5-59061749-G-C

Position:

• chr5-59061749-G-C

Variant summary

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

The NM_001104631.2(PDE4D):​c.809-22778C>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.662 in 151,894 control chromosomes in the GnomAD database, including 33,504 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 0.66 (33504 hom., cov: 32)
• Consequence: PDE4D NM_001104631.2 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.107

Genes affected

PDE4D (HGNC:8783): (phosphodiesterase 4D) This gene encodes one of four mammalian counterparts to the fruit fly 'dunce' gene. The encoded protein has 3',5'-cyclic-AMP phosphodiesterase activity and degrades cAMP, which acts as a signal transduction molecule in multiple cell types. This gene uses different promoters to generate multiple alternatively spliced transcript variants that encode functional proteins.[provided by RefSeq, Sep 2009]

(HGNC:):

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.93).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.862 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
PDE4D	NM_001104631.2	c.809-22778C>G		intron_variant		ENST00000340635.11

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
PDE4D	ENST00000340635.11	c.809-22778C>G		intron_variant		1	NM_001104631.2
	ENST00000500224.2	n.311-1336G>C		intron_variant, non_coding_transcript_variant		3

Frequencies

GnomAD3 genomes AF: 0.663 AC: 100554 AN: 151774 Hom.: 33484 Cov.: 32

Gnomad AFR AF: 0.630

Gnomad AMI AF: 0.708

Gnomad AMR AF: 0.691

Gnomad ASJ AF: 0.730

Gnomad EAS AF: 0.883

Gnomad SAS AF: 0.631

Gnomad FIN AF: 0.627

Gnomad MID AF: 0.697

Gnomad NFE AF: 0.662

Gnomad OTH AF: 0.671

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

GnomAD4 genome AF: 0.662 AC: 100619 AN: 151894 Hom.: 33504 Cov.: 32 AF XY: 0.663 AC XY: 49257 AN XY: 74254

Gnomad4 AFR AF: 0.630

Gnomad4 AMR AF: 0.691

Gnomad4 ASJ AF: 0.730

Gnomad4 EAS AF: 0.883

Gnomad4 SAS AF: 0.631

Gnomad4 FIN AF: 0.627

Gnomad4 NFE AF: 0.662

Gnomad4 OTH AF: 0.675

Alfa AF: 0.655 Hom.: 4088

Bravo AF: 0.671

Asia WGS AF: 0.749 AC: 2606 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.93
CADD	Benign	2.1
DANN	Benign	0.53

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: rs7730070; hg19: chr5-58357576;