rs6776244

Variant names:

• chr3-116050452-G-A
• rs6776244
• NM_002338.5:c.389-30812C>T

Your query was ambiguous. Multiple possible variants found:

• chr3-116050452-G-A
• chr3-116050452-G-C
• chr3-116050452-G-T

Variant summary

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

The NM_002338.5(LSAMP):​c.389-30812C>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.456 in 151,790 control chromosomes in the GnomAD database, including 19,320 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 0.46 (19320 hom., cov: 31)
• Consequence: LSAMP NM_002338.5 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 1.59
• Publications: 4 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]

ENSG00000297753 (HGNC:):

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.77).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.715 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
LSAMP	NM_002338.5	c.389-30812C>T		intron_variant	Intron 2 of 6	ENST00000490035.7	NP_002329.2

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
LSAMP	ENST00000490035.7	c.389-30812C>T		intron_variant	Intron 2 of 6	1	NM_002338.5	ENSP00000419000.1

Frequencies

GnomAD3 genomes AF: 0.456 AC: 69165 AN: 151672 Hom.: 19329 Cov.: 31

Gnomad AFR AF: 0.116

Gnomad AMI AF: 0.660

Gnomad AMR AF: 0.475

Gnomad ASJ AF: 0.642

Gnomad EAS AF: 0.735

Gnomad SAS AF: 0.702

Gnomad FIN AF: 0.615

Gnomad MID AF: 0.653

Gnomad NFE AF: 0.581

Gnomad OTH AF: 0.482

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

GnomAD4 genome AF: 0.456 AC: 69151 AN: 151790 Hom.: 19320 Cov.: 31 AF XY: 0.463 AC XY: 34346 AN XY: 74118

African (AFR) AF: 0.116 AC: 4802 AN: 41398

American (AMR) AF: 0.475 AC: 7241 AN: 15240

Ashkenazi Jewish (ASJ) AF: 0.642 AC: 2226 AN: 3468

East Asian (EAS) AF: 0.734 AC: 3790 AN: 5160

South Asian (SAS) AF: 0.701 AC: 3367 AN: 4800

European-Finnish (FIN) AF: 0.615 AC: 6452 AN: 10486

Middle Eastern (MID) AF: 0.640 AC: 187 AN: 292

European-Non Finnish (NFE) AF: 0.581 AC: 39466 AN: 67934

Other (OTH) AF: 0.485 AC: 1019 AN: 2102

Alfa AF: 0.538 Hom.: 13445

Bravo AF: 0.426

Asia WGS AF: 0.651 AC: 2266 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.77
CADD	Benign	12
DANN	Benign	0.57
PhyloP100		1.6
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: rs6776244; hg19: chr3-115769299;