Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.138946022_138946351delCA2739278055FOXL2c.376_705del (p.Asn126_Gly235del)
3g.138946247_138946370dupCA10654883FOXL2c.353_476dup (p.His159GlnfsTer?)
ClinVar dbSNP
3g.138946312_138946313delCA2586973040FOXL2c.411_412del (p.Met137IlefsTer?)
3g.138946312C>ACA354706340FOXL2c.411G>T (p.Met137Ile)
dbSNP
3g.138946312C=CA1405402457FOXL2c.411G= (p.Met137=)
3g.138946312C>GCA354706338FOXL2c.411G>C (p.Met137Ile)
3g.138946312C>TCA354706330FOXL2c.411G>A (p.Met137Ile)
dbSNP gnomAD v3 gnomAD v4
3g.138946313A>CCA354706343FOXL2c.410T>G (p.Met137Arg)
dbSNP
3g.138946313A>GCA354706345FOXL2c.410T>C (p.Met137Thr)
dbSNP
3g.138946313A>TCA354706346FOXL2c.410T>A (p.Met137Lys)
dbSNP
3g.138946314T>ACA354706349FOXL2c.409A>T (p.Met137Leu)
dbSNP
3g.138946314T>CCA354706350FOXL2c.409A>G (p.Met137Val)
3g.138946314T>GCA354706351FOXL2c.409A>C (p.Met137Leu)
3g.138946315G>ACA2639776FOXL2c.408C>T (p.Asp136=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.138946315G>CCA354706355FOXL2c.408C>G (p.Asp136Glu)
dbSNP
3g.138946315G=CA1405402458FOXL2c.408C= (p.Asp136=)
3g.138946315G>TCA354706357FOXL2c.408C>A (p.Asp136Glu)
3g.138946316T>ACA354706360FOXL2c.407A>T (p.Asp136Val)
dbSNP
3g.138946316T>CCA83970213FOXL2c.407A>G (p.Asp136Gly)
dbSNP
3g.138946316T>GCA83970226FOXL2c.407A>C (p.Asp136Ala)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.138946316T=CA1405402459FOXL2c.407A= (p.Asp136=)
3g.138946317C>ACA354706366FOXL2c.406G>T (p.Asp136Tyr)
3g.138946317C>GCA354706368FOXL2c.406G>C (p.Asp136His)
dbSNP
3g.138946317C>TCA354706364FOXL2c.406G>A (p.Asp136Asn)
dbSNP
3g.138946318T>ACA354706370FOXL2c.405A>T (p.Glu135Asp)
dbSNP
3g.138946318T>CCA436094580FOXL2c.405A>G (p.Glu135=)
gnomAD v4 COSMIC
3g.138946318T>GCA354706369FOXL2c.405A>C (p.Glu135Asp)
3g.138946319T>ACA354706372FOXL2c.404A>T (p.Glu135Val)
dbSNP
3g.138946319T>CCA354706374FOXL2c.404A>G (p.Glu135Gly)
dbSNP COSMIC
3g.138946319T>GCA354706376FOXL2c.404A>C (p.Glu135Ala)
dbSNP gnomAD v4
3g.138946320C>ACA354706378FOXL2c.403G>T (p.Glu135Ter)
dbSNP
3g.138946320C=CA1405402460FOXL2c.403G= (p.Glu135=)
3g.138946320C>GCA354706380FOXL2c.403G>C (p.Glu135Gln)
dbSNP
3g.138946320C>TCA354706382FOXL2c.403G>A (p.Glu135Lys)
dbSNP
3g.138946321G>ACA436094584FOXL2c.402C>T (p.Cys134=)
dbSNP COSMIC
3g.138946321G>CCA16602790FOXL2c.402C>G (p.Cys134Trp)
ClinVar dbSNP COSMIC
3g.138946321G=CA1405402461FOXL2c.402C= (p.Cys134=)
3g.138946321G>TCA354706384FOXL2c.402C>A (p.Cys134Ter)
3g.138946322C>ACA354706386FOXL2c.401G>T (p.Cys134Phe)
dbSNP
3g.138946322C=CA1405402462FOXL2c.401G= (p.Cys134=)
3g.138946322C>GCA2639777FOXL2c.401G>C (p.Cys134Ser)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.138946322C>TCA354706392FOXL2c.401G>A (p.Cys134Tyr)
dbSNP
3g.138946325_138946335delCA2739278056FOXL2c.391_401del (p.Asp131ArgfsTer?)
3g.138946323A>CCA354706397FOXL2c.400T>G (p.Cys134Gly)
dbSNP gnomAD v4
3g.138946323A>GCA354706396FOXL2c.400T>C (p.Cys134Arg)
dbSNP
3g.138946323A>TCA354706394FOXL2c.400T>A (p.Cys134Ser)
dbSNP
3g.138946323_138946324delinsAGCA1405402463FOXL2c.399_400delinsCT (p.Ala133=)
3g.138946324G>ACA83970232FOXL2c.399C>T (p.Ala133=)
dbSNP gnomAD v2 gnomAD v4
3g.138946324G>CCA436094590FOXL2c.399C>G (p.Ala133=)
gnomAD v4
3g.138946324G=CA1405402464FOXL2c.399C= (p.Ala133=)

Number of alleles fetched