F10 — 160 ClinVar variants
All ClinVar germline F10 variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 84 flagged for review →
19 Pathogenic · 25 Likely pathogenic · 9 Conflicting · 17 Benign · 5 Benign/Likely benign · 7 Likely benign · 78 Uncertain significance
Full F10 gene report on Sugi Atlas → Gene function, pathways, protein structure, constraint & interactions⚑ Evidence disagreements 84
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 vs ClinVar 3
ClinVar calls these pathogenic, but the computational predictors lean tolerated — the highest-value review flag.
-
F10 p.Gly21Arg
Pathogenic
Multiple submitters
factor X deficiency
-
F10 p.Thr358Met
Likely pathogenic
Single submitter
congenital factor X deficiency
-
F10 p.Glu72Gln
Pathogenic
No assertion criteria
factor X deficiency
Predictors agree, ClinVar conflicts 5
ClinVar submitters conflict, but the independent predictors unanimously agree — a QC review flag, not a reclassification.
-
F10 p.Gly134Arg
Conflicting
Single submitter
congenital factor X deficiency
-
F10 p.Gly442Asp
Conflicting
Single submitter
congenital factor X deficiency
-
F10 p.Ile451Leu
Conflicting
Single submitter
congenital factor X deficiency
-
F10 p.Lys316Arg
Conflicting
Single submitter
congenital factor X deficiency
-
F10 p.Met48Leu
Conflicting
Single submitter
congenital factor X deficiency
Predictors lean, ClinVar uncertain 48
ClinVar classifies these uncertain (VUS), but the independent predictors unanimously lean one way — a triage signal for review, not a reclassification.
-
F10 p.Arg291Gln
Uncertain significance
Multiple submitters
factor X deficiency
-
F10 p.Gly154Arg
Uncertain significance
Multiple submitters
congenital factor X deficiency
-
F10 p.Pro472Leu
Uncertain significance
Multiple submitters
congenital factor X deficiency
-
F10 p.Thr409Ile
Uncertain significance
Multiple submitters
congenital factor X deficiency
-
F10 p.Ala185Asp
Uncertain significance
Single submitter
Inborn genetic diseases
-
F10 p.Ala250Val
Uncertain significance
Single submitter
Inborn genetic diseases
- F10 p.Ala301Val Uncertain significance Single submitter
-
F10 p.Ala36Glu
Uncertain significance
Single submitter
factor X deficiency
-
F10 p.Ala457Thr
Uncertain significance
Single submitter
Inborn genetic diseases
-
F10 p.Arg179Cys
Uncertain significance
Single submitter
congenital factor X deficiency
- F10 p.Arg182Met Uncertain significance Single submitter
-
F10 p.Arg234Ser
Uncertain significance
Single submitter
congenital factor X deficiency
-
F10 p.Arg27His
Uncertain significance
Single submitter
factor X deficiency
-
F10 p.Arg28Ser
Uncertain significance
Single submitter
factor X deficiency
-
F10 p.Arg28Thr
Uncertain significance
Single submitter
Inborn genetic diseases
-
F10 p.Arg3Cys
Uncertain significance
Single submitter
congenital factor X deficiency
- F10 p.Arg445Pro Uncertain significance Single submitter
-
F10 p.Arg469Lys
Uncertain significance
Single submitter
congenital factor X deficiency
-
F10 p.Asp216Asn
Uncertain significance
Single submitter
congenital factor X deficiency
-
F10 p.Asp413Asn
Uncertain significance
Single submitter
congenital factor X deficiency
- F10 p.Cys110Arg Uncertain significance Single submitter
-
F10 p.Cys277Ser
Uncertain significance
Single submitter
factor X deficiency
-
F10 p.Cys90Gly
Uncertain significance
Single submitter
Inborn genetic diseases
-
F10 p.Gln30Arg
Uncertain significance
Single submitter
factor X deficiency
-
F10 p.Gln89His
Uncertain significance
Single submitter
Inborn genetic diseases
-
F10 p.Glu304Asp
Uncertain significance
Single submitter
Inborn genetic diseases
- F10 p.Glu369Lys Uncertain significance Single submitter
-
F10 p.Glu441Lys
Uncertain significance
Single submitter
congenital factor X deficiency
-
F10 p.Glu66Val
Uncertain significance
Single submitter
congenital factor X deficiency
- F10 p.Gly106Arg Uncertain significance Single submitter
-
F10 p.Gly299Ser
Uncertain significance
Single submitter
Inborn genetic diseases
-
F10 p.Gly365Ala
Uncertain significance
Single submitter
congenital factor X deficiency
-
F10 p.Gly365Arg
Uncertain significance
Single submitter
Inborn genetic diseases
- F10 p.His423Gln Uncertain significance Single submitter
-
F10 p.Ile323Thr
Uncertain significance
Single submitter
Inborn genetic diseases
-
F10 p.Ile397Val
Uncertain significance
Single submitter
Inborn genetic diseases
-
F10 p.Lys410Gln
Uncertain significance
Single submitter
Inborn genetic diseases
-
F10 p.Met336Val
Uncertain significance
Single submitter
Inborn genetic diseases
-
F10 p.Met58Ile
Uncertain significance
Single submitter
Inborn genetic diseases
-
F10 p.Pro195Arg
Uncertain significance
Single submitter
congenital factor X deficiency
- F10 p.Pro331Leu Uncertain significance Single submitter
-
F10 p.Ser11Ile
Uncertain significance
Single submitter
Inborn genetic diseases
-
F10 p.Ser197Thr
Uncertain significance
Single submitter
Inborn genetic diseases
-
F10 p.Thr293Met
Uncertain significance
Single submitter
congenital factor X deficiency
-
F10 p.Thr399Ala
Uncertain significance
Single submitter
Inborn genetic diseases
-
F10 p.Trp81Gly
Uncertain significance
Single submitter
congenital factor X deficiency
-
F10 p.Val424Leu
Uncertain significance
Single submitter
Inborn genetic diseases
-
F10 p.Pro422Ala
Uncertain significance
No assertion criteria
F10-related disorder
Predictors split 28
The independent predictors disagree with each other — read with care.
-
F10 p.Glu306Lys
Uncertain significance
Multiple submitters
congenital factor X deficiency
- F10 p.Ala67Val Uncertain significance Single submitter
-
F10 p.Arg180Gly
Uncertain significance
Single submitter
Inborn genetic diseases
- F10 p.Arg327Trp Uncertain significance Single submitter
-
F10 p.Arg346Cys
Likely pathogenic
Single submitter
congenital factor X deficiency
-
F10 p.Arg366His
Uncertain significance
Single submitter
congenital factor X deficiency
-
F10 p.Asn97Lys
Uncertain significance
Single submitter
Inborn genetic diseases
-
F10 p.Asp159Asn
Uncertain significance
Single submitter
Inborn genetic diseases
-
F10 p.Asp463His
Uncertain significance
Single submitter
factor X deficiency
- F10 p.Cys246Tyr Uncertain significance Single submitter
-
F10 p.Glu142Lys
Conflicting
Single submitter
congenital factor X deficiency
-
F10 p.Glu268Lys
Uncertain significance
Single submitter
Inborn genetic diseases
-
F10 p.Glu294Asp
Uncertain significance
Single submitter
Inborn genetic diseases
-
F10 p.Glu54Gly
Likely pathogenic
Single submitter
congenital factor X deficiency
-
F10 p.Glu54Lys
Conflicting
Single submitter
factor X deficiency
-
F10 p.Gly168Glu
Likely benign
Single submitter
Inborn genetic diseases
-
F10 p.Gly51Glu
Uncertain significance
Single submitter
factor X deficiency
-
F10 p.Ile26Thr
Uncertain significance
Single submitter
Inborn genetic diseases
-
F10 p.Leu10Phe
Uncertain significance
Single submitter
factor X deficiency
-
F10 p.Leu35Pro
Uncertain significance
Single submitter
Inborn genetic diseases
-
F10 p.Ser93Arg
Uncertain significance
Single submitter
Inborn genetic diseases
-
F10 p.Thr483Met
Uncertain significance
Single submitter
Inborn genetic diseases
- F10 p.Tyr108Phe Uncertain significance Single submitter
-
F10 p.Arg287Trp
Pathogenic
No assertion criteria
factor X deficiency
-
F10 p.Asp408Asn
Uncertain significance
No assertion criteria
Abnormal bleeding
-
F10 p.Glu47Gly
Pathogenic
No assertion criteria
factor X deficiency
-
F10 p.Glu69Lys
Likely pathogenic
No assertion criteria
congenital factor X deficiency
-
F10 p.Val338Met
Pathogenic
No assertion criteria
factor X deficiency
All F10 variants
Pathogenic 19
- p.Gly21Arg Multiple submitters factor X deficiency ⚠
- c.71-1G>C Single submitter congenital factor X deficiency
- p.Cys172fs Single submitter factor X deficiency
- p.Gly244Arg Single submitter
- p.Gly406Ser Single submitter congenital factor X deficiency
- p.Trp461Ter Single submitter
- p.Arg287Trp No assertion criteria factor X deficiency ⚠
- p.Arg366Cys No assertion criteria factor X deficiency
- p.Asp103His No assertion criteria factor X deficiency
- p.Asp322Asn No assertion criteria factor X deficiency
- p.Glu47Gly No assertion criteria factor X deficiency ⚠
- p.Glu56fs No assertion criteria congenital factor X deficiency
- p.Glu72Gln No assertion criteria factor X deficiency ⚠
- p.Gly289Arg No assertion criteria Factor x deficiency, autosomal dominant
- p.Ile271_Leu272insTer No assertion criteria factor X deficiency
- p.Pro383Ser No assertion criteria factor X deficiency
- p.Ser374Pro No assertion criteria factor X deficiency
- p.Tyr279Ter No assertion criteria congenital factor X deficiency
- p.Val338Met No assertion criteria factor X deficiency ⚠
Likely pathogenic 25
- p.Gly363Ser Multiple submitters congenital factor X deficiency
- p.Gly450Arg Multiple submitters congenital factor X deficiency
- c.232-2563_503-451del Single submitter congenital factor X deficiency
- c.257-1G>C Single submitter
- c.748-50_865+35del Single submitter Abnormal bleeding
- p.Ala444Val Single submitter congenital factor X deficiency
- p.Arg346Cys Single submitter congenital factor X deficiency ⚠
- p.Arg40Thr Single submitter congenital factor X deficiency
- p.Arg68_Glu69insSerTyrGluGluAlaArg Single submitter congenital factor X deficiency
- p.Asp418His Single submitter congenital factor X deficiency
- p.Asp86Asn Single submitter congenital factor X deficiency
- p.Cys404Arg Single submitter congenital factor X deficiency
- p.Cys90Ter Single submitter congenital factor X deficiency
- p.Gln416Leu Single submitter
- p.Glu54Gly Single submitter congenital factor X deficiency ⚠
- p.Glu56Gly Single submitter congenital factor X deficiency
- p.Leu272Pro Single submitter congenital factor X deficiency
- p.Lys100fs Single submitter congenital factor X deficiency
- p.Lys102fs Single submitter congenital factor X deficiency
- p.Lys83fs Single submitter congenital factor X deficiency
- p.Phe71Ser Single submitter congenital factor X deficiency
- p.Pro383Ala Single submitter congenital factor X deficiency
- p.Thr358Met Single submitter congenital factor X deficiency ⚠
- c.70+1G>A No assertion criteria F10-related disorder
- p.Glu69Lys No assertion criteria congenital factor X deficiency ⚠
Conflicting classifications of pathogenicity 9
- p.Glu142Lys Single submitter congenital factor X deficiency ⚠
- p.Glu54Lys Single submitter factor X deficiency ⚠
- p.Gly134Arg Single submitter congenital factor X deficiency ⚠
- p.Gly442Asp Single submitter congenital factor X deficiency ⚠
- p.Ile451Leu Single submitter congenital factor X deficiency ⚠
- p.Leu19= Single submitter congenital factor X deficiency
- p.Lys316Arg Single submitter congenital factor X deficiency ⚠
- p.Met48Leu Single submitter congenital factor X deficiency ⚠
- p.Pro344= Single submitter congenital factor X deficiency
Benign 17
- c.231+295T>G Multiple submitters
- c.231+64C>T Multiple submitters
- c.231+89G>A Multiple submitters
- c.232-17T>C Multiple submitters congenital factor X deficiency
- c.256+98C>A Multiple submitters
- c.370+65G>A Multiple submitters
- c.865+33A>G Multiple submitters congenital factor X deficiency
- c.865+90G>C Multiple submitters
- p.Arg37= Multiple submitters congenital factor X deficiency
- p.Arg372Pro Multiple submitters congenital factor X deficiency
- p.Gln30His Multiple submitters congenital factor X deficiency
- p.Gly192Arg Multiple submitters congenital factor X deficiency
- p.Thr264= Multiple submitters congenital factor X deficiency
- c.502+288A>G Single submitter
- c.502+307T>C Single submitter
- c.70+270A>G Single submitter
- c.71-42_71-41insAGAGGAGCCTGGGTGA Single submitter
Benign/Likely benign 5
Likely benign 7
- c.747+8T>C Single submitter congenital factor X deficiency
- p.Gln98Glu Single submitter Inborn genetic diseases
- p.Gly168Glu Single submitter Inborn genetic diseases ⚠
- p.Leu10= Single submitter
- p.Lys49= Single submitter
- p.Ser93Asn Single submitter Inborn genetic diseases
- p.Gly259= No assertion criteria F10-related disorder
Uncertain significance 78
- p.Arg291Gln Multiple submitters factor X deficiency ⚠
- p.Glu306Lys Multiple submitters congenital factor X deficiency ⚠
- p.Gly106= Multiple submitters congenital factor X deficiency
- p.Gly154Arg Multiple submitters congenital factor X deficiency ⚠
- p.Pro472Leu Multiple submitters congenital factor X deficiency ⚠
- p.Thr409Ile Multiple submitters congenital factor X deficiency ⚠
- c.257-12C>T Single submitter congenital factor X deficiency
- c.747+11G>A Single submitter congenital factor X deficiency
- c.-10C>G Single submitter congenital factor X deficiency
- c.-60G>A Single submitter congenital factor X deficiency
- p.Ala185Asp Single submitter Inborn genetic diseases ⚠
- p.Ala250Val Single submitter Inborn genetic diseases ⚠
- p.Ala301Val Single submitter ⚠
- p.Ala36Glu Single submitter factor X deficiency ⚠
- p.Ala405= Single submitter congenital factor X deficiency
- p.Ala457Thr Single submitter Inborn genetic diseases ⚠
- p.Ala67Val Single submitter ⚠
- p.Arg179Cys Single submitter congenital factor X deficiency ⚠
- p.Arg180Gly Single submitter Inborn genetic diseases ⚠
- p.Arg182Met Single submitter ⚠
- p.Arg234Ser Single submitter congenital factor X deficiency ⚠
- p.Arg27His Single submitter factor X deficiency ⚠
- p.Arg28Ser Single submitter factor X deficiency ⚠
- p.Arg28Thr Single submitter Inborn genetic diseases ⚠
- p.Arg327Trp Single submitter ⚠
- p.Arg366His Single submitter congenital factor X deficiency ⚠
- p.Arg3Cys Single submitter congenital factor X deficiency ⚠
- p.Arg445Pro Single submitter ⚠
- p.Arg469Lys Single submitter congenital factor X deficiency ⚠
- p.Asn97Lys Single submitter Inborn genetic diseases ⚠
- p.Asp159Asn Single submitter Inborn genetic diseases ⚠
- p.Asp216Asn Single submitter congenital factor X deficiency ⚠
- p.Asp413Asn Single submitter congenital factor X deficiency ⚠
- p.Asp463His Single submitter factor X deficiency ⚠
- p.Cys110Arg Single submitter ⚠
- p.Cys246Tyr Single submitter ⚠
- p.Cys277Ser Single submitter factor X deficiency ⚠
- p.Cys90Gly Single submitter Inborn genetic diseases ⚠
- p.Gln30Arg Single submitter factor X deficiency ⚠
- p.Gln89His Single submitter Inborn genetic diseases ⚠
- p.Glu268Lys Single submitter Inborn genetic diseases ⚠
- p.Glu294Asp Single submitter Inborn genetic diseases ⚠
- p.Glu304Asp Single submitter Inborn genetic diseases ⚠
- p.Glu369Lys Single submitter ⚠
- p.Glu441Lys Single submitter congenital factor X deficiency ⚠
- p.Glu66Val Single submitter congenital factor X deficiency ⚠
- p.Gly106Arg Single submitter ⚠
- p.Gly299Ser Single submitter Inborn genetic diseases ⚠
- p.Gly365Ala Single submitter congenital factor X deficiency ⚠
- p.Gly365Arg Single submitter Inborn genetic diseases ⚠
- p.Gly51Glu Single submitter factor X deficiency ⚠
- p.Gly87= Single submitter congenital factor X deficiency
- p.His423Gln Single submitter ⚠
- p.Ile26Thr Single submitter Inborn genetic diseases ⚠
- p.Ile323Thr Single submitter Inborn genetic diseases ⚠
- p.Ile397Val Single submitter Inborn genetic diseases ⚠
- p.Leu10Phe Single submitter factor X deficiency ⚠
- p.Leu35Pro Single submitter Inborn genetic diseases ⚠
- p.Lys410Gln Single submitter Inborn genetic diseases ⚠
- p.Met336Val Single submitter Inborn genetic diseases ⚠
- p.Met58Ile Single submitter Inborn genetic diseases ⚠
- p.Phe116= Single submitter congenital factor X deficiency
- p.Pro195Arg Single submitter congenital factor X deficiency ⚠
- p.Pro331Leu Single submitter ⚠
- p.Ser11Ile Single submitter Inborn genetic diseases ⚠
- p.Ser197Thr Single submitter Inborn genetic diseases ⚠
- p.Ser93Arg Single submitter Inborn genetic diseases ⚠
- p.Thr211= Single submitter congenital factor X deficiency
- p.Thr293Met Single submitter congenital factor X deficiency ⚠
- p.Thr399Ala Single submitter Inborn genetic diseases ⚠
- p.Thr483Met Single submitter Inborn genetic diseases ⚠
- p.Trp81Gly Single submitter congenital factor X deficiency ⚠
- p.Tyr108Phe Single submitter ⚠
- p.Tyr449= Single submitter congenital factor X deficiency
- p.Val424Leu Single submitter Inborn genetic diseases ⚠
- p.Asp408Asn No assertion criteria Abnormal bleeding ⚠
- p.Pro422Ala No assertion criteria F10-related disorder ⚠
- p.Thr77= No assertion criteria congenital factor X deficiency