rs6464375

chr7-153928758-C-T

Variant summary

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

The ENST00000404039.5(DPP6):c.51+41024C>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.0657 in 152,100 control chromosomes in the GnomAD database, including 343 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 0.066 (343 hom., cov: 30)
• Consequence: DPP6 ENST00000404039.5 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -1.11

Genes affected

DPP6 (HGNC:3010): (dipeptidyl peptidase like 6) This gene encodes a single-pass type II membrane protein that is a member of the peptidase S9B family of serine proteases. This protein has no detectable protease activity, most likely due to the absence of the conserved serine residue normally present in the catalytic domain of serine proteases. However, it does bind specific voltage-gated potassium channels and alters their expression and biophysical properties. Variations in this gene may be associated with susceptibility to amyotrophic lateral sclerosis and with idiopathic ventricular fibrillation. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2014]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-1.0).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.0828 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
DPP6	NM_001039350.3	c.51+41024C>T		intron_variant
DPP6	NM_001364497.2	c.60+179750C>T		intron_variant
DPP6	NM_001364498.2	c.60+179750C>T		intron_variant

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
DPP6	ENST00000404039.5	c.51+41024C>T		intron_variant		1
DPP6	ENST00000706130.1	c.60+179750C>T		intron_variant

Frequencies

GnomAD3 genomes AF: 0.0657 AC: 9982 AN: 151982 Hom.: 343 Cov.: 30

Gnomad AFR AF: 0.0853

Gnomad AMI AF: 0.197

Gnomad AMR AF: 0.0603

Gnomad ASJ AF: 0.0202

Gnomad EAS AF: 0.0414

Gnomad SAS AF: 0.0237

Gnomad FIN AF: 0.0506

Gnomad MID AF: 0.0570

Gnomad NFE AF: 0.0628

Gnomad OTH AF: 0.0605

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

GnomAD4 genome AF: 0.0657 AC: 9987 AN: 152100 Hom.: 343 Cov.: 30 AF XY: 0.0634 AC XY: 4712 AN XY: 74380

Gnomad4 AFR AF: 0.0851

Gnomad4 AMR AF: 0.0605

Gnomad4 ASJ AF: 0.0202

Gnomad4 EAS AF: 0.0413

Gnomad4 SAS AF: 0.0237

Gnomad4 FIN AF: 0.0506

Gnomad4 NFE AF: 0.0629

Gnomad4 OTH AF: 0.0608

Alfa AF: 0.0579 Hom.: 448

Bravo AF: 0.0679

Asia WGS AF: 0.0450 AC: 155 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-1.0
Cadd	Benign	0.40
Dann	Benign	0.36

Splicing

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

Publications

LitVar

Other links and lift over

dbSNP: rs6464375; hg19: chr7-153625843; COSMIC: COSV68054957;