Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
3 | g.138946540_138946552del | CA913189445 | FOXL2 | c.174_186del (p.Tyr59SerfsTer?) | ClinVar dbSNP |
3 | g.138946549_138946581delinsCGAGTACGGGGGCTTCTGCGCCGGGTCCGGCTT | CA1405402560 | FOXL2 | c.142_174delinsAAGCCGGACCCGGCGCAGAAGCCCCCGTACTCG (p.Lys48=) | |
3 | g.138946550_138946581delinsAGCGC | CA273044 | FOXL2 | c.142_173delinsGCGCT (p.Lys48_Ser58delinsAlaLeu) | ClinVar dbSNP |
3 | g.138946552G>A | CA436094489 | FOXL2 | c.171C>T (p.Tyr57=) | dbSNP gnomAD v4 |
3 | g.138946552G>C | CA10654906 | FOXL2 | c.171C>G (p.Tyr57Ter) | ClinVar dbSNP gnomAD v4 |
3 | g.138946552G= | CA1405402563 | FOXL2 | c.171C= (p.Tyr57=) | |
3 | g.138946552G>T | CA354707620 | FOXL2 | c.171C>A (p.Tyr57Ter) | |
3 | g.138946553T>A | CA354707622 | FOXL2 | c.170A>T (p.Tyr57Phe) | dbSNP |
3 | g.138946553T>C | CA354707625 | FOXL2 | c.170A>G (p.Tyr57Cys) | |
3 | g.138946553T>G | CA354707628 | FOXL2 | c.170A>C (p.Tyr57Ser) | |
3 | g.138946554A= | CA1405402564 | FOXL2 | c.169T= (p.Tyr57=) | |
3 | g.138946554A>C | CA354707631 | FOXL2 | c.169T>G (p.Tyr57Asp) | |
3 | g.138946554A>G | CA354707634 | FOXL2 | c.169T>C (p.Tyr57His) | |
3 | g.138946554A>T | CA354707637 | FOXL2 | c.169T>A (p.Tyr57Asn) | ClinVar dbSNP |
3 | g.138946555C>A | CA436094490 | FOXL2 | c.168G>T (p.Pro56=) | gnomAD v4 |
3 | g.138946555C= | CA1405402565 | FOXL2 | c.168G= (p.Pro56=) | |
3 | g.138946555C>G | CA436094491 | FOXL2 | c.168G>C (p.Pro56=) | dbSNP |
3 | g.138946555C>T | CA2639799 | FOXL2 | c.168G>A (p.Pro56=) | dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
3 | g.138946556G>A | CA354707645 | FOXL2 | c.167C>T (p.Pro56Leu) | |
3 | g.138946556G>C | CA354707648 | FOXL2 | c.167C>G (p.Pro56Arg) | |
3 | g.138946556G>T | CA354707650 | FOXL2 | c.167C>A (p.Pro56Gln) | |
3 | g.138946560del | CA2586973053 | FOXL2 | c.167del (p.Pro56ArgfsTer?) | |
3 | g.138946557G>A | CA354707656 | FOXL2 | c.166C>T (p.Pro56Ser) | |
3 | g.138946557G>C | CA354707654 | FOXL2 | c.166C>G (p.Pro56Ala) | dbSNP gnomAD v2 gnomAD v4 |
3 | g.138946557G= | CA1405402566 | FOXL2 | c.166C= (p.Pro56=) | |
3 | g.138946557G>T | CA354707653 | FOXL2 | c.166C>A (p.Pro56Thr) | |
3 | g.138946558G>A | CA2639800 | FOXL2 | c.165C>T (p.Pro55=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
3 | g.138946558G>C | CA436094493 | FOXL2 | c.165C>G (p.Pro55=) | |
3 | g.138946558G= | CA1405402567 | FOXL2 | c.165C= (p.Pro55=) | |
3 | g.138946558G>T | CA436094492 | FOXL2 | c.165C>A (p.Pro55=) | |
3 | g.138946559G>A | CA354707663 | FOXL2 | c.164C>T (p.Pro55Leu) | |
3 | g.138946559G>C | CA354707666 | FOXL2 | c.164C>G (p.Pro55Arg) | |
3 | g.138946559G>T | CA354707669 | FOXL2 | c.164C>A (p.Pro55His) | |
3 | g.138946560G>A | CA354707673 | FOXL2 | c.163C>T (p.Pro55Ser) | dbSNP |
3 | g.138946560G>C | CA354707675 | FOXL2 | c.163C>G (p.Pro55Ala) | |
3 | g.138946560G>T | CA354707677 | FOXL2 | c.163C>A (p.Pro55Thr) | |
3 | g.138946561C>A | CA354707683 | FOXL2 | c.162G>T (p.Lys54Asn) | |
3 | g.138946561C>G | CA354707684 | FOXL2 | c.162G>C (p.Lys54Asn) | |
3 | g.138946561C>T | CA436094494 | FOXL2 | c.162G>A (p.Lys54=) | gnomAD v4 |
3 | g.138946562T>A | CA354707686 | FOXL2 | c.161A>T (p.Lys54Met) | |
3 | g.138946562T>C | CA354707688 | FOXL2 | c.161A>G (p.Lys54Arg) | |
3 | g.138946562T>G | CA354707693 | FOXL2 | c.161A>C (p.Lys54Thr) | |
3 | g.138946563T>A | CA354707718 | FOXL2 | c.160A>T (p.Lys54Ter) | |
3 | g.138946563T>C | CA354707714 | FOXL2 | c.160A>G (p.Lys54Glu) | ClinVar dbSNP gnomAD v4 |
3 | g.138946563T>G | CA354707697 | FOXL2 | c.160A>C (p.Lys54Gln) | |
3 | g.138946563T= | CA1405402568 | FOXL2 | c.160A= (p.Lys54=) | |
3 | g.138946564C>A | CA354707721 | FOXL2 | c.159G>T (p.Gln53His) | |
3 | g.138946564C>G | CA354707724 | FOXL2 | c.159G>C (p.Gln53His) | dbSNP |
3 | g.138946564C>T | CA436094495 | FOXL2 | c.159G>A (p.Gln53=) | gnomAD v4 |
3 | g.138946565T>A | CA354707729 | FOXL2 | c.158A>T (p.Gln53Leu) |