chr20-37862631-C-T

Position:

• chr20-37862631-C-T

Variant summary

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

The NM_030877.5(CTNNBL1):​c.1603+2287C>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.0666 in 152,196 control chromosomes in the GnomAD database, including 424 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 0.067 (424 hom., cov: 31)
• Consequence: CTNNBL1 NM_030877.5 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -3.50

Genes affected

CTNNBL1 (HGNC:15879): (catenin beta like 1) The protein encoded by this gene is a component of the pre-mRNA-processing factor 19-cell division cycle 5-like (PRP19-CDC5L) protein complex, which activates pre-mRNA splicing and is an integral part of the spliceosome. The encoded protein is also a nuclear localization sequence binding protein, and binds to activation-induced deaminase and is important for antibody diversification. This gene may also be associated with the development of obesity. Alternative splicing results in multiple transcript variants. A pseudogene of this gene has been defined on the X chromosome. [provided by RefSeq, Jul 2013]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.99).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.0829 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
CTNNBL1	NM_030877.5	c.1603+2287C>T		intron_variant		ENST00000361383.11	NP_110517.2
CTNNBL1	NM_001281495.2	c.1522+2287C>T		intron_variant			NP_001268424.1
CTNNBL1	XM_011528917.3	c.1273+2287C>T		intron_variant			XP_011527219.1
CTNNBL1	XM_024451947.2	c.1522+2287C>T		intron_variant			XP_024307715.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
CTNNBL1	ENST00000361383.11	c.1603+2287C>T		intron_variant		1	NM_030877.5	ENSP00000355050	P1

Frequencies

GnomAD3 genomes AF: 0.0664 AC: 10104 AN: 152078 Hom.: 420 Cov.: 31

Gnomad AFR AF: 0.0848

Gnomad AMI AF: 0.270

Gnomad AMR AF: 0.0528

Gnomad ASJ AF: 0.0285

Gnomad EAS AF: 0.00945

Gnomad SAS AF: 0.0298

Gnomad FIN AF: 0.0732

Gnomad MID AF: 0.0759

Gnomad NFE AF: 0.0634

Gnomad OTH AF: 0.0665

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

GnomAD4 genome AF: 0.0666 AC: 10129 AN: 152196 Hom.: 424 Cov.: 31 AF XY: 0.0657 AC XY: 4886 AN XY: 74420

Gnomad4 AFR AF: 0.0853

Gnomad4 AMR AF: 0.0528

Gnomad4 ASJ AF: 0.0285

Gnomad4 EAS AF: 0.00947

Gnomad4 SAS AF: 0.0298

Gnomad4 FIN AF: 0.0732

Gnomad4 NFE AF: 0.0634

Gnomad4 OTH AF: 0.0653

Alfa AF: 0.0692 Hom.: 44

Bravo AF: 0.0658

Asia WGS AF: 0.0320 AC: 110 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.99
CADD	Benign	0.17
DANN	Benign	0.55

Splicing

Name	Calibrated prediction	Score	Prediction
SpliceAI score (max)		0.060		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: rs6021428; hg19: chr20-36491033;