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NM_014874.4(MFN2):c.310C>T (p.Arg104Trp) AND Neuropathy, hereditary motor and sensory, type 6A

Germline classification:
Pathogenic (1 submission)
Last evaluated:
Mar 13, 2023
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:
RCV003332995.1

Allele description [Variation Report for NM_014874.4(MFN2):c.310C>T (p.Arg104Trp)]

NM_014874.4(MFN2):c.310C>T (p.Arg104Trp)

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.310C>T (p.Arg104Trp)
Other names:
p.R104W:CGG>TGG; chr1-11992689-C-T; p.Arg104Trp
HGVS:
  • NC_000001.11:g.11992689C>T
  • NG_007945.1:g.17509C>T
  • NM_001127660.2:c.310C>T
  • NM_014874.4:c.310C>TMANE SELECT
  • NP_001121132.1:p.Arg104Trp
  • NP_001121132.1:p.Arg104Trp
  • NP_055689.1:p.Arg104Trp
  • NP_055689.1:p.Arg104Trp
  • LRG_255t1:c.310C>T
  • LRG_255:g.17509C>T
  • LRG_255p1:p.Arg104Trp
  • NC_000001.10:g.12052746C>T
  • NM_001127660.1:c.310C>T
  • NM_014874.3:c.310C>T
Protein change:
R104W; ARG104TRP
Links:
OMIM: 608507.0014; dbSNP: rs119103268
NCBI 1000 Genomes Browser:
rs119103268
Molecular consequence:
  • NM_001127660.2:c.310C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_014874.4:c.310C>T - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:
Neuropathy, hereditary motor and sensory, type 6A (HMSN6A)
Synonyms:
NEUROPATHY, HEREDITARY MOTOR AND SENSORY, TYPE VIA; HMSN VIA; CHARCOT-MARIE-TOOTH DISEASE, TYPE 6A; See all synonyms [MedGen]
Identifiers:
MONDO: MONDO:0011002; MedGen: CN305336; OMIM: 601152

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV004040658Baylor Genetics
criteria provided, single submitter

(ACMG Guidelines, 2015)		Pathogenic
(Mar 13, 2023) 		unknownclinical testing

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

Help

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedunknownunknownnot providednot providednot providednot providednot providedclinical 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, SCV004040658.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testing PubMed (1)
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1unknownunknownnot providednot providednot providednot providednot providednot providednot provided

Last Updated: Sep 29, 2024