NM_001382391.1(CSPP1):c.-125C>A AND Joubert syndrome 21

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Jun 27, 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:: RCV002829378.3

Allele description [Variation Report for NM_001382391.1(CSPP1):c.-125C>A]

NM_001382391.1(CSPP1):c.-125C>A

Gene:

CSPP1:centrosome and spindle pole associated protein 1 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

8q13.1

Genomic location:

Preferred name:

NM_001382391.1(CSPP1):c.-125C>A

HGVS:

NC_000008.11:g.67064424C>A
NG_034100.1:g.5057C>A
NM_001363131.2:c.-125C>A
NM_001363132.2:c.-125C>A
NM_001363133.2:c.-125C>A
NM_001364869.1:c.26C>A
NM_001364870.1:c.26C>A
NM_001382391.1:c.-125C>AMANE SELECT
NM_024790.6:c.26C>A
NP_001351798.1:p.Ala9Asp
NP_001351799.1:p.Ala9Asp
NP_079066.5:p.Ala9Asp
NC_000008.10:g.67976659C>A

Protein change:

A9D

Molecular consequence:

NM_001363131.2:c.-125C>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
NM_001363132.2:c.-125C>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
NM_001363133.2:c.-125C>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
NM_001382391.1:c.-125C>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
NM_001364869.1:c.26C>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001364870.1:c.26C>A - missense variant - [Sequence Ontology: SO:0001583]
NM_024790.6:c.26C>A - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:: Joubert syndrome 21 (JBTS21)
Identifiers:: MONDO: MONDO:0014288; MedGen: C3810212; OMIM: 615636

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV003217984	Labcorp Genetics (formerly Invitae), Labcorp	criteria provided, single submitter (Invitae Variant Classification Sherloc (09022015))	Uncertain significance (Jun 27, 2022)	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

SCV003217984

Labcorp Genetics (formerly Invitae), Labcorp

criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))

Uncertain significance
(Jun 27, 2022)

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 Labcorp Genetics (formerly Invitae), Labcorp, SCV003217984.2

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	not provided	not provided	not provided	clinical testing	PubMed (1)

Description

In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance. Algorithms developed to predict the effect of missense changes on protein structure and function (SIFT, PolyPhen-2, Align-GVGD) all suggest that this variant is likely to be tolerated. This variant has not been reported in the literature in individuals affected with CSPP1-related conditions. This variant is not present in population databases (gnomAD no frequency). This sequence change replaces alanine, which is neutral and non-polar, with aspartic acid, which is acidic and polar, at codon 9 of the CSPP1 protein (p.Ala9Asp).

#	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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