NM_000019.4:c.-9T>A

Variant names:

• chr11-108121598-T-A
• rs3741055
• NM_000019.4:c.-9T>A

Variant summary

Our verdict is Benign. Variant got -20 ACMG points: 0P and 20B. BP4_Strong BP6_Very_Strong BA1

The NM_000019.4(ACAT1):​c.-9T>A variant causes a 5 prime UTR change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.318 in 1,548,816 control chromosomes in the GnomAD database, including 83,240 homozygotes. In-silico tool predicts a benign outcome for this variant. Variant has been reported in ClinVar as Benign (★★).

• Frequency:
  • Genomes: 𝑓 0.27 (6932 hom., cov: 34)
  • Exomes 𝑓: 0.32 (76308 hom.)
• Consequence: ACAT1 NM_000019.4 5_prime_UTR
• Clinical Significance: Benign criteria provided, multiple submitters, no conflicts B:8
• Conservation: PhyloP100: -1.31

Genes affected

ACAT1 (HGNC:93): (acetyl-CoA acetyltransferase 1) This gene encodes a mitochondrially localized enzyme that catalyzes the reversible formation of acetoacetyl-CoA from two molecules of acetyl-CoA. Defects in this gene are associated with 3-ketothiolase deficiency, an inborn error of isoleucine catabolism characterized by urinary excretion of 2-methyl-3-hydroxybutyric acid, 2-methylacetoacetic acid, tiglylglycine, and butanone. [provided by RefSeq, Feb 2009]

ENSG00000255467 (HGNC:):

ACMG classification

Verdict is Benign. Variant got -20 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.76).
• BP6: Variant 11-108121598-T-A is Benign according to our data. Variant chr11-108121598-T-A is described in ClinVar as [Benign]. Clinvar id is 92294.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr11-108121598-T-A is described in Lovd as [Benign].
• BA1: GnomAd4 highest subpopulation (SAS) allele frequency at 95% confidence interval = 0.47 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
ACAT1	NM_000019.4	c.-9T>A		5_prime_UTR_variant	Exon 1 of 12	ENST00000265838.9	NP_000010.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
ACAT1	ENST00000265838	c.-9T>A		5_prime_UTR_variant	Exon 1 of 12	1	NM_000019.4	ENSP00000265838.4

Frequencies

GnomAD3 genomes AF: 0.273 AC: 41578 AN: 152116 Hom.: 6932 Cov.: 34

Gnomad AFR AF: 0.0929

Gnomad AMI AF: 0.216

Gnomad AMR AF: 0.399

Gnomad ASJ AF: 0.381

Gnomad EAS AF: 0.348

Gnomad SAS AF: 0.485

Gnomad FIN AF: 0.309

Gnomad MID AF: 0.532

Gnomad NFE AF: 0.322

Gnomad OTH AF: 0.322

GnomAD3 exomes AF: 0.361 AC: 54490 AN: 150782 Hom.: 10593 AF XY: 0.368 AC XY: 29661 AN XY: 80608

Gnomad AFR exome AF: 0.0814

Gnomad AMR exome AF: 0.470

Gnomad ASJ exome AF: 0.376

Gnomad EAS exome AF: 0.334

Gnomad SAS exome AF: 0.478

Gnomad FIN exome AF: 0.308

Gnomad NFE exome AF: 0.323

Gnomad OTH exome AF: 0.368

GnomAD4 exome AF: 0.323 AC: 451699 AN: 1396582 Hom.: 76308 Cov.: 36 AF XY: 0.329 AC XY: 226982 AN XY: 688990

Gnomad4 AFR exome AF: 0.0827

Gnomad4 AMR exome AF: 0.461

Gnomad4 ASJ exome AF: 0.370

Gnomad4 EAS exome AF: 0.341

Gnomad4 SAS exome AF: 0.481

Gnomad4 FIN exome AF: 0.312

Gnomad4 NFE exome AF: 0.312

Gnomad4 OTH exome AF: 0.329

GnomAD4 genome AF: 0.273 AC: 41580 AN: 152234 Hom.: 6932 Cov.: 34 AF XY: 0.282 AC XY: 20959 AN XY: 74422

Gnomad4 AFR AF: 0.0926

Gnomad4 AMR AF: 0.398

Gnomad4 ASJ AF: 0.381

Gnomad4 EAS AF: 0.347

Gnomad4 SAS AF: 0.486

Gnomad4 FIN AF: 0.309

Gnomad4 NFE AF: 0.322

Gnomad4 OTH AF: 0.327

Alfa AF: 0.314 Hom.: 2527

Bravo AF: 0.269

Asia WGS AF: 0.437 AC: 1517 AN: 3476

ClinVar

Significance: Benign

Submissions summary: Benign:8

Revision: criteria provided, multiple submitters, no conflicts

Submissions by phenotype

not specified Benign:3

Feb 05, 2016

Eurofins Ntd Llc (ga)

Significance: Benign

Review Status: criteria provided, single submitter

Collection Method: clinical testing

- -

-

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

Significance: Benign

Review Status: no assertion criteria provided

Collection Method: clinical testing

- -

-

Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen

Significance: Benign

Review Status: no assertion criteria provided

Collection Method: clinical testing

- -

Deficiency of acetyl-CoA acetyltransferase Benign:3

Jan 13, 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. -

Nov 19, 2019

Natera, Inc.

Significance: Benign

Review Status: no assertion criteria provided

Collection Method: clinical testing

- -

Jul 01, 2021

Genome-Nilou Lab

Significance: Benign

Review Status: criteria provided, single submitter

Collection Method: clinical testing

- -

not provided Benign:2

-

Breakthrough Genomics, Breakthrough Genomics

Significance: Benign

Review Status: criteria provided, single submitter

Collection Method: not provided

- -

Mar 03, 2015

GeneDx

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	-0.76
CADD	Benign	1.0
DANN	Benign	0.71
RBP_binding_hub_radar		0.0
RBP_regulation_power_radar		1.1

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: rs3741055; hg19: chr11-107992325; COSMIC: COSV54920325; COSMIC: COSV54920325;