Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
3 | g.138946420G>A | CA436094746 | FOXL2 | c.303C>T (p.Ser101=) | dbSNP |
3 | g.138946420G>C | CA10654895 | FOXL2 | c.303C>G (p.Ser101Arg) | ClinVar dbSNP |
3 | g.138946420G= | CA1405402501 | FOXL2 | c.303C= (p.Ser101=) | |
3 | g.138946420G>T | CA354706889 | FOXL2 | c.303C>A (p.Ser101Arg) | |
3 | g.138946421C>A | CA354706895 | FOXL2 | c.302G>T (p.Ser101Ile) | |
3 | g.138946421C>G | CA354706899 | FOXL2 | c.302G>C (p.Ser101Thr) | ClinVar dbSNP |
3 | g.138946421C>T | CA354706900 | FOXL2 | c.302G>A (p.Ser101Asn) | dbSNP |
3 | g.138946422T>A | CA354706906 | FOXL2 | c.301A>T (p.Ser101Cys) | |
3 | g.138946422T>C | CA354706909 | FOXL2 | c.301A>G (p.Ser101Gly) | |
3 | g.138946422T>G | CA354706911 | FOXL2 | c.301A>C (p.Ser101Arg) | |
3 | g.138946423A= | CA1405402502 | FOXL2 | c.300T= (p.Asn100=) | |
3 | g.138946423A>C | CA354706915 | FOXL2 | c.300T>G (p.Asn100Lys) | dbSNP |
3 | g.138946423A>G | CA436094750 | FOXL2 | c.300T>C (p.Asn100=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
3 | g.138946423A>T | CA354706919 | FOXL2 | c.300T>A (p.Asn100Lys) | |
3 | g.138946424T>A | CA354706924 | FOXL2 | c.299A>T (p.Asn100Ile) | |
3 | g.138946424T>C | CA354706930 | FOXL2 | c.299A>G (p.Asn100Ser) | |
3 | g.138946424T>G | CA354706927 | FOXL2 | c.299A>C (p.Asn100Thr) | |
3 | g.138946427dup | CA2586973043 | FOXL2 | c.299dup (p.Asn100LysfsTer2) | |
3 | g.138946425T>A | CA354706934 | FOXL2 | c.298A>T (p.Asn100Tyr) | |
3 | g.138946425T>C | CA354706937 | FOXL2 | c.298A>G (p.Asn100Asp) | ClinVar dbSNP |
3 | g.138946425T>G | CA354706940 | FOXL2 | c.298A>C (p.Asn100His) | |
3 | g.138946425T= | CA1405402503 | FOXL2 | c.298A= (p.Asn100=) | |
3 | g.138946426T>A | CA354706944 | FOXL2 | c.297A>T (p.Gln99His) | |
3 | g.138946426T>C | CA436094752 | FOXL2 | c.297A>G (p.Gln99=) | dbSNP COSMIC |
3 | g.138946426T>G | CA354706947 | FOXL2 | c.297A>C (p.Gln99His) | |
3 | g.138946427T>A | CA354706952 | FOXL2 | c.296A>T (p.Gln99Leu) | |
3 | g.138946427T>C | CA354706955 | FOXL2 | c.296A>G (p.Gln99Arg) | |
3 | g.138946427T>G | CA354706957 | FOXL2 | c.296A>C (p.Gln99Pro) | |
3 | g.138946428G>A | CA210688 | FOXL2 | c.295C>T (p.Gln99Ter) | ClinVar dbSNP |
3 | g.138946428G>C | CA354706960 | FOXL2 | c.295C>G (p.Gln99Glu) | dbSNP |
3 | g.138946428G= | CA1405402504 | FOXL2 | c.295C= (p.Gln99=) | |
3 | g.138946428G>T | CA2639784 | FOXL2 | c.295C>A (p.Gln99Lys) | dbSNP ExAC gnomAD v2 gnomAD v4 |
3 | g.138946429C>A | CA354706967 | FOXL2 | c.294G>T (p.Trp98Cys) | dbSNP |
3 | g.138946429C>G | CA354706966 | FOXL2 | c.294G>C (p.Trp98Cys) | |
3 | g.138946429C>T | CA354706964 | FOXL2 | c.294G>A (p.Trp98Ter) | dbSNP |
3 | g.138946431_138946435del | CA2586973044 | FOXL2 | c.290_294del (p.Gly97AlafsTer3) | |
3 | g.138946430C>A | CA354706969 | FOXL2 | c.293G>T (p.Trp98Leu) | dbSNP |
3 | g.138946430C= | CA1405402505 | FOXL2 | c.293G= (p.Trp98=) | |
3 | g.138946430C>G | CA354706971 | FOXL2 | c.293G>C (p.Trp98Ser) | dbSNP |
3 | g.138946430C>T | CA10654896 | FOXL2 | c.293G>A (p.Trp98Ter) | ClinVar dbSNP |
3 | g.138946431A= | CA1405402506 | FOXL2 | c.292T= (p.Trp98=) | |
3 | g.138946431A>C | CA354706975 | FOXL2 | c.292T>G (p.Trp98Gly) | |
3 | g.138946431A>G | CA10654897 | FOXL2 | c.292T>C (p.Trp98Arg) | ClinVar dbSNP |
3 | g.138946431A>T | CA354706977 | FOXL2 | c.292T>A (p.Trp98Arg) | dbSNP |
3 | g.138946432G>A | CA2639785 | FOXL2 | c.291C>T (p.Gly97=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
3 | g.138946432G>C | CA436094760 | FOXL2 | c.291C>G (p.Gly97=) | dbSNP |
3 | g.138946432G= | CA1405402507 | FOXL2 | c.291C= (p.Gly97=) | |
3 | g.138946432G>T | CA436094762 | FOXL2 | c.291C>A (p.Gly97=) | gnomAD v4 |
3 | g.138946433C>A | CA354706981 | FOXL2 | c.290G>T (p.Gly97Val) | dbSNP |
3 | g.138946433C>G | CA354706983 | FOXL2 | c.290G>C (p.Gly97Ala) | dbSNP |