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NM_000540.3(RYR1):c.7835+6_7835+7insGCGGGGCG AND Malignant hyperthermia, susceptibility to, 1

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Mar 28, 2023
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:
RCV004008009.2

Allele description [Variation Report for NM_000540.3(RYR1):c.7835+6_7835+7insGCGGGGCG]

NM_000540.3(RYR1):c.7835+6_7835+7insGCGGGGCG

Gene:
RYR1:ryanodine receptor 1 [Gene - OMIM - HGNC]
Variant type:
Insertion
Cytogenetic location:
19q13.2
Genomic location:
Preferred name:
NM_000540.3(RYR1):c.7835+6_7835+7insGCGGGGCG
HGVS:
  • NC_000019.10:g.38502733_38502734insGCGGGGCG
  • NG_008866.1:g.74034_74035insGCGGGGCG
  • NM_000540.3:c.7835+6_7835+7insGCGGGGCGMANE SELECT
  • NM_001042723.2:c.7835+6_7835+7insGCGGGGCG
  • LRG_766:g.74034_74035insGCGGGGCG
  • NC_000019.9:g.38993372_38993373insGGCGGGGC
  • NC_000019.9:g.38993373_38993374insGCGGGGCG
Molecular consequence:
  • NM_000540.3:c.7835+6_7835+7insGCGGGGCG - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001042723.2:c.7835+6_7835+7insGCGGGGCG - intron variant - [Sequence Ontology: SO:0001627]
Observations:
3

Condition(s)

Name:
Malignant hyperthermia, susceptibility to, 1 (MHS1)
Synonyms:
Anesthesia related hyperthermia; Malignant hyperpyrexia; Fulminating hyperpyrexia; See all synonyms [MedGen]
Identifiers:
MONDO: MONDO:0007783; MedGen: C2930980; Orphanet: 423; OMIM: 145600

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV004817106All of Us Research Program, National Institutes of Health
criteria provided, single submitter

(ACMG Guidelines, 2015)		Uncertain Significance
(Mar 28, 2023) 		germlineclinical testing

PubMed (1)
[See all records that cite this PMID]

Help

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineunknown3not providednot provided108544not providedclinical testing

Citations

PubMed

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.

Richards S, Aziz N, Bale S, Bick D, Das S, Gastier-Foster J, Grody WW, Hegde M, Lyon E, Spector E, Voelkerding K, Rehm HL; ACMG Laboratory Quality Assurance Committee..

Genet Med. 2015 May;17(5):405-24. doi: 10.1038/gim.2015.30. Epub 2015 Mar 5.

PubMed [citation]
PMID:
25741868
PMCID:
PMC4544753

Details of each submission

From All of Us Research Program, National Institutes of Health, SCV004817106.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not provided3not providednot providedclinical testing PubMed (1)
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineunknown108544not providednot provided3not providednot providednot provided

Last Updated: May 7, 2024