15-88852395-A-G

Variant names:

• chr15-88852395-A-G
• rs2280470
• NM_001369268.1:c.2266+362A>G

Variant summary

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

The NM_001369268.1(ACAN):​c.2266+362A>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.674 in 152,032 control chromosomes in the GnomAD database, including 35,646 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 0.67 (35646 hom., cov: 31)
• Consequence: ACAN NM_001369268.1 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.685
• Publications: 27 publications found

Genes affected

ACAN (HGNC:319): (aggrecan) This gene is a member of the aggrecan/versican proteoglycan family. The encoded protein is an integral part of the extracellular matrix in cartilagenous tissue and it withstands compression in cartilage. Mutations in this gene may be involved in skeletal dysplasia and spinal degeneration. Multiple alternatively spliced transcript variants that encode different protein isoforms have been observed in this gene. [provided by RefSeq, Jul 2008]

ACAN Gene-Disease associations (from GenCC):

• osteochondritis dissecans

  Inheritance: AD Classification: DEFINITIVE, SUPPORTIVE Submitted by: Illumina, Orphanet
• short stature and advanced bone age, with or without early-onset osteoarthritis and/or osteochondritis dissecans

  Inheritance: AD Classification: DEFINITIVE Submitted by: Ambry Genetics
• spondyloepiphyseal dysplasia, Kimberley type

  Inheritance: AD Classification: DEFINITIVE, STRONG, SUPPORTIVE, LIMITED Submitted by: G2P, Labcorp Genetics (formerly Invitae), Orphanet, Ambry Genetics
• spondyloepimetaphyseal dysplasia, aggrecan type

  Inheritance: AR Classification: DEFINITIVE, STRONG, SUPPORTIVE, LIMITED Submitted by: Labcorp Genetics (formerly Invitae), G2P, Ambry Genetics, Orphanet
• short stature-advanced bone age-early-onset osteoarthritis syndrome

  Inheritance: AD Classification: SUPPORTIVE Submitted by: Orphanet

ACMG classification

Our verdict: Benign. The variant received -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.99).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.8 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_001369268.1. You can select a different transcript below to see updated ACMG assignments.

RefSeq Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	ACAN	NM_001369268.1	MANE Select	c.2266+362A>G		intron	N/A	NP_001356197.1
	ACAN	NM_001411097.1		c.2266+362A>G		intron	N/A	NP_001398026.1
	ACAN	NM_013227.4		c.2266+362A>G		intron	N/A	NP_037359.3

Ensembl Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	ACAN	ENST00000560601.4	TSL:3 MANE Select	c.2266+362A>G		intron	N/A	ENSP00000453581.2
	ACAN	ENST00000439576.7	TSL:5	c.2266+362A>G		intron	N/A	ENSP00000387356.2
	ACAN	ENST00000561243.7	TSL:5	c.2266+362A>G		intron	N/A	ENSP00000453342.3

Frequencies

GnomAD3 genomes AF: 0.674 AC: 102437 AN: 151914 Hom.: 35629 Cov.: 31

Gnomad AFR AF: 0.808

Gnomad AMI AF: 0.702

Gnomad AMR AF: 0.541

Gnomad ASJ AF: 0.667

Gnomad EAS AF: 0.245

Gnomad SAS AF: 0.575

Gnomad FIN AF: 0.612

Gnomad MID AF: 0.687

Gnomad NFE AF: 0.673

Gnomad OTH AF: 0.672

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

GnomAD4 genome AF: 0.674 AC: 102501 AN: 152032 Hom.: 35646 Cov.: 31 AF XY: 0.664 AC XY: 49333 AN XY: 74312

African (AFR) AF: 0.807 AC: 33485 AN: 41478

American (AMR) AF: 0.540 AC: 8242 AN: 15276

Ashkenazi Jewish (ASJ) AF: 0.667 AC: 2312 AN: 3468

East Asian (EAS) AF: 0.245 AC: 1267 AN: 5174

South Asian (SAS) AF: 0.574 AC: 2764 AN: 4814

European-Finnish (FIN) AF: 0.612 AC: 6462 AN: 10558

Middle Eastern (MID) AF: 0.684 AC: 201 AN: 294

European-Non Finnish (NFE) AF: 0.673 AC: 45713 AN: 67952

Other (OTH) AF: 0.672 AC: 1419 AN: 2112

Alfa AF: 0.665 Hom.: 65911

Bravo AF: 0.669

Asia WGS AF: 0.486 AC: 1693 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.99
CADD	Benign	0.79
DANN	Benign	0.81
PhyloP100		-0.69
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: rs2280470; hg19: chr15-89395626;