NM_002816.5(PSMD12):c.1164_1166delinsTTT (p.Glu388_Ser389delinsAspPhe) AND Stankiewicz-Isidor syndrome

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Jun 1, 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:: RCV003493143.2

Allele description [Variation Report for NM_002816.5(PSMD12):c.1164_1166delinsTTT (p.Glu388_Ser389delinsAspPhe)]

NM_002816.5(PSMD12):c.1164_1166delinsTTT (p.Glu388_Ser389delinsAspPhe)

Gene:

PSMD12:proteasome 26S subunit, non-ATPase 12 [Gene - OMIM - HGNC]

Variant type:

Indel

Cytogenetic location:

17q24.2

Genomic location:

Preferred name:

NM_002816.5(PSMD12):c.1164_1166delinsTTT (p.Glu388_Ser389delinsAspPhe)

HGVS:

NC_000017.11:g.67341048_67341050delinsAAA
NM_001316341.2:c.987_989delinsTTT
NM_002816.5:c.1164_1166delinsTTTMANE SELECT
NM_174871.4:c.1104_1106delinsTTT
NP_001303270.1:p.Glu329_Ser330delinsAspPhe
NP_002807.1:p.Glu388_Ser389delinsAspPhe
NP_777360.1:p.Glu368_Ser369delinsAspPhe
NC_000017.10:g.65337164_65337166delinsAAA

Molecular consequence:

NM_001316341.2:c.987_989delinsTTT - missense variant - [Sequence Ontology: SO:0001583]
NM_002816.5:c.1164_1166delinsTTT - missense variant - [Sequence Ontology: SO:0001583]
NM_174871.4:c.1104_1106delinsTTT - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:: Stankiewicz-Isidor syndrome (STISS)
Identifiers:: MONDO: MONDO:0054591; MedGen: C4479599; OMIM: 617516

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV004236498	Revvity Omics, Revvity	criteria provided, single submitter (ACMG Guidelines, 2015)	Uncertain significance (Jun 1, 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

SCV004236498

Revvity Omics, Revvity

criteria provided, single submitter

(ACMG Guidelines, 2015)

Uncertain significance
(Jun 1, 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

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 Revvity Omics, Revvity, SCV004236498.1

#	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: Mar 16, 2024

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