NM_000540.3(RYR1):c.14196C>A (p.Ile4732=) AND RYR1-related disorder

Germline classification:: Likely benign (2 submissions)
Last evaluated:: Jan 22, 2024
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:: RCV000531112.13

Allele description [Variation Report for NM_000540.3(RYR1):c.14196C>A (p.Ile4732=)]

NM_000540.3(RYR1):c.14196C>A (p.Ile4732=)

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.14196C>A (p.Ile4732=)

HGVS:

NC_000019.10:g.38577941C>A
NG_008866.1:g.149242C>A
NM_000540.3:c.14196C>AMANE SELECT
NM_001042723.2:c.14181C>A
NP_000531.2:p.Ile4732=
NP_000531.2:p.Ile4732=
NP_001036188.1:p.Ile4727=
LRG_766t1:c.14196C>A
LRG_766:g.149242C>A
LRG_766p1:p.Ile4732=
NC_000019.9:g.39068581C>A
NM_000540.2:c.14196C>A

Links:

dbSNP: rs201670423

NCBI 1000 Genomes Browser:

rs201670423

Molecular consequence:

NM_000540.3:c.14196C>A - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001042723.2:c.14181C>A - synonymous variant - [Sequence Ontology: SO:0001819]

Condition(s)

Name:: RYR1-related disorder
Synonyms:: RYR1-Related Disorders; RYR1-related condition
Identifiers:: MedGen: CN239331

Recent activity

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unnamed protein product [Homo sapiens]
unnamed protein product [Homo sapiens]
gi|194376136|dbj|BAG62827.1|

Protein
PREDICTED: Glycine max FT-interacting protein 1 (LOC100814611), mRNA
PREDICTED: Glycine max FT-interacting protein 1 (LOC100814611), mRNA
gi|2027451078|ref|XM_003518028.5|

Nucleotide

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV000659842	Labcorp Genetics (formerly Invitae), Labcorp	criteria provided, single submitter (Invitae Variant Classification Sherloc (09022015))	Likely benign (Jan 22, 2024)	germline	clinical testing	PubMed (1) [See all records that cite this PMID]
SCV004742877	PreventionGenetics, part of Exact Sciences	no assertion criteria provided	Likely benign (Sep 12, 2019)	germline	clinical testing

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV000659842

Labcorp Genetics (formerly Invitae), Labcorp

criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))

Likely benign
(Jan 22, 2024)

germline

clinical testing

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

SCV004742877

PreventionGenetics, part of Exact Sciences

no assertion criteria provided

Likely benign
(Sep 12, 2019)

germline

clinical testing

Help

Summary from all submissions

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

Citations

PubMed

Sherloc: a comprehensive refinement of the ACMG-AMP variant classification criteria.

Nykamp K, Anderson M, Powers M, Garcia J, Herrera B, Ho YY, Kobayashi Y, Patil N, Thusberg J, Westbrook M; Invitae Clinical Genomics Group., Topper S.

Genet Med. 2017 Oct;19(10):1105-1117. doi: 10.1038/gim.2017.37. Epub 2017 May 11. Erratum in: Genet Med. 2020 Jan;22(1):240. doi: 10.1038/s41436-019-0624-9.

PubMed [citation]

PMID:: 28492532
PMCID:: PMC5632818

Details of each submission

From Labcorp Genetics (formerly Invitae), Labcorp, SCV000659842.8

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

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

From PreventionGenetics, part of Exact Sciences, SCV004742877.2

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

Description

This variant is classified as likely benign based on ACMG/AMP sequence variant interpretation guidelines (Richards et al. 2015 PMID: 25741868, with internal and published modifications).

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

Last Updated: Nov 10, 2024

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