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.138946325_138946335del | CA2739278056 | FOXL2 | c.391_401del (p.Asp131ArgfsTer?) | ClinVar |
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 |
3 | g.138946332C>T | CA354706436 | FOXL2 | c.391G>A (p.Asp131Asn) | dbSNP |
3 | g.138946333C>A | CA436094605 | FOXL2 | c.390G>T (p.Leu130=) | |
3 | g.138946333C= | CA1405402467 | FOXL2 | c.390G= (p.Leu130=) | |
3 | g.138946333C>G | CA436094606 | FOXL2 | c.390G>C (p.Leu130=) | COSMIC |
3 | g.138946333C>T | CA2639778 | FOXL2 | c.390G>A (p.Leu130=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
3 | g.138946334A= | CA1405402468 | FOXL2 | c.389T= (p.Leu130=) | |
3 | g.138946334A>C | CA354706443 | FOXL2 | c.389T>G (p.Leu130Arg) | dbSNP |
3 | g.138946334A>G | CA10654884 | FOXL2 | c.389T>C (p.Leu130Pro) | ClinVar dbSNP |
3 | g.138946334A>T | CA10654885 | FOXL2 | c.389T>A (p.Leu130Gln) | ClinVar dbSNP |
3 | g.138946335G>A | CA436094608 | FOXL2 | c.388C>T (p.Leu130=) | gnomAD v4 |
3 | g.138946335G>C | CA354706445 | FOXL2 | c.388C>G (p.Leu130Val) | ClinVar |
3 | g.138946335G>T | CA354706447 | FOXL2 | c.388C>A (p.Leu130Met) | |
3 | g.138946335_138946336delinsGC | CA1405402469 | FOXL2 | c.387_388delinsGC (p.Thr129=) | |
3 | g.138946336del | CA913189441 | FOXL2 | c.387del (p.Leu130TrpfsTer20) | ClinVar dbSNP |
3 | g.138946336C>A | CA436094609 | FOXL2 | c.387G>T (p.Thr129=) | dbSNP gnomAD v4 |
3 | g.138946336C= | CA1405402470 | FOXL2 | c.387G= (p.Thr129=) | |
3 | g.138946336C>G | CA436094610 | FOXL2 | c.387G>C (p.Thr129=) | dbSNP |
3 | g.138946336C>T | CA2639779 | FOXL2 | c.387G>A (p.Thr129=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
3 | g.138946337G>A | CA354706454 | FOXL2 | c.386C>T (p.Thr129Met) | dbSNP gnomAD v4 |
3 | g.138946337G>C | CA354706456 | FOXL2 | c.386C>G (p.Thr129Arg) | dbSNP |
3 | g.138946337G>T | CA354706450 | FOXL2 | c.386C>A (p.Thr129Lys) | |
3 | g.138946338T>A | CA354706458 | FOXL2 | c.385A>T (p.Thr129Ser) | |
3 | g.138946338T>C | CA354706460 | FOXL2 | c.385A>G (p.Thr129Ala) | |
3 | g.138946338T>G | CA354706461 | FOXL2 | c.385A>C (p.Thr129Pro) | |
3 | g.138946338_138946339delinsTC | CA1405402471 | FOXL2 | c.384_385delinsGA (p.Trp128=) | |
3 | g.138946339C>A | CA354706463 | FOXL2 | c.384G>T (p.Trp128Cys) | |
3 | g.138946339C= | CA1405402472 | FOXL2 | c.384G= (p.Trp128=) | |
3 | g.138946339C>G | CA354706464 | FOXL2 | c.384G>C (p.Trp128Cys) | |
3 | g.138946339C>T | CA354706466 | FOXL2 | c.384G>A (p.Trp128Ter) | ClinVar dbSNP |
3 | g.138946340del | CA913189442 | FOXL2 | c.384del (p.Trp128Ter) | ClinVar dbSNP |
3 | g.138946340C>A | CA354706471 | FOXL2 | c.383G>T (p.Trp128Leu) |