rs10501545

Positions:

• chr11-83697919-G-A
• chr11-83697919-G-T

Variant summary

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

The ENST00000376104.7(DLG2):​c.1826-64594C>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.333 in 152,026 control chromosomes in the GnomAD database, including 9,991 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 0.33 (9991 hom., cov: 32)
• Consequence: DLG2 ENST00000376104.7 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.179

Genes affected

DLG2 (HGNC:2901): (discs large MAGUK scaffold protein 2) This gene encodes a member of the membrane-associated guanylate kinase (MAGUK) family. The encoded protein forms a heterodimer with a related family member that may interact at postsynaptic sites to form a multimeric scaffold for the clustering of receptors, ion channels, and associated signaling proteins. Multiple transcript variants encoding different isoforms have been found for this gene. Additional transcript variants have been described, but their full-length nature is not known. [provided by RefSeq, Dec 2008]

DLG2-AS2 (HGNC:40179): (DLG2 antisense RNA 2)

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.92).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.544 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
DLG2	NM_001142699.3	c.1826-64594C>T		intron_variant		ENST00000376104.7	NP_001136171.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
DLG2	ENST00000376104.7	c.1826-64594C>T		intron_variant		1	NM_001142699.3	ENSP00000365272
DLG2-AS2	ENST00000533669.5	n.553+4109G>A		intron_variant, non_coding_transcript_variant		5

Frequencies

GnomAD3 genomes AF: 0.333 AC: 50607 AN: 151908 Hom.: 9958 Cov.: 32

Gnomad AFR AF: 0.549

Gnomad AMI AF: 0.265

Gnomad AMR AF: 0.194

Gnomad ASJ AF: 0.372

Gnomad EAS AF: 0.148

Gnomad SAS AF: 0.340

Gnomad FIN AF: 0.332

Gnomad MID AF: 0.282

Gnomad NFE AF: 0.247

Gnomad OTH AF: 0.302

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

GnomAD4 genome AF: 0.333 AC: 50689 AN: 152026 Hom.: 9991 Cov.: 32 AF XY: 0.334 AC XY: 24846 AN XY: 74338

Gnomad4 AFR AF: 0.550

Gnomad4 AMR AF: 0.194

Gnomad4 ASJ AF: 0.372

Gnomad4 EAS AF: 0.148

Gnomad4 SAS AF: 0.340

Gnomad4 FIN AF: 0.332

Gnomad4 NFE AF: 0.247

Gnomad4 OTH AF: 0.298

Alfa AF: 0.239 Hom.: 761

Bravo AF: 0.328

Asia WGS AF: 0.258 AC: 902 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.92
CADD	Benign	7.6
DANN	Benign	0.51

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: rs10501545; hg19: chr11-83408962;