rs10521946

Positions:

• chrX-28752568-G-A

Variant summary

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

The ENST00000378993.6(IL1RAPL1):​c.-24-36752G>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.217 in 111,619 control chromosomes in the GnomAD database, including 2,095 homozygotes. There are 6,881 hemizygotes in GnomAD. 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 0.22 (2095 hom., 6881 hem., cov: 23)
• Consequence: IL1RAPL1 ENST00000378993.6 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.414

Genes affected

IL1RAPL1 (HGNC:5996): (interleukin 1 receptor accessory protein like 1) The protein encoded by this gene is a member of the interleukin 1 receptor family and is similar to the interleukin 1 accessory proteins. This protein has an N-terminal signal peptide, three extracellular immunoglobulin Ig-like domains, a transmembrane domain, an intracellular Toll/IL-1R domain, and a long C-terminal tail which interacts with multiple signalling molecules. This gene is located at a region on chromosome X that is associated with a non-syndromic form of X-linked intellectual disability. Deletions and mutations in this gene were found in patients with intellectual disability. This gene is expressed at a high level in post-natal brain structures involved in the hippocampal memory system, which suggests a specialized role in the physiological processes underlying memory and learning abilities, and plays a role in synapse formation and stabilization. [provided by RefSeq, Jul 2017]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.77).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.272 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
IL1RAPL1	NM_014271.4	c.-24-36752G>A		intron_variant		ENST00000378993.6	NP_055086.1
IL1RAPL1	XM_017029240.2	c.-25+34021G>A		intron_variant			XP_016884729.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
IL1RAPL1	ENST00000378993.6	c.-24-36752G>A		intron_variant		1	NM_014271.4	ENSP00000368278	P1

Frequencies

GnomAD3 genomes AF: 0.217 AC: 24187 AN: 111565 Hom.: 2094 Cov.: 23 AF XY: 0.203 AC XY: 6861 AN XY: 33797

Gnomad AFR AF: 0.277

Gnomad AMI AF: 0.230

Gnomad AMR AF: 0.144

Gnomad ASJ AF: 0.292

Gnomad EAS AF: 0.0227

Gnomad SAS AF: 0.251

Gnomad FIN AF: 0.191

Gnomad MID AF: 0.391

Gnomad NFE AF: 0.206

Gnomad OTH AF: 0.226

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

GnomAD4 genome AF: 0.217 AC: 24211 AN: 111619 Hom.: 2095 Cov.: 23 AF XY: 0.203 AC XY: 6881 AN XY: 33861

Gnomad4 AFR AF: 0.277

Gnomad4 AMR AF: 0.144

Gnomad4 ASJ AF: 0.292

Gnomad4 EAS AF: 0.0225

Gnomad4 SAS AF: 0.251

Gnomad4 FIN AF: 0.191

Gnomad4 NFE AF: 0.206

Gnomad4 OTH AF: 0.231

Alfa AF: 0.209 Hom.: 16700

Bravo AF: 0.214

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.77
CADD	Benign	3.9
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: rs10521946; hg19: chrX-28770685;