5-11507767-C-T

Position:

• chr5-11507767-C-T

Variant summary

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

The NM_001332.4(CTNND2):​c.287+57177G>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.0343 in 152,282 control chromosomes in the GnomAD database, including 124 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 0.034 (124 hom., cov: 32)
• Consequence: CTNND2 NM_001332.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.453

Genes affected

CTNND2 (HGNC:2516): (catenin delta 2) This gene encodes an adhesive junction associated protein of the armadillo/beta-catenin superfamily and is implicated in brain and eye development and cancer formation. The protein encoded by this gene promotes the disruption of E-cadherin based adherens junction to favor cell spreading upon stimulation by hepatocyte growth factor. This gene is overexpressed in prostate adenocarcinomas and is associated with decreased expression of tumor suppressor E-cadherin in this tissue. This gene resides in a region of the short arm of chromosome 5 that is deleted in Cri du Chat syndrome. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Dec 2013]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.9).
• BA1: GnomAd4 highest subpopulation (SAS) allele frequency at 95% confidence interval = 0.064 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
CTNND2	NM_001332.4	c.287+57177G>A		intron_variant		ENST00000304623.13

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
CTNND2	ENST00000304623.13	c.287+57177G>A		intron_variant		1	NM_001332.4	P1

Frequencies

GnomAD3 genomes AF: 0.0343 AC: 5224 AN: 152164 Hom.: 124 Cov.: 32

Gnomad AFR AF: 0.00922

Gnomad AMI AF: 0.0691

Gnomad AMR AF: 0.0262

Gnomad ASJ AF: 0.0548

Gnomad EAS AF: 0.000963

Gnomad SAS AF: 0.0697

Gnomad FIN AF: 0.0239

Gnomad MID AF: 0.0506

Gnomad NFE AF: 0.0514

Gnomad OTH AF: 0.0402

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

GnomAD4 genome AF: 0.0343 AC: 5222 AN: 152282 Hom.: 124 Cov.: 32 AF XY: 0.0322 AC XY: 2396 AN XY: 74472

Gnomad4 AFR AF: 0.00919

Gnomad4 AMR AF: 0.0262

Gnomad4 ASJ AF: 0.0548

Gnomad4 EAS AF: 0.000966

Gnomad4 SAS AF: 0.0702

Gnomad4 FIN AF: 0.0239

Gnomad4 NFE AF: 0.0513

Gnomad4 OTH AF: 0.0393

Alfa AF: 0.0484 Hom.: 258

Bravo AF: 0.0315

Asia WGS AF: 0.0250 AC: 86 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.90
CADD	Benign	0.64
DANN	Benign	0.49

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: rs17218080; hg19: chr5-11507879;