NM_000540.3(RYR1):c.103T>C (p.Cys35Arg) AND methoxyflurane response - Toxicity - ClinVar

NM_000540.3(RYR1):c.103T>C (p.Cys35Arg) AND methoxyflurane response - Toxicity

Germline classification:: drug response (1 submission)
Last evaluated:: Mar 24, 2021
Review status:: 3 stars out of maximum of 4 stars
reviewed by expert panel

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:: RCV001787934.11

Allele description [Variation Report for NM_000540.3(RYR1):c.103T>C (p.Cys35Arg)]

NM_000540.3(RYR1):c.103T>C (p.Cys35Arg)

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.103T>C (p.Cys35Arg)

Other names:

NM_000540.3(RYR1):c.103T>C

HGVS:

NC_000019.10:g.38440802T>C
NG_008866.1:g.12103T>C
NM_000540.3:c.103T>CMANE SELECT
NM_001042723.2:c.103T>C
NP_000531.2:p.Cys35Arg
NP_000531.2:p.Cys35Arg
NP_001036188.1:p.Cys35Arg
LRG_766t1:c.103T>C
LRG_766:g.12103T>C
LRG_766p1:p.Cys35Arg
NC_000019.9:g.38931442T>C
NM_000540.2:c.103T>C
P21817:p.Cys35Arg
p.(Cys35Arg)

Protein change:

C35R

Links:

PharmGKB: 1445400910PA164749136; PharmGKB: 1445400910PA449461; PharmGKB: 1445400910PA449845; PharmGKB: 1445400910PA450106; PharmGKB: 1445400910PA450434; PharmGKB: 1445400910PA451341; PharmGKB: 1445400910PA451522; UniProtKB: P21817#VAR_005589; dbSNP: rs193922747

NCBI 1000 Genomes Browser:

rs193922747

Molecular consequence:

NM_000540.3:c.103T>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001042723.2:c.103T>C - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:: methoxyflurane response - Toxicity
Identifiers:

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV000925531	PharmGKB	reviewed by expert panel (Pharmacogenomics knowledge for personalized medicine)	drug response (Mar 24, 2021) Condition: methoxyflurane response - Toxicity Drug reported used for: Malignant Hyperthermia	germline	curation	PubMed (7) [See all records that cite these PMIDs] 16163667, 17710899, 20681998, 9066328, 9334205, 9497245, 22992668 Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV000925531

PharmGKB

reviewed by expert panel

(Pharmacogenomics knowledge for personalized medicine)

drug response
(Mar 24, 2021)
Condition: methoxyflurane response - Toxicity
Drug reported used for: Malignant Hyperthermia

germline

curation

PubMed (7)
[See all records that cite these PMIDs]

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	curation

Citations

PubMed

Correlations between genotype and pharmacological, histological, functional, and clinical phenotypes in malignant hyperthermia susceptibility.

Monnier N, Kozak-Ribbens G, Krivosic-Horber R, Nivoche Y, Qi D, Kraev N, Loke J, Sharma P, Tegazzin V, Figarella-Branger D, Roméro N, Mezin P, Bendahan D, Payen JF, Depret T, Maclennan DH, Lunardi J.

Hum Mutat. 2005 Nov;26(5):413-25.

PubMed [citation]

PMID:: 16163667

Molecular genetic detection of susceptibility to malignant hyperthermia in Belgian families.

Heytens L.

Acta Anaesthesiol Belg. 2007;58(2):113-8.

PubMed [citation]

PMID:: 17710899

See all PubMed Citations (7)

Details of each submission

From PharmGKB, SCV000925531.2

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	not provided	not provided	not provided	curation	PubMed (7)

Description

PharmGKB Level of Evidence 1A: Level 1A clinical annotations describe variant-drug combinations that have variant-specific prescribing guidance available in a current clinical guideline annotation or an FDA-approved drug label annotation. Annotations of drug labels or clinical guidelines must give prescribing guidance for specific variants (e.g. CYP2C9*3, HLA-B*57:01) or provide mapping from defined allele functions to diplotypes and phenotypes to be used as supporting evidence for a level 1A clinical annotation. Level 1A clinical annotations must also be supported by at least one publication in addition to a clinical guideline or drug label with variant-specific prescribing guidance.

#	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: Oct 26, 2024

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