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Variant: NM_000540.2(RYR1):c.14825G>T (p.Gly4942Val)

CA024268

133094 (ClinVar)

Gene: RYR1
Condition: malignant hyperthermia, susceptibility to, 1
Inheritance Mode: Autosomal dominant inheritance
UUID: 86e6ae80-88b6-401c-87e1-96be13b84233

HGVS expressions

NM_000540.2:c.14825G>T
NM_000540.2(RYR1):c.14825G>T (p.Gly4942Val)
NC_000019.10:g.38585959G>T
CM000681.2:g.38585959G>T
NC_000019.9:g.39076599G>T
CM000681.1:g.39076599G>T
NC_000019.8:g.43768439G>T
NG_008866.1:g.157260G>T
ENST00000593677.2:n.1761G>T
ENST00000688602.1:n.3158G>T
ENST00000689936.1:n.3130G>T
ENST00000692547.1:n.218G>T
ENST00000359596.8:c.14825G>T
ENST00000355481.8:c.14810G>T
ENST00000359596.7:n.14825G>T
ENST00000360985.7:c.14807G>T
NM_001042723.1:c.14810G>T
NM_000540.3:c.14825G>T
NM_001042723.2:c.14810G>T
NM_000540.3(RYR1):c.14825G>T (p.Gly4942Val)

Uncertain Significance

Met criteria codes 2
PP3_Moderate PM1_Supporting
Not Met criteria codes 1
PS4

Evidence Links 0

Expert Panel

Criteria Specification Information

Criteria Specifications for this VCEP
Evidence submitted by expert panel
Malignant Hyperthermia Susceptibility VCEP
This pathogenicity assessment is relevant only for malignant hyperthermia susceptibility (MHS) inherited in an autosomal dominant pattern. Variants in RYR1 can also cause other myopathies inherited in an autosomal dominant pattern or in an autosomal recessive pattern. Some of these disorders may predispose individuals to malignant hyperthermia. RYR1 variants may also contribute to a malignant hyperthermia reaction in combination with other genetic and non-genetic factors and the clinician needs to consider such factors in making management decisions. This sequence variant predicts a substitution of glycine with valine at codon 4942 of the RYR1 protein, p.(Gly4942Val). This variant was not present in a large population database (gnomAD) at the time this variant was interpreted. To our knowledge this variant has not been reported in the literature in individuals who have a personal or family history of a malignant hyperthermia reaction. No functional studies were identified for this variant. This variant resides in a region of RYR1 considered to be a hotspot for pathogenic variants that contribute to MHS, PM1_Sup (PMID: 21118704). A REVEL score >0.85 (0.922) supports a pathogenic status for this variant, PP3_Moderate. This variant has been classified as a Variant of Unknown Significance. Criteria implemented: PM1_Supporting, PP3_Moderate. 
Met criteria codes
PP3_Moderate
A REVEL score >0.85 (0.922) supports a pathogenic status for this variant, PP3_Moderate.
PM1_Supporting
This variant resides in a region of RYR1 considered to be a hotspot for pathogenic variants that contribute to MHS, PM1_Sup (PMID: 21118704).
Not Met criteria codes
PS4
To our knowledge this variant has not been reported in the literature in individuals who have a personal or family history of a malignant hyperthermia reaction.
Approved on: 2023-04-06
Published on: 2023-04-06
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