rs2859576

Positions:

• chr5-77260492-T-C
• chr5-77260492-T-G

Variant summary

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

The NM_003719.5(PDE8B):​c.339+49228T>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.127 in 151,982 control chromosomes in the GnomAD database, including 1,601 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 0.13 (1601 hom., cov: 32)
• Consequence: PDE8B NM_003719.5 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.127

Genes affected

PDE8B (HGNC:8794): (phosphodiesterase 8B) The protein encoded by this gene is a cyclic nucleotide phosphodiesterase (PDE) that catalyzes the hydrolysis of the second messenger cAMP. The encoded protein, which does not hydrolyze cGMP, is resistant to several PDE inhibitors. Defects in this gene are a cause of autosomal dominant striatal degeneration (ADSD). Several transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Jul 2010]

ENSG00000284762 (HGNC:):

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.89).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.443 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
PDE8B	NM_003719.5	c.339+49228T>C		intron_variant		ENST00000264917.10	NP_003710.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
PDE8B	ENST00000264917.10	c.339+49228T>C		intron_variant		1	NM_003719.5	ENSP00000264917.6
ENSG00000284762	ENST00000646262.1	c.-33-51502T>C		intron_variant				ENSP00000493971.1

Frequencies

GnomAD3 genomes AF: 0.127 AC: 19357 AN: 151866 Hom.: 1597 Cov.: 32

Gnomad AFR AF: 0.127

Gnomad AMI AF: 0.0658

Gnomad AMR AF: 0.135

Gnomad ASJ AF: 0.172

Gnomad EAS AF: 0.459

Gnomad SAS AF: 0.194

Gnomad FIN AF: 0.0793

Gnomad MID AF: 0.0981

Gnomad NFE AF: 0.102

Gnomad OTH AF: 0.128

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

GnomAD4 genome AF: 0.127 AC: 19375 AN: 151982 Hom.: 1601 Cov.: 32 AF XY: 0.129 AC XY: 9549 AN XY: 74294

Gnomad4 AFR AF: 0.127

Gnomad4 AMR AF: 0.136

Gnomad4 ASJ AF: 0.172

Gnomad4 EAS AF: 0.458

Gnomad4 SAS AF: 0.193

Gnomad4 FIN AF: 0.0793

Gnomad4 NFE AF: 0.102

Gnomad4 OTH AF: 0.132

Alfa AF: 0.113 Hom.: 631

Bravo AF: 0.135

Asia WGS AF: 0.292 AC: 1017 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.89
CADD	Benign	7.5
DANN	Benign	0.72

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: rs2859576; hg19: chr5-76556317;