rs16947127

chr16-78117751-T-C

Variant summary

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

The NM_016373.4(WWOX):c.409+2597T>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.139 in 152,200 control chromosomes in the GnomAD database, including 1,741 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 0.14 (1741 hom., cov: 32)
• Consequence: WWOX NM_016373.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.0490

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=-0.85).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.224 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
WWOX	NM_016373.4	c.409+2597T>C		intron_variant		ENST00000566780.6
WWOX	NM_001291997.2	c.70+2597T>C		intron_variant
WWOX	NM_130791.5	c.409+2597T>C		intron_variant
WWOX	NR_120436.3	n.648+2597T>C		intron_variant, non_coding_transcript_variant

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
WWOX	ENST00000566780.6	c.409+2597T>C		intron_variant		1	NM_016373.4	P1

Frequencies

GnomAD3 genomes AF: 0.139 AC: 21192 AN: 152082 Hom.: 1741 Cov.: 32

Gnomad AFR AF: 0.0382

Gnomad AMI AF: 0.170

Gnomad AMR AF: 0.145

Gnomad ASJ AF: 0.161

Gnomad EAS AF: 0.235

Gnomad SAS AF: 0.132

Gnomad FIN AF: 0.192

Gnomad MID AF: 0.133

Gnomad NFE AF: 0.184

Gnomad OTH AF: 0.130

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

GnomAD4 genome AF: 0.139 AC: 21190 AN: 152200 Hom.: 1741 Cov.: 32 AF XY: 0.140 AC XY: 10427 AN XY: 74400

Gnomad4 AFR AF: 0.0381

Gnomad4 AMR AF: 0.145

Gnomad4 ASJ AF: 0.161

Gnomad4 EAS AF: 0.235

Gnomad4 SAS AF: 0.132

Gnomad4 FIN AF: 0.192

Gnomad4 NFE AF: 0.184

Gnomad4 OTH AF: 0.129

Alfa AF: 0.161 Hom.: 277

Bravo AF: 0.131

Asia WGS AF: 0.155 AC: 539 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.85
Cadd	Benign	3.8
Dann	Benign	0.38

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: rs16947127; hg19: chr16-78151648;