13-48664776-A-G

Position:

• chr13-48664776-A-G

Variant summary

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

The NM_001308476.3(CYSLTR2):​c.-266+10759A>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.19 in 151,634 control chromosomes in the GnomAD database, including 3,249 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 0.19 (3249 hom., cov: 32)
• Consequence: CYSLTR2 NM_001308476.3 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.267

Genes affected

CYSLTR2 (HGNC:18274): (cysteinyl leukotriene receptor 2) The cysteinyl leukotrienes LTC4, LTD4, and LTE4 are important mediators of human bronchial asthma. Pharmacologic studies have determined that cysteinyl leukotrienes activate at least 2 receptors, the protein encoded by this gene and CYSLTR1. This encoded receptor is a member of the superfamily of G protein-coupled receptors. It seems to play a major role in endocrine and cardiovascular systems. [provided by RefSeq, Jul 2008]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.8).
• BA1: GnomAd4 highest subpopulation (SAS) allele frequency at 95% confidence interval = 0.261 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
CYSLTR2	NM_001308476.3	c.-266+10759A>G		intron_variant		ENST00000682523.1	NP_001295405.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
CYSLTR2	ENST00000682523.1	c.-266+10759A>G		intron_variant			NM_001308476.3	ENSP00000508181	P1

Frequencies

GnomAD3 genomes AF: 0.190 AC: 28780 AN: 151516 Hom.: 3251 Cov.: 32

Gnomad AFR AF: 0.0580

Gnomad AMI AF: 0.326

Gnomad AMR AF: 0.161

Gnomad ASJ AF: 0.202

Gnomad EAS AF: 0.252

Gnomad SAS AF: 0.274

Gnomad FIN AF: 0.283

Gnomad MID AF: 0.108

Gnomad NFE AF: 0.250

Gnomad OTH AF: 0.195

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

GnomAD4 genome AF: 0.190 AC: 28776 AN: 151634 Hom.: 3249 Cov.: 32 AF XY: 0.194 AC XY: 14376 AN XY: 74106

Gnomad4 AFR AF: 0.0579

Gnomad4 AMR AF: 0.161

Gnomad4 ASJ AF: 0.202

Gnomad4 EAS AF: 0.252

Gnomad4 SAS AF: 0.274

Gnomad4 FIN AF: 0.283

Gnomad4 NFE AF: 0.250

Gnomad4 OTH AF: 0.192

Alfa AF: 0.234 Hom.: 5573

Bravo AF: 0.176

Asia WGS AF: 0.242 AC: 838 AN: 3470

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.80
CADD	Benign	7.6
DANN	Benign	0.81

Splicing

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

Publications

LitVar

Other links and lift over

dbSNP: rs9568079; hg19: chr13-49238912;