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]

Variant: NM_004360.5(CDH1):c.370C>T (p.Arg124Cys)

CA8129836

239905 (ClinVar)

Gene: CDH1
Condition: CDH1-related diffuse gastric and lobular breast cancer
Inheritance Mode: Autosomal dominant inheritance
Link to MONDO
UUID: e554779f-79ec-4bcc-b6dc-93e2ca5df2a7
Approved on: 2023-08-10
Published on: 2023-08-10

HGVS expressions

NM_004360.5:c.370C>T
NM_004360.5(CDH1):c.370C>T (p.Arg124Cys)
NC_000016.10:g.68801876C>T
CM000678.2:g.68801876C>T
NC_000016.9:g.68835779C>T
CM000678.1:g.68835779C>T
NC_000016.8:g.67393280C>T
NG_008021.1:g.69585C>T
ENST00000261769.10:c.370C>T
ENST00000261769.9:c.370C>T
ENST00000422392.6:c.370C>T
ENST00000561751.1:n.137C>T
ENST00000562836.5:n.441C>T
ENST00000564676.5:n.652C>T
ENST00000564745.1:n.365C>T
ENST00000566510.5:c.370C>T
ENST00000566612.5:c.370C>T
ENST00000611625.4:c.370C>T
ENST00000612417.4:c.370C>T
ENST00000621016.4:c.370C>T
NM_004360.3:c.370C>T
NM_001317184.1:c.370C>T
NM_001317185.1:c.-1246C>T
NM_001317186.1:c.-1450C>T
NM_004360.4:c.370C>T
NM_001317184.2:c.370C>T
NM_001317185.2:c.-1246C>T
NM_001317186.2:c.-1450C>T
More

Likely Benign

Met criteria codes 1
BS2
Not Met criteria codes 25
PS1 PS2 PS3 PS4 PP3 PP2 PP4 PP1 PM5 PM4 PM3 PM1 PM6 PM2 PVS1 BA1 BS4 BS3 BS1 BP7 BP5 BP3 BP4 BP1 BP2

Evidence Links 0

Expert Panel

Criteria Specification Information

Criteria Specification: ClinGen CDH1 Expert Panel Specifications to the ACMG/AMP Variant Interpretation Guidelines Version 3.1

Criteria Specification Approval History
Criteria Specifications for this VCEP
Evidence submitted by expert panel
CDH1 VCEP
The c.370C>T (p.Arg124Cys) missense variant has a frequency of 0.039% in South Asians (12/30610 alleles) in the gnomAD v2.1.1 cohort. This variant has been observed in ≥10 (62) individuals without DGC, SRC tumours or LBC and whose families do not suggest HDGC (BS2; PMID: 30287823, SCV000288481.8, SCV000661624.3). In summary, the clinical significance of this variant is classified as of likely benign based the ACMG/AMP criteria applied, as specified by the CDH1 Variant Curation Expert Panel (Variant Interpretation Guidelines Version 3.1): BS2.
Met criteria codes
BS2
PMID: 30287823 - In a Japanese case-control study, this alteration was seen in 2/7051 unselected breast cancer patients and in 8/11,241 controls. Observed in 63 individuals without HDGC phenotypes (PMID: 30287823, SCV000288481.8, SCV000661624.3).
Not Met criteria codes
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 functional studies available.
PS4
PMID: 30287823 - In a Japanese case-control study, this alteration was seen in 2/7051 unselected breast cancer patients and in 8/11,241 controls.
PP3
VarSEAK: Class 1, No splicing effect. No SpliceAI predictions.
PP2
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
PP1
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
PM3
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
PM6
No code specific comments provided, please refer to the summary above or general recommendations provided in the guideline
PM2
gnomAD 2.1.1 = 0.039% in South Asians (12/30610 alleles). gnomAD 3.1 = 0.001314% (total 2/152,212 alleles - 1 East Asian and 1 African-American) - if using this, meets PM2 (<0.002%).
PVS1
No code specific comments provided, please refer to the summary above or general recommendations provided in the guideline
BA1
gnomAD 2.1.1 = 0.039% in South Asians (12/30610 alleles). MAF cut-off 0.2%.
BS4
No code specific comments provided, please refer to the summary above or general recommendations provided in the guideline
BS3
no functional studies available.
BS1
gnomAD 2.1.1 = 0.039% in South Asians (12/30610 alleles). MAF cut-off 0.1%.
BP7
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
BP3
No code specific comments provided, please refer to the summary above or general recommendations provided in the guideline
BP4
VarSEAK: Class 1, No splicing effect. No SpliceAI predictions. SSF - no change. NNSPLICE = 0.89 ⇒ 0.89 (-0.1%) MaxENT = 8.87 ⇒ 8.91 (+0.4%)
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
Curation History
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