NM_002338.5:c.155+177381G>A

Variant names:

• chr3-116267496-C-T
• rs10934326
• NM_002338.5:c.155+177381G>A

Variant summary

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

The NM_002338.5(LSAMP):​c.155+177381G>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.196 in 151,464 control chromosomes in the GnomAD database, including 3,148 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 0.20 (3148 hom., cov: 29)
• Consequence: LSAMP NM_002338.5 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.261
• Publications: 2 publications found

Genes affected

LSAMP (HGNC:6705): (limbic system associated membrane protein) This gene encodes a member of the immunoglobulin LAMP, OBCAM and neurotrimin (IgLON) family of proteins. The encoded preproprotein is proteolytically processed to generate a neuronal surface glycoprotein. This protein may act as a selective homophilic adhesion molecule during axon guidance and neuronal growth in the developing limbic system. The encoded protein may also function as a tumor suppressor and may play a role in neuropsychiatric disorders. Alternative splicing results in multiple transcript variants, at least one of which encodes a preproprotein that is proteolytically processed. [provided by RefSeq, Jan 2016]

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.86).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.231 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_002338.5. 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
	LSAMP	NM_002338.5	MANE Select	c.155+177381G>A		intron	N/A	NP_002329.2
	LSAMP	NM_001318915.2		c.155+177381G>A		intron	N/A	NP_001305844.1

Ensembl Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	LSAMP	ENST00000490035.7	TSL:1 MANE Select	c.155+177381G>A		intron	N/A	ENSP00000419000.1
	LSAMP	ENST00000333617.8	TSL:2	c.107+177381G>A		intron	N/A	ENSP00000328455.4
	LSAMP	ENST00000474851.1	TSL:5	c.257+177381G>A		intron	N/A	ENSP00000418506.1

Frequencies

GnomAD3 genomes AF: 0.196 AC: 29635 AN: 151350 Hom.: 3133 Cov.: 29

Gnomad AFR AF: 0.235

Gnomad AMI AF: 0.220

Gnomad AMR AF: 0.229

Gnomad ASJ AF: 0.126

Gnomad EAS AF: 0.141

Gnomad SAS AF: 0.175

Gnomad FIN AF: 0.274

Gnomad MID AF: 0.177

Gnomad NFE AF: 0.162

Gnomad OTH AF: 0.184

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

GnomAD4 genome AF: 0.196 AC: 29685 AN: 151464 Hom.: 3148 Cov.: 29 AF XY: 0.200 AC XY: 14807 AN XY: 73964

African (AFR) AF: 0.235 AC: 9678 AN: 41252

American (AMR) AF: 0.230 AC: 3498 AN: 15198

Ashkenazi Jewish (ASJ) AF: 0.126 AC: 436 AN: 3464

East Asian (EAS) AF: 0.141 AC: 721 AN: 5126

South Asian (SAS) AF: 0.175 AC: 837 AN: 4790

European-Finnish (FIN) AF: 0.274 AC: 2867 AN: 10450

Middle Eastern (MID) AF: 0.184 AC: 54 AN: 294

European-Non Finnish (NFE) AF: 0.162 AC: 11004 AN: 67872

Other (OTH) AF: 0.185 AC: 389 AN: 2106

Alfa AF: 0.173 Hom.: 3008

Bravo AF: 0.195

Asia WGS AF: 0.172 AC: 598 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.86
CADD	Benign	2.2
DANN	Benign	0.40
PhyloP100		0.26
Mutation Taster		=100/0	polymorphism (auto)

Splicing

Name	Calibrated prediction	Score	Prediction
SpliceAI score (max)		0.010		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: rs10934326; hg19: chr3-115986343; COSMIC: COSV61293800;