Variant 6-137004764-TAAAAA-TAAA details in Genebe, Genetics Data Aggregator

Variant summary

Our verdict is Benign. Variant got -10 ACMG points: 0P and 10B. BP6_ModerateBA1

The NM_014432.4(IL20RA):c.725-6_725-5delTT variant causes a splice region, intron change involving the alteration of a non-conserved nucleotide. 1/1 splice prediction tools predict no significant impact on normal splicing. Variant has been reported in ClinVar as Benign (★).

Frequency

Genomes: 𝑓 0.38 ( 12445 hom., cov: 0)

Exomes 𝑓: 0.42 ( 9676 hom. )

Failed GnomAD Quality Control

Consequence

IL20RA
NM_014432.4 splice_region, intron

Scores

Not classified

Clinical Significance

Benign criteria provided, single submitter B:1

Conservation

PhyloP100: 1.60

Variant links:

Genes affected

IL20RA (HGNC:6003): (interleukin 20 receptor subunit alpha) This gene encodes a member of the type II cytokine receptor family. The encoded protein is a subunit of the receptor for interleukin 20, a cytokine that may be involved in epidermal function. The interleukin 20 receptor is a heterodimeric complex consisting of the encoded protein and interleukin 20 receptor beta. This gene and interleukin 20 receptor beta are highly expressed in skin, and are upregulated in psoriasis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]

IL20RA links:

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ACMG classification

Classification made for transcript

Verdict is Benign. Variant got -10 ACMG points.

BP6

Variant 6-137004764-TAA-T is Benign according to our data. Variant chr6-137004764-TAA-T is described in ClinVar as [Benign]. Clinvar id is 402973.Status of the report is criteria_provided_single_submitter, 1 stars.

BA1

GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.747 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
IL20RA	NM_014432.4 link	c.725-6_725-5delTT		splice_region_variant, intron_variant	Intron 5 of 6	ENST00000316649.10	NP_055247.4	Q9UHF4-1

Ensembl

Gene	Transcript	HGVSc	Effect	Exon rank	TSL	MANE	Protein	UniProt
IL20RA	ENST00000316649.10 link	c.725-6_725-5delTT	splice_region_variant, intron_variant	Intron 5 of 6	1	NM_014432.4	ENSP00000314976.5	Q9UHF4-1
IL20RA	ENST00000367748.4 link	c.392-6_392-5delTT	splice_region_variant, intron_variant	Intron 4 of 5	1		ENSP00000356722.1	Q9UHF4-2
IL20RA	ENST00000541547.5 link	c.578-6_578-5delTT	splice_region_variant, intron_variant	Intron 5 of 6	2		ENSP00000437843.1	Q9UHF4-3
IL20RA	ENST00000468393.5 link	c.392-6_392-5delTT	splice_region_variant, intron_variant	Intron 4 of 4	4		ENSP00000489177.1	A0A0U1RQU9

Frequencies

GnomAD3 genomes

AF:

0.381

AC:

55611

AN:

145974

Hom.:

12458

Cov.:

show subpopulations

Gnomad AFR

AF:

0.123

Gnomad AMI

AF:

0.433

Gnomad AMR

AF:

0.487

Gnomad ASJ

AF:

0.514

Gnomad EAS

AF:

0.768

Gnomad SAS

AF:

0.490

Gnomad FIN

AF:

0.550

Gnomad MID

AF:

0.426

Gnomad NFE

AF:

0.441

Gnomad OTH

AF:

0.392

GnomAD3 exomes

AF:

0.443

AC:

67230

AN:

151602

Hom.:

2410

AF XY:

0.449

AC XY:

37519

AN XY:

83602

show subpopulations

Gnomad AFR exome

AF:

0.158

Gnomad AMR exome

AF:

0.464

Gnomad ASJ exome

AF:

0.450

Gnomad EAS exome

AF:

0.522

Gnomad SAS exome

AF:

0.450

Gnomad FIN exome

AF:

0.492

Gnomad NFE exome

AF:

0.462

Gnomad OTH exome

AF:

0.443

GnomAD4 exome

Data not reliable, filtered out with message: InbreedingCoeff

AF:

0.421

AC:

523531

AN:

1242372

Hom.:

9676

AF XY:

0.423

AC XY:

261743

AN XY:

618700

show subpopulations

Gnomad4 AFR exome

AF:

0.135

Gnomad4 AMR exome

AF:

0.454

Gnomad4 ASJ exome

AF:

0.436

Gnomad4 EAS exome

AF:

0.503

Gnomad4 SAS exome

AF:

0.438

Gnomad4 FIN exome

AF:

0.466

Gnomad4 NFE exome

AF:

0.422

Gnomad4 OTH exome

AF:

0.416

GnomAD4 genome

AF:

0.381

AC:

55582

AN:

146022

Hom.:

12445

Cov.:

AF XY:

0.392

AC XY:

27769

AN XY:

70872

show subpopulations

Gnomad4 AFR

AF:

0.123

Gnomad4 AMR

AF:

0.486

Gnomad4 ASJ

AF:

0.514

Gnomad4 EAS

AF:

0.768

Gnomad4 SAS

AF:

0.490

Gnomad4 FIN

AF:

0.550

Gnomad4 NFE

AF:

0.441

Gnomad4 OTH

AF:

0.392

ClinVar

Significance: Benign

Submissions summary: Benign:1

Revision: criteria provided, single submitter

LINK: link

Submissions by phenotype

not specified

Benign:1

Mar 29, 2016

Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine

Significance: Benign

Review Status: criteria provided, single submitter

Collection Method: clinical testing

Variant identified in a genome or exome case(s) and assessed due to predicted null impact of the variant or pathogenic assertions in the literature or databases. Disclaimer: This variant has not undergone full assessment. The following are preliminary notes: Frequency -

Computational scores

Source: dbNSFP v4.3

Name

Calibrated prediction

Score

Prediction

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

Below is the list of publications found by LitVar. It may be empty.

Variant summary

Frequency

Consequence

Scores

Clinical Significance

Conservation

ACMG classification

Transcripts

RefSeq

Ensembl

Frequencies

ClinVar

Submissions by phenotype

Computational scores

Splicing

Publications

LitVar

Other links and lift over