rs17665435

chr18-62390108-T-Achr18-62390108-T-G

Variant summary

Our verdict is Benign. Variant got -12 ACMG points: 0P and 12B. BP4_Strong BA1

The NM_003839.4(TNFRSF11A):c.*5074T>A variant causes a 3 prime UTR change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.264 in 152,160 control chromosomes in the GnomAD database, including 5,867 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 0.26 (5866 hom., cov: 32)
  • Exomes 𝑓: 0.36 (1 hom.)
• Consequence: TNFRSF11A NM_003839.4 3_prime_UTR
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.878

Genes affected

TNFRSF11A (HGNC:11908): (TNF receptor superfamily member 11a) The protein encoded by this gene is a member of the TNF-receptor superfamily. This receptors can interact with various TRAF family proteins, through which this receptor induces the activation of NF-kappa B and MAPK8/JNK. This receptor and its ligand are important regulators of the interaction between T cells and dendritic cells. This receptor is also an essential mediator for osteoclast and lymph node development. Mutations at this locus have been associated with familial expansile osteolysis, autosomal recessive osteopetrosis, and Paget disease of bone. Alternatively spliced transcript variants have been described for this locus. [provided by RefSeq, Aug 2012]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.78).
• BA1: GnomAd4 highest subpopulation (NFE) allele frequency at 95% confidence interval = 0.327 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
TNFRSF11A	NM_003839.4	c.*5074T>A		3_prime_UTR_variant	10/10	ENST00000586569.3

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
TNFRSF11A	ENST00000586569.3	c.*5074T>A		3_prime_UTR_variant	10/10	1	NM_003839.4	P2

Frequencies

GnomAD3 genomes AF: 0.264 AC: 40075 AN: 152008 Hom.: 5861 Cov.: 32

Gnomad AFR AF: 0.161

Gnomad AMI AF: 0.275

Gnomad AMR AF: 0.280

Gnomad ASJ AF: 0.349

Gnomad EAS AF: 0.0731

Gnomad SAS AF: 0.172

Gnomad FIN AF: 0.319

Gnomad MID AF: 0.263

Gnomad NFE AF: 0.330

Gnomad OTH AF: 0.276

GnomAD4 exome AF: 0.361 AC: 13 AN: 36 Hom.: 1 Cov.: 0 AF XY: 0.250 AC XY: 5 AN XY: 20

Gnomad4 AFR exome AF: 0.00

Gnomad4 FIN exome AF: 0.500

Gnomad4 NFE exome AF: 0.389

Gnomad4 OTH exome AF: 0.00

GnomAD4 genome AF: 0.264 AC: 40125 AN: 152124 Hom.: 5866 Cov.: 32 AF XY: 0.259 AC XY: 19279 AN XY: 74360

Gnomad4 AFR AF: 0.161

Gnomad4 AMR AF: 0.280

Gnomad4 ASJ AF: 0.349

Gnomad4 EAS AF: 0.0734

Gnomad4 SAS AF: 0.174

Gnomad4 FIN AF: 0.319

Gnomad4 NFE AF: 0.330

Gnomad4 OTH AF: 0.278

Alfa AF: 0.197 Hom.: 454

Bravo AF: 0.258

Asia WGS AF: 0.168 AC: 588 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.78
Cadd	Benign	6.2
Dann	Benign	0.89

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: rs17665435; hg19: chr18-60057341;