Evidence Repository - Clinical Genome Resources

The ClinGen Evidence Repository is an FDA-recognized human genetic variant database containing expert-curated assertions regarding variants' pathogenicity and supporting evidence summaries. [Disclaimer]

Link to SEPIO compliant JSON-LD document

Variant: NM_000162.5(GCK):c.1147T>C (p.Ser383Pro)

CA367398737

1256306 (ClinVar)

Gene: GCK

Condition: monogenic diabetes

Inheritance Mode: Semidominant inheritance

Link to MONDO

UUID: 8dcddd9c-1d1a-4e00-97b1-be3a71fb9571

HGVS expressions

NM_000162.5:c.1147T>C

NM_000162.5(GCK):c.1147T>C (p.Ser383Pro)

NC_000007.14:g.44145603A>G

CM000669.2:g.44145603A>G

NC_000007.13:g.44185202A>G

CM000669.1:g.44185202A>G

NC_000007.12:g.44151727A>G

NG_008847.1:g.48821T>C

NG_008847.2:g.57568T>C

ENST00000395796.8:c.*1145T>C

ENST00000616242.5:c.*267T>C

ENST00000683378.1:n.373T>C

ENST00000336642.9:c.181T>C

ENST00000345378.7:c.1150T>C

ENST00000403799.8:c.1147T>C

ENST00000671824.1:c.1210T>C

ENST00000672743.1:n.159T>C

ENST00000673284.1:c.1147T>C

ENST00000336642.8:c.199T>C

ENST00000345378.6:c.1150T>C

ENST00000395796.7:c.1144T>C

ENST00000403799.7:c.1147T>C

ENST00000437084.1:c.1096T>C

ENST00000459642.1:n.527T>C

ENST00000616242.4:c.1144T>C

NM_000162.3:c.1147T>C

NM_033507.1:c.1150T>C

NM_033508.1:c.1144T>C

NM_000162.4:c.1147T>C

NM_001354800.1:c.1147T>C

NM_001354801.1:c.136T>C

NM_001354802.1:c.7T>C

NM_001354803.1:c.181T>C

NM_033507.2:c.1150T>C

NM_033508.2:c.1144T>C

NM_033507.3:c.1150T>C

NM_033508.3:c.1144T>C

NM_001354803.2:c.181T>C

Likely Pathogenic

PM5_Supporting PS4_Moderate PP3 PP2 PM2_Supporting

Evidence Links 0

Expert Panel

Monogenic Diabetes VCEP

Criteria Specification Information

Criteria Specification: ClinGen Monogenic Diabetes Expert Panel Specifications to the ACMG/AMP Variant Interpretation Guidelines for GCK Version 1.3.0

Criteria Specification Approval History

Criteria Specifications for this VCEP

Evidence submitted by expert panel

Monogenic Diabetes VCEP

The c.1147T>C variant in the glucokinase gene, GCK, causes an amino acid change of serine to proline at codon 383 (p. (Ser383Pro)) of NM_000162.5. This variant is absent from gnomAD v2.1.1 (PM2_Supporting). GCK is defined by the ClinGen MDEP as a gene that has a low rate of benign missense variation and has pathogenic missense variants as a common mechanism of disease (PP2) This variant is located in the larger hexokinase domain of the GCK gene (PMID: 31638168) but this variant does not reside in an amino acid that directly binds glucose or ATP, which is defined as critical for the protein’s function by the ClinGen MDEP, so it does not meet PM1. This variant is predicted to be deleterious by computational evidence, with a REVEL score of 0.804 which is greater than the MDEP VCEP threshold of 0.70 (PP3). Another missense variant, c.1148C>T (p.Ser383Leu), has been interpreted as pathogenic by the ClinGen MDEP, but has a greater Grantham distance than p.Ser383Pro (PM5_Supporting). This variant was identified in four unrelated individuals with hyperglycemia (PS4_Moderate; PMID: 36257325, 30663027, internal lab contributors). In summary, c.1147T>C meets the criteria to be classified as likely pathogenic for monogenic diabetes. ACMG/AMP criteria applied, as specified by the ClinGen MDEP VCEP (VCEP specifications version v1.3.0; approved 8/11/2023): PP3, PP2, PM5_Supporting, PM2_Supporting, PS4_Moderate.

PM5_Supporting

Another missense variant, c.1148C>T (p.Ser383Leu), has been interpreted as pathogenic by the ClinGen MDEP, but has a greater Grantham distance than p.Ser383Pro (PM5_Supporting).

PS4_Moderate

This variant was identified in four unrelated individuals with hyperglycemia (PS4_Moderate; PMID: 36257325, 30663027, internal lab contributors).

PP3

REVEL 0.804

PP2

GCK is defined by the ClinGen MDEP as a gene that has a low rate of benign missense variation and has pathogenic missense variants as a common mechanism of disease (PP2).

PM2_Supporting

This variant is absent from gnomAD v2.1.1 (PM2_Supporting).

Approved on: 2024-03-31

Published on: 2024-03-31

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. If you have questions about the information contained on this website, please see a health care professional.