rs2445768

chr15-51343183-A-Cchr15-51343183-A-Gchr15-51343183-A-T

Variant summary

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

The NM_181789.4(GLDN):c.363+1136A>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.3 in 152,136 control chromosomes in the GnomAD database, including 8,814 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 0.30 (8814 hom., cov: 33)
• Consequence: GLDN NM_181789.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -1.19

Genes affected

GLDN (HGNC:29514): (gliomedin) This gene encodes a protein that contains olfactomedin-like and collagen-like domains. The encoded protein, which exists in both transmembrane and secreted forms, promotes formation of the nodes of Ranvier in the peripheral nervous system. Mutations in this gene cause a form of lethal congenital contracture syndrome in human patients. Autoantibodies to the encoded protein have been identified in sera form patients with multifocal motor neuropathy. [provided by RefSeq, May 2017]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.74).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.525 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
GLDN	NM_181789.4	c.363+1136A>C		intron_variant		ENST00000335449.11

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
GLDN	ENST00000335449.11	c.363+1136A>C		intron_variant		2	NM_181789.4	P1
GLDN	ENST00000558286.5	n.174+1136A>C		intron_variant, non_coding_transcript_variant		1
GLDN	ENST00000560690.5	n.140+1098A>C		intron_variant, non_coding_transcript_variant		1
GLDN	ENST00000560215.5	c.250+1136A>C		intron_variant		4

Frequencies

GnomAD3 genomes AF: 0.300 AC: 45560 AN: 152018 Hom.: 8784 Cov.: 33

Gnomad AFR AF: 0.530

Gnomad AMI AF: 0.215

Gnomad AMR AF: 0.268

Gnomad ASJ AF: 0.172

Gnomad EAS AF: 0.492

Gnomad SAS AF: 0.302

Gnomad FIN AF: 0.148

Gnomad MID AF: 0.190

Gnomad NFE AF: 0.184

Gnomad OTH AF: 0.284

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

GnomAD4 genome AF: 0.300 AC: 45657 AN: 152136 Hom.: 8814 Cov.: 33 AF XY: 0.300 AC XY: 22302 AN XY: 74380

Gnomad4 AFR AF: 0.531

Gnomad4 AMR AF: 0.269

Gnomad4 ASJ AF: 0.172

Gnomad4 EAS AF: 0.493

Gnomad4 SAS AF: 0.302

Gnomad4 FIN AF: 0.148

Gnomad4 NFE AF: 0.184

Gnomad4 OTH AF: 0.289

Alfa AF: 0.138 Hom.: 323

Bravo AF: 0.320

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.74
Cadd	Benign	2.9
Dann	Benign	0.67

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: rs2445768; hg19: chr15-51635380;