NM_000162.5(GCK):c.706G>A (p.Glu236Lys) AND Gestational diabetes

Germline classification:: Pathogenic (1 submission)
Last evaluated:: Jul 23, 2013
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:: RCV000117134.6

Allele description [Variation Report for NM_000162.5(GCK):c.706G>A (p.Glu236Lys)]

NM_000162.5(GCK):c.706G>A (p.Glu236Lys)

Gene:

GCK:glucokinase [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

7p13

Genomic location:

Preferred name:

NM_000162.5(GCK):c.706G>A (p.Glu236Lys)

HGVS:

NC_000007.14:g.44147807C>T
NG_008847.2:g.55364G>A
NM_000162.5:c.706G>AMANE SELECT
NM_001354800.1:c.706G>A
NM_033507.3:c.709G>A
NM_033508.3:c.703G>A
NP_000153.1:p.Glu236Lys
NP_001341729.1:p.Glu236Lys
NP_277042.1:p.Glu237Lys
NP_277043.1:p.Glu235Lys
LRG_1074t1:c.706G>A
LRG_1074t2:c.709G>A
LRG_1074:g.55364G>A
LRG_1074p1:p.Glu236Lys
LRG_1074p2:p.Glu237Lys
NC_000007.13:g.44187406C>T
NM_000162.3:c.706G>A

Protein change:

E235K

Links:

dbSNP: rs587780347

NCBI 1000 Genomes Browser:

rs587780347

Molecular consequence:

NM_000162.5:c.706G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001354800.1:c.706G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_033507.3:c.709G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_033508.3:c.703G>A - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:: Gestational diabetes
Synonyms:: Diabetes mellitus, gestational; Maternal diabetes
Identifiers:: MONDO: MONDO:0005406; MedGen: C0085207; Human Phenotype Ontology: HP:0009800

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV000151295	Genetic Services Laboratory, University of Chicago	criteria provided, single submitter (ACMG Guidelines, 2007)	Pathogenic (Jul 23, 2013)	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

SCV000151295

Genetic Services Laboratory, University of Chicago

criteria provided, single submitter

(ACMG Guidelines, 2007)

Pathogenic
(Jul 23, 2013)

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

Citations

PubMed

ACMG recommendations for standards for interpretation and reporting of sequence variations: Revisions 2007.

Richards CS, Bale S, Bellissimo DB, Das S, Grody WW, Hegde MR, Lyon E, Ward BE; Molecular Subcommittee of the ACMG Laboratory Quality Assurance Committee..

Genet Med. 2008 Apr;10(4):294-300. doi: 10.1097/GIM.0b013e31816b5cae.

PubMed [citation]

PMID:: 18414213

Details of each submission

From Genetic Services Laboratory, University of Chicago, SCV000151295.1

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

#	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: Apr 9, 2023

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