NM_000166.6(GJB1):c.578T>G (p.Phe193Cys) AND Charcot-Marie-Tooth disease

Clinical significance:Uncertain significance

Review status:(0/4) 0 stars out of maximum of 4 stars

no assertion criteria provided

Based on:
1 submission [Details]
Record status:
current
Accession:
RCV000789821.1

Allele description [Variation Report for NM_000166.6(GJB1):c.578T>G (p.Phe193Cys)]

NM_000166.6(GJB1):c.578T>G (p.Phe193Cys)

Gene:
GJB1:gap junction protein beta 1 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
Xq13.1
Genomic location:
Preferred name:
NM_000166.6(GJB1):c.578T>G (p.Phe193Cys)
HGVS:
  • NC_000023.11:g.71224285T>G
  • NG_008357.1:g.14074T>G
  • NM_000166.6:c.578T>GMANE SELECT
  • NM_001097642.3:c.578T>G
  • NP_000157.1:p.Phe193Cys
  • NP_001091111.1:p.Phe193Cys
  • LRG_245t2:c.578T>G
  • LRG_245:g.14074T>G
  • LRG_245p2:p.Phe193Cys
  • NC_000023.10:g.70444135T>G
  • NM_000166.5:c.578T>G
Protein change:
F193C
Links:
dbSNP: rs1602349696
NCBI 1000 Genomes Browser:
rs1602349696
Molecular consequence:
  • NM_000166.6:c.578T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001097642.3:c.578T>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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Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV000929205Inherited Neuropathy Consortiumno assertion criteria providedUncertain significancegermlineliterature only

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

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineyesnot providednot providednot providednot providednot providedliterature only

Citations

PubMed

Connexin32 and X-linked Charcot-Marie-Tooth disease.

Bone LJ, DeschĂȘnes SM, Balice-Gordon RJ, Fischbeck KH, Scherer SS.

Neurobiol Dis. 1997;4(3-4):221-30. Review.

PubMed [citation]
PMID:
9361298

Details of each submission

From Inherited Neuropathy Consortium, SCV000929205.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedliterature only PubMed (1)
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineyesnot providednot providednot providednot providednot providednot providednot provided

Last Updated: Oct 24, 2021

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