rs150850549
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Variant summary
Our verdict is Benign. Variant got -17 ACMG points: 0P and 17B. BP4_StrongBP6_Very_StrongBP7BS2
The NM_001098.3(ACO2):āc.84A>Gā(p.Gln28=) variant causes a synonymous change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.000268 in 1,613,976 control chromosomes in the GnomAD database, including 3 homozygotes. In-silico tool predicts a benign outcome for this variant. Variant has been reported in ClinVar as Likely benign (ā ā ).
Frequency
Genomes: š 0.0014 ( 3 hom., cov: 32)
Exomes š: 0.00015 ( 0 hom. )
Consequence
ACO2
NM_001098.3 synonymous
NM_001098.3 synonymous
Scores
2
Clinical Significance
Conservation
PhyloP100: 1.70
Genes affected
ACO2 (HGNC:118): (aconitase 2) The protein encoded by this gene belongs to the aconitase/IPM isomerase family. It is an enzyme that catalyzes the interconversion of citrate to isocitrate via cis-aconitate in the second step of the TCA cycle. This protein is encoded in the nucleus and functions in the mitochondrion. It was found to be one of the mitochondrial matrix proteins that are preferentially degraded by the serine protease 15(PRSS15), also known as Lon protease, after oxidative modification. [provided by RefSeq, Jul 2008]
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ACMG classification
Classification made for transcript
Verdict is Benign. Variant got -17 ACMG points.
BP4
?
Computational evidence support a benign effect (BayesDel_noAF=-0.49).
BP6
?
Variant 22-41499773-A-G is Benign according to our data. Variant chr22-41499773-A-G is described in ClinVar as [Likely_benign]. Clinvar id is 257432.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr22-41499773-A-G is described in Lovd as [Benign].
BP7
?
Synonymous conserved (PhyloP=1.7 with no splicing effect.
BS2
?
High Homozygotes in GnomAd4 at 3 AR gene
Transcripts
RefSeq
Gene | Transcript | HGVSc | HGVSp | Effect | #exon/exons | MANE | UniProt |
---|---|---|---|---|---|---|---|
ACO2 | NM_001098.3 | c.84A>G | p.Gln28= | synonymous_variant | 2/18 | ENST00000216254.9 |
Ensembl
Gene | Transcript | HGVSc | HGVSp | Effect | #exon/exons | TSL | MANE | Appris | UniProt |
---|---|---|---|---|---|---|---|---|---|
ACO2 | ENST00000216254.9 | c.84A>G | p.Gln28= | synonymous_variant | 2/18 | 1 | NM_001098.3 | P3 |
Frequencies
GnomAD3 genomes ? AF: 0.00143 AC: 217AN: 152220Hom.: 3 Cov.: 32
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GnomAD3 exomes AF: 0.000342 AC: 86AN: 251192Hom.: 0 AF XY: 0.000346 AC XY: 47AN XY: 135768
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GnomAD4 exome AF: 0.000146 AC: 213AN: 1461638Hom.: 0 Cov.: 31 AF XY: 0.000129 AC XY: 94AN XY: 727116
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GnomAD4 genome ? AF: 0.00144 AC: 219AN: 152338Hom.: 3 Cov.: 32 AF XY: 0.00125 AC XY: 93AN XY: 74494
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ClinVar
Significance: Benign/Likely benign
Submissions summary: Benign:3
Revision: criteria provided, multiple submitters, no conflicts
LINK: link
Submissions by phenotype
not specified Benign:2
Likely benign, criteria provided, single submitter | clinical testing | GeneDx | Apr 25, 2016 | This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease. - |
Benign, criteria provided, single submitter | clinical testing | PreventionGenetics, part of Exact Sciences | - | - - |
not provided Benign:1
Benign, criteria provided, single submitter | clinical testing | Invitae | Jan 30, 2024 | - - |
Computational scores
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Name
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BayesDel_noAF
Benign
CADD
Benign
DANN
Benign
RBP_binding_hub_radar
RBP_regulation_power_radar
Splicing
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SpliceAI score (max)
Details are displayed if max score is > 0.2
Find out detailed SpliceAI scores and Pangolin per-transcript scores at