Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
3 | g.138946022_138946351del | CA2739278055 | FOXL2 | c.376_705del (p.Asn126_Gly235del) | ClinVar |
3 | g.138946247_138946370dup | CA10654883 | FOXL2 | c.353_476dup (p.His159GlnfsTer?) | ClinVar dbSNP |
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?) | ClinVar |
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=) | |
3 | g.138946324G>T | CA436094591 | FOXL2 | c.399C>A (p.Ala133=) | |
3 | g.138946325del | CA913189440 | FOXL2 | c.399del (p.Cys134AlafsTer16) | ClinVar dbSNP |
3 | g.138946325G>A | CA354706401 | FOXL2 | c.398C>T (p.Ala133Val) | dbSNP |
3 | g.138946325G>C | CA354706403 | FOXL2 | c.398C>G (p.Ala133Gly) | dbSNP gnomAD v4 |
3 | g.138946325G>T | CA354706405 | FOXL2 | c.398C>A (p.Ala133Asp) | |
3 | g.138946326C>A | CA354706407 | FOXL2 | c.397G>T (p.Ala133Ser) | dbSNP COSMIC |
3 | g.138946326C>G | CA354706409 | FOXL2 | c.397G>C (p.Ala133Pro) | dbSNP |
3 | g.138946326C>T | CA354706411 | FOXL2 | c.397G>A (p.Ala133Thr) | dbSNP |
3 | g.138946326delinsAT | CA2586973041 | FOXL2 | c.397delinsAT (p.Ala133IlefsTer?) | |
3 | g.138946327C>A | CA436094596 | FOXL2 | c.396G>T (p.Pro132=) | dbSNP |
3 | g.138946327C>G | CA436094597 | FOXL2 | c.396G>C (p.Pro132=) | dbSNP gnomAD v4 |
3 | g.138946327C>T | CA436094598 | FOXL2 | c.396G>A (p.Pro132=) | dbSNP gnomAD v4 |
3 | g.138946328G>A | CA354706413 | FOXL2 | c.395C>T (p.Pro132Leu) | dbSNP |
3 | g.138946328G>C | CA354706414 | FOXL2 | c.395C>G (p.Pro132Arg) | dbSNP |
3 | g.138946328G>T | CA354706418 | FOXL2 | c.395C>A (p.Pro132Gln) | dbSNP |
3 | g.138946329G>A | CA354706421 | FOXL2 | c.394C>T (p.Pro132Ser) | |
3 | g.138946329G>C | CA354706422 | FOXL2 | c.394C>G (p.Pro132Ala) | |
3 | g.138946329G>T | CA354706424 | FOXL2 | c.394C>A (p.Pro132Thr) | COSMIC |
3 | g.138946330G>A | CA436094600 | FOXL2 | c.393C>T (p.Asp131=) | dbSNP |
3 | g.138946330G>C | CA354706429 | FOXL2 | c.393C>G (p.Asp131Glu) | dbSNP |
3 | g.138946330G= | CA1405402465 | FOXL2 | c.393C= (p.Asp131=) | |
3 | g.138946330G>T | CA354706427 | FOXL2 | c.393C>A (p.Asp131Glu) | |
3 | g.138946331T>A | CA354706430 | FOXL2 | c.392A>T (p.Asp131Val) | |
3 | g.138946331T>C | CA354706431 | FOXL2 | c.392A>G (p.Asp131Gly) | |
3 | g.138946331T>G | CA354706432 | FOXL2 | c.392A>C (p.Asp131Ala) | |
3 | g.138946332C>A | CA354706433 | FOXL2 | c.391G>T (p.Asp131Tyr) | |
3 | g.138946332C= | CA1405402466 | FOXL2 | c.391G= (p.Asp131=) | |
3 | g.138946332C>G | CA354706434 | FOXL2 | c.391G>C (p.Asp131His) | dbSNP |