11-134094614-CTTCTCCTGAACCCTCCTTATTCATCATGTTCCACCTTAAATGTCACTTCCTGAGGGAAGCAT-C

Position:

• chr11-134094614-CTTCTCCTGAACCCTCCTTATTCATCATGTTCCACCTTAAATGTCACTTCCTGAGGGAAGCAT-C

Variant summary

Our verdict is Uncertain significance. Variant got 0 ACMG points: 0P and 0B.

The NM_032801.5(JAM3):​c.76+25456_76+25517delTTCTCCTGAACCCTCCTTATTCATCATGTTCCACCTTAAATGTCACTTCCTGAGGGAAGCAT variant causes a intron change involving the alteration of a non-conserved nucleotide. Variant has been reported in ClinVar as Uncertain significance (no stars).

• Frequency: Genomes: not found (cov: 0)
• Consequence: JAM3 NM_032801.5 intron
• Clinical Significance: Uncertain significance no assertion criteria provided U:1
• Conservation: PhyloP100: 0.349

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]

LOC124902797 (HGNC:):

ACMG classification

Verdict is Uncertain_significance. Variant got 0 ACMG points.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
JAM3	NM_032801.5	c.76+25456_76+25517delTTCTCCTGAACCCTCCTTATTCATCATGTTCCACCTTAAATGTCACTTCCTGAGGGAAGCAT		intron_variant		ENST00000299106.9	NP_116190.3
JAM3	NM_001205329.2	c.76+25456_76+25517delTTCTCCTGAACCCTCCTTATTCATCATGTTCCACCTTAAATGTCACTTCCTGAGGGAAGCAT		intron_variant			NP_001192258.1
LOC124902797	XR_007062960.1	n.10_71delATGCTTCCCTCAGGAAGTGACATTTAAGGTGGAACATGATGAATAAGGAGGGTTCAGGAGAA		non_coding_transcript_exon_variant	1/2

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
JAM3	ENST00000299106.9	c.76+25456_76+25517delTTCTCCTGAACCCTCCTTATTCATCATGTTCCACCTTAAATGTCACTTCCTGAGGGAAGCAT		intron_variant		1	NM_032801.5	ENSP00000299106.4

Frequencies

GnomAD3 genomes Cov.: 0

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

GnomAD4 genome Cov.: 0

ClinVar

Significance: Uncertain significance

Submissions summary: Uncertain:1

Revision: no assertion criteria provided

Submissions by phenotype

Schizophrenia Uncertain:1

Uncertain significance, no assertion criteria provided

case-control

Department of Psychiatry, The University of Hong Kong

Nov 11, 2022

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Computational scores

Source: dbNSFP v4.3

Splicing

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

Publications

No publications associated with this variant yet.

Other links and lift over

hg19: chr11-133964509;