rs10790332

Variant names:

• chr11-119682968-C-T
• rs10790332
• NM_002855.5:c.80-4203G>A

Variant summary

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

The NM_002855.5(NECTIN1):​c.80-4203G>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.343 in 152,136 control chromosomes in the GnomAD database, including 9,730 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 (9730 hom., cov: 32)
• Consequence: NECTIN1 NM_002855.5 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.177
• Publications: 9 publications found

Genes affected

NECTIN1 (HGNC:9706): (nectin cell adhesion molecule 1) This gene encodes an adhesion protein that plays a role in the organization of adherens junctions and tight junctions in epithelial and endothelial cells. The protein is a calcium(2+)-independent cell-cell adhesion molecule that belongs to the immunoglobulin superfamily and has 3 extracellular immunoglobulin-like loops, a single transmembrane domain (in some isoforms), and a cytoplasmic region. This protein acts as a receptor for glycoprotein D (gD) of herpes simplex viruses 1 and 2 (HSV-1, HSV-2), and pseudorabies virus (PRV) and mediates viral entry into epithelial and neuronal cells. Mutations in this gene cause cleft lip and palate/ectodermal dysplasia 1 syndrome (CLPED1) as well as non-syndromic cleft lip with or without cleft palate (CL/P). Alternative splicing results in multiple transcript variants encoding proteins with distinct C-termini. [provided by RefSeq, Oct 2009]

NECTIN1 Gene-Disease associations (from GenCC):

• cleft lip/palate-ectodermal dysplasia syndrome

  Inheritance: AR Classification: STRONG, MODERATE, SUPPORTIVE Submitted by: Ambry Genetics, Labcorp Genetics (formerly Invitae), Orphanet, G2P

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.89).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.463 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_002855.5. 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
	NECTIN1	NM_002855.5	MANE Select	c.80-4203G>A		intron	N/A	NP_002846.3
	NECTIN1	NM_203285.2		c.80-4203G>A		intron	N/A	NP_976030.1
	NECTIN1	NM_203286.2		c.80-4203G>A		intron	N/A	NP_976031.1

Ensembl Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	NECTIN1	ENST00000264025.8	TSL:1 MANE Select	c.80-4203G>A		intron	N/A	ENSP00000264025.3
	NECTIN1	ENST00000340882.2	TSL:1	c.80-4203G>A		intron	N/A	ENSP00000345289.2
	NECTIN1	ENST00000341398.6	TSL:1	n.80-4203G>A		intron	N/A

Frequencies

GnomAD3 genomes AF: 0.343 AC: 52121 AN: 152018 Hom.: 9710 Cov.: 32

Gnomad AFR AF: 0.204

Gnomad AMI AF: 0.254

Gnomad AMR AF: 0.447

Gnomad ASJ AF: 0.318

Gnomad EAS AF: 0.478

Gnomad SAS AF: 0.337

Gnomad FIN AF: 0.445

Gnomad MID AF: 0.389

Gnomad NFE AF: 0.380

Gnomad OTH AF: 0.352

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

GnomAD4 genome AF: 0.343 AC: 52181 AN: 152136 Hom.: 9730 Cov.: 32 AF XY: 0.349 AC XY: 25973 AN XY: 74354

African (AFR) AF: 0.204 AC: 8469 AN: 41516

American (AMR) AF: 0.448 AC: 6843 AN: 15288

Ashkenazi Jewish (ASJ) AF: 0.318 AC: 1103 AN: 3470

East Asian (EAS) AF: 0.478 AC: 2469 AN: 5162

South Asian (SAS) AF: 0.338 AC: 1628 AN: 4818

European-Finnish (FIN) AF: 0.445 AC: 4708 AN: 10584

Middle Eastern (MID) AF: 0.380 AC: 111 AN: 292

European-Non Finnish (NFE) AF: 0.380 AC: 25863 AN: 67984

Other (OTH) AF: 0.358 AC: 755 AN: 2110

Alfa AF: 0.367 Hom.: 5826

Bravo AF: 0.342

Asia WGS AF: 0.416 AC: 1447 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.89
CADD	Benign	3.9
DANN	Benign	0.58
PhyloP100		-0.18
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: rs10790332; hg19: chr11-119553678;