NM_001385028.1:c.-8-31497A>G

Variant names:

• chr15-66159908-T-C
• rs1477798
• NM_001385028.1:c.-8-31497A>G

Variant summary

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

The NM_001385028.1(MEGF11):​c.-8-31497A>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.742 in 151,898 control chromosomes in the GnomAD database, including 41,896 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 0.74 (41896 hom., cov: 30)
• Consequence: MEGF11 NM_001385028.1 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.374
• Publications: 4 publications found

Genes affected

MEGF11 (HGNC:29635): (multiple EGF like domains 11) Predicted to be involved in homotypic cell-cell adhesion and retina layer formation. Predicted to be located in basolateral plasma membrane. Predicted to be integral component of membrane. [provided by Alliance of Genome Resources, Apr 2022]

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.94).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.835 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_001385028.1. 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
	MEGF11	NM_001385028.1	MANE Select	c.-8-31497A>G		intron	N/A	NP_001371957.1
	MEGF11	NM_001387150.1		c.-30-31475A>G		intron	N/A	NP_001374079.1
	MEGF11	NM_032445.3		c.-8-31497A>G		intron	N/A	NP_115821.2

Ensembl Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	MEGF11	ENST00000395614.6	TSL:5 MANE Select	c.-8-31497A>G		intron	N/A	ENSP00000378976.2
	MEGF11	ENST00000422354.6	TSL:1	c.-8-31497A>G		intron	N/A	ENSP00000414475.1
	MEGF11	ENST00000288745.7	TSL:1	c.-26-35908A>G		intron	N/A	ENSP00000288745.3

Frequencies

GnomAD3 genomes AF: 0.742 AC: 112647 AN: 151780 Hom.: 41881 Cov.: 30

Gnomad AFR AF: 0.722

Gnomad AMI AF: 0.720

Gnomad AMR AF: 0.829

Gnomad ASJ AF: 0.732

Gnomad EAS AF: 0.856

Gnomad SAS AF: 0.794

Gnomad FIN AF: 0.752

Gnomad MID AF: 0.794

Gnomad NFE AF: 0.721

Gnomad OTH AF: 0.767

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

GnomAD4 genome AF: 0.742 AC: 112709 AN: 151898 Hom.: 41896 Cov.: 30 AF XY: 0.747 AC XY: 55463 AN XY: 74250

African (AFR) AF: 0.722 AC: 29872 AN: 41400

American (AMR) AF: 0.829 AC: 12665 AN: 15276

Ashkenazi Jewish (ASJ) AF: 0.732 AC: 2539 AN: 3468

East Asian (EAS) AF: 0.856 AC: 4412 AN: 5152

South Asian (SAS) AF: 0.793 AC: 3808 AN: 4802

European-Finnish (FIN) AF: 0.752 AC: 7938 AN: 10560

Middle Eastern (MID) AF: 0.786 AC: 231 AN: 294

European-Non Finnish (NFE) AF: 0.721 AC: 48981 AN: 67924

Other (OTH) AF: 0.761 AC: 1608 AN: 2112

Alfa AF: 0.729 Hom.: 34773

Bravo AF: 0.746

Asia WGS AF: 0.818 AC: 2849 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.94
CADD	Benign	3.6
DANN	Benign	0.33
PhyloP100		-0.37
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: rs1477798; hg19: chr15-66452246;