NM_002691.4(POLD1):c.419A>G (p.His140Arg) AND Colorectal cancer, susceptibility to, 10

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Apr 7, 2023
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:: RCV000794300.7

Allele description [Variation Report for NM_002691.4(POLD1):c.419A>G (p.His140Arg)]

NM_002691.4(POLD1):c.419A>G (p.His140Arg)

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.419A>G (p.His140Arg)

HGVS:

NC_000019.10:g.50401880A>G
NG_033800.1:g.22558A>G
NM_001256849.1:c.419A>G
NM_001308632.1:c.419A>G
NM_002691.2:c.419A>G
NM_002691.4:c.419A>GMANE SELECT
NP_001243778.1:p.His140Arg
NP_001295561.1:p.His140Arg
NP_002682.2:p.His140Arg
LRG_785t1:c.419A>G
LRG_785t2:c.419A>G
LRG_785:g.22558A>G
LRG_785p1:p.His140Arg
LRG_785p2:p.His140Arg
NC_000019.9:g.50905137A>G
NM_002691.3:c.419A>G
NR_046402.2:n.464A>G

Protein change:

H140R

Links:

dbSNP: rs1601198706

NCBI 1000 Genomes Browser:

rs1601198706

Molecular consequence:

NM_001256849.1:c.419A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001308632.1:c.419A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_002691.4:c.419A>G - missense variant - [Sequence Ontology: SO:0001583]
NR_046402.2:n.464A>G - non-coding transcript variant - [Sequence Ontology: SO:0001619]

Condition(s)

Name:: Colorectal cancer, susceptibility to, 10
Synonyms:: COLORECTAL CANCER, SUSCEPTIBILITY TO, ON CHROMOSOME 19q; Colorectal cancer 10
Identifiers:: MONDO: MONDO:0012953; MedGen: C2675481; Orphanet: 220460; OMIM: 612591

Recent activity

Clear Turn Off Turn On

Meckel syndrome, type 1 [Homo sapiens]
Meckel syndrome, type 1 [Homo sapiens]
gi|8923324|ref|NP_060247.1|

Protein
Cell Wall and Surface Molecules of Streptococcus pyogenes: Capsule - Streptococc...
Cell Wall and Surface Molecules of Streptococcus pyogenes: Capsule - Streptococcus pyogenes: Basic Biology to Clinical Manifestations

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

Help

Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV000933698	Labcorp Genetics (formerly Invitae), Labcorp	criteria provided, single submitter (Invitae Variant Classification Sherloc (09022015))	Uncertain significance (Apr 7, 2023)	germline	clinical testing	PubMed (1) [See all records that cite this PMID]

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV000933698

Labcorp Genetics (formerly Invitae), Labcorp

criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))

Uncertain significance
(Apr 7, 2023)

germline

clinical testing

PubMed (1)
[See all records that cite this PMID]

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

Citations

PubMed

Sherloc: a comprehensive refinement of the ACMG-AMP variant classification criteria.

Nykamp K, Anderson M, Powers M, Garcia J, Herrera B, Ho YY, Kobayashi Y, Patil N, Thusberg J, Westbrook M; Invitae Clinical Genomics Group., Topper S.

Genet Med. 2017 Oct;19(10):1105-1117. doi: 10.1038/gim.2017.37. Epub 2017 May 11. Erratum in: Genet Med. 2020 Jan;22(1):240. doi: 10.1038/s41436-019-0624-9.

PubMed [citation]

PMID:: 28492532
PMCID:: PMC5632818

Details of each submission

From Labcorp Genetics (formerly Invitae), Labcorp, SCV000933698.4

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

Description

This sequence change replaces histidine, which is basic and polar, with arginine, which is basic and polar, at codon 140 of the POLD1 protein (p.His140Arg). This variant is not present in population databases (gnomAD no frequency). In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance. Advanced modeling of protein sequence and biophysical properties (such as structural, functional, and spatial information, amino acid conservation, physicochemical variation, residue mobility, and thermodynamic stability) performed at Invitae indicates that this missense variant is not expected to disrupt POLD1 protein function. ClinVar contains an entry for this variant (Variation ID: 641129). This variant has not been reported in the literature in individuals affected with POLD1-related conditions.

#	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: Sep 29, 2024

ClinVar

Relating variation to medicine