NM_003844.4:c.683A>T

Variant names:

• chr8-23200707-T-A
• NM_003844.4:c.683A>T

Variant summary

Our verdict is Uncertain significance. Variant got 1 ACMG points: 2P and 1B. PM2 BP4

The NM_003844.4(TNFRSF10A):​c.683A>T​(p.Glu228Val) 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. 13/21 in silico tools predict a benign outcome for this variant. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar. Another variant affecting the same amino acid position, but resulting in a different missense (i.e. E228A) has been classified as Likely benign.

• Frequency: Genomes: not found (cov: 31)
• Consequence: TNFRSF10A NM_003844.4 missense
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 1.03

Genes affected

TNFRSF10A (HGNC:11904): (TNF receptor superfamily member 10a) The protein encoded by this gene is a member of the TNF-receptor superfamily. This receptor is activated by tumor necrosis factor-related apoptosis inducing ligand (TNFSF10/TRAIL), and thus transduces cell death signal and induces cell apoptosis. Studies with FADD-deficient mice suggested that FADD, a death domain containing adaptor protein, is required for the apoptosis mediated by this protein. [provided by RefSeq, Jul 2008]

ACMG classification

Verdict is Uncertain_significance. Variant got 1 ACMG points.

• PM2: Very rare variant in population databases, with high coverage
• BP4: Computational evidence support a benign effect (MetaRNN=0.27177972).

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
TNFRSF10A	NM_003844.4	c.683A>T	p.Glu228Val	missense_variant	Exon 5 of 10	ENST00000221132.8	NP_003835.3

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
TNFRSF10A	ENST00000221132.8	c.683A>T	p.Glu228Val	missense_variant	Exon 5 of 10	1	NM_003844.4	ENSP00000221132.3
TNFRSF10A	ENST00000613472.1	c.209A>T	p.Glu70Val	missense_variant	Exon 4 of 9	1		ENSP00000480778.1
TNFRSF10A	ENST00000524158.5	c.77A>T	p.Glu26Val	missense_variant	Exon 5 of 7	5		ENSP00000428884.1

Frequencies

GnomAD3 genomes Cov.: 31

GnomAD4 exome Cov.: 53

GnomAD4 genome Cov.: 31

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
AlphaMissense	Benign	0.19
BayesDel_addAF	Benign	-0.036	T
BayesDel_noAF	Benign	-0.29
CADD	Benign	7.4
DANN	Benign	0.95
DEOGEN2	Benign	0.40	T;D;D
Eigen	Benign	-0.97
Eigen_PC	Benign	-1.1
FATHMM_MKL	Benign	0.15	N
LIST_S2	Benign	0.45	T;T;T
M_CAP	Uncertain	0.091	D
MetaRNN	Benign	0.27	T;T;T
MetaSVM	Benign	-0.37	T
MutationAssessor	Benign	0.90	L;.;.
PrimateAI	Benign	0.21	T
PROVEAN	Uncertain	-3.4	D;.;D
REVEL	Benign	0.16
Sift	Uncertain	0.019	D;.;D
Sift4G	Uncertain	0.019	D;D;D
Polyphen		0.76	P;.;.
Vest4		0.24
MutPred		0.48		Loss of sheet (P = 0.0315);.;.;
MVP		0.26
MPC		0.089
ClinPred		0.32	T
GERP RS		0.63
RBP_binding_hub_radar		0.0
RBP_regulation_power_radar		1.1
Varity_R		0.25
gMVP		0.59

Splicing

Name	Calibrated prediction	Score	Prediction
SpliceAI score (max)		0.10		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: chr8-23058220;