rs6984368

chr8-80980674-G-T

Variant summary

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

The NM_018440.4(PAG1):c.877-180C>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.228 in 152,056 control chromosomes in the GnomAD database, including 6,137 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 0.23 (6137 hom., cov: 32)
• Consequence: PAG1 NM_018440.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -1.12

Genes affected

PAG1 (HGNC:30043): (phosphoprotein membrane anchor with glycosphingolipid microdomains 1) The protein encoded by this gene is a type III transmembrane adaptor protein that binds to the tyrosine kinase csk protein. It is thought to be involved in the regulation of T cell activation. [provided by RefSeq, Jul 2008]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.88).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.488 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
PAG1	NM_018440.4	c.877-180C>A		intron_variant		ENST00000220597.4

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
PAG1	ENST00000220597.4	c.877-180C>A		intron_variant		2	NM_018440.4	P1

Frequencies

GnomAD3 genomes AF: 0.227 AC: 34558 AN: 151938 Hom.: 6122 Cov.: 32

Gnomad AFR AF: 0.494

Gnomad AMI AF: 0.171

Gnomad AMR AF: 0.146

Gnomad ASJ AF: 0.183

Gnomad EAS AF: 0.00173

Gnomad SAS AF: 0.175

Gnomad FIN AF: 0.172

Gnomad MID AF: 0.222

Gnomad NFE AF: 0.116

Gnomad OTH AF: 0.232

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

GnomAD4 genome AF: 0.228 AC: 34615 AN: 152056 Hom.: 6137 Cov.: 32 AF XY: 0.226 AC XY: 16774 AN XY: 74332

Gnomad4 AFR AF: 0.494

Gnomad4 AMR AF: 0.145

Gnomad4 ASJ AF: 0.183

Gnomad4 EAS AF: 0.00193

Gnomad4 SAS AF: 0.176

Gnomad4 FIN AF: 0.172

Gnomad4 NFE AF: 0.116

Gnomad4 OTH AF: 0.229

Alfa AF: 0.161 Hom.: 1257

Bravo AF: 0.237

Asia WGS AF: 0.0990 AC: 346 AN: 3476

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.88
Cadd	Benign	0.32
Dann	Benign	0.48

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: rs6984368; hg19: chr8-81892909;