Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
3 | g.138946022_138946351del | CA2739278055 | FOXL2 | c.376_705del (p.Asn126_Gly235del) | ClinVar |
3 | g.138946163C>A | CA354705480 | FOXL2 | c.560G>T (p.Gly187Val) | dbSNP |
3 | g.138946163C= | CA1405402373 | FOXL2 | c.560G= (p.Gly187=) | |
3 | g.138946163C>G | CA354705479 | FOXL2 | c.560G>C (p.Gly187Ala) | dbSNP |
3 | g.138946163C>T | CA117109 | FOXL2 | c.560G>A (p.Gly187Asp) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
3 | g.138946164C>A | CA354705482 | FOXL2 | c.559G>T (p.Gly187Cys) | dbSNP gnomAD v4 |
3 | g.138946164C= | CA1405402374 | FOXL2 | c.559G= (p.Gly187=) | |
3 | g.138946164C>G | CA354705484 | FOXL2 | c.559G>C (p.Gly187Arg) | |
3 | g.138946164C>T | CA354705485 | FOXL2 | c.559G>A (p.Gly187Ser) | dbSNP gnomAD v2 gnomAD v4 |
3 | g.138946165G>A | CA436094328 | FOXL2 | c.558C>T (p.Tyr186=) | gnomAD v4 |
3 | g.138946165G>C | CA354705488 | FOXL2 | c.558C>G (p.Tyr186Ter) | |
3 | g.138946165G>T | CA354705489 | FOXL2 | c.558C>A (p.Tyr186Ter) | |
3 | g.138946165_138946166insACGGC | CA2704129458 | FOXL2 | c.557_558insGCCGT (p.Tyr186Ter) | dbSNP |
3 | g.138946166T>A | CA354705490 | FOXL2 | c.557A>T (p.Tyr186Phe) | dbSNP |
3 | g.138946166T>C | CA354705493 | FOXL2 | c.557A>G (p.Tyr186Cys) | dbSNP gnomAD v4 |
3 | g.138946166T>G | CA354705500 | FOXL2 | c.557A>C (p.Tyr186Ser) | dbSNP |
3 | g.138946167A= | CA1405402375 | FOXL2 | c.556T= (p.Tyr186=) | |
3 | g.138946167A>C | CA354705502 | FOXL2 | c.556T>G (p.Tyr186Asp) | |
3 | g.138946167A>G | CA354705503 | FOXL2 | c.556T>C (p.Tyr186His) | dbSNP gnomAD v3 gnomAD v4 |
3 | g.138946167A>T | CA354705504 | FOXL2 | c.556T>A (p.Tyr186Asn) | |
3 | g.138946167dup | CA2573136579 | FOXL2 | c.556dup (p.Tyr186LeufsTer?) | ClinVar dbSNP |
3 | g.138946168G>A | CA436094329 | FOXL2 | c.555C>T (p.Gly185=) | dbSNP |
3 | g.138946168G>C | CA436094330 | FOXL2 | c.555C>G (p.Gly185=) | dbSNP |
3 | g.138946168G>T | CA436094331 | FOXL2 | c.555C>A (p.Gly185=) | |
3 | g.138946169_138946174dup | CA2667926492 | FOXL2 | c.550_555dup (p.Gly185_Tyr186insAspGly) | gnomAD v4 |
3 | g.138946169C>A | CA354705507 | FOXL2 | c.554G>T (p.Gly185Val) | dbSNP gnomAD v4 |
3 | g.138946169C= | CA1405402376 | FOXL2 | c.554G= (p.Gly185=) | |
3 | g.138946169C>G | CA354705508 | FOXL2 | c.554G>C (p.Gly185Ala) | dbSNP |
3 | g.138946169C>T | CA354705510 | FOXL2 | c.554G>A (p.Gly185Asp) | dbSNP gnomAD v4 |
3 | g.138946170C>A | CA354705534 | FOXL2 | c.553G>T (p.Gly185Cys) | dbSNP |
3 | g.138946170C= | CA1405402377 | FOXL2 | c.553G= (p.Gly185=) | |
3 | g.138946170C>G | CA354705538 | FOXL2 | c.553G>C (p.Gly185Arg) | ClinVar dbSNP gnomAD v4 |
3 | g.138946170C>T | CA354705527 | FOXL2 | c.553G>A (p.Gly185Ser) | dbSNP gnomAD v4 |
3 | g.138946171G>A | CA436094332 | FOXL2 | c.552C>T (p.Asp184=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
3 | g.138946171G>C | CA354705542 | FOXL2 | c.552C>G (p.Asp184Glu) | dbSNP |
3 | g.138946171G= | CA1405402378 | FOXL2 | c.552C= (p.Asp184=) | |
3 | g.138946171G>T | CA354705545 | FOXL2 | c.552C>A (p.Asp184Glu) | dbSNP gnomAD v4 |
3 | g.138946172T>A | CA354705549 | FOXL2 | c.551A>T (p.Asp184Val) | dbSNP |
3 | g.138946172T>C | CA354705552 | FOXL2 | c.551A>G (p.Asp184Gly) | dbSNP gnomAD v4 |
3 | g.138946172T>G | CA354705559 | FOXL2 | c.551A>C (p.Asp184Ala) | ClinVar |
3 | g.138946172dup | CA913189436 | FOXL2 | c.551dup (p.Asp184GlufsTer?) | ClinVar dbSNP |
3 | g.138946173C>A | CA354705565 | FOXL2 | c.550G>T (p.Asp184Tyr) | dbSNP gnomAD v4 |
3 | g.138946173C= | CA1405402379 | FOXL2 | c.550G= (p.Asp184=) | |
3 | g.138946173C>G | CA354705564 | FOXL2 | c.550G>C (p.Asp184His) | dbSNP |
3 | g.138946173C>T | CA354705563 | FOXL2 | c.550G>A (p.Asp184Asn) | dbSNP gnomAD v4 |
3 | g.138946174G>A | CA436094333 | FOXL2 | c.549C>T (p.Ala183=) | dbSNP gnomAD v4 |
3 | g.138946174G>C | CA436094334 | FOXL2 | c.549C>G (p.Ala183=) | dbSNP |
3 | g.138946174G>T | CA436094335 | FOXL2 | c.549C>A (p.Ala183=) | dbSNP gnomAD v4 |
3 | g.138946175dup | CA913189437 | FOXL2 | c.549dup (p.Asp184ArgfsTer?) | ClinVar dbSNP |
3 | g.138946175G>A | CA354705568 | FOXL2 | c.548C>T (p.Ala183Val) | dbSNP gnomAD v4 |