Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
3 | g.138946022_138946351del | CA2739278055 | FOXL2 | c.376_705del (p.Asn126_Gly235del) | |
3 | g.138946247_138946370dup | CA10654883 | FOXL2 | c.353_476dup (p.His159GlnfsTer?) | ClinVar dbSNP |
3 | g.138946312_138946313del | CA2586973040 | FOXL2 | c.411_412del (p.Met137IlefsTer?) | |
3 | g.138946312C>A | CA354706340 | FOXL2 | c.411G>T (p.Met137Ile) | dbSNP |
3 | g.138946312C= | CA1405402457 | FOXL2 | c.411G= (p.Met137=) | |
3 | g.138946312C>G | CA354706338 | FOXL2 | c.411G>C (p.Met137Ile) | |
3 | g.138946312C>T | CA354706330 | FOXL2 | c.411G>A (p.Met137Ile) | dbSNP gnomAD v3 gnomAD v4 |
3 | g.138946313A>C | CA354706343 | FOXL2 | c.410T>G (p.Met137Arg) | dbSNP |
3 | g.138946313A>G | CA354706345 | FOXL2 | c.410T>C (p.Met137Thr) | dbSNP |
3 | g.138946313A>T | CA354706346 | FOXL2 | c.410T>A (p.Met137Lys) | dbSNP |
3 | g.138946314T>A | CA354706349 | FOXL2 | c.409A>T (p.Met137Leu) | dbSNP |
3 | g.138946314T>C | CA354706350 | FOXL2 | c.409A>G (p.Met137Val) | |
3 | g.138946314T>G | CA354706351 | FOXL2 | c.409A>C (p.Met137Leu) | |
3 | g.138946315G>A | CA2639776 | FOXL2 | c.408C>T (p.Asp136=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
3 | g.138946315G>C | CA354706355 | FOXL2 | c.408C>G (p.Asp136Glu) | dbSNP |
3 | g.138946315G= | CA1405402458 | FOXL2 | c.408C= (p.Asp136=) | |
3 | g.138946315G>T | CA354706357 | FOXL2 | c.408C>A (p.Asp136Glu) | |
3 | g.138946316T>A | CA354706360 | FOXL2 | c.407A>T (p.Asp136Val) | dbSNP |
3 | g.138946316T>C | CA83970213 | FOXL2 | c.407A>G (p.Asp136Gly) | dbSNP |
3 | g.138946316T>G | CA83970226 | FOXL2 | c.407A>C (p.Asp136Ala) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
3 | g.138946316T= | CA1405402459 | FOXL2 | c.407A= (p.Asp136=) | |
3 | g.138946317C>A | CA354706366 | FOXL2 | c.406G>T (p.Asp136Tyr) | |
3 | g.138946317C>G | CA354706368 | FOXL2 | c.406G>C (p.Asp136His) | dbSNP |
3 | g.138946317C>T | CA354706364 | FOXL2 | c.406G>A (p.Asp136Asn) | dbSNP |
3 | g.138946318T>A | CA354706370 | FOXL2 | c.405A>T (p.Glu135Asp) | dbSNP |
3 | g.138946318T>C | CA436094580 | FOXL2 | c.405A>G (p.Glu135=) | gnomAD v4 COSMIC |
3 | g.138946318T>G | CA354706369 | FOXL2 | c.405A>C (p.Glu135Asp) | |
3 | g.138946319T>A | CA354706372 | FOXL2 | c.404A>T (p.Glu135Val) | dbSNP |
3 | g.138946319T>C | CA354706374 | FOXL2 | c.404A>G (p.Glu135Gly) | dbSNP COSMIC |
3 | g.138946319T>G | CA354706376 | FOXL2 | c.404A>C (p.Glu135Ala) | dbSNP gnomAD v4 |
3 | g.138946320C>A | CA354706378 | FOXL2 | c.403G>T (p.Glu135Ter) | dbSNP |
3 | g.138946320C= | CA1405402460 | FOXL2 | c.403G= (p.Glu135=) | |
3 | g.138946320C>G | CA354706380 | FOXL2 | c.403G>C (p.Glu135Gln) | dbSNP |
3 | g.138946320C>T | CA354706382 | FOXL2 | c.403G>A (p.Glu135Lys) | dbSNP |
3 | g.138946321G>A | CA436094584 | FOXL2 | c.402C>T (p.Cys134=) | dbSNP COSMIC |
3 | g.138946321G>C | CA16602790 | FOXL2 | c.402C>G (p.Cys134Trp) | ClinVar dbSNP COSMIC |
3 | g.138946321G= | CA1405402461 | FOXL2 | c.402C= (p.Cys134=) | |
3 | g.138946321G>T | CA354706384 | FOXL2 | c.402C>A (p.Cys134Ter) | |
3 | g.138946322C>A | CA354706386 | FOXL2 | c.401G>T (p.Cys134Phe) | dbSNP |
3 | g.138946322C= | CA1405402462 | FOXL2 | c.401G= (p.Cys134=) | |
3 | g.138946322C>G | CA2639777 | FOXL2 | c.401G>C (p.Cys134Ser) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
3 | g.138946322C>T | CA354706392 | FOXL2 | c.401G>A (p.Cys134Tyr) | dbSNP |
3 | g.138946325_138946335del | CA2739278056 | FOXL2 | c.391_401del (p.Asp131ArgfsTer?) | |
3 | g.138946323A>C | CA354706397 | FOXL2 | c.400T>G (p.Cys134Gly) | dbSNP gnomAD v4 |
3 | g.138946323A>G | CA354706396 | FOXL2 | c.400T>C (p.Cys134Arg) | dbSNP |
3 | g.138946323A>T | CA354706394 | FOXL2 | c.400T>A (p.Cys134Ser) | dbSNP |
3 | g.138946323_138946324delinsAG | CA1405402463 | FOXL2 | c.399_400delinsCT (p.Ala133=) | |
3 | g.138946324G>A | CA83970232 | FOXL2 | c.399C>T (p.Ala133=) | dbSNP gnomAD v2 gnomAD v4 |
3 | g.138946324G>C | CA436094590 | FOXL2 | c.399C>G (p.Ala133=) | gnomAD v4 |
3 | g.138946324G= | CA1405402464 | FOXL2 | c.399C= (p.Ala133=) |