| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 3 | g.138946022_138946351del | CA2739278055 | FOXL2 | c.376_705del (p.Asn126_Gly235del) | |
| 3 | g.138946068G>A | CA210680 | FOXL2 | c.655C>T (p.Gln219Ter) | ClinVar dbSNP gnomAD v4 COSMIC |
| 3 | g.138946068G>C | CA354704505 | FOXL2 | c.655C>G (p.Gln219Glu) | dbSNP COSMIC |
| 3 | g.138946068G= | CA1405402329 | FOXL2 | c.655C= (p.Gln219=) | |
| 3 | g.138946068G>T | CA354704507 | FOXL2 | c.655C>A (p.Gln219Lys) | dbSNP gnomAD v4 |
| 3 | g.138946069G>A | CA2639748 | FOXL2 | c.654C>T (p.Cys218=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 3 | g.138946069G>C | CA354704511 | FOXL2 | c.654C>G (p.Cys218Trp) | dbSNP gnomAD v4 |
| 3 | g.138946069G= | CA1405402330 | FOXL2 | c.654C= (p.Cys218=) | |
| 3 | g.138946069G>T | CA354704513 | FOXL2 | c.654C>A (p.Cys218Ter) | dbSNP gnomAD v4 |
| 3 | g.138946070del | CA2667926290 | FOXL2 | c.653del (p.Cys218SerfsTer?) | gnomAD v4 |
| 3 | g.138946070C>A | CA354704527 | FOXL2 | c.653G>T (p.Cys218Phe) | gnomAD v4 |
| 3 | g.138946070C>G | CA354704520 | FOXL2 | c.653G>C (p.Cys218Ser) | |
| 3 | g.138946070C>T | CA354704517 | FOXL2 | c.653G>A (p.Cys218Tyr) | gnomAD v4 |
| 3 | g.138946071A= | CA1405402331 | FOXL2 | c.652T= (p.Cys218=) | |
| 3 | g.138946071A>C | CA354704534 | FOXL2 | c.652T>G (p.Cys218Gly) | dbSNP gnomAD v3 gnomAD v4 |
| 3 | g.138946071A>G | CA354704539 | FOXL2 | c.652T>C (p.Cys218Arg) | dbSNP gnomAD v4 |
| 3 | g.138946071A>T | CA354704538 | FOXL2 | c.652T>A (p.Cys218Ser) | dbSNP gnomAD v4 |
| 3 | g.138946072G>A | CA83969942 | FOXL2 | c.651C>T (p.Ser217=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 3 | g.138946072G>C | CA436094229 | FOXL2 | c.651C>G (p.Ser217=) | dbSNP gnomAD v4 |
| 3 | g.138946072G= | CA1405402332 | FOXL2 | c.651C= (p.Ser217=) | |
| 3 | g.138946072G>T | CA436094228 | FOXL2 | c.651C>A (p.Ser217=) | gnomAD v4 |
| 3 | g.138946078_138946099dup | CA10654874 | FOXL2 | c.630_651dup (p.Cys218LeufsTer28) | ClinVar dbSNP |
| 3 | g.138946073G>A | CA347073 | FOXL2 | c.650C>T (p.Ser217Phe) | ClinVar dbSNP gnomAD v4 |
| 3 | g.138946073G>C | CA354704540 | FOXL2 | c.650C>G (p.Ser217Cys) | |
| 3 | g.138946073G= | CA1405402333 | FOXL2 | c.650C= (p.Ser217=) | |
| 3 | g.138946073G>T | CA354704542 | FOXL2 | c.650C>A (p.Ser217Tyr) | gnomAD v4 |
| 3 | g.138946074A>C | CA354704549 | FOXL2 | c.649T>G (p.Ser217Ala) | dbSNP |
| 3 | g.138946074A>G | CA354704554 | FOXL2 | c.649T>C (p.Ser217Pro) | dbSNP gnomAD v4 |
| 3 | g.138946074A>T | CA354704567 | FOXL2 | c.649T>A (p.Ser217Thr) | dbSNP gnomAD v4 |
| 3 | g.138946075G>A | CA83969953 | FOXL2 | c.648C>T (p.Ala216=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 3 | g.138946075G>C | CA436094234 | FOXL2 | c.648C>G (p.Ala216=) | dbSNP |
| 3 | g.138946075G= | CA1405402334 | FOXL2 | c.648C= (p.Ala216=) | |
| 3 | g.138946075G>T | CA436094233 | FOXL2 | c.648C>A (p.Ala216=) | dbSNP gnomAD v4 |
| 3 | g.138946076G>A | CA10654875 | FOXL2 | c.647C>T (p.Ala216Val) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 3 | g.138946076G>C | CA354704576 | FOXL2 | c.647C>G (p.Ala216Gly) | dbSNP |
| 3 | g.138946076G= | CA1405402335 | FOXL2 | c.647C= (p.Ala216=) | |
| 3 | g.138946076G>T | CA354704580 | FOXL2 | c.647C>A (p.Ala216Asp) | dbSNP |
| 3 | g.138946077C>A | CA354704587 | FOXL2 | c.646G>T (p.Ala216Ser) | dbSNP gnomAD v4 |
| 3 | g.138946077C>G | CA354704588 | FOXL2 | c.646G>C (p.Ala216Pro) | dbSNP |
| 3 | g.138946077C>T | CA354704593 | FOXL2 | c.646G>A (p.Ala216Thr) | dbSNP gnomAD v4 |
| 3 | g.138946078A>C | CA354704602 | FOXL2 | c.645T>G (p.Tyr215Ter) | gnomAD v4 |
| 3 | g.138946078A>G | CA436094240 | FOXL2 | c.645T>C (p.Tyr215=) | dbSNP gnomAD v4 |
| 3 | g.138946078A>T | CA354704603 | FOXL2 | c.645T>A (p.Tyr215Ter) | dbSNP |
| 3 | g.138946079T>A | CA354704605 | FOXL2 | c.644A>T (p.Tyr215Phe) | dbSNP |
| 3 | g.138946079T>C | CA10654876 | FOXL2 | c.644A>G (p.Tyr215Cys) | ClinVar dbSNP gnomAD v4 |
| 3 | g.138946079T>G | CA354704608 | FOXL2 | c.644A>C (p.Tyr215Ser) | dbSNP |
| 3 | g.138946079T= | CA1405402336 | FOXL2 | c.644A= (p.Tyr215=) | |
| 3 | g.138946080A>C | CA354704609 | FOXL2 | c.643T>G (p.Tyr215Asp) | gnomAD v4 |
| 3 | g.138946080A>G | CA354704612 | FOXL2 | c.643T>C (p.Tyr215His) | gnomAD v4 |
| 3 | g.138946080A>T | CA354704616 | FOXL2 | c.643T>A (p.Tyr215Asn) | dbSNP gnomAD v4 |