NM_014780.5(CUL7):c.3398G>A (p.Arg1133Gln) AND CUL7-related disorder

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Dec 15, 2023
Review status:: (0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided

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:: RCV003902024.2

Allele description [Variation Report for NM_014780.5(CUL7):c.3398G>A (p.Arg1133Gln)]

NM_014780.5(CUL7):c.3398G>A (p.Arg1133Gln)

Gene:

CUL7:cullin 7 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

6p21.1

Genomic location:

Preferred name:

NM_014780.5(CUL7):c.3398G>A (p.Arg1133Gln)

HGVS:

NC_000006.12:g.43043138C>T
NG_016205.1:g.15808G>A
NM_001168370.2:c.3494G>A
NM_001374872.1:c.3494G>A
NM_001374873.1:c.3398G>A
NM_001374874.1:c.3395G>A
NM_014780.5:c.3398G>AMANE SELECT
NP_001161842.2:p.Arg1165Gln
NP_001361801.1:p.Arg1165Gln
NP_001361802.1:p.Arg1133Gln
NP_001361803.1:p.Arg1132Gln
NP_055595.2:p.Arg1133Gln
NC_000006.11:g.43010876C>T
NM_014780.4:c.3398G>A

Protein change:

R1132Q

Molecular consequence:

NM_001168370.2:c.3494G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001374872.1:c.3494G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001374873.1:c.3398G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001374874.1:c.3395G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_014780.5:c.3398G>A - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:: CUL7-related disorder
Synonyms:: CUL7-related condition
Identifiers:

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV004717081	PreventionGenetics, part of Exact Sciences	no assertion criteria provided	Uncertain significance (Dec 15, 2023)	germline	clinical testing

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV004717081

PreventionGenetics, part of Exact Sciences

no assertion criteria provided

Uncertain significance
(Dec 15, 2023)

germline

clinical testing

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 PreventionGenetics, part of Exact Sciences, SCV004717081.2

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

Description

The CUL7 c.3398G>A variant is predicted to result in the amino acid substitution p.Arg1133Gln. To our knowledge, this variant has not been reported in the literature. This variant is reported in 0.0062% of alleles in individuals of African descent in gnomAD. At this time, the clinical significance of this variant is uncertain due to the absence of conclusive functional and genetic evidence.

#	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 13, 2024

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