rs2618661

chr1-237548344-T-C

Variant summary

Our verdict is Benign. Variant got -14 ACMG points: 0P and 14B. BP4_Strong BP6_Moderate BA1

The NM_001035.3(RYR2):c.2907-87T>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.938 in 1,393,984 control chromosomes in the GnomAD database, including 617,586 homozygotes. In-silico tool predicts a benign outcome for this variant. Variant has been reported in ClinVar as Benign (★).

• Frequency:
  • Genomes: 𝑓 0.86 (57878 hom., cov: 32)
  • Exomes 𝑓: 0.95 (559708 hom.)
• Consequence: RYR2 NM_001035.3 intron
• Clinical Significance: Benign criteria provided, single submitter B:1
• Conservation: PhyloP100: -0.220

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]

ACMG classification

Verdict is Benign. Variant got -14 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.86).
• BP6: Variant 1-237548344-T-C is Benign according to our data. Variant chr1-237548344-T-C is described in ClinVar as [Benign]. Clinvar id is 671749.Status of the report is criteria_provided_single_submitter, 1 stars.
• BA1: GnomAd4 highest subpopulation (SAS) allele frequency at 95% confidence interval = 0.952 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
RYR2	NM_001035.3	c.2907-87T>C		intron_variant		ENST00000366574.7

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
RYR2	ENST00000366574.7	c.2907-87T>C		intron_variant		1	NM_001035.3	P1
RYR2	ENST00000659194.3	c.2907-87T>C		intron_variant
RYR2	ENST00000660292.2	c.2907-87T>C		intron_variant
RYR2	ENST00000609119.2	c.2907-87T>C		intron_variant, NMD_transcript_variant		5

Frequencies

GnomAD3 genomes AF: 0.858 AC: 130456 AN: 152084 Hom.: 57852 Cov.: 32

Gnomad AFR AF: 0.606

Gnomad AMI AF: 0.954

Gnomad AMR AF: 0.931

Gnomad ASJ AF: 0.965

Gnomad EAS AF: 0.888

Gnomad SAS AF: 0.962

Gnomad FIN AF: 0.976

Gnomad MID AF: 0.883

Gnomad NFE AF: 0.958

Gnomad OTH AF: 0.885

GnomAD4 exome AF: 0.948 AC: 1176738 AN: 1241784 Hom.: 559708 AF XY: 0.949 AC XY: 583517 AN XY: 614856

Gnomad4 AFR exome AF: 0.594

Gnomad4 AMR exome AF: 0.951

Gnomad4 ASJ exome AF: 0.960

Gnomad4 EAS exome AF: 0.885

Gnomad4 SAS exome AF: 0.968

Gnomad4 FIN exome AF: 0.972

Gnomad4 NFE exome AF: 0.959

Gnomad4 OTH exome AF: 0.932

GnomAD4 genome AF: 0.858 AC: 130526 AN: 152200 Hom.: 57878 Cov.: 32 AF XY: 0.861 AC XY: 64064 AN XY: 74428

Gnomad4 AFR AF: 0.606

Gnomad4 AMR AF: 0.931

Gnomad4 ASJ AF: 0.965

Gnomad4 EAS AF: 0.889

Gnomad4 SAS AF: 0.962

Gnomad4 FIN AF: 0.976

Gnomad4 NFE AF: 0.958

Gnomad4 OTH AF: 0.884

Alfa AF: 0.902 Hom.: 10644

Bravo AF: 0.842

Asia WGS AF: 0.913 AC: 3173 AN: 3478

ClinVar

Significance: Benign

Submissions summary: Benign:1

Revision: criteria provided, single submitter

Submissions by phenotype

not provided Benign:1

Benign, criteria provided, single submitter

clinical testing

GeneDx

Jun 15, 2018

This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease. -

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.86
Cadd	Benign	2.4
Dann	Benign	0.46

Splicing

Name	Calibrated prediction	Score	Prediction
SpliceAI score (max)		0.010		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: rs2618661; hg19: chr1-237711644;