rs10264296

chr7-78763071-C-T

Variant summary

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

The NM_012301.4(MAGI2):c.419-135832G>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.397 in 151,980 control chromosomes in the GnomAD database, including 12,677 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 0.40 (12677 hom., cov: 32)
• Consequence: MAGI2 NM_012301.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.0220

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]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.76).
• BA1: GnomAd4 highest subpopulation (NFE) allele frequency at 95% confidence interval = 0.476 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
MAGI2	NM_012301.4	c.419-135832G>A		intron_variant		ENST00000354212.9

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
MAGI2	ENST00000354212.9	c.419-135832G>A		intron_variant		1	NM_012301.4	P4

Frequencies

GnomAD3 genomes AF: 0.398 AC: 60394 AN: 151862 Hom.: 12676 Cov.: 32

Gnomad AFR AF: 0.269

Gnomad AMI AF: 0.432

Gnomad AMR AF: 0.398

Gnomad ASJ AF: 0.470

Gnomad EAS AF: 0.352

Gnomad SAS AF: 0.293

Gnomad FIN AF: 0.410

Gnomad MID AF: 0.392

Gnomad NFE AF: 0.480

Gnomad OTH AF: 0.434

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

GnomAD4 genome AF: 0.397 AC: 60397 AN: 151980 Hom.: 12677 Cov.: 32 AF XY: 0.391 AC XY: 29072 AN XY: 74300

Gnomad4 AFR AF: 0.268

Gnomad4 AMR AF: 0.397

Gnomad4 ASJ AF: 0.470

Gnomad4 EAS AF: 0.352

Gnomad4 SAS AF: 0.293

Gnomad4 FIN AF: 0.410

Gnomad4 NFE AF: 0.480

Gnomad4 OTH AF: 0.431

Alfa AF: 0.415 Hom.: 1994

Bravo AF: 0.398

Asia WGS AF: 0.299 AC: 1038 AN: 3476

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.76
Cadd	Benign	14
Dann	Benign	0.71

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: rs10264296; hg19: chr7-78392387;