X-78272820-G-C

Position:

• chrX-78272820-G-C

Variant summary

Our verdict is Uncertain significance. Variant got 1 ACMG points: 2P and 1B. PM2 BP4

The NM_006639.4(CYSLTR1):​c.927C>G​(p.Phe309Leu) variant causes a missense change involving the alteration of a non-conserved nucleotide. The variant was absent in control chromosomes in GnomAD project. In-silico tool predicts a benign outcome for this variant. 12/20 in silico tools predict a benign outcome for this variant. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar.

• Frequency: Genomes: not found (cov: 22)
• Consequence: CYSLTR1 NM_006639.4 missense
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.281

Genes affected

CYSLTR1 (HGNC:17451): (cysteinyl leukotriene receptor 1) This gene encodes a member of the G-protein coupled receptor 1 family. The encoded protein is a receptor for cysteinyl leukotrienes, and is involved in mediating bronchoconstriction via activation of a phosphatidylinositol-calcium second messenger system. Activation of the encoded receptor results in contraction and proliferation of bronchial smooth muscle cells, eosinophil migration, and damage to the mucus layer in the lung. Upregulation of this gene is associated with asthma and dysregulation may also be implicated in cancer. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2013]

ACMG classification

Verdict is Uncertain_significance. Variant got 1 ACMG points.

• PM2: Very rare variant in population databases, with high coverage
• BP4: Computational evidence support a benign effect (MetaRNN=0.2882983).

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
CYSLTR1	NM_006639.4	c.927C>G	p.Phe309Leu	missense_variant	3/3	ENST00000373304.4
CYSLTR1	NM_001282186.2	c.927C>G	p.Phe309Leu	missense_variant	2/2
CYSLTR1	NM_001282187.2	c.927C>G	p.Phe309Leu	missense_variant	4/4
CYSLTR1	NM_001282188.2	c.927C>G	p.Phe309Leu	missense_variant	4/4

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
CYSLTR1	ENST00000373304.4	c.927C>G	p.Phe309Leu	missense_variant	3/3	1	NM_006639.4	P1
CYSLTR1	ENST00000614798.1	c.927C>G	p.Phe309Leu	missense_variant	2/2	1		P1

Frequencies

GnomAD3 genomes Cov.: 22

GnomAD4 exome Cov.: 44

GnomAD4 genome Cov.: 22

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
AlphaMissense	Uncertain	0.42
BayesDel_addAF	Benign	-0.44	T
BayesDel_noAF	Benign	-0.87
CADD	Benign	7.1
DANN	Benign	0.82
DEOGEN2	Benign	0.15	T;T
FATHMM_MKL	Benign	0.29	N
M_CAP	Benign	0.0016	T
MetaRNN	Benign	0.29	T;T
MetaSVM	Benign	-0.98	T
MutationAssessor	Benign	0.0	N;N
MutationTaster	Benign	0.18	P
PrimateAI	Uncertain	0.58	T
PROVEAN	Benign	-0.51	N;.
REVEL	Benign	0.042
Sift	Benign	0.47	T;.
Sift4G	Benign	0.25	T;T
Polyphen		0.0	B;B
Vest4		0.18
MutPred		0.45		Loss of methylation at R310 (P = 0.0758);Loss of methylation at R310 (P = 0.0758);
MVP		0.94
MPC		0.0077
ClinPred		0.091	T
GERP RS		3.0
Varity_R		0.071
gMVP		0.21

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: rs320995; hg19: chrX-77528317;