NM_002691.4(POLD1):c.2585C>G (p.Ala862Gly) AND Hereditary cancer-predisposing syndrome

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Aug 22, 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:: RCV002426087.1

Allele description [Variation Report for NM_002691.4(POLD1):c.2585C>G (p.Ala862Gly)]

NM_002691.4(POLD1):c.2585C>G (p.Ala862Gly)

Gene:

POLD1:DNA polymerase delta 1, catalytic subunit [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

19q13.33

Genomic location:

Preferred name:

NM_002691.4(POLD1):c.2585C>G (p.Ala862Gly)

HGVS:

NC_000019.10:g.50415458C>G
NG_033800.1:g.36136C>G
NM_001256849.1:c.2585C>G
NM_001308632.1:c.2663C>G
NM_002691.4:c.2585C>GMANE SELECT
NP_001243778.1:p.Ala862Gly
NP_001295561.1:p.Ala888Gly
NP_002682.2:p.Ala862Gly
LRG_785t1:c.2585C>G
LRG_785t2:c.2663C>G
LRG_785:g.36136C>G
LRG_785p1:p.Ala862Gly
LRG_785p2:p.Ala888Gly
NC_000019.9:g.50918715C>G
NM_002691.2:c.2585C>G
NR_046402.2:n.2630C>G

Protein change:

A862G

Molecular consequence:

NM_001256849.1:c.2585C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001308632.1:c.2663C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_002691.4:c.2585C>G - missense variant - [Sequence Ontology: SO:0001583]
NR_046402.2:n.2630C>G - non-coding transcript variant - [Sequence Ontology: SO:0001619]

Observations:

Condition(s)

Name:: Hereditary cancer-predisposing syndrome
Synonyms:: Neoplastic Syndromes, Hereditary; Tumor predisposition; Cancer predisposition; See all synonyms [MedGen]
Identifiers:: MONDO: MONDO:0015356; MeSH: D009386; MedGen: C0027672

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV002743956	Ambry Genetics	criteria provided, single submitter (Ambry General Variant Classification Scheme_2022)	Uncertain significance (Aug 22, 2022)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV002743956

Ambry Genetics

criteria provided, single submitter

(Ambry General Variant Classification Scheme_2022)

Uncertain significance
(Aug 22, 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	1	not provided	not provided	1	not provided	clinical testing

Details of each submission

From Ambry Genetics, SCV002743956.1

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

Description

The p.A862G variant (also known as c.2585C>G), located in coding exon 20 of the POLD1 gene, results from a C to G substitution at nucleotide position 2585. The alanine at codon 862 is replaced by glycine, an amino acid with similar properties. This amino acid position is conserved. In addition, this alteration is predicted to be tolerated by in silico analysis. Since supporting evidence is limited at this time, 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	1	not provided	not provided		1	not provided	not provided	not provided

Last Updated: Dec 24, 2023

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