NM_053051.5(CNTROB):c.392G>A (p.Arg131Gln) AND not specified

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Mar 7, 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:: RCV004071263.1

Allele description [Variation Report for NM_053051.5(CNTROB):c.392G>A (p.Arg131Gln)]

NM_053051.5(CNTROB):c.392G>A (p.Arg131Gln)

Gene:

CNTROB:centrobin, centriole duplication and spindle assembly protein [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

17p13.1

Genomic location:

Preferred name:

NM_053051.5(CNTROB):c.392G>A (p.Arg131Gln)

HGVS:

NC_000017.11:g.7934501G>A
NG_029754.1:g.7372G>A
NG_029754.2:g.7422G>A
NM_001037144.7:c.392G>A
NM_001330124.3:c.392G>A
NM_001353202.2:c.392G>A
NM_001353203.2:c.392G>A
NM_001353204.2:c.-295G>A
NM_001353205.2:c.125G>A
NM_001353206.2:c.392G>A
NM_001353207.1:c.392G>A
NM_001353208.2:c.392G>A
NM_001353209.1:c.392G>A
NM_053051.5:c.392G>AMANE SELECT
NP_001032221.1:p.Arg131Gln
NP_001317053.1:p.Arg131Gln
NP_001340131.1:p.Arg131Gln
NP_001340132.1:p.Arg131Gln
NP_001340134.1:p.Arg42Gln
NP_001340135.1:p.Arg131Gln
NP_001340136.1:p.Arg131Gln
NP_001340137.1:p.Arg131Gln
NP_001340138.1:p.Arg131Gln
NP_444279.2:p.Arg131Gln
NC_000017.10:g.7837819G>A
NM_001037144.5:c.392G>A

Protein change:

R131Q

Molecular consequence:

NM_001353204.2:c.-295G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
NM_001037144.7:c.392G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001330124.3:c.392G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001353202.2:c.392G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001353203.2:c.392G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001353205.2:c.125G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001353206.2:c.392G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001353207.1:c.392G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001353208.2:c.392G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001353209.1:c.392G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_053051.5:c.392G>A - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Synonyms:: AllHighlyPenetrant
Identifiers:: MedGen: CN169374

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Bacillus cereus ATCC 10987 plasmid pBc10987, complete sequence
Bacillus cereus ATCC 10987 plasmid pBc10987, complete sequence
gi|42741405|gb|AE017195.1|

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV003526673	Ambry Genetics	criteria provided, single submitter (Ambry Variant Classification Scheme 2023)	Uncertain significance (Mar 7, 2024)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV003526673

Ambry Genetics

criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)

Uncertain significance
(Mar 7, 2024)

germline

clinical testing

Citation Link

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

Details of each submission

From Ambry Genetics, SCV003526673.2

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

Description

The c.392G>A (p.R131Q) alteration is located in exon 3 (coding exon 3) of the CNTROB gene. This alteration results from a G to A substitution at nucleotide position 392, causing the arginine (R) at amino acid position 131 to be replaced by a glutamine (Q). Based on insufficient or conflicting evidence, the clinical significance of this alteration remains unclear.

#	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: Oct 26, 2024

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