rs720308

Positions:

• chr19-35307157-A-G

Variant summary

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

The NM_002361.4(MAG):​c.1232-2717A>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.132 in 152,282 control chromosomes in the GnomAD database, including 1,434 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 0.13 (1434 hom., cov: 33)
• Consequence: MAG NM_002361.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.256

Genes affected

MAG (HGNC:6783): (myelin associated glycoprotein) The protein encoded by this gene is a type I membrane protein and member of the immunoglobulin superfamily. It is thought to be involved in the process of myelination. It is a lectin that binds to sialylated glycoconjugates and mediates certain myelin-neuron cell-cell interactions. Three alternatively spliced transcripts encoding different isoforms have been described for this gene. [provided by RefSeq, Nov 2010]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.88).
• BA1: GnomAd4 highest subpopulation (SAS) allele frequency at 95% confidence interval = 0.178 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
MAG	NM_002361.4	c.1232-2717A>G		intron_variant		ENST00000392213.8	NP_002352.1
MAG	NM_001199216.2	c.1157-2717A>G		intron_variant			NP_001186145.1
MAG	NM_080600.3	c.1232-2717A>G		intron_variant			NP_542167.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
MAG	ENST00000392213.8	c.1232-2717A>G		intron_variant		1	NM_002361.4	ENSP00000376048	P1
MAG	ENST00000361922.8	c.1232-2717A>G		intron_variant		1		ENSP00000355234
MAG	ENST00000537831.2	c.1157-2717A>G		intron_variant		1		ENSP00000440695

Frequencies

GnomAD3 genomes AF: 0.132 AC: 20129 AN: 152162 Hom.: 1430 Cov.: 33

Gnomad AFR AF: 0.102

Gnomad AMI AF: 0.155

Gnomad AMR AF: 0.182

Gnomad ASJ AF: 0.178

Gnomad EAS AF: 0.159

Gnomad SAS AF: 0.186

Gnomad FIN AF: 0.109

Gnomad MID AF: 0.155

Gnomad NFE AF: 0.134

Gnomad OTH AF: 0.137

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

GnomAD4 genome AF: 0.132 AC: 20154 AN: 152282 Hom.: 1434 Cov.: 33 AF XY: 0.134 AC XY: 9961 AN XY: 74452

Gnomad4 AFR AF: 0.102

Gnomad4 AMR AF: 0.182

Gnomad4 ASJ AF: 0.178

Gnomad4 EAS AF: 0.158

Gnomad4 SAS AF: 0.188

Gnomad4 FIN AF: 0.109

Gnomad4 NFE AF: 0.134

Gnomad4 OTH AF: 0.136

Alfa AF: 0.141 Hom.: 1624

Bravo AF: 0.135

Asia WGS AF: 0.174 AC: 605 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.88
CADD	Benign	5.6
DANN	Benign	0.66

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: rs720308; hg19: chr19-35798060;