rs199569629

Positions:

• chr1-237801846-G-T

Variant summary

Our verdict is Likely benign. Variant got -6 ACMG points: 0P and 6B. BP4_Strong BP6_Moderate

The NM_001035.3(RYR2):​c.14091-10G>T variant causes a intron change involving the alteration of a non-conserved nucleotide. In-silico tool predicts a benign outcome for this variant. Variant has been reported in ClinVar as Likely benign (★).

• Frequency:
  • Genomes: 𝑓 0.00034 (0 hom., cov: 32)
  • Exomes 𝑓: 0.0015 (0 hom.)
  • Failed GnomAD Quality Control
• Consequence: RYR2 NM_001035.3 intron
• Scores: Splicing: ADA: 0.00004461
• Clinical Significance: Likely benign criteria provided, single submitter B:1
• Conservation: PhyloP100: -0.0720

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 Likely_benign. Variant got -6 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.82).
• BP6: Variant 1-237801846-G-T is Benign according to our data. Variant chr1-237801846-G-T is described in ClinVar as [Likely_benign]. Clinvar id is 463574.Status of the report is criteria_provided_single_submitter, 1 stars.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
RYR2	NM_001035.3	c.14091-10G>T		intron_variant		ENST00000366574.7	NP_001026.2

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
RYR2	ENST00000366574.7	c.14091-10G>T		intron_variant		1	NM_001035.3	ENSP00000355533.2
RYR2	ENST00000609119.2	n.*5183-10G>T		intron_variant		5		ENSP00000499659.2

Frequencies

GnomAD3 genomes AF: 0.00 AC: 44 AN: 130532 Hom.: 0 Cov.: 32 FAILED QC

Gnomad AFR AF: 0.000203

Gnomad AMI AF: 0.00

Gnomad AMR AF: 0.000151

Gnomad ASJ AF: 0.00

Gnomad EAS AF: 0.00

Gnomad SAS AF: 0.00

Gnomad FIN AF: 0.00262

Gnomad MID AF: 0.00

Gnomad NFE AF: 0.000215

Gnomad OTH AF: 0.000564

GnomAD4 exome Data not reliable, filtered out with message: AS_VQSR AF: 0.00147 AC: 1872 AN: 1271770 Hom.: 0 Cov.: 26 AF XY: 0.00159 AC XY: 1005 AN XY: 630910

Gnomad4 AFR exome AF: 0.00428

Gnomad4 AMR exome AF: 0.0123

Gnomad4 ASJ exome AF: 0.00259

Gnomad4 EAS exome AF: 0.000275

Gnomad4 SAS exome AF: 0.00647

Gnomad4 FIN exome AF: 0.00285

Gnomad4 NFE exome AF: 0.000642

Gnomad4 OTH exome AF: 0.00153

GnomAD4 genome Data not reliable, filtered out with message: AS_VQSR AF: 0.000337 AC: 44 AN: 130532 Hom.: 0 Cov.: 32 AF XY: 0.000429 AC XY: 27 AN XY: 62956

Gnomad4 AFR AF: 0.000203

Gnomad4 AMR AF: 0.000151

Gnomad4 ASJ AF: 0.00

Gnomad4 EAS AF: 0.00

Gnomad4 SAS AF: 0.00

Gnomad4 FIN AF: 0.00262

Gnomad4 NFE AF: 0.000215

Gnomad4 OTH AF: 0.000564

Alfa AF: 0.00404 Hom.: 0

ClinVar

Significance: Likely benign

Submissions summary: Benign:1

Revision: criteria provided, single submitter

Submissions by phenotype

Catecholaminergic polymorphic ventricular tachycardia 1 Benign:1

Likely benign, criteria provided, single submitter

clinical testing

Labcorp Genetics (formerly Invitae), Labcorp

Oct 11, 2023

- -

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.82
CADD	Benign	10
DANN	Benign	0.55

Splicing

Name	Calibrated prediction	Score	Prediction
dbscSNV1_ADA	Benign	0.000045
dbscSNV1_RF	Benign	0.0020
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: rs199569629; hg19: chr1-237965146;