rs7233791

Variant names:

• chr18-49783514-G-A
• rs7233791
• NM_006111.3:c.*333C>T

Your query was ambiguous. Multiple possible variants found:

• chr18-49783514-G-A
• chr18-49783514-G-C

Variant summary

Our verdict is Uncertain significance. The variant received 0 ACMG points: 2P and 2B. PM2 BP4_Moderate

The NM_006111.3(ACAA2):​c.*333C>T variant causes a 3 prime UTR change. The variant allele was found at a frequency of 0.0000265 in 188,466 control chromosomes in the GnomAD database, with no homozygous occurrence. 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 0.000020 (0 hom., cov: 33)
  • Exomes 𝑓: 0.000055 (0 hom.)
• Consequence: ACAA2 NM_006111.3 3_prime_UTR
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 4.03
• Publications: 8 publications found

Genes affected

ACAA2 (HGNC:83): (acetyl-CoA acyltransferase 2) The encoded protein catalyzes the last step of the mitochondrial fatty acid beta-oxidation spiral. Unlike most mitochondrial matrix proteins, it contains a non-cleavable amino-terminal targeting signal. [provided by RefSeq, Jul 2008]

ACMG classification

Our verdict: Uncertain_significance. The variant received 0 ACMG points.

• PM2: Very rare variant in population databases, with high coverage
• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.19).

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
ACAA2	NM_006111.3	c.*333C>T		3_prime_UTR_variant	Exon 10 of 10	ENST00000285093.15	NP_006102.2

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
ACAA2	ENST00000285093.15	c.*333C>T		3_prime_UTR_variant	Exon 10 of 10	1	NM_006111.3	ENSP00000285093.8
ACAA2	ENST00000591171.1	n.1841C>T		non_coding_transcript_exon_variant	Exon 2 of 2	2
ACAA2	ENST00000587994.5	c.*333C>T		3_prime_UTR_variant	Exon 10 of 10	5		ENSP00000466015.1
ACAA2	ENST00000589432.5	c.*333C>T		3_prime_UTR_variant	Exon 10 of 10	5		ENSP00000466466.1

Frequencies

GnomAD3 genomes AF: 0.0000197 AC: 3 AN: 152058 Hom.: 0 Cov.: 33

Gnomad AFR AF: 0.00

Gnomad AMI AF: 0.00

Gnomad AMR AF: 0.00

Gnomad ASJ AF: 0.00

Gnomad EAS AF: 0.00

Gnomad SAS AF: 0.00

Gnomad FIN AF: 0.00

Gnomad MID AF: 0.00

Gnomad NFE AF: 0.0000441

Gnomad OTH AF: 0.00

GnomAD4 exome AF: 0.0000549 AC: 2 AN: 36408 Hom.: 0 Cov.: 0 AF XY: 0.0000537 AC XY: 1 AN XY: 18610

African (AFR) AF: 0.00 AC: 0 AN: 1540

American (AMR) AF: 0.00 AC: 0 AN: 2608

Ashkenazi Jewish (ASJ) AF: 0.00 AC: 0 AN: 1236

East Asian (EAS) AF: 0.000370 AC: 1 AN: 2706

South Asian (SAS) AF: 0.00 AC: 0 AN: 1392

European-Finnish (FIN) AF: 0.00 AC: 0 AN: 1602

Middle Eastern (MID) AF: 0.00 AC: 0 AN: 184

European-Non Finnish (NFE) AF: 0.0000439 AC: 1 AN: 22762

Other (OTH) AF: 0.00 AC: 0 AN: 2378

GnomAD4 genome AF: 0.0000197 AC: 3 AN: 152058 Hom.: 0 Cov.: 33 AF XY: 0.0000269 AC XY: 2 AN XY: 74282

African (AFR) AF: 0.00 AC: 0 AN: 41384

American (AMR) AF: 0.00 AC: 0 AN: 15272

Ashkenazi Jewish (ASJ) AF: 0.00 AC: 0 AN: 3472

East Asian (EAS) AF: 0.00 AC: 0 AN: 5194

South Asian (SAS) AF: 0.00 AC: 0 AN: 4822

European-Finnish (FIN) AF: 0.00 AC: 0 AN: 10588

Middle Eastern (MID) AF: 0.00 AC: 0 AN: 316

European-Non Finnish (NFE) AF: 0.0000441 AC: 3 AN: 68006

Other (OTH) AF: 0.00 AC: 0 AN: 2092

Alfa AF: 0.00 Hom.: 5

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.19
CADD	Benign	16
DANN	Benign	0.92
PhyloP100		4.0

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: rs7233791; hg19: chr18-47309884;