rs10791345

Positions:

• chr11-134142118-G-A

Variant summary

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

The NM_032801.5(JAM3):​c.256+1348G>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.176 in 152,054 control chromosomes in the GnomAD database, including 2,466 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 0.18 (2466 hom., cov: 32)
• Consequence: JAM3 NM_032801.5 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.847

Genes affected

JAM3 (HGNC:15532): (junctional adhesion molecule 3) Tight junctions represent one mode of cell-to-cell adhesion in epithelial or endothelial cell sheets, forming continuous seals around cells and serving as a physical barrier to prevent solutes and water from passing freely through the paracellular space. The protein encoded by this immunoglobulin superfamily gene member is localized in the tight junctions between high endothelial cells. Unlike other proteins in this family, the this protein is unable to adhere to leukocyte cell lines and only forms weak homotypic interactions. The encoded protein is a member of the junctional adhesion molecule protein family and acts as a receptor for another member of this family. A mutation in an intron of this gene is associated with hemorrhagic destruction of the brain, subependymal calcification, and congenital cataracts. Alternative splicing results in multiple transcript variants.[provided by RefSeq, Apr 2011]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.84).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.208 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
JAM3	NM_032801.5	c.256+1348G>A		intron_variant		ENST00000299106.9
JAM3	NM_001205329.2	c.256+1348G>A		intron_variant

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
JAM3	ENST00000299106.9	c.256+1348G>A		intron_variant		1	NM_032801.5	P1

Frequencies

GnomAD3 genomes AF: 0.176 AC: 26734 AN: 151936 Hom.: 2458 Cov.: 32

Gnomad AFR AF: 0.212

Gnomad AMI AF: 0.142

Gnomad AMR AF: 0.164

Gnomad ASJ AF: 0.121

Gnomad EAS AF: 0.142

Gnomad SAS AF: 0.0754

Gnomad FIN AF: 0.243

Gnomad MID AF: 0.0696

Gnomad NFE AF: 0.161

Gnomad OTH AF: 0.152

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

GnomAD4 genome AF: 0.176 AC: 26768 AN: 152054 Hom.: 2466 Cov.: 32 AF XY: 0.179 AC XY: 13269 AN XY: 74320

Gnomad4 AFR AF: 0.212

Gnomad4 AMR AF: 0.164

Gnomad4 ASJ AF: 0.121

Gnomad4 EAS AF: 0.142

Gnomad4 SAS AF: 0.0765

Gnomad4 FIN AF: 0.243

Gnomad4 NFE AF: 0.161

Gnomad4 OTH AF: 0.151

Alfa AF: 0.160 Hom.: 989

Bravo AF: 0.173

Asia WGS AF: 0.0980 AC: 341 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.84
CADD	Benign	12
DANN	Benign	0.54

Splicing

Name	Calibrated prediction	Score	Prediction
SpliceAI score (max)		0.070		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: rs10791345; hg19: chr11-134012013;