Variant chr5-35878410-G-A details in Genebe, Genetics Data Aggregator

Variant summary

Our verdict is Benign. Variant got -20 ACMG points: 0P and 20B. BP4_StrongBP6_Very_StrongBA1

The NM_002185.5(IL7R):c.*1924G>A variant causes a 3 prime UTR change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.132 in 232,966 control chromosomes in the GnomAD database, including 2,066 homozygotes. In-silico tool predicts a benign outcome for this variant. Variant has been reported in ClinVar as Benign (★★).

Frequency

Genomes: 𝑓 0.13 ( 1318 hom., cov: 33)

Exomes 𝑓: 0.13 ( 748 hom. )

Consequence

IL7R
NM_002185.5 3_prime_UTR

Scores

Clinical Significance

Benign criteria provided, multiple submitters, no conflicts B:2

Conservation

PhyloP100: -1.61

Variant links:

Genes affected

IL7R (HGNC:6024): (interleukin 7 receptor) The protein encoded by this gene is a receptor for interleukin 7 (IL7). The function of this receptor requires the interleukin 2 receptor, gamma chain (IL2RG), which is a common gamma chain shared by the receptors of various cytokines, including interleukins 2, 4, 7, 9, and 15. This protein has been shown to play a critical role in V(D)J recombination during lymphocyte development. Defects in this gene may be associated with severe combined immunodeficiency (SCID). Alternatively spliced transcript variants have been found. [provided by RefSeq, Dec 2015]

IL7R links:

Genome browser will be placed here

ACMG classification

Classification made for transcript

Verdict is Benign. Variant got -20 ACMG points.

BP4

Computational evidence support a benign effect (BayesDel_noAF=-0.95).

BP6

Variant 5-35878410-G-A is Benign according to our data. Variant chr5-35878410-G-A is described in ClinVar as [Benign]. Clinvar id is 353301.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars.

BA1

GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.138 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	Effect	#exon/exons	MANE
IL7R	NM_002185.5 linkuse as main transcript	c.*1924G>A	3_prime_UTR_variant	8/8	ENST00000303115.8
IL7R	NM_001410734.1 linkuse as main transcript	c.*2421G>A	3_prime_UTR_variant	7/7
IL7R	NR_120485.3 linkuse as main transcript	n.3128G>A	non_coding_transcript_exon_variant	6/6

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
IL7R	ENST00000303115.8 linkuse as main transcript	c.*1924G>A		3_prime_UTR_variant	8/8	1	NM_002185.5	P1	P16871-1

Frequencies

GnomAD3 genomes

AF:

0.131

AC:

19948

AN:

152060

Hom.:

1318

Cov.:

show subpopulations

Gnomad AFR

AF:

0.132

Gnomad AMI

AF:

0.147

Gnomad AMR

AF:

0.143

Gnomad ASJ

AF:

0.131

Gnomad EAS

AF:

0.144

Gnomad SAS

AF:

0.0636

Gnomad FIN

AF:

0.100

Gnomad MID

AF:

0.127

Gnomad NFE

AF:

0.136

Gnomad OTH

AF:

0.146

GnomAD4 exome

AF:

0.134

AC:

10808

AN:

80788

Hom.:

748

Cov.:

AF XY:

0.134

AC XY:

4968

AN XY:

37124

show subpopulations

Gnomad4 AFR exome

AF:

0.133

Gnomad4 AMR exome

AF:

0.157

Gnomad4 ASJ exome

AF:

0.116

Gnomad4 EAS exome

AF:

0.112

Gnomad4 SAS exome

AF:

0.0500

Gnomad4 FIN exome

AF:

0.138

Gnomad4 NFE exome

AF:

0.139

Gnomad4 OTH exome

AF:

0.144

GnomAD4 genome

AF:

0.131

AC:

19940

AN:

152178

Hom.:

1318

Cov.:

AF XY:

0.128

AC XY:

9513

AN XY:

74394

show subpopulations

Gnomad4 AFR

AF:

0.131

Gnomad4 AMR

AF:

0.143

Gnomad4 ASJ

AF:

0.131

Gnomad4 EAS

AF:

0.144

Gnomad4 SAS

AF:

0.0628

Gnomad4 FIN

AF:

0.100

Gnomad4 NFE

AF:

0.136

Gnomad4 OTH

AF:

0.144

Alfa

AF:

0.134

Hom.:

213

Bravo

AF:

0.139

Asia WGS

AF:

0.108

AC:

374

AN:

3478

ClinVar

Significance: Benign

Submissions summary: Benign:2

Revision: criteria provided, multiple submitters, no conflicts

LINK: link

Submissions by phenotype

not provided

Benign:1

Benign, criteria provided, single submitter

not provided

Breakthrough Genomics, Breakthrough Genomics

- -

Immunodeficiency 104

Benign:1

Benign, criteria provided, single submitter

clinical testing

Illumina Laboratory Services, Illumina

Jan 13, 2018

This variant was observed in the ICSL laboratory as part of a predisposition screen in an ostensibly healthy population. It had not been previously curated by ICSL or reported in the Human Gene Mutation Database (HGMD: prior to June 1st, 2018), and was therefore a candidate for classification through an automated scoring system. Utilizing variant allele frequency, disease prevalence and penetrance estimates, and inheritance mode, an automated score was calculated to assess if this variant is too frequent to cause the disease. Based on the score and internal cut-off values, a variant classified as benign is not then subjected to further curation. The score for this variant resulted in a classification of benign for this disease. -

Computational scores

Source: dbNSFP v4.3

Name

Calibrated prediction

Score

Prediction

BayesDel_noAF

Benign

-0.95

CADD

Benign

0.075

DANN

Benign

0.41

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