rs798285

Variant names:

• chr7-78310679-C-A
• rs798285
• NM_012301.4:c.1408+33099G>T

Your query was ambiguous. Multiple possible variants found:

• chr7-78310679-C-A
• chr7-78310679-C-G

Variant summary

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

The ENST00000354212.9(MAGI2):​c.1408+33099G>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.513 in 151,746 control chromosomes in the GnomAD database, including 20,533 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 0.51 (20533 hom., cov: 30)
• Consequence: MAGI2 ENST00000354212.9 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.0640
• Publications: 4 publications found

Genes affected

MAGI2 (HGNC:18957): (membrane associated guanylate kinase, WW and PDZ domain containing 2) The protein encoded by this gene interacts with atrophin-1. Atrophin-1 contains a polyglutamine repeat, expansion of which is responsible for dentatorubral and pallidoluysian atrophy. This encoded protein is characterized by two WW domains, a guanylate kinase-like domain, and multiple PDZ domains. It has structural similarity to the membrane-associated guanylate kinase homologue (MAGUK) family. [provided by RefSeq, Jul 2008]

MAGI2 Gene-Disease associations (from GenCC):

• nephrotic syndrome 15

  Inheritance: AR Classification: STRONG, LIMITED Submitted by: Ambry Genetics, Labcorp Genetics (formerly Invitae)
• familial idiopathic steroid-resistant nephrotic syndrome

  Inheritance: AD Classification: SUPPORTIVE Submitted by: Orphanet
• genetic developmental and epileptic encephalopathy

  Inheritance: AD Classification: LIMITED Submitted by: G2P
• epilepsy

  Inheritance: AD Classification: NO_KNOWN Submitted by: ClinGen

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.9).
• BA1: GnomAd4 highest subpopulation (NFE) allele frequency at 95% confidence interval = 0.567 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: ENST00000354212.9. 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
	MAGI2	NM_012301.4	MANE Select	c.1408+33099G>T		intron	N/A	NP_036433.2
	MAGI2	NM_001301128.2		c.1408+33099G>T		intron	N/A	NP_001288057.1

Ensembl Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	MAGI2	ENST00000354212.9	TSL:1 MANE Select	c.1408+33099G>T		intron	N/A	ENSP00000346151.4
	MAGI2	ENST00000419488.5	TSL:1	c.1408+33099G>T		intron	N/A	ENSP00000405766.1
	MAGI2	ENST00000519748.5	TSL:1	c.235+33099G>T		intron	N/A	ENSP00000486774.1

Frequencies

GnomAD3 genomes AF: 0.513 AC: 77832 AN: 151626 Hom.: 20533 Cov.: 30

Gnomad AFR AF: 0.406

Gnomad AMI AF: 0.493

Gnomad AMR AF: 0.547

Gnomad ASJ AF: 0.608

Gnomad EAS AF: 0.375

Gnomad SAS AF: 0.565

Gnomad FIN AF: 0.510

Gnomad MID AF: 0.589

Gnomad NFE AF: 0.572

Gnomad OTH AF: 0.533

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

GnomAD4 genome AF: 0.513 AC: 77847 AN: 151746 Hom.: 20533 Cov.: 30 AF XY: 0.511 AC XY: 37874 AN XY: 74108

African (AFR) AF: 0.406 AC: 16786 AN: 41356

American (AMR) AF: 0.547 AC: 8339 AN: 15246

Ashkenazi Jewish (ASJ) AF: 0.608 AC: 2108 AN: 3466

East Asian (EAS) AF: 0.377 AC: 1930 AN: 5126

South Asian (SAS) AF: 0.565 AC: 2715 AN: 4804

European-Finnish (FIN) AF: 0.510 AC: 5352 AN: 10488

Middle Eastern (MID) AF: 0.592 AC: 173 AN: 292

European-Non Finnish (NFE) AF: 0.572 AC: 38883 AN: 67952

Other (OTH) AF: 0.528 AC: 1113 AN: 2108

Alfa AF: 0.552 Hom.: 76242

Bravo AF: 0.507

Asia WGS AF: 0.460 AC: 1601 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.90
CADD	Benign	1.2
DANN	Benign	0.56
PhyloP100		0.064
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: rs798285; hg19: chr7-77939996;