rs2918215

chr3-115828629-C-T

Variant summary

Our verdict is Benign. Variant got -12 ACMG points: 0P and 12B. BP4_Strong BA1

The NM_002338.5(LSAMP):c.919+13216G>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.148 in 152,250 control chromosomes in the GnomAD database, including 1,942 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 0.15 (1942 hom., cov: 32)
• Consequence: LSAMP NM_002338.5 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.207

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]

LOC124906269 (HGNC:):

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.7).
• BA1: GnomAd4 highest subpopulation (AMR) allele frequency at 95% confidence interval = 0.272 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
LSAMP	NM_002338.5	c.919+13216G>A		intron_variant		ENST00000490035.7
LOC124906269	XR_007096010.1	n.58+37471C>T		intron_variant, non_coding_transcript_variant

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
LSAMP	ENST00000490035.7	c.919+13216G>A		intron_variant		1	NM_002338.5	P1
LSAMP	ENST00000333617.8	c.907+5933G>A		intron_variant		2
LSAMP	ENST00000475403.2	n.225+5933G>A		intron_variant, non_coding_transcript_variant		3

Frequencies

GnomAD3 genomes AF: 0.148 AC: 22450 AN: 152132 Hom.: 1937 Cov.: 32

Gnomad AFR AF: 0.155

Gnomad AMI AF: 0.121

Gnomad AMR AF: 0.279

Gnomad ASJ AF: 0.0960

Gnomad EAS AF: 0.230

Gnomad SAS AF: 0.160

Gnomad FIN AF: 0.141

Gnomad MID AF: 0.158

Gnomad NFE AF: 0.110

Gnomad OTH AF: 0.152

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

GnomAD4 genome AF: 0.148 AC: 22473 AN: 152250 Hom.: 1942 Cov.: 32 AF XY: 0.153 AC XY: 11403 AN XY: 74434

Gnomad4 AFR AF: 0.155

Gnomad4 AMR AF: 0.279

Gnomad4 ASJ AF: 0.0960

Gnomad4 EAS AF: 0.230

Gnomad4 SAS AF: 0.160

Gnomad4 FIN AF: 0.141

Gnomad4 NFE AF: 0.110

Gnomad4 OTH AF: 0.154

Alfa AF: 0.125 Hom.: 171

Bravo AF: 0.159

Asia WGS AF: 0.180 AC: 625 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.70
Cadd	Benign	5.1
Dann	Benign	0.66

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

Publications

LitVar

Other links and lift over

dbSNP: rs2918215; hg19: chr3-115547476;