rs2129821

Positions:

• chr3-57101952-C-A
• chr3-57101952-C-G

Variant summary

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

The NM_017563.5(IL17RD):​c.979+527G>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.908 in 152,130 control chromosomes in the GnomAD database, including 63,231 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 0.91 (63231 hom., cov: 31)
• Consequence: IL17RD NM_017563.5 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -1.04

Genes affected

IL17RD (HGNC:17616): (interleukin 17 receptor D) This gene encodes a membrane protein belonging to the interleukin-17 receptor (IL-17R) protein family. The encoded protein is a component of the interleukin-17 receptor signaling complex, and the interaction between this protein and IL-17R does not require the interleukin. The gene product also affects fibroblast growth factor signaling, inhibiting or stimulating growth through MAPK/ERK signaling. Alternate splicing generates multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Jan 2016]

IL17RD (HGNC:):

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.96).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.958 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
IL17RD	NM_017563.5	c.979+527G>T		intron_variant		ENST00000296318.12	NP_060033.3

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
IL17RD	ENST00000296318.12	c.979+527G>T		intron_variant		1	NM_017563.5	ENSP00000296318.7
IL17RD	ENST00000320057.9	c.547+527G>T		intron_variant		1		ENSP00000322250.5
IL17RD	ENST00000463523.5	c.547+527G>T		intron_variant		1		ENSP00000417516.1
IL17RD	ENST00000469841.5	n.916+527G>T		intron_variant		2

Frequencies

GnomAD3 genomes AF: 0.908 AC: 138021 AN: 152012 Hom.: 63170 Cov.: 31

Gnomad AFR AF: 0.966

Gnomad AMI AF: 0.941

Gnomad AMR AF: 0.911

Gnomad ASJ AF: 0.845

Gnomad EAS AF: 0.503

Gnomad SAS AF: 0.950

Gnomad FIN AF: 0.934

Gnomad MID AF: 0.908

Gnomad NFE AF: 0.899

Gnomad OTH AF: 0.899

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

GnomAD4 genome AF: 0.908 AC: 138140 AN: 152130 Hom.: 63231 Cov.: 31 AF XY: 0.908 AC XY: 67547 AN XY: 74358

Gnomad4 AFR AF: 0.966

Gnomad4 AMR AF: 0.911

Gnomad4 ASJ AF: 0.845

Gnomad4 EAS AF: 0.503

Gnomad4 SAS AF: 0.951

Gnomad4 FIN AF: 0.934

Gnomad4 NFE AF: 0.899

Gnomad4 OTH AF: 0.897

Alfa AF: 0.886 Hom.: 3342

Bravo AF: 0.905

Asia WGS AF: 0.765 AC: 2663 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.96
CADD	Benign	0.21
DANN	Benign	0.63

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: rs2129821; hg19: chr3-57135980;