NM_002529.4(NTRK1):c.1733T>G (p.Val578Gly) 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:: RCV000789625.1

Allele description [Variation Report for NM_002529.4(NTRK1):c.1733T>G (p.Val578Gly)]

NM_002529.4(NTRK1):c.1733T>G (p.Val578Gly)

Gene:

NTRK1:neurotrophic receptor tyrosine kinase 1 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

1q23.1

Genomic location:

Preferred name:

NM_002529.4(NTRK1):c.1733T>G (p.Val578Gly)

HGVS:

NC_000001.11:g.156876500T>G
NG_007493.1:g.65751T>G
NM_001007792.1:c.1625T>G
NM_001012331.2:c.1715T>G
NM_002529.4:c.1733T>GMANE SELECT
NP_001007793.1:p.Val542Gly
NP_001012331.1:p.Val572Gly
NP_001012331.1:p.Val572Gly
NP_002520.2:p.Val578Gly
LRG_261t1:c.1625T>G
LRG_261t2:c.1715T>G
LRG_261:g.65751T>G
LRG_261p1:p.Val542Gly
LRG_261p2:p.Val572Gly
NC_000001.10:g.156846292T>G
NM_001012331.1:c.1715T>G

Protein change:

V542G

Links:

dbSNP: rs1571699872

NCBI 1000 Genomes Browser:

rs1571699872

Molecular consequence:

NM_001007792.1:c.1625T>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001012331.2:c.1715T>G - missense variant - [Sequence Ontology: SO:0001583]
NM_002529.4:c.1733T>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
SCV000928992	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

SCV000928992

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

Novel missense, insertion and deletion mutations in the neurotrophic tyrosine kinase receptor type 1 gene (NTRK1) associated with congenital insensitivity to pain with anhidrosis.

Huehne K, Zweier C, Raab K, Odent S, Bonnaure-Mallet M, Sixou JL, Landrieu P, Goizet C, Sarlangue J, Baumann M, Eggermann T, Rauch A, Ruppert S, Stettner GM, Rautenstrauss B.

Neuromuscul Disord. 2008 Feb;18(2):159-66. Epub 2008 Feb 20.

PubMed [citation]

PMID:: 18077166

Details of each submission

From Inherited Neuropathy Consortium, SCV000928992.1

#	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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