rs10496236

Positions:

• chr2-80072228-C-A

Variant summary

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

The NM_001282597.3(CTNNA2):​c.1056+162431C>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.163 in 152,130 control chromosomes in the GnomAD database, including 2,837 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 0.16 (2837 hom., cov: 32)
• Consequence: CTNNA2 NM_001282597.3 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 1.20

Genes affected

CTNNA2 (HGNC:2510): (catenin alpha 2) Enables actin filament binding activity. Involved in negative regulation of Arp2/3 complex-mediated actin nucleation; regulation of neuron migration; and regulation of neuron projection development. Located in cytoplasm. Implicated in complex cortical dysplasia with other brain malformations. [provided by Alliance of Genome Resources, Apr 2022]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.91).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.441 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
CTNNA2	NM_001282597.3	c.1056+162431C>A		intron_variant		ENST00000402739.9	NP_001269526.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
CTNNA2	ENST00000402739.9	c.1056+162431C>A		intron_variant		1	NM_001282597.3	ENSP00000384638
CTNNA2	ENST00000496558.5	c.1056+162431C>A		intron_variant		1		ENSP00000419295	P1
CTNNA2	ENST00000466387.5	c.1056+162431C>A		intron_variant		2		ENSP00000418191	P1
CTNNA2	ENST00000629316.2	c.1056+162431C>A		intron_variant		2		ENSP00000486160

Frequencies

GnomAD3 genomes AF: 0.163 AC: 24719 AN: 152012 Hom.: 2833 Cov.: 32

Gnomad AFR AF: 0.106

Gnomad AMI AF: 0.0789

Gnomad AMR AF: 0.342

Gnomad ASJ AF: 0.183

Gnomad EAS AF: 0.457

Gnomad SAS AF: 0.213

Gnomad FIN AF: 0.227

Gnomad MID AF: 0.123

Gnomad NFE AF: 0.121

Gnomad OTH AF: 0.182

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

GnomAD4 genome AF: 0.163 AC: 24749 AN: 152130 Hom.: 2837 Cov.: 32 AF XY: 0.174 AC XY: 12955 AN XY: 74350

Gnomad4 AFR AF: 0.106

Gnomad4 AMR AF: 0.342

Gnomad4 ASJ AF: 0.183

Gnomad4 EAS AF: 0.456

Gnomad4 SAS AF: 0.213

Gnomad4 FIN AF: 0.227

Gnomad4 NFE AF: 0.121

Gnomad4 OTH AF: 0.189

Alfa AF: 0.150 Hom.: 3681

Bravo AF: 0.175

Asia WGS AF: 0.330 AC: 1147 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.91
CADD	Benign	12
DANN	Benign	0.74

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: rs10496236; hg19: chr2-80299354;