LYN — 298 ClinVar variants
All ClinVar germline LYN variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 104 flagged for review →
4 Pathogenic · 2 Conflicting · 10 Benign · 2 Benign/Likely benign · 154 Likely benign · 126 Uncertain significance
Full LYN gene report on Sugi Atlas → Gene function, pathways, protein structure, constraint & interactions⚑ Evidence disagreements 104
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 1
ClinVar submitters conflict, but the independent predictors unanimously agree — a QC review flag, not a reclassification.
-
LYN p.Val465Met
Conflicting
Single submitter
Inborn genetic diseases
Predictors lean, ClinVar uncertain 78
ClinVar classifies these uncertain (VUS), but the independent predictors unanimously lean one way — a triage signal for review, not a reclassification.
-
LYN p.Ala150Thr
Uncertain significance
Multiple submitters
Inborn genetic diseases
-
LYN p.Ala70Thr
Uncertain significance
Multiple submitters
Inborn genetic diseases
-
LYN p.Glu47Asp
Uncertain significance
Multiple submitters
Inborn genetic diseases
- LYN p.Ile227Val Uncertain significance Multiple submitters
-
LYN p.Thr30Ala
Uncertain significance
Multiple submitters
Inborn genetic diseases
-
LYN p.Val45Ile
Uncertain significance
Multiple submitters
Inborn genetic diseases
- LYN p.Ala150Ser Uncertain significance Single submitter
- LYN p.Ala215Thr Uncertain significance Single submitter
- LYN p.Ala273Val Uncertain significance Single submitter
-
LYN p.Ala307Thr
Uncertain significance
Single submitter
Inborn genetic diseases
- LYN p.Ala450Gly Uncertain significance Single submitter
- LYN p.Ala455Thr Uncertain significance Single submitter
- LYN p.Arg25Cys Uncertain significance Single submitter
- LYN p.Arg25His Uncertain significance Single submitter
- LYN p.Arg311Lys Uncertain significance Single submitter
- LYN p.Arg360Gln Uncertain significance Single submitter
-
LYN p.Arg360Leu
Uncertain significance
Single submitter
Inborn genetic diseases
- LYN p.Arg366Gln Uncertain significance Single submitter
- LYN p.Arg366Trp Uncertain significance Single submitter
- LYN p.Arg464Cys Uncertain significance Single submitter
- LYN p.Asn268Ser Uncertain significance Single submitter
- LYN p.Asp133Gly Uncertain significance Single submitter
- LYN p.Asp15Gly Uncertain significance Single submitter
-
LYN p.Asp189Ala
Uncertain significance
Single submitter
Inborn genetic diseases
-
LYN p.Asp238Val
Uncertain significance
Single submitter
Inborn genetic diseases
- LYN p.Asp334His Uncertain significance Single submitter
- LYN p.Asp334Val Uncertain significance Single submitter
- LYN p.Asp451Glu Uncertain significance Single submitter
- LYN p.Asp470Gly Uncertain significance Single submitter
- LYN p.Asp66Val Uncertain significance Single submitter
- LYN p.Cys203Phe Uncertain significance Single submitter
- LYN p.Cys219Phe Uncertain significance Single submitter
- LYN p.Gln41Arg Uncertain significance Single submitter
- LYN p.Glu159Lys Uncertain significance Single submitter
- LYN p.Glu260Lys Uncertain significance Single submitter
- LYN p.Glu313Asp Uncertain significance Single submitter
- LYN p.Glu62Lys Uncertain significance Single submitter
- LYN p.Glu88Asp Uncertain significance Single submitter
-
LYN p.Gly163Val
Uncertain significance
Single submitter
autoinflammatory disease, systemic, with vasculitis
-
LYN p.Gly402Asp
Uncertain significance
Single submitter
Inborn genetic diseases
- LYN p.Gly76Ser Uncertain significance Single submitter
- LYN p.Gly8Glu Uncertain significance Single submitter
- LYN p.His96Gln Uncertain significance Single submitter
- LYN p.Ile134Met Uncertain significance Single submitter
- LYN p.Ile134Val Uncertain significance Single submitter
- LYN p.Ile227Phe Uncertain significance Single submitter
- LYN p.Ile317Val Uncertain significance Single submitter
- LYN p.Ile4Val Uncertain significance Single submitter
- LYN p.Leu105Pro Uncertain significance Single submitter
- LYN p.Leu106Ser Uncertain significance Single submitter
- LYN p.Leu374Gln Uncertain significance Single submitter
-
LYN p.Lys109Asn
Uncertain significance
Single submitter
Inborn genetic diseases
- LYN p.Lys120Arg Uncertain significance Single submitter
- LYN p.Lys132Arg Uncertain significance Single submitter
- LYN p.Lys338Arg Uncertain significance Single submitter
- LYN p.Met207Leu Uncertain significance Single submitter
-
LYN p.Met380Val
Uncertain significance
Single submitter
Inborn genetic diseases
- LYN p.Met478Thr Uncertain significance Single submitter
- LYN p.Pro202Ala Uncertain significance Single submitter
- LYN p.Pro202Ser Uncertain significance Single submitter
- LYN p.Pro73Ala Uncertain significance Single submitter
- LYN p.Pro79Leu Uncertain significance Single submitter
- LYN p.Ser11Gly Uncertain significance Single submitter
- LYN p.Ser205Gly Uncertain significance Single submitter
- LYN p.Ser83Cys Uncertain significance Single submitter
- LYN p.Thr126Ile Uncertain significance Single submitter
- LYN p.Thr200Ser Uncertain significance Single submitter
- LYN p.Thr21Ser Uncertain significance Single submitter
- LYN p.Thr296Ala Uncertain significance Single submitter
-
LYN p.Thr310Ser
Uncertain significance
Single submitter
autoinflammatory disease, systemic, with vasculitis
- LYN p.Thr37Ala Uncertain significance Single submitter
-
LYN p.Trp480Cys
Uncertain significance
Single submitter
Inborn genetic diseases
- LYN p.Tyr265Cys Uncertain significance Single submitter
- LYN p.Val426Met Uncertain significance Single submitter
- LYN p.Val437Ala Uncertain significance Single submitter
-
LYN p.Val45Phe
Uncertain significance
Single submitter
Inborn genetic diseases
- LYN p.Val496Ile Uncertain significance Single submitter
- LYN p.Val92Ile Uncertain significance Single submitter
Predictors split 25
The independent predictors disagree with each other — read with care.
-
LYN p.Arg360Trp
Uncertain significance
Multiple submitters
Inborn genetic diseases
- LYN p.Ala139Thr Uncertain significance Single submitter
-
LYN p.Arg244Trp
Uncertain significance
Single submitter
Inborn genetic diseases
- LYN p.Arg447Thr Uncertain significance Single submitter
- LYN p.Asn395Ser Uncertain significance Single submitter
- LYN p.Asn416Thr Uncertain significance Single submitter
- LYN p.Asp206Asn Uncertain significance Single submitter
-
LYN p.Glu312Lys
Uncertain significance
Single submitter
Inborn genetic diseases
- LYN p.Glu482Gly Uncertain significance Single submitter
- LYN p.Gly76Val Uncertain significance Single submitter
- LYN p.His176Pro Uncertain significance Single submitter
- LYN p.Leu379Phe Uncertain significance Single submitter
- LYN p.Lys120Ile Uncertain significance Single submitter
- LYN p.Lys230Asn Uncertain significance Single submitter
- LYN p.Lys91Asn Uncertain significance Single submitter
- LYN p.Phe56Leu Uncertain significance Single submitter
- LYN p.Pro52Arg Uncertain significance Single submitter
-
LYN p.Ser326Cys
Uncertain significance
Single submitter
Inborn genetic diseases
- LYN p.Ser457Cys Uncertain significance Single submitter
- LYN p.Ser457Phe Uncertain significance Single submitter
- LYN p.Thr107Arg Uncertain significance Single submitter
- LYN p.Thr37Met Uncertain significance Single submitter
- LYN p.Val68Ala Uncertain significance Single submitter
-
LYN p.Tyr508His
Pathogenic
No assertion criteria
autoinflammatory disease, systemic, with vasculitis
-
LYN p.Tyr508Phe
Pathogenic
No assertion criteria
autoinflammatory disease, systemic, with vasculitis
All LYN variants
Pathogenic 4
- p.Gln507Ter No assertion criteria autoinflammatory disease, systemic, with vasculitis
- p.Tyr508His No assertion criteria autoinflammatory disease, systemic, with vasculitis ⚠
- p.Tyr508Phe No assertion criteria autoinflammatory disease, systemic, with vasculitis ⚠
- p.Tyr508Ter No assertion criteria autoinflammatory disease, systemic, with vasculitis
Conflicting classifications of pathogenicity 2
- c.133-4G>A Single submitter
- p.Val465Met Single submitter Inborn genetic diseases ⚠
Benign 10
- p.Gly254= Multiple submitters
- p.Ile358= Multiple submitters
- p.Lys233= Multiple submitters
- c.1337-10dup Single submitter
- c.488-11del Single submitter
- c.488-5del Single submitter
- c.973+14A>G Single submitter
- p.Ile247= Single submitter
- p.Lys338= Single submitter
- p.Tyr473= Single submitter
Likely benign 154
- c.179-3del Multiple submitters
- p.Asp138= Multiple submitters
- p.Glu223= Multiple submitters
- p.Gly163= Multiple submitters
- p.Pro79= Multiple submitters
- p.Thr410= Multiple submitters
- p.Thr502= Multiple submitters
- c.1050+13A>G Single submitter
- c.1050+18C>T Single submitter
- c.1050+47del Single submitter autoinflammatory disease, systemic, with vasculitis
- c.1050+8_1050+9del Single submitter
- c.1051-14A>G Single submitter
- c.1051-20G>T Single submitter
- c.1051-8G>A Single submitter
- c.1204+13A>G Single submitter
- c.1204+14A>G Single submitter
- c.1204+8G>A Single submitter
- c.1205-17C>T Single submitter
- c.1205-19del Single submitter
- c.132+13T>A Single submitter
- c.132+17_132+18del Single submitter
- c.132+17A>G Single submitter
- c.133-14A>T Single submitter
- c.133-17C>A Single submitter
- c.133-5C>T Single submitter
- c.1336+16C>T Single submitter
- c.1336+18A>G Single submitter
- c.1337-16T>C Single submitter
- c.1337-16T>G Single submitter
- c.1337-17G>A Single submitter
- c.178+12T>C Single submitter
- c.178+13A>T Single submitter
- c.178+14G>A Single submitter
- c.178+19A>G Single submitter
- c.179-19C>T Single submitter
- c.179-4T>C Single submitter
- c.179-8A>C Single submitter
- c.284+12C>G Single submitter
- c.284+14A>G Single submitter
- c.284+15del Single submitter
- c.284+18C>T Single submitter
- c.284+19G>T Single submitter
- c.284+7G>T Single submitter
- c.284+8CT[4] Single submitter
- c.284+9T>C Single submitter
- c.285-15G>A Single submitter
- c.285-16T>G Single submitter
- c.285-19A>T Single submitter
- c.383+10C>G Single submitter
- c.384-18G>A Single submitter
- c.384-19T>C Single submitter
- c.487+14C>A Single submitter
- c.487+7A>G Single submitter
- c.488-11T>G Single submitter
- c.488-18_488-17insAA Single submitter
- c.488-5C>T Single submitter
- c.488-9C>T Single submitter
- c.638-12del Single submitter
- c.638-13C>T Single submitter
- c.638-9T>A Single submitter
- c.790+10C>T Single submitter
- c.790+11G>A Single submitter
- c.790+15C>T Single submitter
- c.790+16G>A Single submitter
- c.790+18G>T Single submitter
- c.790+19G>A Single submitter
- c.790+20A>T Single submitter
- c.791-20G>A Single submitter
- c.791-8C>A Single submitter
- c.973+10T>C Single submitter
- c.974-12C>T Single submitter
- c.974-18T>C Single submitter
- p.Ala102= Single submitter
- p.Ala139= Single submitter
- p.Ala239= Single submitter
- p.Ala286= Single submitter
- p.Ala291= Single submitter
- p.Ala349= Single submitter
- p.Ala356= Single submitter
- p.Ala399= Single submitter
- p.Ala414= Single submitter
- p.Ala503= Single submitter
- p.Arg186= Single submitter
- p.Arg369= Single submitter
- p.Arg464= Single submitter
- p.Asn190= Single submitter
- p.Asn395= Single submitter
- p.Asp14= Single submitter
- p.Asp173= Single submitter
- p.Asp18= Single submitter
- p.Asp300= Single submitter
- p.Asp346= Single submitter
- p.Asp80= Single submitter
- p.Asp81= Single submitter
- p.Gln42= Single submitter
- p.Gln494= Single submitter
- p.Gln509= Single submitter
- p.Gln54= Single submitter
- p.Glu28Gly Single submitter
- p.Glu353= Single submitter
- p.Glu47= Single submitter
- p.Glu505= Single submitter
- p.Gly336= Single submitter
- p.Gly53= Single submitter
- p.His78= Single submitter
- p.Ile113= Single submitter
- p.Ile195= Single submitter
- p.Ile204= Single submitter
- p.Ile242= Single submitter
- p.Ile431= Single submitter
- p.Leu12= Single submitter
- p.Leu222= Single submitter
- p.Leu293= Single submitter
- p.Leu297= Single submitter
- p.Leu302= Single submitter
- p.Leu432= Single submitter
- p.Leu51= Single submitter
- p.Lys108= Single submitter
- p.Lys224= Single submitter
- p.Lys251= Single submitter
- p.Lys343= Single submitter
- p.Lys404= Single submitter
- p.Lys483= Single submitter
- p.Lys86= Single submitter
- p.Lys91= Single submitter
- p.Phe330= Single submitter
- p.Phe417= Single submitter
- p.Pro146= Single submitter
- p.Pro174= Single submitter
- p.Pro229= Single submitter
- p.Pro52= Single submitter
- p.Ser205= Single submitter
- p.Ser326= Single submitter
- p.Ser376= Single submitter
- p.Ser457= Single submitter
- p.Ser495= Single submitter
- p.Thr107= Single submitter
- p.Thr160= Single submitter
- p.Thr270= Single submitter
- p.Thr281= Single submitter
- p.Thr296= Single submitter
- p.Thr319= Single submitter
- p.Thr37= Single submitter
- p.Thr438= Single submitter
- p.Thr448= Single submitter
- p.Thr454= Single submitter
- p.Thr504= Single submitter
- p.Tyr117= Single submitter
- p.Tyr193= Single submitter
- p.Tyr265= Single submitter
- p.Tyr266= Single submitter
- p.Tyr306= Single submitter
- p.Tyr434= Single submitter
- p.Val92= Single submitter
Uncertain significance 126
- p.Ala150Thr Multiple submitters Inborn genetic diseases ⚠
- p.Ala70Thr Multiple submitters Inborn genetic diseases ⚠
- p.Arg360Trp Multiple submitters Inborn genetic diseases ⚠
- p.Glu47Asp Multiple submitters Inborn genetic diseases ⚠
- p.Ile227Val Multiple submitters ⚠
- p.Ser333Asn Multiple submitters Inborn genetic diseases
- p.Thr30Ala Multiple submitters Inborn genetic diseases ⚠
- p.Val45Ile Multiple submitters Inborn genetic diseases ⚠
- c.1050+6A>G Single submitter
- c.1204+5G>A Single submitter
- c.1336+2T>A Single submitter
- c.178+4T>C Single submitter
- c.179-3T>C Single submitter
- c.285-3T>C Single submitter
- c.383+1G>A Single submitter
- c.488-3T>C Single submitter
- c.790+5dup Single submitter
- c.791-9_791-8delinsAA Single submitter
- c.974-3T>C Single submitter
- p.Ala139Ser Single submitter
- p.Ala139Thr Single submitter ⚠
- p.Ala150Ser Single submitter ⚠
- p.Ala152Thr Single submitter
- p.Ala215Thr Single submitter ⚠
- p.Ala273Val Single submitter ⚠
- p.Ala307Thr Single submitter Inborn genetic diseases ⚠
- p.Ala450Gly Single submitter ⚠
- p.Ala455Thr Single submitter ⚠
- p.Arg170Lys Single submitter
- p.Arg244Trp Single submitter Inborn genetic diseases ⚠
- p.Arg25Cys Single submitter ⚠
- p.Arg25His Single submitter ⚠
- p.Arg311Lys Single submitter ⚠
- p.Arg360Gln Single submitter ⚠
- p.Arg360Leu Single submitter Inborn genetic diseases ⚠
- p.Arg366Gln Single submitter ⚠
- p.Arg366Trp Single submitter ⚠
- p.Arg447Thr Single submitter ⚠
- p.Arg464Cys Single submitter ⚠
- p.Asn268Ser Single submitter ⚠
- p.Asn395Ser Single submitter ⚠
- p.Asn416Thr Single submitter ⚠
- p.Asp133Gly Single submitter ⚠
- p.Asp15Gly Single submitter ⚠
- p.Asp178Gly Single submitter
- p.Asp189Ala Single submitter Inborn genetic diseases ⚠
- p.Asp206Asn Single submitter ⚠
- p.Asp238Val Single submitter Inborn genetic diseases ⚠
- p.Asp334His Single submitter ⚠
- p.Asp334Val Single submitter ⚠
- p.Asp451Glu Single submitter ⚠
- p.Asp470Gly Single submitter ⚠
- p.Asp66Val Single submitter ⚠
- p.Cys203Phe Single submitter ⚠
- p.Cys219Phe Single submitter ⚠
- p.Gln41Arg Single submitter ⚠
- p.Glu159Lys Single submitter ⚠
- p.Glu260Lys Single submitter ⚠
- p.Glu312Lys Single submitter Inborn genetic diseases ⚠
- p.Glu313Asp Single submitter ⚠
- p.Glu377Lys Single submitter
- p.Glu482Gly Single submitter ⚠
- p.Glu62Lys Single submitter ⚠
- p.Glu88Asp Single submitter ⚠
- p.Gly163Val Single submitter autoinflammatory disease, systemic, with vasculitis ⚠
- p.Gly402Asp Single submitter Inborn genetic diseases ⚠
- p.Gly446= Single submitter
- p.Gly76Ser Single submitter ⚠
- p.Gly76Val Single submitter ⚠
- p.Gly8Glu Single submitter ⚠
- p.His176Pro Single submitter ⚠
- p.His96Gln Single submitter ⚠
- p.Ile134Met Single submitter ⚠
- p.Ile134Val Single submitter ⚠
- p.Ile227Phe Single submitter ⚠
- p.Ile317Val Single submitter ⚠
- p.Ile4Val Single submitter ⚠
- p.Leu105Pro Single submitter ⚠
- p.Leu106Ser Single submitter ⚠
- p.Leu374Gln Single submitter ⚠
- p.Leu379Phe Single submitter ⚠
- p.Lys109Asn Single submitter Inborn genetic diseases ⚠
- p.Lys120Arg Single submitter ⚠
- p.Lys120Ile Single submitter ⚠
- p.Lys132Arg Single submitter ⚠
- p.Lys230Asn Single submitter ⚠
- p.Lys338Arg Single submitter ⚠
- p.Lys91Asn Single submitter ⚠
- p.Met1Thr Single submitter
- p.Met207Leu Single submitter ⚠
- p.Met380fs Single submitter
- p.Met380Val Single submitter Inborn genetic diseases ⚠
- p.Met478Thr Single submitter ⚠
- p.Phe56Leu Single submitter ⚠
- p.Pro202Ala Single submitter ⚠
- p.Pro202Ser Single submitter ⚠
- p.Pro52Arg Single submitter ⚠
- p.Pro73Ala Single submitter ⚠
- p.Pro79Leu Single submitter ⚠
- p.Ser11Gly Single submitter ⚠
- p.Ser164Asn Single submitter
- p.Ser205Gly Single submitter ⚠
- p.Ser326Cys Single submitter Inborn genetic diseases ⚠
- p.Ser457Cys Single submitter ⚠
- p.Ser457Phe Single submitter ⚠
- p.Ser83Cys Single submitter ⚠
- p.Thr107Arg Single submitter ⚠
- p.Thr126Ile Single submitter ⚠
- p.Thr200Ser Single submitter ⚠
- p.Thr21Ser Single submitter ⚠
- p.Thr296Ala Single submitter ⚠
- p.Thr310Ser Single submitter autoinflammatory disease, systemic, with vasculitis ⚠
- p.Thr37Ala Single submitter ⚠
- p.Thr37Met Single submitter ⚠
- p.Trp480Cys Single submitter Inborn genetic diseases ⚠
- p.Tyr265Cys Single submitter ⚠
- p.Tyr460fs Single submitter
- p.Val169Leu Single submitter
- p.Val24= Single submitter
- p.Val339Gly Single submitter
- p.Val426Met Single submitter ⚠
- p.Val437Ala Single submitter ⚠
- p.Val45Phe Single submitter Inborn genetic diseases ⚠
- p.Val496Ile Single submitter ⚠
- p.Val68Ala Single submitter ⚠
- p.Val92Ile Single submitter ⚠