NM_006346.4(PIBF1):c.1223+15dup AND Joubert syndrome 33

Germline classification:: Benign (1 submission)
Last evaluated:: Jan 21, 2022
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:: RCV002507978.1

Allele description [Variation Report for NM_006346.4(PIBF1):c.1223+15dup]

NM_006346.4(PIBF1):c.1223+15dup

Gene:

PIBF1:progesterone immunomodulatory binding factor 1 [Gene - OMIM - HGNC]

Variant type:

Duplication

Cytogenetic location:

13q22.1

Genomic location:

Preferred name:

NM_006346.4(PIBF1):c.1223+15dup

HGVS:

NC_000013.11:g.72835383dup
NG_053118.1:g.58360dup
NM_001349655.2:c.1223+15dup
NM_006346.4:c.1223+15dupMANE SELECT
NC_000013.10:g.73409508_73409509insA
NC_000013.10:g.73409521dup

Links:

dbSNP: rs200683940

NCBI 1000 Genomes Browser:

rs200683940

Molecular consequence:

NM_001349655.2:c.1223+15dup - intron variant - [Sequence Ontology: SO:0001627]
NM_006346.4:c.1223+15dup - intron variant - [Sequence Ontology: SO:0001627]

Condition(s)

Name:: Joubert syndrome 33
Identifiers:: MONDO: MONDO:0033311; MedGen: C4540389; OMIM: 617767

Recent activity

Clear Turn Off Turn On

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

Help

Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV002804451	Fulgent Genetics, Fulgent Genetics	criteria provided, single submitter (ACMG Guidelines, 2015)	Benign (Jan 21, 2022)	unknown	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

SCV002804451

Fulgent Genetics, Fulgent Genetics

criteria provided, single submitter

(ACMG Guidelines, 2015)

Benign
(Jan 21, 2022)

unknown

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	unknown	unknown	not provided	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 Fulgent Genetics, Fulgent Genetics, SCV002804451.1

#	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	unknown	unknown	not provided	not provided	not provided		not provided	not provided	not provided	not provided

Last Updated: Sep 29, 2024

ClinVar

Relating variation to medicine