NM_181882.3(PRX):c.979del (p.Asp327fs) AND Charcot-Marie-Tooth disease type 4F

Germline classification:: Pathogenic (1 submission)
Last evaluated:: Jan 1, 2019
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:: RCV000785029.3

Allele description [Variation Report for NM_181882.3(PRX):c.979del (p.Asp327fs)]

NM_181882.3(PRX):c.979del (p.Asp327fs)

Gene:

PRX:periaxin [Gene - OMIM - HGNC]

Variant type:

Deletion

Cytogenetic location:

19q13.2

Genomic location:

Preferred name:

NM_181882.3(PRX):c.979del (p.Asp327fs)

HGVS:

NC_000019.10:g.40397374del
NG_007979.1:g.20992del
NM_020956.2:c.*1184del
NM_181882.3:c.979delMANE SELECT
NP_870998.2:p.Asp327fs
LRG_265t1:c.*1184del
LRG_265:g.20992del
NC_000019.9:g.40903281del
NM_181882.2:c.979delG

Protein change:

D327fs

Links:

dbSNP: rs1568708792

NCBI 1000 Genomes Browser:

rs1568708792

Molecular consequence:

NM_020956.2:c.*1184del - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
NM_181882.3:c.979del - frameshift variant - [Sequence Ontology: SO:0001589]

Observations:

Condition(s)

Name:: Charcot-Marie-Tooth disease type 4F
Synonyms:: Charcot-Marie-Tooth disease, demyelinating, type 4F; CHARCOT-MARIE-TOOTH DISEASE, TYPE 4F, LATE-ONSET
Identifiers:: MONDO: MONDO:0013959; MedGen: C3540453; Orphanet: 99952; OMIM: 614895

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV000923581	Genomic Research Center, Shahid Beheshti University of Medical Sciences	criteria provided, single submitter (ACMG Guidelines, 2015)	Pathogenic (Jan 1, 2019)	inherited	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

SCV000923581

Genomic Research Center, Shahid Beheshti University of Medical Sciences

criteria provided, single submitter

(ACMG Guidelines, 2015)

Pathogenic
(Jan 1, 2019)

inherited

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	inherited	yes	1	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 Genomic Research Center, Shahid Beheshti University of Medical Sciences, SCV000923581.1

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

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

Last Updated: May 24, 2022

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