| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 3 | g.138946410_138946412del | CA10654891 | FOXL2 | c.313_315del (p.Asn105del) | ClinVar dbSNP |
| 3 | g.138946412T>A | CA354706808 | FOXL2 | c.311A>T (p.His104Leu) | dbSNP |
| 3 | g.138946412T>C | CA10654892 | FOXL2 | c.311A>G (p.His104Arg) | ClinVar dbSNP |
| 3 | g.138946412T>G | CA354706813 | FOXL2 | c.311A>C (p.His104Pro) | |
| 3 | g.138946412T= | CA1405402499 | FOXL2 | c.311A= (p.His104=) | |
| 3 | g.138946413G>A | CA354706817 | FOXL2 | c.310C>T (p.His104Tyr) | |
| 3 | g.138946413G>C | CA354706821 | FOXL2 | c.310C>G (p.His104Asp) | |
| 3 | g.138946413G>T | CA354706824 | FOXL2 | c.310C>A (p.His104Asn) | |
| 3 | g.138946414G>A | CA436094734 | FOXL2 | c.309C>T (p.Arg103=) | |
| 3 | g.138946414G>C | CA436094737 | FOXL2 | c.309C>G (p.Arg103=) | |
| 3 | g.138946414G>T | CA436094738 | FOXL2 | c.309C>A (p.Arg103=) | |
| 3 | g.138946415C>A | CA10654893 | FOXL2 | c.308G>T (p.Arg103Leu) | ClinVar dbSNP |
| 3 | g.138946415C= | CA1405402500 | FOXL2 | c.308G= (p.Arg103=) | |
| 3 | g.138946415C>G | CA354706831 | FOXL2 | c.308G>C (p.Arg103Pro) | dbSNP |
| 3 | g.138946415C>T | CA10654894 | FOXL2 | c.308G>A (p.Arg103His) | ClinVar dbSNP |
| 3 | g.138946416G>A | CA354706841 | FOXL2 | c.307C>T (p.Arg103Cys) | |
| 3 | g.138946416G>C | CA354706844 | FOXL2 | c.307C>G (p.Arg103Gly) | |
| 3 | g.138946416G>T | CA354706856 | FOXL2 | c.307C>A (p.Arg103Ser) | COSMIC |
| 3 | g.138946417G>A | CA436094740 | FOXL2 | c.306C>T (p.Ile102=) | dbSNP |
| 3 | g.138946417G>C | CA354706862 | FOXL2 | c.306C>G (p.Ile102Met) | dbSNP |
| 3 | g.138946417G>T | CA436094741 | FOXL2 | c.306C>A (p.Ile102=) | dbSNP gnomAD v4 |
| 3 | g.138946418A>C | CA354706866 | FOXL2 | c.305T>G (p.Ile102Ser) | dbSNP |
| 3 | g.138946418A>G | CA354706870 | FOXL2 | c.305T>C (p.Ile102Thr) | dbSNP |
| 3 | g.138946418A>T | CA354706874 | FOXL2 | c.305T>A (p.Ile102Asn) | dbSNP |
| 3 | g.138946419T>A | CA354706878 | FOXL2 | c.304A>T (p.Ile102Phe) | |
| 3 | g.138946419T>C | CA354706881 | FOXL2 | c.304A>G (p.Ile102Val) | |
| 3 | g.138946419T>G | CA354706884 | FOXL2 | c.304A>C (p.Ile102Leu) | dbSNP |
| 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) |