CADM3 — 82 ClinVar variants
All ClinVar germline CADM3 variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 66 flagged for review →
1 Likely pathogenic · 2 Conflicting · 1 Benign · 11 Likely benign · 67 Uncertain significance
Full CADM3 gene report on Sugi Atlas → Gene function, pathways, protein structure, constraint & interactions⚑ Evidence disagreements 66
Variants where the independent computational evidence doesn't line up with the clinical picture — a QC signal for a second look, not a reclassification.
Predictors agree, ClinVar conflicts 2
ClinVar submitters conflict, but the independent predictors unanimously agree — a QC review flag, not a reclassification.
-
CADM3 p.Arg257His
Conflicting
Single submitter
Inborn genetic diseases
-
CADM3 p.Asp240Glu
Conflicting
Single submitter
Inborn genetic diseases
Predictors lean, ClinVar uncertain 36
ClinVar classifies these uncertain (VUS), but the independent predictors unanimously lean one way — a triage signal for review, not a reclassification.
-
CADM3 p.Tyr354Cys
Uncertain significance
Multiple submitters
Charcot-Marie-Tooth disease, axonal, type 2FF
-
CADM3 p.Ala20Gly
Uncertain significance
Single submitter
Inborn genetic diseases
-
CADM3 p.Ala20Ser
Uncertain significance
Single submitter
Inborn genetic diseases
-
CADM3 p.Ala219Val
Uncertain significance
Single submitter
Inborn genetic diseases
- CADM3 p.Ala331Asp Uncertain significance Single submitter
-
CADM3 p.Arg178His
Uncertain significance
Single submitter
Inborn genetic diseases
-
CADM3 p.Asn25His
Uncertain significance
Single submitter
Inborn genetic diseases
-
CADM3 p.Asn317Asp
Uncertain significance
Single submitter
Inborn genetic diseases
-
CADM3 p.Asp30Ala
Uncertain significance
Single submitter
Inborn genetic diseases
-
CADM3 p.Asp54Asn
Uncertain significance
Single submitter
Inborn genetic diseases
-
CADM3 p.Asp57Asn
Uncertain significance
Single submitter
Inborn genetic diseases
-
CADM3 p.Gln51Arg
Uncertain significance
Single submitter
Inborn genetic diseases
-
CADM3 p.Glu56Lys
Uncertain significance
Single submitter
Inborn genetic diseases
-
CADM3 p.Gly156Glu
Uncertain significance
Single submitter
Inborn genetic diseases
-
CADM3 p.Gly247Ser
Uncertain significance
Single submitter
Charcot-Marie-Tooth disease, axonal, type 2FF
-
CADM3 p.Gly334Cys
Uncertain significance
Single submitter
Charcot-Marie-Tooth disease, axonal, type 2FF
-
CADM3 p.His213Leu
Uncertain significance
Single submitter
Inborn genetic diseases
-
CADM3 p.His243Gln
Uncertain significance
Single submitter
Inborn genetic diseases
-
CADM3 p.His330Tyr
Uncertain significance
Single submitter
Inborn genetic diseases
-
CADM3 p.His365Asn
Uncertain significance
Single submitter
Inborn genetic diseases
-
CADM3 p.His91Tyr
Uncertain significance
Single submitter
Inborn genetic diseases
-
CADM3 p.Ile207Val
Uncertain significance
Single submitter
Inborn genetic diseases
-
CADM3 p.Met278Ile
Uncertain significance
Single submitter
Inborn genetic diseases
-
CADM3 p.Pro4Ser
Uncertain significance
Single submitter
Inborn genetic diseases
-
CADM3 p.Ser31Asn
Uncertain significance
Single submitter
Inborn genetic diseases
-
CADM3 p.Ser370Thr
Uncertain significance
Single submitter
Inborn genetic diseases
-
CADM3 p.Thr119Ile
Uncertain significance
Single submitter
Inborn genetic diseases
-
CADM3 p.Thr361Ile
Uncertain significance
Single submitter
Inborn genetic diseases
-
CADM3 p.Thr378Met
Uncertain significance
Single submitter
Inborn genetic diseases
-
CADM3 p.Trp19Arg
Uncertain significance
Single submitter
Inborn genetic diseases
-
CADM3 p.Trp19Ser
Uncertain significance
Single submitter
Inborn genetic diseases
-
CADM3 p.Trp34Arg
Uncertain significance
Single submitter
Inborn genetic diseases
- CADM3 p.Tyr311Phe Uncertain significance Single submitter
-
CADM3 p.Val124Ile
Uncertain significance
Single submitter
Inborn genetic diseases
-
CADM3 p.Val46Met
Uncertain significance
Single submitter
Inborn genetic diseases
-
CADM3 p.Gly128Arg
Uncertain significance
No assertion criteria
prostate cancer
Predictors split 28
The independent predictors disagree with each other — read with care.
-
CADM3 p.Leu13Gln
Uncertain significance
Multiple submitters
Inborn genetic diseases
-
CADM3 p.Tyr138Cys
Likely pathogenic
Multiple submitters
Charcot-Marie-Tooth disease, axonal, type 2FF
-
CADM3 p.Ala331Thr
Uncertain significance
Single submitter
Inborn genetic diseases
-
CADM3 p.Ala376Val
Uncertain significance
Single submitter
Inborn genetic diseases
-
CADM3 p.Arg143Trp
Uncertain significance
Single submitter
Inborn genetic diseases
-
CADM3 p.Arg200Trp
Uncertain significance
Single submitter
Inborn genetic diseases
-
CADM3 p.Arg245His
Uncertain significance
Single submitter
Inborn genetic diseases
-
CADM3 p.Asn184Ser
Uncertain significance
Single submitter
Inborn genetic diseases
-
CADM3 p.Asn382Ser
Uncertain significance
Single submitter
Inborn genetic diseases
-
CADM3 p.Asp54Tyr
Uncertain significance
Single submitter
Inborn genetic diseases
-
CADM3 p.Cys17Tyr
Uncertain significance
Single submitter
Inborn genetic diseases
-
CADM3 p.Gln197Arg
Uncertain significance
Single submitter
Inborn genetic diseases
-
CADM3 p.Gln84Glu
Uncertain significance
Single submitter
Inborn genetic diseases
-
CADM3 p.Glu175Lys
Uncertain significance
Single submitter
Inborn genetic diseases
-
CADM3 p.Gly2Val
Uncertain significance
Single submitter
Inborn genetic diseases
-
CADM3 p.Gly386Arg
Uncertain significance
Single submitter
Inborn genetic diseases
-
CADM3 p.Ile349Leu
Uncertain significance
Single submitter
Inborn genetic diseases
-
CADM3 p.Leu10Phe
Uncertain significance
Single submitter
Inborn genetic diseases
-
CADM3 p.Pro33Leu
Uncertain significance
Single submitter
Inborn genetic diseases
- CADM3 p.Pro4Thr Uncertain significance Single submitter
-
CADM3 p.Ser140Pro
Uncertain significance
Single submitter
Inborn genetic diseases
-
CADM3 p.Ser191Arg
Uncertain significance
Single submitter
Inborn genetic diseases
- CADM3 p.Ser193Leu Likely benign Single submitter
-
CADM3 p.Thr199Ala
Uncertain significance
Single submitter
Inborn genetic diseases
-
CADM3 p.Thr87Ile
Uncertain significance
Single submitter
Inborn genetic diseases
-
CADM3 p.Thr89Met
Uncertain significance
Single submitter
Inborn genetic diseases
-
CADM3 p.Val194Leu
Uncertain significance
Single submitter
Inborn genetic diseases
-
CADM3 p.Val208Met
Uncertain significance
Single submitter
Inborn genetic diseases
All CADM3 variants
Likely pathogenic 1
- p.Tyr138Cys Multiple submitters Charcot-Marie-Tooth disease, axonal, type 2FF ⚠
Conflicting classifications of pathogenicity 2
- p.Arg257His Single submitter Inborn genetic diseases ⚠
- p.Asp240Glu Single submitter Inborn genetic diseases ⚠
Benign 1
- c.-12C>T Single submitter
Likely benign 11
Uncertain significance 67
- c.89-2102C>T Multiple submitters Inborn genetic diseases
- p.Leu13Gln Multiple submitters Inborn genetic diseases ⚠
- p.Tyr354Cys Multiple submitters Charcot-Marie-Tooth disease, axonal, type 2FF ⚠
- c.229+11A>G Single submitter Charcot-Marie-Tooth disease, axonal, type 2FF
- c.382+1G>A Single submitter
- c.383del Single submitter Charcot-Marie-Tooth disease, axonal, type 2FF
- c.89-2133A>T Single submitter Inborn genetic diseases
- p.Ala20Gly Single submitter Inborn genetic diseases ⚠
- p.Ala20Ser Single submitter Inborn genetic diseases ⚠
- p.Ala219Val Single submitter Inborn genetic diseases ⚠
- p.Ala331Asp Single submitter ⚠
- p.Ala331Thr Single submitter Inborn genetic diseases ⚠
- p.Ala376Val Single submitter Inborn genetic diseases ⚠
- p.Arg143Trp Single submitter Inborn genetic diseases ⚠
- p.Arg178His Single submitter Inborn genetic diseases ⚠
- p.Arg200Trp Single submitter Inborn genetic diseases ⚠
- p.Arg245His Single submitter Inborn genetic diseases ⚠
- p.Asn184Ser Single submitter Inborn genetic diseases ⚠
- p.Asn25His Single submitter Inborn genetic diseases ⚠
- p.Asn317Asp Single submitter Inborn genetic diseases ⚠
- p.Asn382Ser Single submitter Inborn genetic diseases ⚠
- p.Asp30Ala Single submitter Inborn genetic diseases ⚠
- p.Asp54Asn Single submitter Inborn genetic diseases ⚠
- p.Asp54Tyr Single submitter Inborn genetic diseases ⚠
- p.Asp57Asn Single submitter Inborn genetic diseases ⚠
- p.Cys17Tyr Single submitter Inborn genetic diseases ⚠
- p.Gln197Arg Single submitter Inborn genetic diseases ⚠
- p.Gln51Arg Single submitter Inborn genetic diseases ⚠
- p.Gln84Glu Single submitter Inborn genetic diseases ⚠
- p.Glu175Lys Single submitter Inborn genetic diseases ⚠
- p.Glu56Lys Single submitter Inborn genetic diseases ⚠
- p.Gly156Glu Single submitter Inborn genetic diseases ⚠
- p.Gly247Ser Single submitter Charcot-Marie-Tooth disease, axonal, type 2FF ⚠
- p.Gly2Val Single submitter Inborn genetic diseases ⚠
- p.Gly334Cys Single submitter Charcot-Marie-Tooth disease, axonal, type 2FF ⚠
- p.Gly386Arg Single submitter Inborn genetic diseases ⚠
- p.His213Leu Single submitter Inborn genetic diseases ⚠
- p.His243Gln Single submitter Inborn genetic diseases ⚠
- p.His330Tyr Single submitter Inborn genetic diseases ⚠
- p.His365Asn Single submitter Inborn genetic diseases ⚠
- p.His91Tyr Single submitter Inborn genetic diseases ⚠
- p.Ile207Val Single submitter Inborn genetic diseases ⚠
- p.Ile349Leu Single submitter Inborn genetic diseases ⚠
- p.Leu10Phe Single submitter Inborn genetic diseases ⚠
- p.Met278Ile Single submitter Inborn genetic diseases ⚠
- p.Pro33Leu Single submitter Inborn genetic diseases ⚠
- p.Pro4Ser Single submitter Inborn genetic diseases ⚠
- p.Pro4Thr Single submitter ⚠
- p.Ser140Pro Single submitter Inborn genetic diseases ⚠
- p.Ser191Arg Single submitter Inborn genetic diseases ⚠
- p.Ser31Asn Single submitter Inborn genetic diseases ⚠
- p.Ser370Thr Single submitter Inborn genetic diseases ⚠
- p.Thr119Ile Single submitter Inborn genetic diseases ⚠
- p.Thr199Ala Single submitter Inborn genetic diseases ⚠
- p.Thr361Ile Single submitter Inborn genetic diseases ⚠
- p.Thr378Met Single submitter Inborn genetic diseases ⚠
- p.Thr87Ile Single submitter Inborn genetic diseases ⚠
- p.Thr89Met Single submitter Inborn genetic diseases ⚠
- p.Trp19Arg Single submitter Inborn genetic diseases ⚠
- p.Trp19Ser Single submitter Inborn genetic diseases ⚠
- p.Trp34Arg Single submitter Inborn genetic diseases ⚠
- p.Tyr311Phe Single submitter ⚠
- p.Val124Ile Single submitter Inborn genetic diseases ⚠
- p.Val194Leu Single submitter Inborn genetic diseases ⚠
- p.Val208Met Single submitter Inborn genetic diseases ⚠
- p.Val46Met Single submitter Inborn genetic diseases ⚠
- p.Gly128Arg No assertion criteria prostate cancer ⚠