NM_012301.4:c.538+23984A>T

Variant names:

• chr7-78603136-T-A
• rs22535
• NM_012301.4:c.538+23984A>T

Variant summary

Our verdict is Benign. The variant received -10 ACMG points: 0P and 10B. BP4_Moderate BA1

The NM_012301.4(MAGI2):​c.538+23984A>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.748 in 152,106 control chromosomes in the GnomAD database, including 42,939 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 0.75 (42939 hom., cov: 33)
• Consequence: MAGI2 NM_012301.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.582
• Publications: 1 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 -10 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.37).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.778 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_012301.4. 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.538+23984A>T		intron	N/A	NP_036433.2
	MAGI2	NM_001301128.2		c.538+23984A>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.538+23984A>T		intron	N/A	ENSP00000346151.4
	MAGI2	ENST00000419488.5	TSL:1	c.538+23984A>T		intron	N/A	ENSP00000405766.1
	MAGI2	ENST00000522391.3	TSL:5	c.538+23984A>T		intron	N/A	ENSP00000428389.1

Frequencies

GnomAD3 genomes AF: 0.748 AC: 113744 AN: 151988 Hom.: 42898 Cov.: 33

Gnomad AFR AF: 0.785

Gnomad AMI AF: 0.861

Gnomad AMR AF: 0.649

Gnomad ASJ AF: 0.804

Gnomad EAS AF: 0.508

Gnomad SAS AF: 0.724

Gnomad FIN AF: 0.698

Gnomad MID AF: 0.785

Gnomad NFE AF: 0.772

Gnomad OTH AF: 0.748

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

GnomAD4 genome AF: 0.748 AC: 113837 AN: 152106 Hom.: 42939 Cov.: 33 AF XY: 0.741 AC XY: 55090 AN XY: 74340

African (AFR) AF: 0.785 AC: 32568 AN: 41486

American (AMR) AF: 0.648 AC: 9910 AN: 15286

Ashkenazi Jewish (ASJ) AF: 0.804 AC: 2786 AN: 3464

East Asian (EAS) AF: 0.507 AC: 2611 AN: 5146

South Asian (SAS) AF: 0.726 AC: 3501 AN: 4822

European-Finnish (FIN) AF: 0.698 AC: 7381 AN: 10576

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

European-Non Finnish (NFE) AF: 0.772 AC: 52484 AN: 68004

Other (OTH) AF: 0.747 AC: 1580 AN: 2116

Alfa AF: 0.680 Hom.: 2000

Bravo AF: 0.741

Asia WGS AF: 0.609 AC: 2119 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.37
CADD	Benign	13
DANN	Benign	0.75
PhyloP100		0.58
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: rs22535; hg19: chr7-78232453;