rs6420411

chr16-78843721-A-Cchr16-78843721-A-Gchr16-78843721-A-T

Variant summary

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

The NM_016373.4(WWOX):c.1057-367887A>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.696 in 151,992 control chromosomes in the GnomAD database, including 37,126 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 0.70 (37126 hom., cov: 33)
• Consequence: WWOX NM_016373.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.120

Genes affected

WWOX (HGNC:12799): (WW domain containing oxidoreductase) This gene encodes a member of the short-chain dehydrogenases/reductases (SDR) protein family. This gene spans the FRA16D common chromosomal fragile site and appears to function as a tumor suppressor gene. Expression of the encoded protein is able to induce apoptosis, while defects in this gene are associated with multiple types of cancer. Disruption of this gene is also associated with autosomal recessive spinocerebellar ataxia 12. Disruption of a similar gene in mouse results in impaired steroidogenesis, additionally suggesting a metabolic function for the protein. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2014]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.9).
• BA1: GnomAd4 highest subpopulation (NFE) allele frequency at 95% confidence interval = 0.723 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
WWOX	NM_016373.4	c.1057-367887A>C		intron_variant		ENST00000566780.6
WWOX	NM_001291997.2	c.718-367887A>C		intron_variant

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
WWOX	ENST00000566780.6	c.1057-367887A>C		intron_variant		1	NM_016373.4	P1

Frequencies

GnomAD3 genomes AF: 0.696 AC: 105736 AN: 151874 Hom.: 37105 Cov.: 33

Gnomad AFR AF: 0.659

Gnomad AMI AF: 0.664

Gnomad AMR AF: 0.706

Gnomad ASJ AF: 0.753

Gnomad EAS AF: 0.489

Gnomad SAS AF: 0.641

Gnomad FIN AF: 0.722

Gnomad MID AF: 0.768

Gnomad NFE AF: 0.729

Gnomad OTH AF: 0.720

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

GnomAD4 genome AF: 0.696 AC: 105803 AN: 151992 Hom.: 37126 Cov.: 33 AF XY: 0.694 AC XY: 51523 AN XY: 74280

Gnomad4 AFR AF: 0.660

Gnomad4 AMR AF: 0.706

Gnomad4 ASJ AF: 0.753

Gnomad4 EAS AF: 0.489

Gnomad4 SAS AF: 0.642

Gnomad4 FIN AF: 0.722

Gnomad4 NFE AF: 0.729

Gnomad4 OTH AF: 0.713

Alfa AF: 0.724 Hom.: 46344

Bravo AF: 0.696

Asia WGS AF: 0.570 AC: 1986 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.90
Cadd	Benign	1.0
Dann	Benign	0.54

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: rs6420411; hg19: chr16-78877618;