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LYFE SCIENCES
Project: HERA
NM_004360.5:c.1239C>T
p.Tyr413=  ·  CDH1
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Classification rationale
1

The CDH1 NM_004360.5:c.1239C>T (p.Tyr413=, p.Y413=) variant has not been observed in COSMIC and has been reported in ClinVar predominantly as benign or likely benign.

clinvar ↗ oncokb ↗
2

This variant is present in gnomAD above the CDH1 BS1 threshold of 0.1%, reaching 0.11215% in African/African American individuals in gnomAD v2.1 and 0.16258% in African/African American individuals in gnomAD v4.1, but it remains below the BA1 threshold of 0.2%.

cspec ↗ gnomad_v2 ↗ gnomad_v4 ↗
3

In gnomAD v4.1, this variant is also observed in the homozygous state in 3 individuals, supporting BP2 under the CDH1 specification.

cspec ↗ gnomad_v4 ↗
4

In silico splicing evidence does not support a splice-altering effect, with SpliceAI showing a maximum delta score of 0.01, which is consistent with applying BP7 for this synonymous internal exonic variant and does not support PP3.

cspec ↗ spliceai ↗
Applied criteria
Met
Not met
Not assessed
N/A
Very strong
Strong
Moderate
Supporting
Pathogenic evidence
PVS
PVS1
PS
PS1
PS2
PS3
PS4
PM
PM1
PM2
PM3
PM4
PM5
PM6
PP
PP1
PP2
PP3
PP4
PP5
Benign evidence
BA
BA1
BS
BS1
BS2
BS3
BS4
BP
BP1
BP2
BP3
BP4
BP5
BP6
BP7
PVS1
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Rationale
Select a criterion to inspect its explanation.
Evidence used
  • —
Gaps remaining
  • —
Rule
—
Publications
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Research and evidence
gnomAD v2.1 evidence
v2.1
gnomAD v4.1 evidence
v4.1
01
Population
gnomAD v2.1This variant is present in gnomAD v2.1 (AF= 0.000134328; MAF= 0.01343%, 38/282890 alleles, homozygotes = 0) and has highest observed frequency in the African/African American population (AF= 0.00112153; MAF= 0.11215%, 28/24966 alleles, homozygotes = 0); grpmax FAF= 0.00081502.
gnomAD v4.1This variant is present in gnomAD v4.1 (AF= 9.29301e-05; MAF= 0.00929%, 150/1614116 alleles, homozygotes = 3) and has highest observed frequency in the African/African American population (AF= 0.0016258; MAF= 0.16258%, 122/75040 alleles, homozygotes = 3); grpmax FAF= 0.00139058.
gnomAD v2 ↗ gnomAD v4 ↗
ClinVar evidence
02
ClinVar
This variant has been reported in ClinVar as Benign (9 clinical laboratories) and as Likely benign (5 clinical laboratories). (ClinVarID = 184347)
ClinVar ↗
Functional evidence
03
Functional
OncoKB: Unknown Oncogenic Effect
OncoKB identified curated literature and non-variant-specific oncogenicity context for review; listed oncogenicity label: Unknown Oncogenic Effect.
OncoKB ↗
In silico evidence
04
In silico
SpliceAI predicts no significant splice impact for this variant (max delta score = 0.01).
SpliceAI ↗
COSMIC evidence
05
COSMIC
This variant does not lie in a statistically significant hotspot. This variant has not previously been reported in somatic cancers (COSMIC).
COSMIC ↗
Cancer hotspots evidence
06
Cancer hotspots Not found
This variant does not lie in a statistically significant hotspot.
ResidueY413
Hotspots ↗