NM_000540.3(RYR1):c.1825A>G (p.Asn609Asp) AND not provided

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: May 17, 2017
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:: RCV000494299.1

Allele description [Variation Report for NM_000540.3(RYR1):c.1825A>G (p.Asn609Asp)]

NM_000540.3(RYR1):c.1825A>G (p.Asn609Asp)

Gene:

RYR1:ryanodine receptor 1 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

19q13.2

Genomic location:

Preferred name:

NM_000540.3(RYR1):c.1825A>G (p.Asn609Asp)

HGVS:

NC_000019.10:g.38457530A>G
NG_008866.1:g.28831A>G
NM_000540.3:c.1825A>GMANE SELECT
NM_001042723.2:c.1825A>G
NP_000531.2:p.Asn609Asp
NP_000531.2:p.Asn609Asp
NP_001036188.1:p.Asn609Asp
LRG_766t1:c.1825A>G
LRG_766:g.28831A>G
LRG_766p1:p.Asn609Asp
NC_000019.9:g.38948170A>G
NM_000540.2:c.1825A>G

Protein change:

N609D

Links:

dbSNP: rs1131691719

NCBI 1000 Genomes Browser:

rs1131691719

Molecular consequence:

NM_000540.3:c.1825A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001042723.2:c.1825A>G - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Synonyms:: none provided
Identifiers:: MedGen: CN517202

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV000582706	GeneDx	criteria provided, single submitter (GeneDx Variant Classification (06012015))	Uncertain significance (May 17, 2017)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV000582706

GeneDx

criteria provided, single submitter

(GeneDx Variant Classification (06012015))

Uncertain significance
(May 17, 2017)

germline

clinical testing

Citation Link

Help

Summary from all submissions

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

Details of each submission

From GeneDx, SCV000582706.3

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

Description

The N609D variant in the RYR1 gene has not been reported previously as a pathogenic variant, nor as a benign variant, to our knowledge. The N609D variant is not observed in large population cohorts (Lek et al., 2016; 1000 Genomes Consortium et al., 2015; Exome Variant Server). The N609D variant is a semi-conservative amino acid substitution, which may impact secondary protein structure as these residues differ in some properties. This substitution occurs at a position that is conserved across species. In silico analysis predicts this variant is probably damaging to the protein structure/function. We interpret N609D as a variant of uncertain significance.

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

Last Updated: Nov 5, 2022

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