rs780161535

Variant names:

• chr19-6667440-C-G
• rs780161535
• NM_001376887.1:c.229G>C

Your query was ambiguous. Multiple possible variants found:

• chr19-6667440-C-G
• chr19-6667440-C-T

Variant summary

Our verdict is Uncertain significance. Variant got 0 ACMG points: 2P and 2B. PM2 BP4_Moderate

The NM_001376887.1(TNFSF14):​c.229G>C​(p.Ala77Pro) 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. 14/20 in silico tools predict a benign outcome for this variant. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar.

• Frequency: Genomes: not found (cov: 32)
• Consequence: TNFSF14 NM_001376887.1 missense
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -1.48

Genes affected

TNFSF14 (HGNC:11930): (TNF superfamily member 14) The protein encoded by this gene is a member of the tumor necrosis factor (TNF) ligand family. This protein is a ligand for TNFRSF14, which is a member of the tumor necrosis factor receptor superfamily, and which is also known as a herpesvirus entry mediator (HVEM). This protein may function as a costimulatory factor for the activation of lymphoid cells and as a deterrent to infection by herpesvirus. This protein has been shown to stimulate the proliferation of T cells, and trigger apoptosis of various tumor cells. This protein is also reported to prevent tumor necrosis factor alpha mediated apoptosis in primary hepatocyte. Two alternatively spliced transcript variant encoding distinct isoforms have been reported. [provided by RefSeq, Jul 2008]

ACMG classification

Verdict is Uncertain_significance. Variant got 0 ACMG points.

• PM2: Very rare variant in population databases, with high coverage
• BP4: Computational evidence support a benign effect (MetaRNN=0.0753994).

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
TNFSF14	NM_001376887.1	c.229G>C	p.Ala77Pro	missense_variant	Exon 2 of 4	ENST00000675206.1	NP_001363816.1
TNFSF14	NM_003807.5	c.229G>C	p.Ala77Pro	missense_variant	Exon 3 of 5		NP_003798.2
TNFSF14	NM_172014.3	c.121G>C	p.Ala41Pro	missense_variant	Exon 2 of 4		NP_742011.2

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
TNFSF14	ENST00000675206.1	c.229G>C	p.Ala77Pro	missense_variant	Exon 2 of 4		NM_001376887.1	ENSP00000502837.1
TNFSF14	ENST00000599359.1	c.229G>C	p.Ala77Pro	missense_variant	Exon 3 of 5	1		ENSP00000469049.1
TNFSF14	ENST00000245912.7	c.121G>C	p.Ala41Pro	missense_variant	Exon 2 of 4	1		ENSP00000245912.3

Frequencies

GnomAD3 genomes Cov.: 32

GnomAD4 exome Cov.: 31

GnomAD4 genome Cov.: 32

Bravo AF: 0.00000378

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
AlphaMissense	Benign	0.081
BayesDel_addAF	Benign	-0.18	T
BayesDel_noAF	Benign	-0.50
CADD	Benign	0.30
DANN	Benign	0.88
DEOGEN2	Benign	0.17	.;T
Eigen	Benign	-1.5
Eigen_PC	Benign	-1.7
FATHMM_MKL	Benign	0.056	N
LIST_S2	Benign	0.37	T;T
M_CAP	Benign	0.0088	T
MetaRNN	Benign	0.075	T;T
MetaSVM	Benign	-1.0	T
MutationAssessor	Benign	1.9	.;L
PrimateAI	Benign	0.30	T
REVEL	Benign	0.037
Sift4G	Benign	0.062	T;T
Polyphen		0.087	B;B
Vest4		0.17
MutPred		0.46		.;Gain of glycosylation at A77 (P = 0.0062);
MVP		0.28
MPC		0.51
ClinPred		0.57	D
GERP RS		-8.4
RBP_binding_hub_radar		0.0
RBP_regulation_power_radar		1.1
Varity_R		0.081
gMVP		0.36

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

LitVar

Other links and lift over

dbSNP: rs780161535; hg19: chr19-6667451;