chr9-28374102-C-T

Variant names:

• chr9-28374102-C-T
• rs10968542
• NM_001258282.3:c.-227-1234G>A

Variant summary

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

The NM_001258282.3(LINGO2):​c.-227-1234G>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.344 in 151,260 control chromosomes in the GnomAD database, including 10,288 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 0.34 (10288 hom., cov: 29)
• Consequence: LINGO2 NM_001258282.3 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.629
• Publications: 1 publications found

Genes affected

LINGO2 (HGNC:21207): (leucine rich repeat and Ig domain containing 2) Predicted to act upstream of or within positive regulation of synapse assembly. Predicted to be integral component of membrane. Predicted to be active in extracellular matrix and extracellular space. [provided by Alliance of Genome Resources, Apr 2022]

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.91).
• BA1: GnomAd4 highest subpopulation (NFE) allele frequency at 95% confidence interval = 0.419 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_001258282.3. 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
	LINGO2	NM_001258282.3	MANE Select	c.-227-1234G>A		intron	N/A	NP_001245211.1
	LINGO2	NM_001354574.2		c.-194-78736G>A		intron	N/A	NP_001341503.1
	LINGO2	NM_001354575.2		c.-227-1234G>A		intron	N/A	NP_001341504.1

Ensembl Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	LINGO2	ENST00000698399.1	MANE Select	c.-227-1234G>A		intron	N/A	ENSP00000513694.1
	LINGO2	ENST00000379992.6	TSL:5	c.-278-1234G>A		intron	N/A	ENSP00000369328.1
	LINGO2	ENST00000698400.1		c.-442-1234G>A		intron	N/A	ENSP00000513695.1

Frequencies

GnomAD3 genomes AF: 0.344 AC: 52044 AN: 151158 Hom.: 10291 Cov.: 29

Gnomad AFR AF: 0.156

Gnomad AMI AF: 0.318

Gnomad AMR AF: 0.351

Gnomad ASJ AF: 0.445

Gnomad EAS AF: 0.274

Gnomad SAS AF: 0.336

Gnomad FIN AF: 0.570

Gnomad MID AF: 0.321

Gnomad NFE AF: 0.424

Gnomad OTH AF: 0.355

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

GnomAD4 genome AF: 0.344 AC: 52042 AN: 151260 Hom.: 10288 Cov.: 29 AF XY: 0.350 AC XY: 25832 AN XY: 73838

African (AFR) AF: 0.156 AC: 6433 AN: 41280

American (AMR) AF: 0.351 AC: 5316 AN: 15156

Ashkenazi Jewish (ASJ) AF: 0.445 AC: 1542 AN: 3466

East Asian (EAS) AF: 0.274 AC: 1397 AN: 5092

South Asian (SAS) AF: 0.336 AC: 1610 AN: 4794

European-Finnish (FIN) AF: 0.570 AC: 5891 AN: 10338

Middle Eastern (MID) AF: 0.319 AC: 92 AN: 288

European-Non Finnish (NFE) AF: 0.424 AC: 28739 AN: 67848

Other (OTH) AF: 0.351 AC: 733 AN: 2090

Alfa AF: 0.404 Hom.: 5592

Bravo AF: 0.324

Asia WGS AF: 0.269 AC: 936 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.91
CADD	Benign	1.5
DANN	Benign	0.90
PhyloP100		-0.63
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: rs10968542; hg19: chr9-28374100; COSMIC: COSV66143801;