chr8-97926160-C-A

Variant names:

• chr8-97926160-C-A
• rs1378124
• NM_002380.5:c.143-4793C>A

Variant summary

Our verdict is Likely benign. The variant received -2 ACMG points: 2P and 4B. PM2 BP4_Strong

The NM_002380.5(MATN2):​c.143-4793C>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant was absent in control chromosomes in GnomAD project. 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: not found (cov: 31)
• Consequence: MATN2 NM_002380.5 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.630
• Publications: 4 publications found

Genes affected

MATN2 (HGNC:6908): (matrilin 2) This gene encodes a member of the von Willebrand factor A domain containing protein family. This family of proteins is thought to be involved in the formation of filamentous networks in the extracellular matrices of various tissues. This protein contains five von Willebrand factor A domains. The specific function of this gene has not yet been determined. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]

ACMG classification

Our verdict: Likely_benign. The variant received -2 ACMG points.

• PM2: Very rare variant in population databases, with high coverage
• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.64).

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
MATN2	NM_002380.5	c.143-4793C>A		intron_variant	Intron 2 of 18	ENST00000254898.7	NP_002371.3
MATN2	NM_030583.4	c.143-4793C>A		intron_variant	Intron 2 of 18		NP_085072.2
MATN2	NM_001317748.2	c.143-4793C>A		intron_variant	Intron 2 of 17		NP_001304677.1
MATN2	XM_005250920.3	c.143-4793C>A		intron_variant	Intron 2 of 17		XP_005250977.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
MATN2	ENST00000254898.7	c.143-4793C>A		intron_variant	Intron 2 of 18	1	NM_002380.5	ENSP00000254898.6
MATN2	ENST00000520016.5	c.143-4793C>A		intron_variant	Intron 1 of 17	1		ENSP00000430487.1
MATN2	ENST00000521689.5	c.143-4793C>A		intron_variant	Intron 2 of 18	1		ENSP00000429977.1
MATN2	ENST00000524308.5	c.143-4793C>A		intron_variant	Intron 2 of 17	1		ENSP00000430221.1
MATN2	ENST00000522025.6	c.-117-4378C>A		intron_variant	Intron 1 of 17	5		ENSP00000429010.1

Frequencies

GnomAD3 genomes Cov.: 31

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

GnomAD4 genome Cov.: 31

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.64
CADD	Benign	5.9
DANN	Benign	0.82
PhyloP100		-0.63

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: rs1378124; hg19: chr8-98938388;