NM_080916.3(DGUOK):c.800T>C (p.Met267Thr) AND Inborn genetic diseases

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Jul 20, 2021
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:: RCV002713791.2

Allele description [Variation Report for NM_080916.3(DGUOK):c.800T>C (p.Met267Thr)]

NM_080916.3(DGUOK):c.800T>C (p.Met267Thr)

Genes:

DGUOK-AS1:DGUOK antisense RNA 1 [Gene - HGNC]
DGUOK:deoxyguanosine kinase [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

2p13.1

Genomic location:

Preferred name:

NM_080916.3(DGUOK):c.800T>C (p.Met267Thr)

HGVS:

NC_000002.12:g.73958238T>C
NG_008044.1:g.36413T>C
NM_001318859.2:c.518T>C
NM_001318860.2:c.509T>C
NM_001318861.2:c.509T>C
NM_001318862.2:c.491T>C
NM_001318863.2:c.491T>C
NM_080916.3:c.800T>CMANE SELECT
NM_080918.3:c.536T>C
NP_001305788.1:p.Met173Thr
NP_001305789.1:p.Met170Thr
NP_001305790.1:p.Met170Thr
NP_001305791.1:p.Met164Thr
NP_001305792.1:p.Met164Thr
NP_550438.1:p.Met267Thr
NP_550440.1:p.Met179Thr
NC_000002.11:g.74185365T>C
NM_080916.1:c.800T>C
NR_134893.2:n.454T>C
NR_134894.2:n.602T>C
NR_134895.2:n.266T>C
NR_134896.2:n.436T>C
NR_134897.2:n.646T>C
NR_134898.2:n.570T>C

Protein change:

M164T

Molecular consequence:

NM_001318859.2:c.518T>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001318860.2:c.509T>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001318861.2:c.509T>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001318862.2:c.491T>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001318863.2:c.491T>C - missense variant - [Sequence Ontology: SO:0001583]
NM_080916.3:c.800T>C - missense variant - [Sequence Ontology: SO:0001583]
NM_080918.3:c.536T>C - missense variant - [Sequence Ontology: SO:0001583]
NR_134893.2:n.454T>C - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NR_134894.2:n.602T>C - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NR_134895.2:n.266T>C - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NR_134896.2:n.436T>C - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NR_134897.2:n.646T>C - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NR_134898.2:n.570T>C - non-coding transcript variant - [Sequence Ontology: SO:0001619]

Condition(s)

Name:: Inborn genetic diseases
Identifiers:: MeSH: D030342; MedGen: C0950123

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV003566690	Ambry Genetics	criteria provided, single submitter (Ambry Variant Classification Scheme 2023)	Uncertain significance (Jul 20, 2021)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV003566690

Ambry Genetics

criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)

Uncertain significance
(Jul 20, 2021)

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, SCV003566690.2

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

Description

The c.800T>C (p.M267T) alteration is located in exon 6 (coding exon 6) of the DGUOK gene. This alteration results from a T to C substitution at nucleotide position 800, causing the methionine (M) at amino acid position 267 to be replaced by a threonine (T). 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 1, 2024

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