.;D;.;.;.;T;D;D;D;D
M_CAP	Uncertain	0.11	D
MetaRNN	Uncertain	0.71	D;D;D;D;D;D;D;D;D;D;D;D;D
MetaSVM	Uncertain	0.095	D
MutationAssessor	Benign	2.0	M;M;M;M;M;M;M;M;.;.;M;.;.
PrimateAI	Uncertain	0.54	T
PROVEAN	Benign	-1.5	.;.;N;N;N;.;.;.;.;.;.;.;.
REVEL	Uncertain	0.55
Sift	Uncertain	0.022	.;.;D;T;D;.;.;.;.;.;.;.;.
Sift4G	Uncertain	0.029	D;D;T;D;T;D;D;D;.;.;T;.;T
Polyphen		0.41	B;B;.;B;.;B;B;B;.;.;.;.;.
Vest4		0.71
MutPred		0.67		Loss of glycosylation at T75 (P = 0.0916);Loss of glycosylation at T75 (P = 0.0916);Loss of glycosylation at T75 (P = 0.0916);Loss of glycosylation at T75 (P = 0.0916);Loss of glycosylation at T75 (P = 0.0916);Loss of glycosylation at T75 (P = 0.0916);Loss of glycosylation at T75 (P = 0.0916);Loss of glycosylation at T75 (P = 0.0916);Loss of glycosylation at T75 (P = 0.0916);Loss of glycosylation at T75 (P = 0.0916);Loss of glycosylation at T75 (P = 0.0916);Loss of glycosylation at T75 (P = 0.0916);Loss of glycosylation at T75 (P = 0.0916);
MVP		0.93
MPC		0.27
ClinPred		0.84	D
GERP RS		4.4
RBP_binding_hub_radar		0.0
RBP_regulation_power_radar		1.1
Varity_R		0.11
gMVP		0.68

Splicing

Name	Calibrated prediction	Score	Prediction
SpliceAI score (max)		0.030		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: rs371334679; hg19: chr16-11647540;