rs2829866

Positions:

• chr21-25686759-T-A
• chr21-25686759-T-C

Variant summary

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

The NM_021219.4(JAM2):​c.133+2811T>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.355 in 152,136 control chromosomes in the GnomAD database, including 10,095 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 0.36 (10095 hom., cov: 33)
• Consequence: JAM2 NM_021219.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 1.33

Genes affected

JAM2 (HGNC:14686): (junctional adhesion molecule 2) This gene belongs to the immunoglobulin superfamily, and the junctional adhesion molecule (JAM) family. The protein encoded by this gene is a type I membrane protein that is localized at the tight junctions of both epithelial and endothelial cells. It acts as an adhesive ligand for interacting with a variety of immune cell types, and may play a role in lymphocyte homing to secondary lymphoid organs. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jul 2012]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.85).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.457 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
JAM2	NM_021219.4	c.133+2811T>A		intron_variant		ENST00000480456.6	NP_067042.1
JAM2	NM_001270407.2	c.133+2811T>A		intron_variant			NP_001257336.1
JAM2	NM_001270408.2	c.133+2811T>A		intron_variant			NP_001257337.1
JAM2	NR_072999.2	n.697+2811T>A		intron_variant, non_coding_transcript_variant

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
JAM2	ENST00000480456.6	c.133+2811T>A		intron_variant		1	NM_021219.4	ENSP00000420419	P1
JAM2	ENST00000400532.5	c.133+2811T>A		intron_variant		1		ENSP00000383376
JAM2	ENST00000312957.9	c.133+2811T>A		intron_variant		2		ENSP00000318416

Frequencies

GnomAD3 genomes AF: 0.355 AC: 54010 AN: 152018 Hom.: 10082 Cov.: 33

Gnomad AFR AF: 0.462

Gnomad AMI AF: 0.128

Gnomad AMR AF: 0.308

Gnomad ASJ AF: 0.295

Gnomad EAS AF: 0.362

Gnomad SAS AF: 0.453

Gnomad FIN AF: 0.301

Gnomad MID AF: 0.329

Gnomad NFE AF: 0.309

Gnomad OTH AF: 0.338

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

GnomAD4 genome AF: 0.355 AC: 54061 AN: 152136 Hom.: 10095 Cov.: 33 AF XY: 0.354 AC XY: 26300 AN XY: 74396

Gnomad4 AFR AF: 0.462

Gnomad4 AMR AF: 0.309

Gnomad4 ASJ AF: 0.295

Gnomad4 EAS AF: 0.361

Gnomad4 SAS AF: 0.452

Gnomad4 FIN AF: 0.301

Gnomad4 NFE AF: 0.309

Gnomad4 OTH AF: 0.338

Alfa AF: 0.194 Hom.: 383

Bravo AF: 0.360

Asia WGS AF: 0.433 AC: 1502 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.85
CADD	Benign	15
DANN	Benign	0.80

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: rs2829866; hg19: chr21-27059071;