rs4498351

Variant names:

• chr6-46709046-T-A
• rs4498351
• NM_005084.4:c.869+281A>T

Your query was ambiguous. Multiple possible variants found:

• chr6-46709046-T-A
• chr6-46709046-T-G

Variant summary

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

The NM_005084.4(PLA2G7):​c.869+281A>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.414 in 151,868 control chromosomes in the GnomAD database, including 13,507 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 0.41 (13507 hom., cov: 32)
• Consequence: PLA2G7 NM_005084.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.834
• Publications: 15 publications found

Genes affected

PLA2G7 (HGNC:9040): (phospholipase A2 group VII) The protein encoded by this gene is a secreted enzyme that catalyzes the degradation of platelet-activating factor to biologically inactive products. Defects in this gene are a cause of platelet-activating factor acetylhydrolase deficiency. Two transcript variants encoding the same protein have been found for this gene.[provided by RefSeq, Dec 2009]

ACMG classification

Our verdict: Benign. The variant received -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 = 0.548 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
PLA2G7	NM_005084.4	c.869+281A>T		intron_variant	Intron 9 of 11	ENST00000274793.12	NP_005075.3

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
PLA2G7	ENST00000274793.12	c.869+281A>T		intron_variant	Intron 9 of 11	1	NM_005084.4	ENSP00000274793.7
PLA2G7	ENST00000537365.1	c.869+281A>T		intron_variant	Intron 9 of 11	1		ENSP00000445666.1

Frequencies

GnomAD3 genomes AF: 0.414 AC: 62875 AN: 151750 Hom.: 13503 Cov.: 32

Gnomad AFR AF: 0.313

Gnomad AMI AF: 0.327

Gnomad AMR AF: 0.421

Gnomad ASJ AF: 0.407

Gnomad EAS AF: 0.564

Gnomad SAS AF: 0.234

Gnomad FIN AF: 0.431

Gnomad MID AF: 0.389

Gnomad NFE AF: 0.475

Gnomad OTH AF: 0.414

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

GnomAD4 genome AF: 0.414 AC: 62911 AN: 151868 Hom.: 13507 Cov.: 32 AF XY: 0.411 AC XY: 30541 AN XY: 74224

African (AFR) AF: 0.313 AC: 12966 AN: 41418

American (AMR) AF: 0.421 AC: 6420 AN: 15256

Ashkenazi Jewish (ASJ) AF: 0.407 AC: 1411 AN: 3466

East Asian (EAS) AF: 0.565 AC: 2913 AN: 5158

South Asian (SAS) AF: 0.235 AC: 1131 AN: 4818

European-Finnish (FIN) AF: 0.431 AC: 4536 AN: 10534

Middle Eastern (MID) AF: 0.401 AC: 118 AN: 294

European-Non Finnish (NFE) AF: 0.475 AC: 32255 AN: 67910

Other (OTH) AF: 0.411 AC: 863 AN: 2102

Alfa AF: 0.450 Hom.: 2183

Bravo AF: 0.412

Asia WGS AF: 0.361 AC: 1252 AN: 3472

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.93
CADD	Benign	0.87
DANN	Benign	0.43
PhyloP100		-0.83
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: rs4498351; hg19: chr6-46676783;