NM_001029883.3(PCARE):c.2415del (p.Pro807fs) AND Retinitis pigmentosa 54

Germline classification:: Likely pathogenic (1 submission)
Last evaluated:: May 31, 2021
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:: RCV001591905.1

Allele description [Variation Report for NM_001029883.3(PCARE):c.2415del (p.Pro807fs)]

NM_001029883.3(PCARE):c.2415del (p.Pro807fs)

Gene:

PCARE:photoreceptor cilium actin regulator [Gene - OMIM - HGNC]

Variant type:

Deletion

Cytogenetic location:

2p23.2

Genomic location:

Preferred name:

NM_001029883.3(PCARE):c.2415del (p.Pro807fs)

HGVS:

NC_000002.12:g.29071849del
NG_021427.1:g.7415del
NM_001029883.3:c.2415delMANE SELECT
NP_001025054.1:p.Pro807fs
NC_000002.11:g.29294715del

Protein change:

P807fs

Links:

dbSNP: rs1412522034

NCBI 1000 Genomes Browser:

rs1412522034

Molecular consequence:

NM_001029883.3:c.2415del - frameshift variant - [Sequence Ontology: SO:0001589]

Observations:

Condition(s)

Name:: Retinitis pigmentosa 54 (RP54)
Identifiers:: MONDO: MONDO:0013263; MedGen: C3150691; Orphanet: 791; OMIM: 613428

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV001816051	DBGen Ocular Genomics	criteria provided, single submitter (ACMG Guidelines, 2015)	Likely pathogenic (May 31, 2021)	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

SCV001816051

DBGen Ocular Genomics

criteria provided, single submitter

(ACMG Guidelines, 2015)

Likely pathogenic
(May 31, 2021)

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
unspecified	germline	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 DBGen Ocular Genomics, SCV001816051.1

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

Last Updated: Dec 24, 2023

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