The ClinGen Evidence Repository is an FDA-recognized human genetic variant database containing expert-curated assertions regarding variants' pathogenicity and supporting evidence summaries. [Disclaimer]
  • No ClinVar Id was directly found from the curated document


Variant: NM_001354803.2:c.340A>T

CA367397094

Gene: GCK (HGNC:2645)
Condition: monogenic diabetes (MONDO:0015967)
Inheritance Mode: Semidominant inheritance
UUID: b9fdf1be-e713-4663-99b7-34a1f581d8a7
Approved on: 2024-01-22
Published on: 2024-01-22

HGVS expressions

NM_001354803.2:c.340A>T
NC_000007.14:g.44145228T>A
CM000669.2:g.44145228T>A
NC_000007.13:g.44184827T>A
CM000669.1:g.44184827T>A
NC_000007.12:g.44151352T>A
NG_008847.1:g.49196A>T
NG_008847.2:g.57943A>T
ENST00000395796.8:c.*1304A>T
ENST00000616242.5:c.*426A>T
ENST00000683378.1:n.532A>T
ENST00000336642.9:c.340A>T
ENST00000345378.7:c.1309A>T
ENST00000403799.8:c.1306A>T
ENST00000671824.1:c.1369A>T
ENST00000672743.1:n.318A>T
ENST00000673284.1:c.1306A>T
ENST00000336642.8:c.358A>T
ENST00000345378.6:c.1309A>T
ENST00000395796.7:c.1303A>T
ENST00000403799.7:c.1306A>T
ENST00000437084.1:c.1255A>T
ENST00000459642.1:n.686A>T
ENST00000616242.4:c.1303A>T
NM_000162.3:c.1306A>T
NM_033507.1:c.1309A>T
NM_033508.1:c.1303A>T
NM_000162.4:c.1306A>T
NM_001354800.1:c.1306A>T
NM_001354801.1:c.295A>T
NM_001354802.1:c.166A>T
NM_001354803.1:c.340A>T
NM_033507.2:c.1309A>T
NM_033508.2:c.1303A>T
NM_000162.5:c.1306A>T
NM_033507.3:c.1309A>T
NM_033508.3:c.1303A>T
More

Likely Pathogenic

Met criteria codes 7
PS4_Moderate PP4_Moderate PP3 PP2 PP1 PM5_Supporting PM2_Supporting
Not Met criteria codes 1
PM1

Evidence Links 0

Expert Panel

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.1306A>T variant in the glucokinase gene, GCK, causes an amino acid change of isoleucine to phenylalanine at codon 436 (p.(Ile436Phe)) of NM_000162.5. 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 predicted to be deleterious by computational evidence, with a REVEL score of 0.8259, which is greater than the MDEP VCEP threshold of 0.70 (PP3). This variant is absent in gnomAD v2.1.1 (PM2_Supporting), and was identified in 6 unrelated individuals with hyperglycemia (PS4_Moderate; internal lab contributors). Three of these individuals had a clinical history highly specific for GCK-hyperglycemia (FBG 5.5-8 mmol/L and HbA1c 5.6 - 7.6% and negative antibodies) (PP4_Moderate; internal lab contributor). This variant segregated with diabetes/hyperglycemia, with 2 informative meioses in 2 families (PP1; internal lab contributor). Additionally, another missense variant, c.1307T>A (p.Ile436Asn), has been classified as likely pathogenic by the ClinGen MDEP but has a greater Grantham distance than p.Ile436Phe (PM5_Supporting). Taken together, this evidence supports the classification of c.1306A>T as likely pathogenic for monogenic diabetes. ACMG/AMP criteria applied, as specified by the ClinGen MDEP (specification version 1.3.0, approved 8/11/2023): PP4_Moderate, PS4_Moderate, PP1, PP2, PP3, PM2_Supporting, PM5_Supporting.
Met criteria codes
PS4_Moderate
This variant was identified in 6 unrelated individuals with hyperglycemia (PS4_Moderate; internal lab contributors).
PP4_Moderate
This variant was identified in 3 individuals with a clinical history highly specific for GCK-hyperglycemia (FBG 5.5-8 mmol/L and HbA1c 5.6 - 7.6% and negative antibodies) (PP4_Moderate; internal lab contributors).
PP3
This variant is predicted to be deleterious by computational evidence, with a REVEL score of 0.8259, which is greater than the MDEP VCEP threshold of 0.70 (PP3).
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).
PP1
This variant segregated with diabetes/hyperglycemia, with 2 informative meioses in 2 families (PP1; internal lab contributor).
PM5_Supporting
Another missense variant, c.1307T>A (p.Ile436Asn), has been classified as pathogenic by the ClinGen MDEP but has a greater Grantham distance than p.Ile436Phe (PM5_Supporting).
PM2_Supporting
This variant is absent in gnomAD v2.1.1 (PM2_Supporting).
Not Met criteria codes
PM1
No code specific comments provided, please refer to the summary above or general recommendations provided in the guideline
Curation History
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.
ClinGen Terms of Use.
¤ Powered by BCM's Genboree.