rs793722

chr6-24352135-G-Achr6-24352135-G-Cchr6-24352135-G-T

Variant summary

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

The NM_016356.5(DCDC2):c.348+1434C>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.562 in 151,952 control chromosomes in the GnomAD database, including 25,806 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 0.56 (25806 hom., cov: 32)
• Consequence: DCDC2 NM_016356.5 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.781

Genes affected

DCDC2 (HGNC:18141): (doublecortin domain containing 2) This gene encodes a doublecortin domain-containing family member. The doublecortin domain has been demonstrated to bind tubulin and enhance microtubule polymerization. This family member is thought to function in neuronal migration where it may affect the signaling of primary cilia. Mutations in this gene have been associated with reading disability (RD) type 2, also referred to as developmental dyslexia. Alternatively spliced transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jan 2013]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.93).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.778 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
DCDC2	NM_016356.5	c.348+1434C>T		intron_variant		ENST00000378454.8
DCDC2	NM_001195610.2	c.348+1434C>T		intron_variant

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
DCDC2	ENST00000378454.8	c.348+1434C>T		intron_variant		1	NM_016356.5	P1

Frequencies

GnomAD3 genomes AF: 0.562 AC: 85368 AN: 151834 Hom.: 25786 Cov.: 32

Gnomad AFR AF: 0.325

Gnomad AMI AF: 0.685

Gnomad AMR AF: 0.677

Gnomad ASJ AF: 0.605

Gnomad EAS AF: 0.798

Gnomad SAS AF: 0.706

Gnomad FIN AF: 0.582

Gnomad MID AF: 0.630

Gnomad NFE AF: 0.645

Gnomad OTH AF: 0.571

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

GnomAD4 genome AF: 0.562 AC: 85404 AN: 151952 Hom.: 25806 Cov.: 32 AF XY: 0.567 AC XY: 42100 AN XY: 74244

Gnomad4 AFR AF: 0.325

Gnomad4 AMR AF: 0.678

Gnomad4 ASJ AF: 0.605

Gnomad4 EAS AF: 0.798

Gnomad4 SAS AF: 0.705

Gnomad4 FIN AF: 0.582

Gnomad4 NFE AF: 0.645

Gnomad4 OTH AF: 0.576

Alfa AF: 0.596 Hom.: 3484

Bravo AF: 0.558

Asia WGS AF: 0.714 AC: 2483 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.93
Cadd	Benign	0.18
Dann	Benign	0.70

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: rs793722; hg19: chr6-24352363;