NM_000162.5(GCK):c.59T>C (p.Leu20Pro) AND not provided

Germline classification:: Likely pathogenic (1 submission)
Last evaluated:: Jul 19, 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:: RCV003231847.2

Allele description [Variation Report for NM_000162.5(GCK):c.59T>C (p.Leu20Pro)]

NM_000162.5(GCK):c.59T>C (p.Leu20Pro)

Gene:

GCK:glucokinase [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

7p13

Genomic location:

Preferred name:

NM_000162.5(GCK):c.59T>C (p.Leu20Pro)

HGVS:

NC_000007.14:g.44153450A>G
NG_008847.2:g.49721T>C
NM_000162.5:c.59T>CMANE SELECT
NM_001354800.1:c.59T>C
NM_033507.3:c.62T>C
NM_033508.3:c.56T>C
NP_000153.1:p.Leu20Pro
NP_001341729.1:p.Leu20Pro
NP_277042.1:p.Leu21Pro
NP_277043.1:p.Leu19Pro
LRG_1074t1:c.59T>C
LRG_1074t2:c.62T>C
LRG_1074:g.49721T>C
LRG_1074p1:p.Leu20Pro
LRG_1074p2:p.Leu21Pro
NC_000007.13:g.44193049A>G
NM_000162.3:c.59T>C

Protein change:

L19P

Molecular consequence:

NM_000162.5:c.59T>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001354800.1:c.59T>C - missense variant - [Sequence Ontology: SO:0001583]
NM_033507.3:c.62T>C - missense variant - [Sequence Ontology: SO:0001583]
NM_033508.3:c.56T>C - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Synonyms:: none provided
Identifiers:: MedGen: CN517202

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV003929953	GeneDx	criteria provided, single submitter (GeneDx Variant Classification Process June 2021)	Likely pathogenic (Jul 19, 2023)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV003929953

GeneDx

criteria provided, single submitter

(GeneDx Variant Classification Process June 2021)

Likely pathogenic
(Jul 19, 2023)

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	yes	not provided	not provided	not provided	not provided	not provided	clinical testing

Details of each submission

From GeneDx, SCV003929953.2

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

Description

Not observed at significant frequency in large population cohorts (gnomAD); In silico analysis supports that this missense variant has a deleterious effect on protein structure/function; Missense variants in this gene are often considered pathogenic (HGMD); This variant is associated with the following publications: (PMID: 32041611, 27634015, 17573900)

#	Sample				Method		Observation
#	Origin	Affected	Number tested	Tissue	Purpose	Method	Individuals	Allele frequency	Families	Co-occurrences
1	germline	yes	not provided	not provided	not provided		not provided	not provided	not provided	not provided

Last Updated: Jul 29, 2023

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