NM_001376887.1:c.147C>G

Variant names:

• chr19-6669923-G-C
• rs2291668
• NM_001376887.1:c.147C>G

Variant summary

Our verdict is Likely benign. The variant received -3 ACMG points: 2P and 5B. PM2 BP4_Strong BP7

The NM_001376887.1(TNFSF14):​c.147C>G​(p.Ala49Ala) variant causes a synonymous 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. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar.

• Frequency: Genomes: not found (cov: 31)
• Consequence: TNFSF14 NM_001376887.1 synonymous
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -4.93
• Publications: 22 publications found

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

Our verdict: Likely_benign. The variant received -3 ACMG points.

• PM2: Very rare variant in population databases, with high coverage
• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.82).
• BP7: Synonymous conserved (PhyloP=-4.93 with no splicing effect.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
TNFSF14	NM_001376887.1	c.147C>G	p.Ala49Ala	synonymous_variant	Exon 1 of 4	ENST00000675206.1	NP_001363816.1
TNFSF14	NM_003807.5	c.147C>G	p.Ala49Ala	synonymous_variant	Exon 2 of 5		NP_003798.2
TNFSF14	NM_172014.3	c.111+36C>G		intron_variant	Intron 1 of 3		NP_742011.2

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
TNFSF14	ENST00000675206.1	c.147C>G	p.Ala49Ala	synonymous_variant	Exon 1 of 4		NM_001376887.1	ENSP00000502837.1
TNFSF14	ENST00000599359.1	c.147C>G	p.Ala49Ala	synonymous_variant	Exon 2 of 5	1		ENSP00000469049.1
TNFSF14	ENST00000245912.7	c.111+36C>G		intron_variant	Intron 1 of 3	1		ENSP00000245912.3
TNFSF14	ENST00000850589.1	n.147C>G		non_coding_transcript_exon_variant	Exon 1 of 5			ENSP00000520876.1

Frequencies

GnomAD3 genomes Cov.: 31

GnomAD4 exome Cov.: 35

GnomAD4 genome Cov.: 31

Alfa AF: 0.00 Hom.: 1593

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.82
CADD	Benign	0.21
DANN	Benign	0.41
PhyloP100		-4.9
PromoterAI		-0.030	Neutral

Splicing

Name	Calibrated prediction	Score	Prediction
SpliceAI score (max)		0.16		Details are displayed if max score is > 0.2

Find out detailed SpliceAI scores and Pangolin per-transcript scores at spliceailookup.broadinstitute.org

Other links and lift over

dbSNP: rs2291668; hg19: chr19-6669934;