chr7-78103956-A-C

Position:

• chr7-78103956-A-C

Variant summary

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

The NM_012301.4(MAGI2):​c.3567+21738T>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.412 in 152,058 control chromosomes in the GnomAD database, including 13,772 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 0.41 (13772 hom., cov: 32)
• Consequence: MAGI2 NM_012301.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.344

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=-0.81).
• BA1: GnomAd4 highest subpopulation (NFE) allele frequency at 95% confidence interval = 0.491 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
MAGI2	NM_012301.4	c.3567+21738T>G		intron_variant		ENST00000354212.9

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
MAGI2	ENST00000354212.9	c.3567+21738T>G		intron_variant		1	NM_012301.4	P4

Frequencies

GnomAD3 genomes AF: 0.412 AC: 62535 AN: 151940 Hom.: 13761 Cov.: 32

Gnomad AFR AF: 0.288

Gnomad AMI AF: 0.455

Gnomad AMR AF: 0.329

Gnomad ASJ AF: 0.350

Gnomad EAS AF: 0.246

Gnomad SAS AF: 0.458

Gnomad FIN AF: 0.560

Gnomad MID AF: 0.320

Gnomad NFE AF: 0.495

Gnomad OTH AF: 0.396

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

GnomAD4 genome AF: 0.412 AC: 62584 AN: 152058 Hom.: 13772 Cov.: 32 AF XY: 0.412 AC XY: 30619 AN XY: 74344

Gnomad4 AFR AF: 0.289

Gnomad4 AMR AF: 0.328

Gnomad4 ASJ AF: 0.350

Gnomad4 EAS AF: 0.246

Gnomad4 SAS AF: 0.460

Gnomad4 FIN AF: 0.560

Gnomad4 NFE AF: 0.495

Gnomad4 OTH AF: 0.394

Alfa AF: 0.465 Hom.: 9466

Bravo AF: 0.386

Asia WGS AF: 0.362 AC: 1259 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.81
CADD	Benign	8.5
DANN	Benign	0.63

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: rs3807736; hg19: chr7-77733273;