chr6-136160474-G-T

Variant names:

• chr6-136160474-G-T
• rs9321552
• NM_018945.4:c.711+4716G>T

Variant summary

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

The NM_018945.4(PDE7B):​c.711+4716G>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.24 in 152,048 control chromosomes in the GnomAD database, including 12,047 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 0.24 (12047 hom., cov: 32)
• Consequence: PDE7B NM_018945.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.287
• Publications: 5 publications found

Genes affected

PDE7B (HGNC:8792): (phosphodiesterase 7B) The 3',5'-cyclic nucleotides cAMP and cGMP function as second messengers in a wide variety of signal transduction pathways. 3',5'-cyclic nucleotide phosphodiesterases (PDEs) catalyze the hydrolysis of cAMP and cGMP to the corresponding 5'-monophosphates and provide a mechanism to downregulate cAMP and cGMP signaling. This gene encodes a cAMP-specific phosphodiesterase, a member of the cyclic nucleotide phosphodiesterase family.[provided by RefSeq, Apr 2009]

PDE7B-AS1 (HGNC:56334): (PDE7B antisense RNA 1)

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.97).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.734 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_018945.4. You can select a different transcript below to see updated ACMG assignments.

RefSeq Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	PDE7B	NM_018945.4	MANE Select	c.711+4716G>T		intron	N/A	NP_061818.1

Ensembl Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	PDE7B	ENST00000308191.11	TSL:1 MANE Select	c.711+4716G>T		intron	N/A	ENSP00000310661.6
	PDE7B	ENST00000615259.4	TSL:1	c.867+4716G>T		intron	N/A	ENSP00000482117.1
	PDE7B-AS1	ENST00000417643.5	TSL:5	n.155+1778C>A		intron	N/A

Frequencies

GnomAD3 genomes AF: 0.239 AC: 36331 AN: 151930 Hom.: 11992 Cov.: 32

Gnomad AFR AF: 0.740

Gnomad AMI AF: 0.00

Gnomad AMR AF: 0.214

Gnomad ASJ AF: 0.0156

Gnomad EAS AF: 0.102

Gnomad SAS AF: 0.0625

Gnomad FIN AF: 0.0572

Gnomad MID AF: 0.0665

Gnomad NFE AF: 0.00797

Gnomad OTH AF: 0.211

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

GnomAD4 genome AF: 0.240 AC: 36461 AN: 152048 Hom.: 12047 Cov.: 32 AF XY: 0.236 AC XY: 17562 AN XY: 74346

African (AFR) AF: 0.741 AC: 30692 AN: 41420

American (AMR) AF: 0.214 AC: 3267 AN: 15264

Ashkenazi Jewish (ASJ) AF: 0.0156 AC: 54 AN: 3472

East Asian (EAS) AF: 0.102 AC: 527 AN: 5170

South Asian (SAS) AF: 0.0623 AC: 300 AN: 4814

European-Finnish (FIN) AF: 0.0572 AC: 606 AN: 10598

Middle Eastern (MID) AF: 0.0714 AC: 21 AN: 294

European-Non Finnish (NFE) AF: 0.00797 AC: 542 AN: 67996

Other (OTH) AF: 0.214 AC: 452 AN: 2110

Alfa AF: 0.164 Hom.: 1144

Bravo AF: 0.277

Asia WGS AF: 0.172 AC: 599 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.97
CADD	Benign	0.30
DANN	Benign	0.59
PhyloP100		-0.29
Mutation Taster		=100/0	polymorphism (auto)

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

Other links and lift over

dbSNP: rs9321552; hg19: chr6-136481612;