rs3136604

Variant names:

• chr3-172508291-G-A
• rs3136604
• NM_003810.4:c.418+926C>T

Your query was ambiguous. Multiple possible variants found:

• chr3-172508291-G-A
• chr3-172508291-G-T

Variant summary

Our verdict is Benign. The variant received -12 ACMG points: 0P and 12B. BP4_Strong BA1

The NM_003810.4(TNFSF10):​c.418+926C>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.226 in 132,748 control chromosomes in the GnomAD database, including 3,352 homozygotes. 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: 𝑓 0.23 (3352 hom., cov: 30)
• Consequence: TNFSF10 NM_003810.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -2.28
• Publications: 1 publications found

Genes affected

TNFSF10 (HGNC:11925): (TNF superfamily member 10) The protein encoded by this gene is a cytokine that belongs to the tumor necrosis factor (TNF) ligand family. This protein preferentially induces apoptosis in transformed and tumor cells, but does not appear to kill normal cells although it is expressed at a significant level in most normal tissues. This protein binds to several members of TNF receptor superfamily including TNFRSF10A/TRAILR1, TNFRSF10B/TRAILR2, TNFRSF10C/TRAILR3, TNFRSF10D/TRAILR4, and possibly also to TNFRSF11B/OPG. The activity of this protein may be modulated by binding to the decoy receptors TNFRSF10C/TRAILR3, TNFRSF10D/TRAILR4, and TNFRSF11B/OPG that cannot induce apoptosis. The binding of this protein to its receptors has been shown to trigger the activation of MAPK8/JNK, caspase 8, and caspase 3. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2010]

ACMG classification

Our verdict: Benign. The variant received -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-1.0).
• BA1: GnomAd4 highest subpopulation (NFE) allele frequency at 95% confidence interval = 0.253 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_003810.4. You can select a different transcript below to see updated ACMG assignments.

RefSeq Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	TNFSF10	NM_003810.4	MANE Select	c.418+926C>T		intron	N/A	NP_003801.1	Q6IBA9
	TNFSF10	NM_001190942.2		c.271-1372C>T		intron	N/A	NP_001177871.1	P50591-2
	TNFSF10	NR_033994.2		n.421+926C>T		intron	N/A

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	TNFSF10	ENST00000241261.7	TSL:1 MANE Select	c.418+926C>T		intron	N/A	ENSP00000241261.2	P50591-1
	TNFSF10	ENST00000420541.6	TSL:1	c.271-1372C>T		intron	N/A	ENSP00000389931.2	P50591-2
	TNFSF10	ENST00000855872.1		c.520+926C>T		intron	N/A	ENSP00000525931.1

Frequencies

GnomAD3 genomes AF: 0.226 AC: 29945 AN: 132644 Hom.: 3353 Cov.: 30

Gnomad AFR AF: 0.146

Gnomad AMI AF: 0.331

Gnomad AMR AF: 0.205

Gnomad ASJ AF: 0.335

Gnomad EAS AF: 0.146

Gnomad SAS AF: 0.221

Gnomad FIN AF: 0.298

Gnomad MID AF: 0.438

Gnomad NFE AF: 0.257

Gnomad OTH AF: 0.261

We have no GnomAD4 exomes data on this position. Probably position not covered by the project.

GnomAD4 genome AF: 0.226 AC: 29948 AN: 132748 Hom.: 3352 Cov.: 30 AF XY: 0.228 AC XY: 14714 AN XY: 64420

African (AFR) AF: 0.146 AC: 4634 AN: 31766

American (AMR) AF: 0.204 AC: 2803 AN: 13720

Ashkenazi Jewish (ASJ) AF: 0.335 AC: 1101 AN: 3284

East Asian (EAS) AF: 0.147 AC: 650 AN: 4422

South Asian (SAS) AF: 0.221 AC: 923 AN: 4174

European-Finnish (FIN) AF: 0.298 AC: 2714 AN: 9104

Middle Eastern (MID) AF: 0.428 AC: 119 AN: 278

European-Non Finnish (NFE) AF: 0.257 AC: 16253 AN: 63324

Other (OTH) AF: 0.258 AC: 478 AN: 1850

Alfa AF: 0.106 Hom.: 179

Bravo AF: 0.186

Asia WGS AF: 0.116 AC: 406 AN: 3472

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-1.0
CADD	Benign	0.95
DANN	Benign	0.48
PhyloP100		-2.3
Mutation Taster		=100/0	polymorphism (auto)

Splicing

Name	Calibrated prediction	Score	Prediction
SpliceAI score (max)		0.040		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: rs3136604; hg19: chr3-172226081;