NM_005055.5(RAPSN):c.172C>T (p.Arg58Cys) AND Congenital myasthenic syndrome 11

Germline classification:: Benign (2 submissions)
Last evaluated:: Jul 10, 2021
Review status:: 2 stars out of maximum of 4 stars
criteria provided, multiple submitters, no conflicts

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:: RCV000390783.8

Allele description [Variation Report for NM_005055.5(RAPSN):c.172C>T (p.Arg58Cys)]

NM_005055.5(RAPSN):c.172C>T (p.Arg58Cys)

Gene:

RAPSN:receptor associated protein of the synapse [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

11p11.2

Genomic location:

Preferred name:

NM_005055.5(RAPSN):c.172C>T (p.Arg58Cys)

HGVS:

NC_000011.10:g.47448793G>A
NG_008312.1:g.5386C>T
NM_005055.5:c.172C>TMANE SELECT
NM_032645.5:c.172C>T
NP_005046.2:p.Arg58Cys
NP_116034.2:p.Arg58Cys
NC_000011.9:g.47470345G>A
NM_005055.4:c.172C>T

Protein change:

R58C

Links:

dbSNP: rs34312154

NCBI 1000 Genomes Browser:

rs34312154

Molecular consequence:

NM_005055.5:c.172C>T - missense variant - [Sequence Ontology: SO:0001583]
NM_032645.5:c.172C>T - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:: Congenital myasthenic syndrome 11
Synonyms:: MYASTHENIC SYNDROME, CONGENITAL, Ie; Myasthenic syndrome, congenital, 11, associated with acetylcholine receptor deficiency
Identifiers:: MONDO: MONDO:0014588; MedGen: C4225367; Orphanet: 590; OMIM: 616326

Recent activity

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753136[uid] (1)
Taxonomy
PREDICTED: Cucurbita moschata enolase 1, chloroplastic (LOC111437858), mRNA
PREDICTED: Cucurbita moschata enolase 1, chloroplastic (LOC111437858), mRNA
gi|1279761307|ref|XM_023075941.1|

Nucleotide
Phosphaenus hemipterus 18S ribosomal RNA gene, partial sequence
Phosphaenus hemipterus 18S ribosomal RNA gene, partial sequence
gi|151933847|gb|EU009246.1|

Nucleotide
Phosphaenus hemipterus voucher ZFMK-TIS-2503782 cytochrome oxidase subunit 1 (CO...
Phosphaenus hemipterus voucher ZFMK-TIS-2503782 cytochrome oxidase subunit 1 (COI) gene, partial cds; mitochondrial
gi|1169317297|gnl|uoguelph|GCOL5376 OI-5P|gb|KU915622.1|

Nucleotide
Phosphaenus hemipterus clone PphLUC luciferase gene, partial cds
Phosphaenus hemipterus clone PphLUC luciferase gene, partial cds
gi|198409928|gb|EU684086.1|

Nucleotide

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV000372482	Illumina Laboratory Services, Illumina	criteria provided, single submitter (ICSL Variant Classification Criteria 13 December 2019)	Benign (Jan 12, 2018)	germline	clinical testing	Citation Link,
SCV001755014	Genome-Nilou Lab	criteria provided, single submitter (ACMG Guidelines, 2015)	Benign (Jul 10, 2021)	germline	clinical testing	PubMed (1) [See all records that cite this PMID]

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV000372482

Illumina Laboratory Services, Illumina

criteria provided, single submitter

(ICSL Variant Classification Criteria 13 December 2019)

Benign
(Jan 12, 2018)

germline

clinical testing

Citation Link,

SCV001755014

Genome-Nilou Lab

criteria provided, single submitter

(ACMG Guidelines, 2015)

Benign
(Jul 10, 2021)

germline

clinical testing

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

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
not provided	germline	no	not provided	not provided	not provided	not provided	not provided	clinical 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 Illumina Laboratory Services, Illumina, SCV000372482.3

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

Description

This variant was observed in the ICSL laboratory as part of a predisposition screen in an ostensibly healthy population. It had not been previously curated by ICSL or reported in the Human Gene Mutation Database (HGMD: prior to June 1st, 2018), and was therefore a candidate for classification through an automated scoring system. Utilizing variant allele frequency, disease prevalence and penetrance estimates, and inheritance mode, an automated score was calculated to assess if this variant is too frequent to cause the disease. Based on the score and internal cut-off values, a variant classified as benign is not then subjected to further curation. The score for this variant resulted in a classification of benign for this disease.

#	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 Genome-Nilou Lab, SCV001755014.1

#	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	no	not provided	not provided	not provided		not provided	not provided	not provided	not provided

Last Updated: Sep 29, 2024

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