NM_021224.6(ZNF462):c.1151del (p.Asn384fs) AND Weiss-Kruszka syndrome

Germline classification:: Pathogenic (1 submission)
Last evaluated:: Dec 4, 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:: RCV003448888.1

Allele description [Variation Report for NM_021224.6(ZNF462):c.1151del (p.Asn384fs)]

NM_021224.6(ZNF462):c.1151del (p.Asn384fs)

Gene:

ZNF462:zinc finger protein 462 [Gene - OMIM - HGNC]

Variant type:

Deletion

Cytogenetic location:

9q31.2

Genomic location:

Preferred name:

NM_021224.6(ZNF462):c.1151del (p.Asn384fs)

HGVS:

NC_000009.12:g.106925063del
NG_052913.1:g.66967del
NM_001347997.2:c.1151del
NM_021224.6:c.1151delMANE SELECT
NP_001334926.1:p.Asn384fs
NP_067047.4:p.Asn384fs
NC_000009.11:g.109687344del

Protein change:

N384fs

Molecular consequence:

NM_001347997.2:c.1151del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_021224.6:c.1151del - frameshift variant - [Sequence Ontology: SO:0001589]

Observations:

Condition(s)

Name:: Weiss-Kruszka syndrome
Identifiers:: MONDO: MONDO:0032836; MedGen: C5231429; OMIM: 618619

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV004176712	Laboratory of Molecular and Physiopathological Bases of Osteochondrodysplasia, Imagine Institute	criteria provided, single submitter (ACMG Guidelines, 2015)	Pathogenic (Dec 4, 2023)	de novo	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

SCV004176712

Laboratory of Molecular and Physiopathological Bases of Osteochondrodysplasia, Imagine Institute

criteria provided, single submitter

(ACMG Guidelines, 2015)

Pathogenic
(Dec 4, 2023)

de novo

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	de novo	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 Laboratory of Molecular and Physiopathological Bases of Osteochondrodysplasia, Imagine Institute, SCV004176712.1

#	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	de novo	yes	not provided	not provided	not provided		1	not provided	not provided	not provided

Last Updated: Oct 13, 2024

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