Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.138945277_138946050delinsGCGGCTGCAGCAGCTGCGGCTGCAGCCGCGGGCCCCGGTAGCCCTGGCGCGGCCGCTGTGGTCAAGGGGCTGGCGGGCCCGGCCGCCTCGTACGGGCCGTACACACGCGTGCAGAGCATGGCGCTGCCCCCCGGCGTAGTGAACTCGTACAATGGCCTGGGAGGCCCGCCGGCCGCACCCCCGCCTCCGCCGCACCCCCACCCGCATCCGCACGCACACCATCTGCACGCGGCCGCCGCACCGCCGCCTGCCCCACCGCACCACGGGGCCGCCGCGCCGCCGCCGGGCCAGCTCAGCCCTGCCAGCCCAGCCACCGCCGCGCCCCCGGCGCCCGCGCCCACCAGTGCGCCGGGCCTGCAGTTCGCTTGTGCCCGGCAGCCCGAGCTCGCCATGATGCATTGCTCTTACTGGGACCACGACAGCAAGACCGGCGCGCTGCATTCGCGCCTCGATCTCTGAGAGCCCACCGCATGCCGGTGCAGACGGATGCGAGGATGCAGGGACGCGCGACGCCGGCCCCGGTCGCAGCCGACGACGCCGCCGCCAGCCTGACCTCACACCCTCTGGGCCCGCCTCTGGAGCCAGCGCCCAGGGTCCCTCTGTGCTTTTTCGCTTTCCTAAGCTCCTGTCGCTCCTCTTTGTCCCCTCAGTTTATGTCCTCCTGTGCTCACCTCCCTGACCTCTGTGACCTTGCACTCCCCTGGCCTGAAGCTGCCTCTCTGCGCGCTTTCTACTGGGCTCGTCTCTTTCCGGAGCCCCAGCGTCTCCTGCCCACA2580068839FOXL2c.673_*315delinsTGGGCAGGAGACGCTGGGGCTCCGGAAAGAGACGAGCCCAGTAGAAAGCGCGCAGAGAGGCAGCTTCAGGCCAGGGGAGTGCAAGGTCACAGAGGTCAGGGAGGTGAGCACAGGAGGACATAAACTGAGGGGACAAAGAGGAGCGACAGGAGCTTAGGAAAGCGAAAAAGCACAGAGGGACCCTGGGCGCTGGCTCCAGAGGCGGGCCCAGAGGGTGTGAGGTCAGGCTGGCGGCGGCGTCGTCGGCTGCGACCGGGGCCGGCGTCGCGCGTCCCTGCATCCTCGCATCCGTCTGCACCGGCATGCGGTGGGCTCTCAGAGATCGAGGCGCGAATGCAGCGCGCCGGTCTTGCTGTCGTGGTCCCAGTAAGAGCAATGCATCATGGCGAGCTCGGGCTGCCGGGCACAAGCGAACTGCAGGCCCGGCGCACTGGTGGGCGCGGGCGCCGGGGGCGCGGCGGTGGCTGGGCTGGCAGGGCTGAGCTGGCCCGGCGGCGGCGCGGCGGCCCCGTGGTGCGGTGGGGCAGGCGGCGGTGCGGCGGCCGCGTGCAGATGGTGTGCGTGCGGATGCGGGTGGGGGTGCGGCGGAGGCGGGGGTGCGGCCGGCGGGCCTCCCAGGCCATTGTACGAGTTCACTACGCCGGGGGGCAGCGCCATGCTCTGCACGCGTGTGTACGGCCCGTACGAGGCGGCCGGGCCCGCCAGCCCCTTGACCACAGCGGCCGCGCCAGGGCTACCGGGGCCCGCGGCTGCAGCCGCAGCTGCTGCAGCCGC (n.[c.673_*315delinsTGGGCAGGAGACGCTGGGGCTCCGGAAAGAGACGAGCCCAGTAGAAAGCGCGCAGAGAGGCAGCTTCAGGCCAGGGGAGTGCAAGGTCACAGAGGTCAGGGAGGTGAGCACAGGAGGACATAAACTGAGGGGACAAAGAGGAGCGACAGGAGCTTAGGAAAGCGAAAAAGCACAGAGGGACCCTGGGCGCTGGCTCCAGAGGCGGGCCCAGAGGGTGTGAGGTCAGGCTGGCGGCGGCGTCGTCGGCTGCGACCGGGGCCGGCGTCGCGCGTCCCTGCATCCTCGCATCCGTCTGCACCGGCATGCGGTGGGCTCTCAGAGATCGAGGCGCGAATGCAGCGCGCCGGTCTTGCTGTCGTGGTCCCAGTAAGAGCAATGCATCATGGCGAGCTCGGGCTGCCGGGCACAAGCGAACTGCAGGCCCGGCGCACTGGTGGGCGCGGGCGCCGGGGGCGCGGCGGTGGCTGGGCTGGCAGGGCTGAGCTGGCCCGGCGGCGGCGCGGCGGCCCCGTGGTGCGGTGGGGCAGGCGGCGGTGCGGCGGCCGCGTGCAGATGGTGTGCGTGCGGATGCGGGTGGGGGTGCGGCGGAGGCGGGGGTGCGGCCGGCGGGCCTCCCAGGCCATTGTACGAGTTCACTACGCCGGGGGGCAGCGCCATGCTCTGCACGCGTGTGTACGGCCCGTACGAGGCGGCCGGGCCCGCCAGCCCCTTGACCACAGCGGCCGCGCCAGGGCTACCGGGGCCCGCGGCTGCAGCCGCAGCTGCTGCAGCCGC;Ala225TrpfsTer41])
ClinVar
3g.138945725_138945788delinsGGGGGCGCGGCGGTGGCTGGGCTGGCAGGGCTGAGCTGGCCCGGCGGCGGCGCGGCGGCCCCGTCA1405402122FOXL2c.935_998delinsACGGGGCCGCCGCGCCGCCGCCGGGCCAGCTCAGCCCTGCCAGCCCAGCCACCGCCGCGCCCCC (p.His312=)
3g.138945726_138945788delinsCGCCGCCGCCCA913189428FOXL2c.935_997delinsGGCGGCGGCG (p.His312ArgfsTer?)
ClinVar dbSNP
3g.138945774_138945776dupCA899582006FOXL2c.955_957dup (p.Pro319_Gly320insPro)
dbSNP gnomAD v3 gnomAD v4
3g.138945774_138945776delCA546892572FOXL2c.955_957del (p.Pro319del)
dbSNP gnomAD v2
3g.138945773_138945783delCA2586973007FOXL2c.947_957del (p.Ala316GlyfsTer?)
3g.138945775_138945810delCA1054107766FOXL2c.921_956del (p.Ala308_Pro319del)
gnomAD v3 gnomAD v4
3g.138945776_138945783dupCA2586973009FOXL2c.948_955dup (p.Pro319ArgfsTer?)
gnomAD v4
3g.138945776_138945783delCA913189429FOXL2c.948_955del (p.Pro317GlyfsTer?)
ClinVar dbSNP
3g.138945776G>ACA83969672FOXL2c.947C>T (p.Ala316Val)
dbSNP gnomAD v3 gnomAD v4
3g.138945776G>CCA354701623FOXL2c.947C>G (p.Ala316Gly)
3g.138945776G=CA1405402155FOXL2c.947C= (p.Ala316=)
3g.138945776G>TCA354701629FOXL2c.947C>A (p.Ala316Glu)
gnomAD v4
3g.138945785_138945820delCA1054107772FOXL2c.912_947del (p.Pro305_Ala316del)
gnomAD v3 gnomAD v4
3g.138945776_138945777insGTAGTTGCCCTTCTCA2510773779FOXL2c.946_947insAGAAGGGCAACTAC (p.Ala316GlufsTer?)
3g.138945777C>ACA354701654FOXL2c.946G>T (p.Ala316Ser)
gnomAD v4
3g.138945777C=CA1405402156FOXL2c.946G= (p.Ala316=)
3g.138945777C>GCA354701650FOXL2c.946G>C (p.Ala316Pro)
3g.138945777C>TCA354701638FOXL2c.946G>A (p.Ala316Thr)
dbSNP gnomAD v4
3g.138945777dupCA1054107776FOXL2c.946dup (p.Ala316GlyfsTer?)
gnomAD v3 gnomAD v4
3g.138945777_138945778insCCACCACA917019810FOXL2c.945_946insTGGTGG (p.Ala315_Ala316insTrpTrp)
dbSNP
3g.138945778G>ACA436094063FOXL2c.945C>T (p.Ala315=)
dbSNP gnomAD v4
3g.138945778G>CCA436094064FOXL2c.945C>G (p.Ala315=)
gnomAD v4
3g.138945778G=CA1405402157FOXL2c.945C= (p.Ala315=)
3g.138945778G>TCA436094065FOXL2c.945C>A (p.Ala315=)
3g.138945778_138945779insTCA917019811FOXL2c.944_945insA (p.Ala316ArgfsTer?)
dbSNP
3g.138945779G>ACA354701659FOXL2c.944C>T (p.Ala315Val)
gnomAD v4
3g.138945779G>CCA354701660FOXL2c.944C>G (p.Ala315Gly)
3g.138945779G>TCA354701663FOXL2c.944C>A (p.Ala315Asp)
3g.138945779_138945780insTAGTTGCCCTTCTCGAACATGTCTTCGCAGGCCGGGTCCAGCGTCCAGTAGTTGCCCTTGCGCTCGCCGCCGCCCTCGCGCA2604860301FOXL2c.944_945insGCGAGGGCGGCGGCGAGCGCAAGGGCAACTACTGGACGCTGGACCCGGCCTGCGAAGACATGTTCGAGAAGGGCAACTAC (p.Ala316ArgfsTer?)
gnomAD v3 gnomAD v4
3g.138945780_138945787dupCA913189430FOXL2c.937_944dup (p.Ala316GlyfsTer?)
ClinVar dbSNP
3g.138945779_138945780insTAGTTGCCCTTCTCA2572466992FOXL2c.943_944insAGAAGGGCAACTA (p.Ala315GlufsTer?)
3g.138945780C>ACA354701667FOXL2c.943G>T (p.Ala315Ser)
gnomAD v4
3g.138945780C>GCA354701670FOXL2c.943G>C (p.Ala315Pro)
3g.138945780C>TCA354701676FOXL2c.943G>A (p.Ala315Thr)
dbSNP gnomAD v4
3g.138945781G>ACA83969673FOXL2c.942C>T (p.Ala314=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.138945781G>CCA436094069FOXL2c.942C>G (p.Ala314=)
3g.138945781G=CA1405402158FOXL2c.942C= (p.Ala314=)
3g.138945781G>TCA436094070FOXL2c.942C>A (p.Ala314=)
gnomAD v4
3g.138945782G>ACA354701680FOXL2c.941C>T (p.Ala314Val)
dbSNP gnomAD v4
3g.138945782G>CCA354701684FOXL2c.941C>G (p.Ala314Gly)
dbSNP
3g.138945782G=CA1405402159FOXL2c.941C= (p.Ala314=)
3g.138945782G>TCA354701693FOXL2c.941C>A (p.Ala314Asp)
3g.138945783C>ACA354701698FOXL2c.940G>T (p.Ala314Ser)
3g.138945783C=CA1405402160FOXL2c.940G= (p.Ala314=)
3g.138945783C>GCA354701705FOXL2c.940G>C (p.Ala314Pro)
dbSNP
3g.138945783C>TCA354701709FOXL2c.940G>A (p.Ala314Thr)
dbSNP gnomAD v4
3g.138945786delCA2667925279FOXL2c.940del (p.Ala314ProfsTer?)
gnomAD v4
3g.138945784C>ACA436094072FOXL2c.939G>T (p.Gly313=)
gnomAD v4
3g.138945784C>GCA436094074FOXL2c.939G>C (p.Gly313=)

Number of alleles fetched