NM_001303256.3(MORC2):c.328C>T (p.Arg110Cys) AND Charcot-Marie-Tooth disease axonal type 2Z

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: May 7, 2018
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:: RCV001333922.2

Allele description [Variation Report for NM_001303256.3(MORC2):c.328C>T (p.Arg110Cys)]

NM_001303256.3(MORC2):c.328C>T (p.Arg110Cys)

Gene:

MORC2:MORC family CW-type zinc finger 2 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

22q12.2

Genomic location:

Preferred name:

NM_001303256.3(MORC2):c.328C>T (p.Arg110Cys)

HGVS:

NC_000022.11:g.30946439G>A
NG_046752.1:g.27059C>T
NM_001303256.3:c.328C>TMANE SELECT
NM_001303257.2:c.328C>T
NM_014941.3:c.142C>T
NP_001290185.1:p.Arg110Cys
NP_001290186.1:p.Arg110Cys
NP_055756.1:p.Arg48Cys
NC_000022.10:g.31342426G>A
NM_001303256.1:c.328C>T
NM_001303256.2:c.328C>T

Protein change:

R110C

Links:

dbSNP: rs2040817364

NCBI 1000 Genomes Browser:

rs2040817364

Molecular consequence:

NM_001303256.3:c.328C>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001303257.2:c.328C>T - missense variant - [Sequence Ontology: SO:0001583]
NM_014941.3:c.142C>T - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:: Charcot-Marie-Tooth disease axonal type 2Z
Synonyms:: CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL DOMINANT, TYPE 2Z; CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 2Z
Identifiers:: MONDO: MONDO:0014736; MedGen: C5569025; OMIM: 616688

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV001526633	Baylor Genetics	criteria provided, single submitter (ACMG Guidelines, 2015)	Uncertain significance (May 7, 2018)	de novo	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

SCV001526633

Baylor Genetics

criteria provided, single submitter

(ACMG Guidelines, 2015)

Uncertain significance
(May 7, 2018)

de novo

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	de novo	yes	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 Baylor Genetics, SCV001526633.1

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

Description

This variant was determined to be of uncertain significance according to ACMG Guidelines, 2015 [PMID:25741868].

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

Last Updated: Oct 20, 2024

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