NM_012179.4(FBXO7):c.1183-7del AND Parkinsonian-pyramidal syndrome

Germline classification:: Benign (1 submission)
Last evaluated:: Nov 24, 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:: RCV003611363.1

Allele description [Variation Report for NM_012179.4(FBXO7):c.1183-7del]

NM_012179.4(FBXO7):c.1183-7del

Gene:

FBXO7:F-box protein 7 [Gene - OMIM - HGNC]

Variant type:

Deletion

Cytogenetic location:

22q12.3

Genomic location:

Preferred name:

NM_012179.4(FBXO7):c.1183-7del

HGVS:

NC_000022.11:g.32498137del
NG_016001.2:g.28418del
NM_001033024.2:c.946-7del
NM_001257990.2:c.841-7del
NM_012179.4:c.1183-7delMANE SELECT
NC_000022.10:g.32894119del
NC_000022.10:g.32894124del

Molecular consequence:

NM_001033024.2:c.946-7del - intron variant - [Sequence Ontology: SO:0001627]
NM_001257990.2:c.841-7del - intron variant - [Sequence Ontology: SO:0001627]
NM_012179.4:c.1183-7del - intron variant - [Sequence Ontology: SO:0001627]

Condition(s)

Name:: Parkinsonian-pyramidal syndrome
Synonyms:: PARKINSON DISEASE 15, AUTOSOMAL RECESSIVE; Pallidopyramidal syndrome; Pallido-pyramidal disease; See all synonyms [MedGen]
Identifiers:: MONDO: MONDO:0009830; MedGen: C1850100; Orphanet: 171695; OMIM: 260300

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV004511142	Invitae	criteria provided, single submitter (Invitae Variant Classification Sherloc (09022015))	Benign (Nov 24, 2023)	germline	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

SCV004511142

Invitae

criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))

Benign
(Nov 24, 2023)

germline

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	germline	unknown	not provided	not provided	not provided	not provided	not provided	clinical testing

Citations

PubMed

Sherloc: a comprehensive refinement of the ACMG-AMP variant classification criteria.

Nykamp K, Anderson M, Powers M, Garcia J, Herrera B, Ho YY, Kobayashi Y, Patil N, Thusberg J, Westbrook M; Invitae Clinical Genomics Group., Topper S.

Genet Med. 2017 Oct;19(10):1105-1117. doi: 10.1038/gim.2017.37. Epub 2017 May 11. Erratum in: Genet Med. 2020 Jan;22(1):240. doi: 10.1038/s41436-019-0624-9.

PubMed [citation]

PMID:: 28492532
PMCID:: PMC5632818

Details of each submission

From Invitae, SCV004511142.1

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	not provided	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	germline	unknown	not provided	not provided	not provided		not provided	not provided	not provided	not provided

Last Updated: Feb 28, 2024

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