NM_014874.4(MFN2):c.1066A>G (p.Thr356Ala) AND Charcot-Marie-Tooth disease

Germline classification:: Uncertain significance (1 submission)
Review status:: (0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided

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:: RCV000789414.1

Allele description [Variation Report for NM_014874.4(MFN2):c.1066A>G (p.Thr356Ala)]

NM_014874.4(MFN2):c.1066A>G (p.Thr356Ala)

Gene:

MFN2:mitofusin 2 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

1p36.22

Genomic location:

Preferred name:

NM_014874.4(MFN2):c.1066A>G (p.Thr356Ala)

HGVS:

NC_000001.11:g.12002009A>G
NG_007945.1:g.26829A>G
NM_001127660.2:c.1066A>G
NM_014874.4:c.1066A>GMANE SELECT
NP_001121132.1:p.Thr356Ala
NP_055689.1:p.Thr356Ala
NP_055689.1:p.Thr356Ala
LRG_255t1:c.1066A>G
LRG_255:g.26829A>G
LRG_255p1:p.Thr356Ala
NC_000001.10:g.12062066A>G
NM_014874.3:c.1066A>G

Protein change:

T356A

Links:

dbSNP: rs1569853967

NCBI 1000 Genomes Browser:

rs1569853967

Molecular consequence:

NM_001127660.2:c.1066A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_014874.4:c.1066A>G - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:: Charcot-Marie-Tooth disease
Synonyms:: Charcot-Marie-Tooth Neuropathy
Identifiers:: MONDO: MONDO:0015626; MedGen: C0007959; OMIM: PS118220

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV000928769	Inherited Neuropathy Consortium	no assertion criteria provided	Uncertain significance	germline	literature only	PubMed (1) [See all records that cite this PMID]

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV000928769

Inherited Neuropathy Consortium

no assertion criteria provided

Uncertain significance

germline

literature only

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	yes	not provided	not provided	not provided	not provided	not provided	literature only

Citations

PubMed

A novel mutation of the MFN2 gene in a Chinese family with Charcot-Marie-Tooth disease.

Wang YW, Han WT, Jiang M, Lu CX, Li XF, Zhang X, Li JX.

Genet Mol Res. 2012 May 18;11(2):1454-9. doi: 10.4238/2012.May.18.5.

PubMed [citation]

PMID:: 22653593

Details of each submission

From Inherited Neuropathy Consortium, SCV000928769.1

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	not provided	not provided	not provided	literature only	PubMed (1)

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

Last Updated: Apr 23, 2022

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