NM_000537.4(REN):c.241_243dup (p.Tyr81_Met82insTyr) AND Intellectual disability, X-linked 61

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Mar 29, 2024
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:: RCV003989850.2

Allele description [Variation Report for NM_000537.4(REN):c.241_243dup (p.Tyr81_Met82insTyr)]

NM_000537.4(REN):c.241_243dup (p.Tyr81_Met82insTyr)

Gene:

REN:renin [Gene - OMIM - HGNC]

Variant type:

Duplication

Cytogenetic location:

1q32.1

Genomic location:

Preferred name:

NM_000537.4(REN):c.241_243dup (p.Tyr81_Met82insTyr)

HGVS:

NC_000001.11:g.204162021_204162023dup
NG_012122.1:g.9317_9319dup
NM_000537.4:c.241_243dupMANE SELECT
NP_000528.1:p.Tyr81_Met82insTyr
NC_000001.10:g.204131146_204131147insGTA
NC_000001.10:g.204131149_204131151dup

Molecular consequence:

NM_000537.4:c.241_243dup - inframe_insertion - [Sequence Ontology: SO:0001821]

Condition(s)

Name:: Intellectual disability, X-linked 61 (TOKAS)
Synonyms:: TONNE-KALSCHEUER SYNDROME
Identifiers:: MONDO: MONDO:0010506; MedGen: C4283894; OMIM: 300978

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV004807683	Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center	criteria provided, single submitter (ACMG Guidelines, 2015)	Uncertain significance (Mar 29, 2024)	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

SCV004807683

Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center

criteria provided, single submitter

(ACMG Guidelines, 2015)

Uncertain significance
(Mar 29, 2024)

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

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 Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center, SCV004807683.1

#	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: Sep 29, 2024

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Relating variation to medicine