NM_015018.4(DOP1A):c.3124A>G (p.Ser1042Gly) AND not specified

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Oct 3, 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:: RCV004384081.1

Allele description [Variation Report for NM_015018.4(DOP1A):c.3124A>G (p.Ser1042Gly)]

NM_015018.4(DOP1A):c.3124A>G (p.Ser1042Gly)

Gene:

DOP1A:DOP1 leucine zipper like protein A [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

6q14.1

Genomic location:

Preferred name:

NM_015018.4(DOP1A):c.3124A>G (p.Ser1042Gly)

HGVS:

NC_000006.12:g.83135872A>G
NM_001199942.2:c.3097A>G
NM_001385856.1:c.3094A>G
NM_001385857.1:c.3094A>G
NM_001385858.1:c.2641A>G
NM_001385859.1:c.2299A>G
NM_001385860.1:c.3094A>G
NM_001385861.1:c.3094A>G
NM_001385863.1:c.3097A>G
NM_001385864.1:c.1588A>G
NM_001385865.1:c.3097A>G
NM_015018.4:c.3124A>GMANE SELECT
NP_001186871.1:p.Ser1033Gly
NP_001372785.1:p.Ser1032Gly
NP_001372786.1:p.Ser1032Gly
NP_001372787.1:p.Ser881Gly
NP_001372788.1:p.Ser767Gly
NP_001372789.1:p.Ser1032Gly
NP_001372790.1:p.Ser1032Gly
NP_001372792.1:p.Ser1033Gly
NP_001372793.1:p.Ser530Gly
NP_001372794.1:p.Ser1033Gly
NP_055833.2:p.Ser1042Gly
NC_000006.11:g.83845591A>G
NM_001199942.1:c.3097A>G
NR_169790.1:n.3352A>G
NR_169791.1:n.3352A>G

Protein change:

S1032G

Molecular consequence:

NM_001199942.2:c.3097A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001385856.1:c.3094A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001385857.1:c.3094A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001385858.1:c.2641A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001385859.1:c.2299A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001385860.1:c.3094A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001385861.1:c.3094A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001385863.1:c.3097A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001385864.1:c.1588A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001385865.1:c.3097A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_015018.4:c.3124A>G - missense variant - [Sequence Ontology: SO:0001583]
NR_169790.1:n.3352A>G - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NR_169791.1:n.3352A>G - non-coding transcript variant - [Sequence Ontology: SO:0001619]

Condition(s)

Synonyms:: AllHighlyPenetrant
Identifiers:: MedGen: CN169374

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV004861370	Ambry Genetics	criteria provided, single submitter (Ambry Variant Classification Scheme 2023)	Uncertain significance (Oct 3, 2022)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV004861370

Ambry Genetics

criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)

Uncertain significance
(Oct 3, 2022)

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, SCV004861370.1

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

Description

The c.3097A>G (p.S1033G) alteration is located in exon 20 (coding exon 18) of the DOPEY1 gene. This alteration results from a A to G substitution at nucleotide position 3097, causing the serine (S) at amino acid position 1033 to be replaced by a glycine (G). 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: May 7, 2024

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