NM_001035.3:c.385-1433T>G

Variant names:

• chr1-237373284-T-G
• rs6670163
• NM_001035.3:c.385-1433T>G

Variant summary

Our verdict is Benign. The variant received -12 ACMG points: 0P and 12B. BP4_Strong BA1

The NM_001035.3(RYR2):​c.385-1433T>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.232 in 152,000 control chromosomes in the GnomAD database, including 4,167 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 0.23 (4167 hom., cov: 32)
• Consequence: RYR2 NM_001035.3 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.560
• Publications: 3 publications found

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 Gene-Disease associations (from GenCC):

• arrhythmogenic right ventricular dysplasia 2

  Inheritance: AD Classification: DEFINITIVE, NO_KNOWN Submitted by: Laboratory for Molecular Medicine, Ambry Genetics
• catecholaminergic polymorphic ventricular tachycardia

  Inheritance: AD Classification: DEFINITIVE, SUPPORTIVE Submitted by: Orphanet, ClinGen, G2P
• catecholaminergic polymorphic ventricular tachycardia 1

  Inheritance: AD Classification: STRONG Submitted by: Genomics England PanelApp, Labcorp Genetics (formerly Invitae)
• hypertrophic cardiomyopathy

  Inheritance: AD Classification: LIMITED Submitted by: ClinGen
• arrhythmogenic right ventricular cardiomyopathy

  Inheritance: AD Classification: NO_KNOWN Submitted by: ClinGen

ACMG classification

Our verdict: Benign. The variant received -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.95).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.383 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
RYR2	NM_001035.3	c.385-1433T>G		intron_variant	Intron 6 of 104	ENST00000366574.7	NP_001026.2

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
RYR2	ENST00000366574.7	c.385-1433T>G		intron_variant	Intron 6 of 104	1	NM_001035.3	ENSP00000355533.2
RYR2	ENST00000661330.2	c.385-1433T>G		intron_variant	Intron 6 of 105			ENSP00000499393.2
RYR2	ENST00000609119.2	n.385-1433T>G		intron_variant	Intron 6 of 103	5		ENSP00000499659.2

Frequencies

GnomAD3 genomes AF: 0.232 AC: 35182 AN: 151882 Hom.: 4162 Cov.: 32

Gnomad AFR AF: 0.212

Gnomad AMI AF: 0.266

Gnomad AMR AF: 0.283

Gnomad ASJ AF: 0.209

Gnomad EAS AF: 0.398

Gnomad SAS AF: 0.133

Gnomad FIN AF: 0.260

Gnomad MID AF: 0.232

Gnomad NFE AF: 0.222

Gnomad OTH AF: 0.255

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

GnomAD4 genome AF: 0.232 AC: 35208 AN: 152000 Hom.: 4167 Cov.: 32 AF XY: 0.233 AC XY: 17332 AN XY: 74300

African (AFR) AF: 0.212 AC: 8789 AN: 41464

American (AMR) AF: 0.284 AC: 4326 AN: 15252

Ashkenazi Jewish (ASJ) AF: 0.209 AC: 727 AN: 3472

East Asian (EAS) AF: 0.398 AC: 2046 AN: 5146

South Asian (SAS) AF: 0.134 AC: 649 AN: 4826

European-Finnish (FIN) AF: 0.260 AC: 2750 AN: 10566

Middle Eastern (MID) AF: 0.219 AC: 64 AN: 292

European-Non Finnish (NFE) AF: 0.222 AC: 15083 AN: 67954

Other (OTH) AF: 0.251 AC: 531 AN: 2116

Alfa AF: 0.176 Hom.: 2159

Bravo AF: 0.239

Asia WGS AF: 0.239 AC: 831 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.95
CADD	Benign	5.5
DANN	Benign	0.46
PhyloP100		0.56
Mutation Taster		=100/0	polymorphism (auto)

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

Other links and lift over

dbSNP: rs6670163; hg19: chr1-237536584;