NM_130810.4:c.406-2878G>A

Variant names:

• chr15-55470039-C-T
• rs7182524
• NM_130810.4:c.406-2878G>A

Variant summary

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

The NM_130810.4(DNAAF4):​c.406-2878G>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.0542 in 151,408 control chromosomes in the GnomAD database, including 291 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 0.054 (291 hom., cov: 29)
• Consequence: DNAAF4 NM_130810.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.691
• Publications: 2 publications found

Genes affected

DNAAF4 (HGNC:21493): (dynein axonemal assembly factor 4) This gene encodes a tetratricopeptide repeat domain-containing protein. The encoded protein interacts with estrogen receptors and the heat shock proteins, Hsp70 and Hsp90. An homologous protein in rat has been shown to function in neuronal migration in the developing neocortex. A chromosomal translocation involving this gene is associated with a susceptibility to developmental dyslexia. Mutations in this gene are associated with deficits in reading and spelling. Alternative splicing results in multiple transcript variants. Read-through transcription also exists between this gene and the downstream cell cycle progression 1 (CCPG1) gene. [provided by RefSeq, Mar 2011]

DNAAF4-CCPG1 (HGNC:43019): (DNAAF4-CCPG1 readthrough (NMD candidate)) This locus represents naturally occurring read-through transcription between the neighboring dyslexia susceptibility 1 candidate 1 (DYX1C1) and cell cycle progression 1 (CCPG1) genes on chromosome 15. The read-through transcript is a candidate for nonsense-mediated mRNA decay (NMD), and is thus unlikely to produce a protein product. [provided by RefSeq, Mar 2011]

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.94).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.138 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_130810.4. You can select a different transcript below to see updated ACMG assignments.

RefSeq Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	DNAAF4	NM_130810.4	MANE Select	c.406-2878G>A		intron	N/A	NP_570722.2
	DNAAF4	NM_001033560.2		c.406-2878G>A		intron	N/A	NP_001028732.1
	DNAAF4	NM_001033559.3		c.406-2878G>A		intron	N/A	NP_001028731.1

Ensembl Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	DNAAF4	ENST00000321149.7	TSL:1 MANE Select	c.406-2878G>A		intron	N/A	ENSP00000323275.3
	DNAAF4	ENST00000448430.6	TSL:1	c.406-2878G>A		intron	N/A	ENSP00000403412.2
	DNAAF4	ENST00000457155.6	TSL:1	c.406-2878G>A		intron	N/A	ENSP00000402640.2

Frequencies

GnomAD3 genomes AF: 0.0542 AC: 8205 AN: 151302 Hom.: 290 Cov.: 29

Gnomad AFR AF: 0.0304

Gnomad AMI AF: 0.0548

Gnomad AMR AF: 0.0501

Gnomad ASJ AF: 0.0638

Gnomad EAS AF: 0.146

Gnomad SAS AF: 0.140

Gnomad FIN AF: 0.0342

Gnomad MID AF: 0.0791

Gnomad NFE AF: 0.0589

Gnomad OTH AF: 0.0550

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

GnomAD4 genome AF: 0.0542 AC: 8209 AN: 151408 Hom.: 291 Cov.: 29 AF XY: 0.0542 AC XY: 4008 AN XY: 73980

African (AFR) AF: 0.0306 AC: 1259 AN: 41188

American (AMR) AF: 0.0499 AC: 760 AN: 15218

Ashkenazi Jewish (ASJ) AF: 0.0638 AC: 221 AN: 3462

East Asian (EAS) AF: 0.147 AC: 755 AN: 5146

South Asian (SAS) AF: 0.140 AC: 672 AN: 4798

European-Finnish (FIN) AF: 0.0342 AC: 357 AN: 10440

Middle Eastern (MID) AF: 0.0714 AC: 21 AN: 294

European-Non Finnish (NFE) AF: 0.0589 AC: 3995 AN: 67854

Other (OTH) AF: 0.0568 AC: 119 AN: 2096

Alfa AF: 0.0491 Hom.: 29

Bravo AF: 0.0524

Asia WGS AF: 0.115 AC: 398 AN: 3464

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.94
CADD	Benign	2.3
DANN	Benign	0.42
PhyloP100		-0.69
Mutation Taster		=100/0	polymorphism (auto)

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

Other links and lift over

dbSNP: rs7182524; hg19: chr15-55762237;