5-60413925-C-T

Variant names:

• chr5-60413925-C-T
• rs16878037
• ENST00000502484.6:c.-90+74017G>A

Variant summary

Our verdict is Benign. The variant received -12 ACMG points: 0P and 12B. BP4_Strong BA1

The NM_001165899.2(PDE4D):​c.-90+74017G>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.0571 in 152,246 control chromosomes in the GnomAD database, including 339 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 0.057 (339 hom., cov: 32)
• Consequence: PDE4D NM_001165899.2 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.245
• Publications: 8 publications found

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]

PDE4D Gene-Disease associations (from GenCC):

• acrodysostosis 2 with or without hormone resistance

  Inheritance: AD Classification: DEFINITIVE, STRONG, MODERATE Submitted by: Labcorp Genetics (formerly Invitae), Ambry Genetics, G2P
• acrodysostosis

  Inheritance: AD Classification: SUPPORTIVE Submitted by: Orphanet
• acrodysostosis with multiple hormone resistance

  Inheritance: AD Classification: SUPPORTIVE Submitted by: Orphanet
• chromosome 5q12 deletion syndrome

  Inheritance: Unknown Classification: SUPPORTIVE Submitted by: Orphanet

ACMG classification

Our verdict: Benign. The variant received -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.9).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.136 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_001165899.2. You can select a different transcript below to see updated ACMG assignments.

RefSeq Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	PDE4D	NM_001165899.2		c.-90+74017G>A		intron	N/A	NP_001159371.1	Q08499-11
	PDE4D	NM_001364599.1		c.-90+82214G>A		intron	N/A	NP_001351528.1	Q08499-11
	PDE4D	NM_001349241.2		c.-193+74017G>A		intron	N/A	NP_001336170.1

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	PDE4D	ENST00000502484.6	TSL:1	c.-90+74017G>A		intron	N/A	ENSP00000423094.2	Q08499-11
	PDE4D	ENST00000509355.5	TSL:1	n.157+74017G>A		intron	N/A
	PDE4D	ENST00000505507.6	TSL:4	c.-213+74017G>A		intron	N/A	ENSP00000425910.2	D6RIG1

Frequencies

GnomAD3 genomes AF: 0.0572 AC: 8695 AN: 152128 Hom.: 338 Cov.: 32

Gnomad AFR AF: 0.0904

Gnomad AMI AF: 0.0362

Gnomad AMR AF: 0.0494

Gnomad ASJ AF: 0.0424

Gnomad EAS AF: 0.145

Gnomad SAS AF: 0.0762

Gnomad FIN AF: 0.0241

Gnomad MID AF: 0.0285

Gnomad NFE AF: 0.0373

Gnomad OTH AF: 0.0445

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

GnomAD4 genome AF: 0.0571 AC: 8694 AN: 152246 Hom.: 339 Cov.: 32 AF XY: 0.0573 AC XY: 4261 AN XY: 74414

African (AFR) AF: 0.0903 AC: 3751 AN: 41530

American (AMR) AF: 0.0492 AC: 752 AN: 15290

Ashkenazi Jewish (ASJ) AF: 0.0424 AC: 147 AN: 3470

East Asian (EAS) AF: 0.145 AC: 752 AN: 5186

South Asian (SAS) AF: 0.0763 AC: 368 AN: 4824

European-Finnish (FIN) AF: 0.0241 AC: 255 AN: 10602

Middle Eastern (MID) AF: 0.0238 AC: 7 AN: 294

European-Non Finnish (NFE) AF: 0.0373 AC: 2537 AN: 68026

Other (OTH) AF: 0.0436 AC: 92 AN: 2112

Alfa AF: 0.0407 Hom.: 247

Bravo AF: 0.0608

Asia WGS AF: 0.103 AC: 358 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.90
CADD	Benign	1.5
DANN	Benign	0.52
PhyloP100		-0.24
Mutation Taster		=100/0	polymorphism (auto)

Splicing

Find out detailed SpliceAI scores and Pangolin per-transcript scores at spliceailookup.broadinstitute.org

Other links and lift over

dbSNP: rs16878037; hg19: chr5-59709752;