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

Variant: NM_004360.4(CDH1):c.1147C>T (p.Gln383Ter)

CA169687

142888 (ClinVar)

Gene: CDH1
Condition: hereditary diffuse gastric cancer
Inheritance Mode: Autosomal dominant inheritance
Link to MONDO
UUID: 85e6ec9e-bbed-4967-a6af-72d3f6999902
Approved on: 2019-08-20
Published on: 2019-09-11

HGVS expressions

NM_004360.4:c.1147C>T
NM_004360.4(CDH1):c.1147C>T (p.Gln383Ter)
NC_000016.10:g.68813322C>T
CM000678.2:g.68813322C>T
NC_000016.9:g.68847225C>T
CM000678.1:g.68847225C>T
NC_000016.8:g.67404726C>T
NG_008021.1:g.81031C>T
ENST00000261769.10:c.1147C>T
ENST00000261769.9:c.1147C>T
ENST00000422392.6:c.1137+1059C>T
ENST00000562836.5:n.1218C>T
ENST00000565810.1:n.191C>T
ENST00000566510.5:c.991C>T
ENST00000566612.5:c.1147C>T
ENST00000611625.4:c.1147C>T
ENST00000612417.4:c.1147C>T
ENST00000621016.4:c.1147C>T
NM_004360.3:c.1147C>T
NM_001317184.1:c.1137+1059C>T
NM_001317185.1:c.-469C>T
NM_001317186.1:c.-673C>T
NM_004360.5:c.1147C>T
NM_001317184.2:c.1137+1059C>T
NM_001317185.2:c.-469C>T
NM_001317186.2:c.-673C>T
More

Pathogenic

Met criteria codes 3
PM2 PS4_Supporting PVS1
Not Met criteria codes 23
BA1 PS1 PS2 PS3 PP1 PP2 PP3 PP4 PM1 PM3 PM5 PM4 PM6 BS2 BS1 BS4 BS3 BP4 BP3 BP1 BP2 BP5 BP7

Evidence Links 1

Expert Panel

Criteria Specification Information

Criteria Specifications for this VCEP
Evidence submitted by expert panel
CDH1 VCEP
The c.1147C>T (p.Gln383Ter) variant is predicted to result in a premature stop codon that leads to a truncated or absent protein (PVS1). This variant is absent in the gnomAD cohort (PM2; http://gnomad.broadinstitute.org). The variant has been reported in at least one family meeting HDGC clinical criteria (PS4_Supporting; PMID 23709761). In summary, this variant meets criteria to be classified as pathogenic based on the ACMG/AMP criteria applied as specified by the CDH1 Variant Curation Expert Panel: PVS1, PM2, PS4_Supporting.
Met criteria codes
PM2
Absent in gnomAD
PS4_Supporting
One French family that meets HDGC clinical criteria. Two DGCs in family, one of them < age 50 (PMID: 23709761). One family that does not meet HDGC clinical criteria, with an index case with ductal breast cancer age 36 (DOI: 10.1200/PO.16.00021 JCO Precision Oncology - published online March 29, 2017).
French index case with DGC dx age 24 and a family member dx with DGC age 43. PubMed:23709761
PVS1
Predicted null variant in exon 9 of 16. Protein is expected to undergo NMD.
Not Met criteria codes
BA1
No code specific comments provided, please refer to the summary above or general recommendations provided in the guideline
PS1
No code specific comments provided, please refer to the summary above or general recommendations provided in the guideline
PS2
No code specific comments provided, please refer to the summary above or general recommendations provided in the guideline
PS3
No code specific comments provided, please refer to the summary above or general recommendations provided in the guideline
PP1
No code specific comments provided, please refer to the summary above or general recommendations provided in the guideline
PP2
No code specific comments provided, please refer to the summary above or general recommendations provided in the guideline
PP3
No code specific comments provided, please refer to the summary above or general recommendations provided in the guideline
PP4
No code specific comments provided, please refer to the summary above or general recommendations provided in the guideline
PM1
No code specific comments provided, please refer to the summary above or general recommendations provided in the guideline
PM3
No code specific comments provided, please refer to the summary above or general recommendations provided in the guideline
PM5
No code specific comments provided, please refer to the summary above or general recommendations provided in the guideline
PM4
No code specific comments provided, please refer to the summary above or general recommendations provided in the guideline
PM6
No code specific comments provided, please refer to the summary above or general recommendations provided in the guideline
BS2
No code specific comments provided, please refer to the summary above or general recommendations provided in the guideline
BS1
No code specific comments provided, please refer to the summary above or general recommendations provided in the guideline
BS4
No code specific comments provided, please refer to the summary above or general recommendations provided in the guideline
BS3
No code specific comments provided, please refer to the summary above or general recommendations provided in the guideline
BP4
No code specific comments provided, please refer to the summary above or general recommendations provided in the guideline
BP3
No code specific comments provided, please refer to the summary above or general recommendations provided in the guideline
BP1
No code specific comments provided, please refer to the summary above or general recommendations provided in the guideline
BP2
No code specific comments provided, please refer to the summary above or general recommendations provided in the guideline
BP5
No code specific comments provided, please refer to the summary above or general recommendations provided in the guideline
BP7
No code specific comments provided, please refer to the summary above or general recommendations provided in the guideline
Curation History
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