NM_001035.3(RYR2):c.13081G>A (p.Glu4361Lys) AND Ventricular arrhythmias due to cardiac ryanodine receptor calcium release deficiency syndrome

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Oct 27, 2021
Review status:: 1 star out of maximum of 4 stars
criteria provided, single submitter

Somatic classification of clinical impact:: None
Review status:: (0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided

Somatic classification of oncogenicity:: None
Review status:: (0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided

Record status:: current
Accession:: RCV002054173.10

Allele description [Variation Report for NM_001035.3(RYR2):c.13081G>A (p.Glu4361Lys)]

NM_001035.3(RYR2):c.13081G>A (p.Glu4361Lys)

Genes:

LOC126806068:BRD4-independent group 4 enhancer GRCh37_chr1:237947411-237948610 [Gene]
RYR2:ryanodine receptor 2 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

1q43

Genomic location:

Preferred name:

NM_001035.3(RYR2):c.13081G>A (p.Glu4361Lys)

Other names:

p.E4361K:GAG>AAG

HGVS:

NC_000001.11:g.237784793G>A
NG_008799.3:g.747610G>A
NM_001035.3:c.13081G>AMANE SELECT
NP_001026.2:p.Glu4361Lys
LRG_402t1:c.13081G>A
LRG_402:g.747610G>A
LRG_402p1:p.Glu4361Lys
NC_000001.10:g.237948093G>A
NG_008799.2:g.747392G>A
NM_001035.2:c.13081G>A

Protein change:

E4361K

Links:

dbSNP: rs794728795

NCBI 1000 Genomes Browser:

rs794728795

Molecular consequence:

NM_001035.3:c.13081G>A - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:: Ventricular arrhythmias due to cardiac ryanodine receptor calcium release deficiency syndrome
Synonyms:: Autosomal dominant cardiac arrhythmia (Kuhn)
Identifiers:: MONDO: MONDO:0020745; MedGen: C5542154; OMIM: 115000

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV002320706	Center For Human Genetics And Laboratory Diagnostics, Dr. Klein, Dr. Rost And Colleagues	criteria provided, single submitter (ACGS Guidelines, 2020)	Uncertain significance (Oct 27, 2021)	unknown	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV002320706

Center For Human Genetics And Laboratory Diagnostics, Dr. Klein, Dr. Rost And Colleagues

criteria provided, single submitter

(ACGS Guidelines, 2020)

Uncertain significance
(Oct 27, 2021)

unknown

clinical testing

Citation Link

Help

Summary from all submissions

Ethnicity	Origin	Affected	Individuals	Families	Chromosomes tested	Number Tested	Family history	Method
not provided	unknown	yes	not provided	not provided	not provided	not provided	not provided	clinical testing

Details of each submission

From Center For Human Genetics And Laboratory Diagnostics, Dr. Klein, Dr. Rost And Colleagues, SCV002320706.1

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	not provided	not provided	not provided	clinical testing	not provided

#	Sample				Method		Observation
#	Origin	Affected	Number tested	Tissue	Purpose	Method	Individuals	Allele frequency	Families	Co-occurrences
1	unknown	yes	not provided	not provided	not provided		not provided	not provided	not provided	not provided

Last Updated: Nov 24, 2024

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