1-237136049-T-C

Position:

• chr1-237136049-T-C

Variant summary

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

The NM_001035.3(RYR2):​c.48+93480T>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.67 in 152,094 control chromosomes in the GnomAD database, including 34,213 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 0.67 (34213 hom., cov: 33)
• Consequence: RYR2 NM_001035.3 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.0510

Genes affected

RYR2 (HGNC:10484): (ryanodine receptor 2) This gene encodes a ryanodine receptor found in cardiac muscle sarcoplasmic reticulum. The encoded protein is one of the components of a calcium channel, composed of a tetramer of the ryanodine receptor proteins and a tetramer of FK506 binding protein 1B proteins, that supplies calcium to cardiac muscle. Mutations in this gene are associated with stress-induced polymorphic ventricular tachycardia and arrhythmogenic right ventricular dysplasia. [provided by RefSeq, Jul 2008]

RYR2 (HGNC:):

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.99).
• BA1: GnomAd4 highest subpopulation (SAS) allele frequency at 95% confidence interval = 0.73 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
RYR2	NM_001035.3	c.48+93480T>C		intron_variant		ENST00000366574.7	NP_001026.2

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
RYR2	ENST00000366574.7	c.48+93480T>C		intron_variant		1	NM_001035.3	ENSP00000355533.2
RYR2	ENST00000609119.2	n.48+93480T>C		intron_variant		5		ENSP00000499659.2
RYR2	ENST00000660292.2	c.48+93480T>C		intron_variant				ENSP00000499787.2
RYR2	ENST00000659194.3	c.48+93480T>C		intron_variant				ENSP00000499653.3

Frequencies

GnomAD3 genomes AF: 0.670 AC: 101861 AN: 151974 Hom.: 34185 Cov.: 33

Gnomad AFR AF: 0.632

Gnomad AMI AF: 0.737

Gnomad AMR AF: 0.687

Gnomad ASJ AF: 0.622

Gnomad EAS AF: 0.587

Gnomad SAS AF: 0.750

Gnomad FIN AF: 0.685

Gnomad MID AF: 0.674

Gnomad NFE AF: 0.690

Gnomad OTH AF: 0.675

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

GnomAD4 genome AF: 0.670 AC: 101935 AN: 152094 Hom.: 34213 Cov.: 33 AF XY: 0.670 AC XY: 49849 AN XY: 74372

Gnomad4 AFR AF: 0.631

Gnomad4 AMR AF: 0.687

Gnomad4 ASJ AF: 0.622

Gnomad4 EAS AF: 0.587

Gnomad4 SAS AF: 0.750

Gnomad4 FIN AF: 0.685

Gnomad4 NFE AF: 0.690

Gnomad4 OTH AF: 0.677

Alfa AF: 0.685 Hom.: 35330

Bravo AF: 0.667

Asia WGS AF: 0.695 AC: 2417 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.99
CADD	Benign	2.1
DANN	Benign	0.62

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: rs1337797; hg19: chr1-237299349;