NM_004556.3:c.1078A>G

Variant names:

• chr6-44259227-T-C
• NM_004556.3:c.1078A>G

Variant summary

Our verdict is Likely benign. Variant got -4 ACMG points: 2P and 6B. PM2 BP4_Strong BP6_Moderate

The NM_004556.3(NFKBIE):​c.1078A>G​(p.Thr360Ala) variant causes a missense change involving the alteration of a non-conserved nucleotide. The variant was absent in control chromosomes in GnomAD project. In-silico tool predicts a benign outcome for this variant. 15/21 in silico tools predict a benign outcome for this variant. Variant has been reported in ClinVar as Likely benign (★).

• Frequency: Genomes: not found (cov: 32)
• Consequence: NFKBIE NM_004556.3 missense
• Clinical Significance: Likely benign criteria provided, single submitter B:1
• Conservation: PhyloP100: 0.480

Genes affected

NFKBIE (HGNC:7799): (NFKB inhibitor epsilon) The protein encoded by this gene binds to components of NF-kappa-B, trapping the complex in the cytoplasm and preventing it from activating genes in the nucleus. Phosphorylation of the encoded protein targets it for destruction by the ubiquitin pathway, which activates NF-kappa-B by making it available to translocate to the nucleus. [provided by RefSeq, Sep 2011]

ACMG classification

Verdict is Likely_benign. Variant got -4 ACMG points.

• PM2: Very rare variant in population databases, with high coverage
• BP4: Computational evidence support a benign effect (MetaRNN=0.05132091).
• BP6: Variant 6-44259227-T-C is Benign according to our data. Variant chr6-44259227-T-C is described in ClinVar as [Likely_benign]. Clinvar id is 3405240.Status of the report is criteria_provided_single_submitter, 1 stars.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
NFKBIE	NM_004556.3	c.1078A>G	p.Thr360Ala	missense_variant	Exon 6 of 6	ENST00000619360.6	NP_004547.3

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
NFKBIE	ENST00000619360.6	c.1078A>G	p.Thr360Ala	missense_variant	Exon 6 of 6	1	NM_004556.3	ENSP00000480216.1
NFKBIE	ENST00000275015.9	c.1495A>G	p.Thr499Ala	missense_variant	Exon 6 of 6	1		ENSP00000275015.3
NFKBIE	ENST00000443607.2	c.160A>G	p.Thr54Ala	missense_variant	Exon 2 of 3	3		ENSP00000394658.2

Frequencies

GnomAD3 genomes Cov.: 32

GnomAD4 exome Cov.: 30

GnomAD4 genome Cov.: 32

ClinVar

Significance: Likely benign

Submissions summary: Benign:1

Revision: criteria provided, single submitter

Submissions by phenotype

not specified Benign:1

Jul 02, 2024

Ambry Genetics

Significance: Likely benign

Review Status: criteria provided, single submitter

Collection Method: clinical testing

This alteration is classified as likely benign based on a combination of the following: seen in unaffected individuals, population frequency, intact protein function, lack of segregation with disease, co-occurrence, RNA analysis, in silico models, amino acid conservation, lack of disease association in case-control studies, and/or the mechanism of disease or impacted region is inconsistent with a known cause of pathogenicity. -

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
AlphaMissense	Benign	0.060
BayesDel_addAF	Benign	-0.34	T
BayesDel_noAF	Benign	-0.73
CADD	Benign	11
DANN	Benign	0.67
DEOGEN2	Benign	0.0051	T;T;T
Eigen	Benign	-0.80
Eigen_PC	Benign	-0.68
FATHMM_MKL	Benign	0.083	N
LIST_S2	Benign	0.35	T;T;T
M_CAP	Benign	0.0064	T
MetaRNN	Benign	0.051	T;T;T
MetaSVM	Benign	-0.99	T
MutationAssessor	Benign	0.0	.;N;.
PrimateAI	Benign	0.32	T
PROVEAN	Benign	-0.33	.;N;N
REVEL	Benign	0.022
Sift	Benign	0.18	.;T;T
Sift4G	Benign	0.43	T;T;T
Polyphen		0.0020	.;B;.
Vest4		0.013
MutPred		0.28		.;Gain of ubiquitination at K494 (P = 0.0941);.;
MVP		0.16
MPC		0.75
ClinPred		0.034	T
GERP RS		1.4
Varity_R		0.075
gMVP		0.48

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

No publications associated with this variant yet.

Other links and lift over

hg19: chr6-44226964;