rs1713239

chr1-206864130-G-Cchr1-206864130-G-T

Variant summary

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

The NM_001385166.1(IL20):c.-171+523G>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.872 in 152,152 control chromosomes in the GnomAD database, including 58,225 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 0.87 (58225 hom., cov: 30)
• Consequence: IL20 NM_001385166.1 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.345

Genes affected

IL20 (HGNC:):

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.98).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.953 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
IL20	NM_001385166.1	c.-171+523G>C		intron_variant
IL20	NM_001385167.1	c.-252+523G>C		intron_variant

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt

Frequencies

GnomAD3 genomes AF: 0.872 AC: 132531 AN: 152034 Hom.: 58171 Cov.: 30

Gnomad AFR AF: 0.960

Gnomad AMI AF: 0.858

Gnomad AMR AF: 0.799

Gnomad ASJ AF: 0.908

Gnomad EAS AF: 0.657

Gnomad SAS AF: 0.778

Gnomad FIN AF: 0.823

Gnomad MID AF: 0.886

Gnomad NFE AF: 0.863

Gnomad OTH AF: 0.857

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

GnomAD4 genome AF: 0.872 AC: 132640 AN: 152152 Hom.: 58225 Cov.: 30 AF XY: 0.866 AC XY: 64377 AN XY: 74374

Gnomad4 AFR AF: 0.961

Gnomad4 AMR AF: 0.798

Gnomad4 ASJ AF: 0.908

Gnomad4 EAS AF: 0.657

Gnomad4 SAS AF: 0.777

Gnomad4 FIN AF: 0.823

Gnomad4 NFE AF: 0.863

Gnomad4 OTH AF: 0.858

Alfa AF: 0.873 Hom.: 7291

Bravo AF: 0.873

Asia WGS AF: 0.765 AC: 2659 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.98
Cadd	Benign	1.0
Dann	Benign	0.38

Splicing

Find out detailed SpliceAI scores and Pangolin per-transcript scores at spliceailookup.broadinstitute.org

Publications

LitVar

Other links and lift over

dbSNP: rs1713239; hg19: chr1-207037475; COSMIC: COSV65584356;