Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
3 | g.138946382_138946385delinsTTGA | CA1405402487 | FOXL2 | c.338_341delinsTCAA (p.Ile113=) | |
3 | g.138946386_138946388del | CA913189444 | FOXL2 | c.338_340del (p.Ile113del) | ClinVar dbSNP |
3 | g.138946384_138946385delinsGA | CA1405402489 | FOXL2 | c.338_339delinsTC (p.Ile113=) | |
3 | g.138946385del | CA10654887 | FOXL2 | c.338del (p.Ile113ThrfsTer?) | ClinVar dbSNP |
3 | g.138946385A>C | CA354706642 | FOXL2 | c.338T>G (p.Ile113Ser) | |
3 | g.138946385A>G | CA354706643 | FOXL2 | c.338T>C (p.Ile113Thr) | dbSNP |
3 | g.138946385A>T | CA354706641 | FOXL2 | c.338T>A (p.Ile113Asn) | dbSNP |
3 | g.138946386T>A | CA354706644 | FOXL2 | c.337A>T (p.Ile113Phe) | dbSNP |
3 | g.138946386T>C | CA354706645 | FOXL2 | c.337A>G (p.Ile113Val) | gnomAD v4 |
3 | g.138946386T>G | CA354706646 | FOXL2 | c.337A>C (p.Ile113Leu) | gnomAD v4 |
3 | g.138946387G>A | CA436094693 | FOXL2 | c.336C>T (p.Phe112=) | dbSNP |
3 | g.138946387G>C | CA354706648 | FOXL2 | c.336C>G (p.Phe112Leu) | dbSNP |
3 | g.138946387G>T | CA354706649 | FOXL2 | c.336C>A (p.Phe112Leu) | gnomAD v4 |
3 | g.138946388A>C | CA354706652 | FOXL2 | c.335T>G (p.Phe112Cys) | |
3 | g.138946388A>G | CA354706654 | FOXL2 | c.335T>C (p.Phe112Ser) | dbSNP |
3 | g.138946388A>T | CA354706655 | FOXL2 | c.335T>A (p.Phe112Tyr) | dbSNP |
3 | g.138946389A>C | CA354706656 | FOXL2 | c.334T>G (p.Phe112Val) | |
3 | g.138946389A>G | CA354706658 | FOXL2 | c.334T>C (p.Phe112Leu) | |
3 | g.138946389A>T | CA354706661 | FOXL2 | c.334T>A (p.Phe112Ile) | |
3 | g.138946390G>A | CA436094697 | FOXL2 | c.333C>T (p.Cys111=) | dbSNP gnomAD v4 |
3 | g.138946390G>C | CA354706662 | FOXL2 | c.333C>G (p.Cys111Trp) | |
3 | g.138946390G>T | CA354706663 | FOXL2 | c.333C>A (p.Cys111Ter) | |
3 | g.138946391C>A | CA354706669 | FOXL2 | c.332G>T (p.Cys111Phe) | dbSNP |
3 | g.138946391C>G | CA354706668 | FOXL2 | c.332G>C (p.Cys111Ser) | |
3 | g.138946391C>T | CA354706665 | FOXL2 | c.332G>A (p.Cys111Tyr) | dbSNP |
3 | g.138946392A>C | CA354706671 | FOXL2 | c.331T>G (p.Cys111Gly) | dbSNP |
3 | g.138946392A>G | CA354706674 | FOXL2 | c.331T>C (p.Cys111Arg) | |
3 | g.138946392A>T | CA354706676 | FOXL2 | c.331T>A (p.Cys111Ser) | dbSNP |
3 | g.138946392dup | CA2586973042 | FOXL2 | c.331dup (p.Cys111LeufsTer?) | |
3 | g.138946393C>A | CA354706677 | FOXL2 | c.330G>T (p.Glu110Asp) | |
3 | g.138946393C>G | CA354706678 | FOXL2 | c.330G>C (p.Glu110Asp) | |
3 | g.138946393C>T | CA436094703 | FOXL2 | c.330G>A (p.Glu110=) | |
3 | g.138946394T>A | CA354706680 | FOXL2 | c.329A>T (p.Glu110Val) | dbSNP |
3 | g.138946394T>C | CA354706681 | FOXL2 | c.329A>G (p.Glu110Gly) | |
3 | g.138946394T>G | CA354706682 | FOXL2 | c.329A>C (p.Glu110Ala) | |
3 | g.138946395C>A | CA354706683 | FOXL2 | c.328G>T (p.Glu110Ter) | |
3 | g.138946395C= | CA1405402490 | FOXL2 | c.328G= (p.Glu110=) | |
3 | g.138946395C>G | CA2639783 | FOXL2 | c.328G>C (p.Glu110Gln) | dbSNP ExAC gnomAD v2 gnomAD v4 |
3 | g.138946395C>T | CA354706685 | FOXL2 | c.328G>A (p.Glu110Lys) | dbSNP |
3 | g.138946396G>A | CA436094704 | FOXL2 | c.327C>T (p.Asn109=) | dbSNP gnomAD v4 |
3 | g.138946396G>C | CA354706686 | FOXL2 | c.327C>G (p.Asn109Lys) | dbSNP |
3 | g.138946396G>T | CA354706690 | FOXL2 | c.327C>A (p.Asn109Lys) | |
3 | g.138946397T>A | CA354706693 | FOXL2 | c.326A>T (p.Asn109Ile) | dbSNP |
3 | g.138946397T>C | CA354706696 | FOXL2 | c.326A>G (p.Asn109Ser) | dbSNP gnomAD v3 gnomAD v4 |
3 | g.138946397T>G | CA354706695 | FOXL2 | c.326A>C (p.Asn109Thr) | dbSNP |
3 | g.138946397T= | CA1405402491 | FOXL2 | c.326A= (p.Asn109=) | |
3 | g.138946398T>A | CA354706698 | FOXL2 | c.325A>T (p.Asn109Tyr) | dbSNP |
3 | g.138946398T>C | CA354706702 | FOXL2 | c.325A>G (p.Asn109Asp) | dbSNP |
3 | g.138946398T>G | CA354706700 | FOXL2 | c.325A>C (p.Asn109His) | |
3 | g.138946399G>A | CA436094707 | FOXL2 | c.324C>T (p.Leu108=) | dbSNP |