NM_001387274.1:c.2591+35007C>G

Variant names:

• chr11-31029462-G-C
• rs288458
• NM_001387274.1:c.2591+35007C>G

Variant summary

Our verdict is Benign. The variant received -12 ACMG points: 0P and 12B. BP4_Strong BA1

The NM_001387274.1(DCDC1):​c.2591+35007C>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.0771 in 152,078 control chromosomes in the GnomAD database, including 601 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 0.077 (601 hom., cov: 32)
• Consequence: DCDC1 NM_001387274.1 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.451
• Publications: 2 publications found

Genes affected

DCDC1 (HGNC:20625): (doublecortin domain containing 1) This gene encodes a member of the doublecortin family. The protein encoded by this gene is a hydrophilic, intracellular protein. It contains a single doublecortin domain and is unable to bind microtubules and to regulate microtubule polymerization. This gene is mainly expressed in adult testis. It does not have a mouse homolog. [provided by RefSeq, Sep 2010]

ACMG classification

Our verdict: Benign. The variant received -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.84).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.25 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
DCDC1	NM_001387274.1	c.2591+35007C>G		intron_variant	Intron 20 of 38	ENST00000684477.1	NP_001374203.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
DCDC1	ENST00000684477.1	c.2591+35007C>G		intron_variant	Intron 20 of 38		NM_001387274.1	ENSP00000507427.1
DCDC1	ENST00000597505.5	c.2591+35007C>G		intron_variant	Intron 18 of 35	5		ENSP00000472625.1
DCDC1	ENST00000342355.8	n.*1666+35007C>G		intron_variant	Intron 20 of 21	2		ENSP00000343496.4
DCDC1	ENST00000437348.5	n.1299+35007C>G		intron_variant	Intron 10 of 11	5

Frequencies

GnomAD3 genomes AF: 0.0772 AC: 11725 AN: 151960 Hom.: 602 Cov.: 32

Gnomad AFR AF: 0.0435

Gnomad AMI AF: 0.129

Gnomad AMR AF: 0.0701

Gnomad ASJ AF: 0.0746

Gnomad EAS AF: 0.261

Gnomad SAS AF: 0.158

Gnomad FIN AF: 0.0740

Gnomad MID AF: 0.158

Gnomad NFE AF: 0.0788

Gnomad OTH AF: 0.0815

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

GnomAD4 genome AF: 0.0771 AC: 11721 AN: 152078 Hom.: 601 Cov.: 32 AF XY: 0.0788 AC XY: 5857 AN XY: 74318

African (AFR) AF: 0.0434 AC: 1803 AN: 41528

American (AMR) AF: 0.0700 AC: 1069 AN: 15280

Ashkenazi Jewish (ASJ) AF: 0.0746 AC: 259 AN: 3472

East Asian (EAS) AF: 0.262 AC: 1352 AN: 5168

South Asian (SAS) AF: 0.158 AC: 761 AN: 4824

European-Finnish (FIN) AF: 0.0740 AC: 782 AN: 10568

Middle Eastern (MID) AF: 0.170 AC: 50 AN: 294

European-Non Finnish (NFE) AF: 0.0789 AC: 5357 AN: 67924

Other (OTH) AF: 0.0806 AC: 170 AN: 2108

Alfa AF: 0.0729 Hom.: 63

Bravo AF: 0.0771

Asia WGS AF: 0.206 AC: 709 AN: 3460

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.84
CADD	Benign	0.39
DANN	Benign	0.47
PhyloP100		0.45
Mutation Taster		=100/0	polymorphism (auto)

Splicing

Find out detailed SpliceAI scores and Pangolin per-transcript scores at spliceailookup.broadinstitute.org

Other links and lift over

dbSNP: rs288458; hg19: chr11-31051009;