chr1-229432890-C-G

Variant names:

Variant summary

Our verdict is Benign. Variant got -20 ACMG points: 0P and 20B. BP4_StrongBP6_Very_StrongBA1

The NM_001100.4(ACTA1):c.130-10G>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.179 in 1,613,784 control chromosomes in the GnomAD database, including 26,922 homozygotes. In-silico tool predicts a benign outcome for this variant. Variant has been reported in ClinVar as Benign (★★).

Frequency

Genomes: 𝑓 0.20 ( 3445 hom., cov: 32)

Exomes 𝑓: 0.18 ( 23477 hom. )

Consequence

ACTA1
NM_001100.4 intron

Scores

Splicing: ADA: 0.00004224

Clinical Significance

Benign criteria provided, multiple submitters, no conflicts B:12

Conservation

PhyloP100: 0.0250

Variant links:

Genes affected

ACTA1 (HGNC:129): (actin alpha 1, skeletal muscle) The product encoded by this gene belongs to the actin family of proteins, which are highly conserved proteins that play a role in cell motility, structure and integrity. Alpha, beta and gamma actin isoforms have been identified, with alpha actins being a major constituent of the contractile apparatus, while beta and gamma actins are involved in the regulation of cell motility. This actin is an alpha actin that is found in skeletal muscle. Mutations in this gene cause a variety of myopathies, including nemaline myopathy, congenital myopathy with excess of thin myofilaments, congenital myopathy with cores, and congenital myopathy with fiber-type disproportion, diseases that lead to muscle fiber defects with manifestations such as hypotonia. [provided by RefSeq, Sep 2019]

ACTA1 links:

Genome browser will be placed here

ACMG classification

Classification made for transcript

Verdict is Benign. Variant got -20 ACMG points.

BP4

Computational evidence support a benign effect (BayesDel_noAF=-0.87).

BP6

Variant 1-229432890-C-G is Benign according to our data. Variant chr1-229432890-C-G is described in ClinVar as [Benign]. Clinvar id is 93546.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr1-229432890-C-G is described in Lovd as [Benign].

BA1

GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.27 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
ACTA1	NM_001100.4 link	c.130-10G>C		intron_variant	Intron 2 of 6	ENST00000366684.7	NP_001091.1	P68133

Ensembl

Gene	Transcript	HGVSc	Effect	Exon rank	TSL	MANE	Protein	UniProt
ACTA1	ENST00000366684.7 link	c.130-10G>C	intron_variant	Intron 2 of 6	1	NM_001100.4	ENSP00000355645.3	P68133
ACTA1	ENST00000366683.4 link	c.130-10G>C	intron_variant	Intron 2 of 6	5		ENSP00000355644.4	A6NL76
ACTA1	ENST00000684723.1 link	c.-6-10G>C	intron_variant	Intron 1 of 5			ENSP00000508084.1	A0A804HKV3

Frequencies

GnomAD3 genomes

AF:

0.204

AC:

31037

AN:

151926

Hom.:

3433

Cov.:

show subpopulations

Gnomad AFR

AF:

0.274

Gnomad AMI

AF:

0.225

Gnomad AMR

AF:

0.235

Gnomad ASJ

AF:

0.304

Gnomad EAS

AF:

0.159

Gnomad SAS

AF:

0.152

Gnomad FIN

AF:

0.115

Gnomad MID

AF:

0.259

Gnomad NFE

AF:

0.170

Gnomad OTH

AF:

0.229

GnomAD3 exomes

AF:

0.189

AC:

47303

AN:

250232

Hom.:

4658

AF XY:

0.186

AC XY:

25179

AN XY:

135480

show subpopulations

Gnomad AFR exome

AF:

0.272

Gnomad AMR exome

AF:

0.251

Gnomad ASJ exome

AF:

0.302

Gnomad EAS exome

AF:

0.174

Gnomad SAS exome

AF:

0.164

Gnomad FIN exome

AF:

0.117

Gnomad NFE exome

AF:

0.172

Gnomad OTH exome

AF:

0.181

GnomAD4 exome

AF:

0.176

AC:

257719

AN:

1461740

Hom.:

23477

Cov.:

AF XY:

0.176

AC XY:

127952

AN XY:

727162

show subpopulations

Gnomad4 AFR exome

AF:

0.281

Gnomad4 AMR exome

AF:

0.256

Gnomad4 ASJ exome

AF:

0.299

Gnomad4 EAS exome

AF:

0.155

Gnomad4 SAS exome

AF:

0.162

Gnomad4 FIN exome

AF:

0.116

Gnomad4 NFE exome

AF:

0.171

Gnomad4 OTH exome

AF:

0.185

GnomAD4 genome

AF:

0.204

AC:

31080

AN:

152044

Hom.:

3445

Cov.:

AF XY:

0.202

AC XY:

15031

AN XY:

74342

show subpopulations

Gnomad4 AFR

AF:

0.274

Gnomad4 AMR

AF:

0.235

Gnomad4 ASJ

AF:

0.304

Gnomad4 EAS

AF:

0.158

Gnomad4 SAS

AF:

0.151

Gnomad4 FIN

AF:

0.115

Gnomad4 NFE

AF:

0.170

Gnomad4 OTH

AF:

0.230

Alfa

AF:

0.199

Hom.:

561

Bravo

AF:

0.221

Asia WGS

AF:

0.164

AC:

568

AN:

3478

ClinVar

Significance: Benign

Submissions summary: Benign:12

Revision: criteria provided, multiple submitters, no conflicts

LINK: link

Submissions by phenotype

not specified

Benign:6

PreventionGenetics, part of Exact Sciences

Significance: Benign

Review Status: criteria provided, single submitter

Collection Method: clinical testing

- -

Genetic Services Laboratory, University of Chicago

Significance: Likely benign

Review Status: no assertion criteria provided

Collection Method: clinical testing

Likely benign based on allele frequency in 1000 Genomes Project or ESP global frequency and its presence in a patient with a rare or unrelated disease phenotype. NOT Sanger confirmed. -

Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+

Significance: Benign

Review Status: no assertion criteria provided

Collection Method: clinical testing

- -

Jan 13, 2015

Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine

Significance: Benign

Review Status: criteria provided, single submitter

Collection Method: clinical testing

c.130-10G>C in intron 2 of ACTA1: This variant is not expected to have clinical significance because it has been identified in 26.2% (1154/4406) of African Amer ican chromosomes from a broad population by the NHLBI Exome Sequencing Project ( http://evs.gs.washington.edu/EVS; dbSNP rs41271481). -

Aug 22, 2013

Eurofins Ntd Llc (ga)

Significance: Benign

Review Status: criteria provided, single submitter

Collection Method: clinical testing

- -

Genome Diagnostics Laboratory, University Medical Center Utrecht

Significance: Benign

Review Status: no assertion criteria provided

Collection Method: clinical testing

- -

Actin accumulation myopathy

Benign:2

Feb 03, 2025

Labcorp Genetics (formerly Invitae), Labcorp

Significance: Benign

Review Status: criteria provided, single submitter

Collection Method: clinical testing

- -

Jan 12, 2018

Illumina Laboratory Services, Illumina

Significance: Benign

Review Status: criteria provided, single submitter

Collection Method: clinical testing

This variant was observed in the ICSL laboratory as part of a predisposition screen in an ostensibly healthy population. It had not been previously curated by ICSL or reported in the Human Gene Mutation Database (HGMD: prior to June 1st, 2018), and was therefore a candidate for classification through an automated scoring system. Utilizing variant allele frequency, disease prevalence and penetrance estimates, and inheritance mode, an automated score was calculated to assess if this variant is too frequent to cause the disease. Based on the score and internal cut-off values, a variant classified as benign is not then subjected to further curation. The score for this variant resulted in a classification of benign for this disease. -

not provided

Benign:2

Mar 03, 2015

GeneDx

Significance: Benign

Review Status: criteria provided, single submitter

Collection Method: clinical testing

- -

Breakthrough Genomics, Breakthrough Genomics

Significance: Benign

Review Status: criteria provided, single submitter

Collection Method: not provided

- -

Congenital myopathy with fiber type disproportion

Benign:1

Jan 12, 2018

Illumina Laboratory Services, Illumina

Significance: Benign

Review Status: criteria provided, single submitter

Collection Method: clinical testing

Familial restrictive cardiomyopathy

Benign:1

Jan 12, 2018

Illumina Laboratory Services, Illumina

Significance: Benign

Review Status: criteria provided, single submitter

Collection Method: clinical testing

Computational scores

Source: dbNSFP v4.3

Name

Calibrated prediction

Score

Prediction

BayesDel_noAF

Benign

-0.87

CADD

Benign

4.8

DANN

Benign

0.55

Splicing

Name

Calibrated prediction

Score

Prediction

dbscSNV1_ADA

Benign

0.000042

dbscSNV1_RF

Benign

0.086

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

Below is the list of publications found by LitVar. It may be empty.

Variant summary

Frequency

Consequence

Scores

Clinical Significance

Conservation

ACMG classification

Transcripts

RefSeq

Ensembl

Frequencies

ClinVar

Submissions by phenotype

Computational scores

Splicing

Publications

LitVar

Other links and lift over