19-50406261-C-G

Variant names:

• chr19-50406261-C-G
• rs376711125
• NM_002691.4:c.1322C>G

Variant summary

Our verdict is Likely benign. The variant received -1 ACMG points: 2P and 3B. PM2 BP4_Moderate BP6

The NM_002691.4(POLD1):​c.1322C>G​(p.Thr441Arg) variant causes a missense change involving the alteration of a non-conserved nucleotide. The variant was absent in control chromosomes in GnomAD project. In-silico tool predicts a benign outcome for this variant. 13/22 in silico tools predict a benign outcome for this variant. Variant has been reported in ClinVar as Conflicting classifications of pathogenicity (no stars). Another variant affecting the same amino acid position, but resulting in a different missense (i.e. T441M) has been classified as Likely benign.

• Frequency: Genomes: not found (cov: 32)
• Consequence: POLD1 NM_002691.4 missense
• Clinical Significance: Conflicting classifications of pathogenicity criteria provided, conflicting classifications U:1 B:1
• Conservation: PhyloP100: 0.922
• Publications: 0 publications found

Genes affected

POLD1 (HGNC:9175): (DNA polymerase delta 1, catalytic subunit) This gene encodes the 125-kDa catalytic subunit of DNA polymerase delta. DNA polymerase delta possesses both polymerase and 3' to 5' exonuclease activity and plays a critical role in DNA replication and repair. Alternatively spliced transcript variants have been observed for this gene, and a pseudogene of this gene is located on the long arm of chromosome 6. [provided by RefSeq, Mar 2012]

POLD1 Gene-Disease associations (from GenCC):

• POLD1-related polyposis and colorectal cancer syndrome

  Inheritance: AD Classification: DEFINITIVE Submitted by: ClinGen
• colorectal cancer, susceptibility to, 10

  Inheritance: AD Classification: STRONG, MODERATE Submitted by: Labcorp Genetics (formerly Invitae), Ambry Genetics, Genomics England PanelApp
• mandibular hypoplasia-deafness-progeroid syndrome

  Inheritance: AD, AR Classification: STRONG, SUPPORTIVE, LIMITED Submitted by: Labcorp Genetics (formerly Invitae), PanelApp Australia, Genomics England PanelApp, Ambry Genetics, Orphanet, G2P
• Polymerase proofreading-related adenomatous polyposis

  Inheritance: AD Classification: SUPPORTIVE Submitted by: Orphanet
• immunodeficiency 120

  Inheritance: AR Classification: LIMITED Submitted by: Ambry Genetics
• non-severe combined immunodeficiency due to polymerase delta deficiency

  Inheritance: AR Classification: LIMITED Submitted by: ClinGen

ACMG classification

Our verdict: Likely_benign. The variant received -1 ACMG points.

• PM2: Very rare variant in population databases, with high coverage
• BP4: Computational evidence support a benign effect (MetaRNN=0.20041311).
• BP6: Variant 19-50406261-C-G is Benign according to our data. Variant chr19-50406261-C-G is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 2989261. Variant chr19-50406261-C-G is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 2989261. Variant chr19-50406261-C-G is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 2989261. Variant chr19-50406261-C-G is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 2989261. Variant chr19-50406261-C-G is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 2989261. Variant chr19-50406261-C-G is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 2989261. Variant chr19-50406261-C-G is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 2989261. Variant chr19-50406261-C-G is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 2989261. Variant chr19-50406261-C-G is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 2989261. Variant chr19-50406261-C-G is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 2989261. Variant chr19-50406261-C-G is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 2989261. Variant chr19-50406261-C-G is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 2989261. Variant chr19-50406261-C-G is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 2989261. Variant chr19-50406261-C-G is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 2989261. Variant chr19-50406261-C-G is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 2989261. Variant chr19-50406261-C-G is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 2989261. Variant chr19-50406261-C-G is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 2989261. Variant chr19-50406261-C-G is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 2989261. Variant chr19-50406261-C-G is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 2989261. Variant chr19-50406261-C-G is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 2989261. Variant chr19-50406261-C-G is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 2989261. Variant chr19-50406261-C-G is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 2989261. Variant chr19-50406261-C-G is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 2989261. Variant chr19-50406261-C-G is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 2989261. Variant chr19-50406261-C-G is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 2989261. Variant chr19-50406261-C-G is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 2989261. Variant chr19-50406261-C-G is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 2989261. Variant chr19-50406261-C-G is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 2989261. Variant chr19-50406261-C-G is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 2989261. Variant chr19-50406261-C-G is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 2989261. Variant chr19-50406261-C-G is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 2989261. Variant chr19-50406261-C-G is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 2989261. Variant chr19-50406261-C-G is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 2989261. Variant chr19-50406261-C-G is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 2989261. Variant chr19-50406261-C-G is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 2989261. Variant chr19-50406261-C-G is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 2989261. Variant chr19-50406261-C-G is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 2989261. Variant chr19-50406261-C-G is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 2989261. Variant chr19-50406261-C-G is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 2989261. Variant chr19-50406261-C-G is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 2989261. Variant chr19-50406261-C-G is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 2989261. Variant chr19-50406261-C-G is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 2989261. Variant chr19-50406261-C-G is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 2989261.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
POLD1	NM_002691.4	c.1322C>G	p.Thr441Arg	missense_variant	Exon 11 of 27	ENST00000440232.7	NP_002682.2

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
POLD1	ENST00000440232.7	c.1322C>G	p.Thr441Arg	missense_variant	Exon 11 of 27	1	NM_002691.4	ENSP00000406046.1

Frequencies

GnomAD3 genomes Cov.: 32

GnomAD4 exome Cov.: 36

GnomAD4 genome Cov.: 32

ClinVar

Significance: Conflicting classifications of pathogenicity

Submissions summary: Uncertain:1 Benign:1

Revision: criteria provided, conflicting classifications

Submissions by phenotype

Colorectal cancer, susceptibility to, 10 Uncertain:1

Nov 18, 2024

Labcorp Genetics (formerly Invitae), Labcorp

Significance: Uncertain significance

Review Status: criteria provided, single submitter

Collection Method: clinical testing

This sequence change replaces threonine, which is neutral and polar, with arginine, which is basic and polar, at codon 441 of the POLD1 protein (p.Thr441Arg). This variant is not present in population databases (gnomAD no frequency). This variant has not been reported in the literature in individuals affected with POLD1-related conditions. ClinVar contains an entry for this variant (Variation ID: 2989261). Invitae Evidence Modeling of protein sequence and biophysical properties (such as structural, functional, and spatial information, amino acid conservation, physicochemical variation, residue mobility, and thermodynamic stability) indicates that this missense variant is not expected to disrupt POLD1 protein function with a negative predictive value of 80%. 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. -

Hereditary cancer-predisposing syndrome Benign:1

Feb 06, 2025

Ambry Genetics

Significance: Likely benign

Review Status: criteria provided, single submitter

Collection Method: clinical testing

This alteration is classified as likely benign based on a combination of the following: seen in unaffected individuals, population frequency, intact protein function, lack of segregation with disease, co-occurrence, RNA analysis, in silico models, amino acid conservation, lack of disease association in case-control studies, and/or the mechanism of disease or impacted region is inconsistent with a known cause of pathogenicity. -

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
AlphaMissense	Uncertain	0.47
BayesDel_addAF	Benign	-0.22	T
BayesDel_noAF	Benign	-0.56
CADD	Benign	18
DANN	Uncertain	0.98
DEOGEN2	Benign	0.12	T;.;.;T
Eigen	Benign	-0.90
Eigen_PC	Benign	-0.78
FATHMM_MKL	Uncertain	0.88	D
LIST_S2	Pathogenic	0.98	.;.;D;D
M_CAP	Benign	0.012	T
MetaRNN	Benign	0.20	T;T;T;T
MetaSVM	Benign	-1.0	T
MutationAssessor	Benign	0.55	N;.;.;N
PhyloP100		0.92
PrimateAI	Uncertain	0.49	T
PROVEAN	Benign	-0.61	N;.;.;.
REVEL	Benign	0.063
Sift	Uncertain	0.022	D;.;.;.
Sift4G	Uncertain	0.046	D;T;T;D
Polyphen		0.0040	B;.;.;B
Vest4		0.44
MutPred		0.44		Gain of MoRF binding (P = 0.0336);Gain of MoRF binding (P = 0.0336);Gain of MoRF binding (P = 0.0336);Gain of MoRF binding (P = 0.0336);
MVP		0.26
MPC		1.1
ClinPred		0.53	D
GERP RS		-2.9
Varity_R		0.53
gMVP		0.74
Mutation Taster		=82/18	polymorphism

Splicing

Name	Calibrated prediction	Score	Prediction
SpliceAI score (max)		0.0		Details are displayed if max score is > 0.2

Find out detailed SpliceAI scores and Pangolin per-transcript scores at spliceailookup.broadinstitute.org

Other links and lift over

dbSNP: rs376711125; hg19: chr19-50909518;