19-38653527-A-G

Position:

• chr19-38653527-A-G

Variant summary

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

The ENST00000252699.7(ACTN4):​c.162+5620A>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.388 in 151,942 control chromosomes in the GnomAD database, including 12,502 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 0.39 (12502 hom., cov: 32)
• Consequence: ACTN4 ENST00000252699.7 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 1.00

Genes affected

ACTN4 (HGNC:166): (actinin alpha 4) Alpha actinins belong to the spectrin gene superfamily which represents a diverse group of cytoskeletal proteins, including the alpha and beta spectrins and dystrophins. Alpha actinin is an actin-binding protein with multiple roles in different cell types. In nonmuscle cells, the cytoskeletal isoform is found along microfilament bundles and adherens-type junctions, where it is involved in binding actin to the membrane. In contrast, skeletal, cardiac, and smooth muscle isoforms are localized to the Z-disc and analogous dense bodies, where they help anchor the myofibrillar actin filaments. This gene encodes a nonmuscle, alpha actinin isoform which is concentrated in the cytoplasm, and thought to be involved in metastatic processes. Mutations in this gene have been associated with focal and segmental glomerulosclerosis. [provided by RefSeq, Jul 2008]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.82).
• BA1: GnomAd4 highest subpopulation (NFE) allele frequency at 95% confidence interval = 0.467 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
ACTN4	NM_004924.6	c.162+5620A>G		intron_variant		ENST00000252699.7	NP_004915.2

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
ACTN4	ENST00000252699.7	c.162+5620A>G		intron_variant		1	NM_004924.6	ENSP00000252699	A1

Frequencies

GnomAD3 genomes AF: 0.388 AC: 58949 AN: 151830 Hom.: 12512 Cov.: 32

Gnomad AFR AF: 0.227

Gnomad AMI AF: 0.518

Gnomad AMR AF: 0.356

Gnomad ASJ AF: 0.417

Gnomad EAS AF: 0.442

Gnomad SAS AF: 0.382

Gnomad FIN AF: 0.499

Gnomad MID AF: 0.236

Gnomad NFE AF: 0.471

Gnomad OTH AF: 0.366

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

GnomAD4 genome AF: 0.388 AC: 58934 AN: 151942 Hom.: 12502 Cov.: 32 AF XY: 0.387 AC XY: 28762 AN XY: 74274

Gnomad4 AFR AF: 0.226

Gnomad4 AMR AF: 0.355

Gnomad4 ASJ AF: 0.417

Gnomad4 EAS AF: 0.442

Gnomad4 SAS AF: 0.382

Gnomad4 FIN AF: 0.499

Gnomad4 NFE AF: 0.471

Gnomad4 OTH AF: 0.363

Alfa AF: 0.432 Hom.: 3666

Bravo AF: 0.368

Asia WGS AF: 0.341 AC: 1187 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.82
CADD	Benign	8.4
DANN	Benign	0.71

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: rs979972; hg19: chr19-39144167;