Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
3 | g.138946022_138946351del | CA2739278055 | FOXL2 | c.376_705del (p.Asn126_Gly235del) | ClinVar |
3 | g.138946078_138946099dup | CA10654874 | FOXL2 | c.630_651dup (p.Cys218LeufsTer28) | ClinVar 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 |
3 | g.138946081G>A | CA436094243 | FOXL2 | c.642C>T (p.Pro214=) | dbSNP gnomAD v4 |
3 | g.138946081G>C | CA436094246 | FOXL2 | c.642C>G (p.Pro214=) | dbSNP |
3 | g.138946081G= | CA1405402337 | FOXL2 | c.642C= (p.Pro214=) | |
3 | g.138946081G>T | CA436094244 | FOXL2 | c.642C>A (p.Pro214=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
3 | g.138946083_138946089del | CA2586973030 | FOXL2 | c.636_642del (p.Tyr215ProfsTer?) | |
3 | g.138946082G>A | CA354704620 | FOXL2 | c.641C>T (p.Pro214Leu) | dbSNP |
3 | g.138946082G>C | CA354704624 | FOXL2 | c.641C>G (p.Pro214Arg) | dbSNP |
3 | g.138946082G>T | CA354704638 | FOXL2 | c.641C>A (p.Pro214His) | dbSNP |
3 | g.138946083G>A | CA354704645 | FOXL2 | c.640C>T (p.Pro214Ser) | dbSNP gnomAD v4 COSMIC |
3 | g.138946083G>C | CA354704649 | FOXL2 | c.640C>G (p.Pro214Ala) | dbSNP |
3 | g.138946083G>T | CA354704651 | FOXL2 | c.640C>A (p.Pro214Thr) | dbSNP gnomAD v4 |
3 | g.138946084C>A | CA354704664 | FOXL2 | c.639G>T (p.Met213Ile) | gnomAD v4 |
3 | g.138946084C>G | CA354704660 | FOXL2 | c.639G>C (p.Met213Ile) | |
3 | g.138946084C>T | CA354704656 | FOXL2 | c.639G>A (p.Met213Ile) | gnomAD v4 |
3 | g.138946085A>C | CA354704671 | FOXL2 | c.638T>G (p.Met213Arg) | gnomAD v4 |
3 | g.138946085A>G | CA354704675 | FOXL2 | c.638T>C (p.Met213Thr) | dbSNP gnomAD v4 |
3 | g.138946085A>T | CA354704681 | FOXL2 | c.638T>A (p.Met213Lys) | dbSNP gnomAD v4 |
3 | g.138946086T>A | CA354704689 | FOXL2 | c.637A>T (p.Met213Leu) | |
3 | g.138946086T>C | CA354704692 | FOXL2 | c.637A>G (p.Met213Val) | dbSNP gnomAD v4 |
3 | g.138946086T>G | CA354704694 | FOXL2 | c.637A>C (p.Met213Leu) | gnomAD v4 |
3 | g.138946086T= | CA1405402338 | FOXL2 | c.637A= (p.Met213=) | |
3 | g.138946087G>A | CA83969990 | FOXL2 | c.636C>T (p.Pro212=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
3 | g.138946087G>C | CA436094252 | FOXL2 | c.636C>G (p.Pro212=) | dbSNP |
3 | g.138946087G= | CA1405402339 | FOXL2 | c.636C= (p.Pro212=) | |
3 | g.138946087G>T | CA436094253 | FOXL2 | c.636C>A (p.Pro212=) | dbSNP gnomAD v4 |
3 | g.138946089del | CA2667926350 | FOXL2 | c.636del (p.Met213CysfsTer?) | gnomAD v4 |
3 | g.138946088G>A | CA354704700 | FOXL2 | c.635C>T (p.Pro212Leu) | dbSNP gnomAD v4 |
3 | g.138946088G>C | CA354704703 | FOXL2 | c.635C>G (p.Pro212Arg) | dbSNP gnomAD v4 |
3 | g.138946088G>T | CA354704706 | FOXL2 | c.635C>A (p.Pro212His) | dbSNP gnomAD v4 |
3 | g.138946089G>A | CA354704711 | FOXL2 | c.634C>T (p.Pro212Ser) | dbSNP gnomAD v2 gnomAD v4 |
3 | g.138946089G>C | CA2639749 | FOXL2 | c.634C>G (p.Pro212Ala) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
3 | g.138946089G= | CA1405402340 | FOXL2 | c.634C= (p.Pro212=) | |
3 | g.138946089G>T | CA354704718 | FOXL2 | c.634C>A (p.Pro212Thr) | dbSNP |
3 | g.138946090T>A | CA436094255 | FOXL2 | c.633A>T (p.Ser211=) | gnomAD v4 |
3 | g.138946090T>C | CA436094256 | FOXL2 | c.633A>G (p.Ser211=) | gnomAD v4 |