NM_001378615.1(CC2D2A):c.2326G>A (p.Gly776Arg) AND CC2D2A-related disorder

Germline classification:: Uncertain significance (2 submissions)
Last evaluated:: Apr 27, 2017
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:: RCV001150183.6

Allele description [Variation Report for NM_001378615.1(CC2D2A):c.2326G>A (p.Gly776Arg)]

NM_001378615.1(CC2D2A):c.2326G>A (p.Gly776Arg)

Gene:

CC2D2A:coiled-coil and C2 domain containing 2A [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

4p15.32

Genomic location:

Preferred name:

NM_001378615.1(CC2D2A):c.2326G>A (p.Gly776Arg)

HGVS:

NC_000004.12:g.15550968G>A
NG_013035.1:g.86103G>A
NM_001080522.2:c.2326G>A
NM_001378615.1:c.2326G>AMANE SELECT
NM_001378617.1:c.2179G>A
NP_001073991.2:p.Gly776Arg
NP_001365544.1:p.Gly776Arg
NP_001365546.1:p.Gly727Arg
LRG_697t1:c.2326G>A
LRG_697:g.86103G>A
LRG_697p1:p.Gly776Arg
NC_000004.11:g.15552591G>A

Protein change:

G727R

Links:

dbSNP: rs200764366

NCBI 1000 Genomes Browser:

rs200764366

Molecular consequence:

NM_001080522.2:c.2326G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001378615.1:c.2326G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001378617.1:c.2179G>A - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:: CC2D2A-related disorder
Synonyms:: CC2D2A-Related Disorders; CC2D2A-related condition
Identifiers:: MedGen: CN239313

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV001311196	Illumina Laboratory Services, Illumina	criteria provided, single submitter (ICSL Variant Classification Criteria 13 December 2019)	Uncertain significance (Apr 27, 2017)	germline	clinical testing	Citation Link,
SCV004745419	PreventionGenetics, part of Exact Sciences	no assertion criteria provided	Likely benign (Feb 7, 2022)	germline	clinical testing

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV001311196

Illumina Laboratory Services, Illumina

criteria provided, single submitter

(ICSL Variant Classification Criteria 13 December 2019)

Uncertain significance
(Apr 27, 2017)

germline

clinical testing

Citation Link,

SCV004745419

PreventionGenetics, part of Exact Sciences

no assertion criteria provided

Likely benign
(Feb 7, 2022)

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 Illumina Laboratory Services, Illumina, SCV001311196.1

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

Description

This variant was observed as part of a predisposition screen in an ostensibly healthy population. A literature search was performed for the gene, cDNA change, and amino acid change (where applicable). No publications were found based on this search. Allele frequency data from public databases did not allow this variant to be ruled in or out of causing disease. Therefore, this variant is classified as a variant of unknown significance.

#	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

From PreventionGenetics, part of Exact Sciences, SCV004745419.2

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

Description

This variant is classified as likely benign based on ACMG/AMP sequence variant interpretation guidelines (Richards et al. 2015 PMID: 25741868, with internal and published modifications).

#	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: Nov 24, 2024

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