Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
11 | g.69810459T>A | CA381663578 | FGF3 | c.566A>T (p.Glu189Val) n.413A>T | |
11 | g.69810459T>C | CA381663579 | FGF3 | c.566A>G (p.Glu189Gly) n.413A>G | |
11 | g.69810459T>G | CA381663577 | FGF3 | c.566A>C (p.Glu189Ala) n.413A>C | |
11 | g.69810460C>A | CA381663580 | FGF3 | c.565G>T (p.Glu189Ter) n.412G>T | gnomAD v4 |
11 | g.69810460C= | CA1980742034 | FGF3 | c.565G= (p.Glu189=) n.412G= | |
11 | g.69810460C>G | CA381663581 | FGF3 | c.565G>C (p.Glu189Gln) n.412G>C | |
11 | g.69810460C>T | CA381663582 | FGF3 | c.565G>A (p.Glu189Lys) n.412G>A | dbSNP gnomAD v2 gnomAD v4 COSMIC |
11 | g.69810461G>A | CA223497052 | FGF3 | c.564C>T (p.His188=) n.411C>T | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.69810461G>C | CA381663583 | FGF3 | c.564C>G (p.His188Gln) n.411C>G | dbSNP |
11 | g.69810461G= | CA1980742035 | FGF3 | c.564C= (p.His188=) n.411C= | |
11 | g.69810461G>T | CA6157035 | FGF3 | c.564C>A (p.His188Gln) n.411C>A | dbSNP ExAC gnomAD v2 gnomAD v4 |
11 | g.69810462T>A | CA381663584 | FGF3 | c.563A>T (p.His188Leu) n.410A>T | |
11 | g.69810462T>C | CA381663586 | FGF3 | c.563A>G (p.His188Arg) n.410A>G | dbSNP gnomAD v2 |
11 | g.69810462T>G | CA381663585 | FGF3 | c.563A>C (p.His188Pro) n.410A>C | |
11 | g.69810462T= | CA1980742036 | FGF3 | c.563A= (p.His188=) n.410A= | |
11 | g.69810463G>A | CA381663587 | FGF3 | c.562C>T (p.His188Tyr) n.409C>T | |
11 | g.69810463G>C | CA381663588 | FGF3 | c.562C>G (p.His188Asp) n.409C>G | |
11 | g.69810463G>T | CA381663589 | FGF3 | c.562C>A (p.His188Asn) n.409C>A | gnomAD v4 |
11 | g.69810464G>A | CA475468028 | FGF3 | c.561C>T (p.Asp187=) n.408C>T | gnomAD v4 |
11 | g.69810464G>C | CA381663590 | FGF3 | c.561C>G (p.Asp187Glu) n.408C>G | |
11 | g.69810464G= | CA1980742037 | FGF3 | c.561C= (p.Asp187=) n.408C= | |
11 | g.69810464G>T | CA381663591 | FGF3 | c.561C>A (p.Asp187Glu) n.408C>A | dbSNP gnomAD v2 gnomAD v4 |
11 | g.69810465T>A | CA381663593 | FGF3 | c.560A>T (p.Asp187Val) n.407A>T | |
11 | g.69810465T>C | CA381663594 | FGF3 | c.560A>G (p.Asp187Gly) n.407A>G | gnomAD v4 |
11 | g.69810465T>G | CA381663592 | FGF3 | c.560A>C (p.Asp187Ala) n.407A>C | |
11 | g.69810466C>A | CA381663595 | FGF3 | c.559G>T (p.Asp187Tyr) n.406G>T | gnomAD v4 |
11 | g.69810466C= | CA1980742038 | FGF3 | c.559G= (p.Asp187=) n.406G= | |
11 | g.69810466C>G | CA381663596 | FGF3 | c.559G>C (p.Asp187His) n.406G>C | |
11 | g.69810466C>T | CA381663597 | FGF3 | c.559G>A (p.Asp187Asn) n.406G>A | dbSNP gnomAD v3 gnomAD v4 |
11 | g.69810467C>A | CA381663598 | FGF3 | c.558G>T (p.Arg186Ser) n.405G>T | |
11 | g.69810467C>G | CA381663599 | FGF3 | c.558G>C (p.Arg186Ser) n.405G>C | |
11 | g.69810467C>T | CA475468029 | FGF3 | c.558G>A (p.Arg186=) n.405G>A | |
11 | g.69810468C>A | CA381663602 | FGF3 | c.557G>T (p.Arg186Met) n.404G>T | gnomAD v4 |
11 | g.69810468C>G | CA381663601 | FGF3 | c.557G>C (p.Arg186Thr) n.404G>C | |
11 | g.69810468C>T | CA381663600 | FGF3 | c.557G>A (p.Arg186Lys) n.404G>A | |
11 | g.69810469T>A | CA381663603 | FGF3 | c.556A>T (p.Arg186Trp) n.403A>T | |
11 | g.69810469T>C | CA381663604 | FGF3 | c.556A>G (p.Arg186Gly) n.403A>G | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.69810469T>G | CA475468030 | FGF3 | c.556A>C (p.Arg186=) n.403A>C | |
11 | g.69810469T= | CA1980742039 | FGF3 | c.556A= (p.Arg186=) n.403A= | |
11 | g.69810470G>A | CA475468031 | FGF3 | c.555C>T (p.His185=) n.402C>T | |
11 | g.69810470G>C | CA381663605 | FGF3 | c.555C>G (p.His185Gln) n.402C>G | |
11 | g.69810470G>T | CA381663606 | FGF3 | c.555C>A (p.His185Gln) n.402C>A | |
11 | g.69810471T>A | CA381663607 | FGF3 | c.554A>T (p.His185Leu) n.401A>T | |
11 | g.69810471T>C | CA381663608 | FGF3 | c.554A>G (p.His185Arg) n.401A>G | gnomAD v4 |
11 | g.69810471T>G | CA6157036 | FGF3 | c.554A>C (p.His185Pro) n.401A>C | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.69810471T= | CA1980742040 | FGF3 | c.554A= (p.His185=) n.401A= | |
11 | g.69810472G>A | CA381663609 | FGF3 | c.553C>T (p.His185Tyr) n.400C>T | gnomAD v4 |
11 | g.69810472G>C | CA381663611 | FGF3 | c.553C>G (p.His185Asp) n.400C>G | |
11 | g.69810472G>T | CA381663610 | FGF3 | c.553C>A (p.His185Asn) n.400C>A | |
11 | g.69810473G>A | CA475468032 | FGF3 | c.552C>T (p.Asp184=) n.399C>T | |
11 | g.69810473G>C | CA381663612 | FGF3 | c.552C>G (p.Asp184Glu) n.399C>G | |
11 | g.69810473G>T | CA381663613 | FGF3 | c.552C>A (p.Asp184Glu) n.399C>A | |
11 | g.69810474T>A | CA381663614 | FGF3 | c.551A>T (p.Asp184Val) n.398A>T | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.69810474T>C | CA6157037 | FGF3 | c.551A>G (p.Asp184Gly) n.398A>G | dbSNP ExAC gnomAD v2 |
11 | g.69810474T>G | CA381663615 | FGF3 | c.551A>C (p.Asp184Ala) n.398A>C | dbSNP |
11 | g.69810474T= | CA1980742041 | FGF3 | c.551A= (p.Asp184=) n.398A= | |
11 | g.69810475C>A | CA381663616 | FGF3 | c.550G>T (p.Asp184Tyr) n.397G>T | |
11 | g.69810475C>G | CA381663617 | FGF3 | c.550G>C (p.Asp184His) n.397G>C | |
11 | g.69810475C>T | CA381663618 | FGF3 | c.550G>A (p.Asp184Asn) n.397G>A | gnomAD v4 COSMIC |
11 | g.69810476C>A | CA475468033 | FGF3 | c.549G>T (p.Leu183=) n.396G>T | |
11 | g.69810476C>G | CA475468034 | FGF3 | c.549G>C (p.Leu183=) n.396G>C | |
11 | g.69810476C>T | CA475468035 | FGF3 | c.549G>A (p.Leu183=) n.396G>A | gnomAD v4 |
11 | g.69810477A= | CA1980742042 | FGF3 | c.548T= (p.Leu183=) n.395T= | |
11 | g.69810477A>C | CA381663619 | FGF3 | c.548T>G (p.Leu183Arg) n.395T>G | |
11 | g.69810477A>G | CA6157038 | FGF3 | c.548T>C (p.Leu183Pro) n.395T>C | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.69810477A>T | CA381663620 | FGF3 | c.548T>A (p.Leu183Gln) n.395T>A | |
11 | g.69810478G>A | CA475468036 | FGF3 | c.547C>T (p.Leu183=) n.394C>T | dbSNP gnomAD v4 |
11 | g.69810478G>C | CA381663621 | FGF3 | c.547C>G (p.Leu183Val) n.394C>G | gnomAD v4 |
11 | g.69810478G>T | CA381663622 | FGF3 | c.547C>A (p.Leu183Met) n.394C>A | |
11 | g.69810479C>A | CA475468037 | FGF3 | c.546G>T (p.Val182=) n.393G>T | |
11 | g.69810479C= | CA1980742043 | FGF3 | c.546G= (p.Val182=) n.393G= | |
11 | g.69810479C>G | CA475468038 | FGF3 | c.546G>C (p.Val182=) n.393G>C | |
11 | g.69810479C>T | CA475468039 | FGF3 | c.546G>A (p.Val182=) n.393G>A | dbSNP gnomAD v2 gnomAD v4 COSMIC |
11 | g.69810480A>C | CA381663623 | FGF3 | c.545T>G (p.Val182Gly) n.392T>G | |
11 | g.69810480A>G | CA381663625 | FGF3 | c.545T>C (p.Val182Ala) n.392T>C | |
11 | g.69810480A>T | CA381663624 | FGF3 | c.545T>A (p.Val182Glu) n.392T>A | |
11 | g.69810481C>A | CA381663626 | FGF3 | c.544G>T (p.Val182Leu) n.391G>T | gnomAD v4 |
11 | g.69810481C= | CA1980742044 | FGF3 | c.544G= (p.Val182=) n.391G= | |
11 | g.69810481C>G | CA381663627 | FGF3 | c.544G>C (p.Val182Leu) n.391G>C | gnomAD v4 |
11 | g.69810481C>T | CA6157039 | FGF3 | c.544G>A (p.Val182Met) n.391G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
11 | g.69810482G>A | CA475468040 | FGF3 | c.543C>T (p.Arg181=) n.390C>T | dbSNP gnomAD v3 gnomAD v4 COSMIC |
11 | g.69810482G>C | CA475468041 | FGF3 | c.543C>G (p.Arg181=) n.390C>G | |
11 | g.69810482G= | CA1980742045 | FGF3 | c.543C= (p.Arg181=) n.390C= | |
11 | g.69810482G>T | CA475468042 | FGF3 | c.543C>A (p.Arg181=) n.390C>A | gnomAD v4 |
11 | g.69810483C>A | CA381663628 | FGF3 | c.542G>T (p.Arg181Leu) n.389G>T | dbSNP gnomAD v2 |
11 | g.69810483C= | CA1980742046 | FGF3 | c.542G= (p.Arg181=) n.389G= | |
11 | g.69810483C>G | CA381663629 | FGF3 | c.542G>C (p.Arg181Pro) n.389G>C | dbSNP |
11 | g.69810483C>T | CA6157040 | FGF3 | c.542G>A (p.Arg181His) n.389G>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
11 | g.69810484G>A | CA6157041 | FGF3 | c.541C>T (p.Arg181Cys) n.388C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
11 | g.69810484G>C | CA381663630 | FGF3 | c.541C>G (p.Arg181Gly) n.388C>G | |
11 | g.69810484G= | CA1980742047 | FGF3 | c.541C= (p.Arg181=) n.388C= | |
11 | g.69810484G>T | CA381663631 | FGF3 | c.541C>A (p.Arg181Ser) n.388C>A | gnomAD v4 |
11 | g.69810485G>A | CA475468043 | FGF3 | c.540C>T (p.Pro180=) n.387C>T | dbSNP |
11 | g.69810485G>C | CA475468044 | FGF3 | c.540C>G (p.Pro180=) n.387C>G | |
11 | g.69810485G>T | CA475468045 | FGF3 | c.540C>A (p.Pro180=) n.387C>A | |
11 | g.69810486G>A | CA381663632 | FGF3 | c.539C>T (p.Pro180Leu) n.386C>T | |
11 | g.69810486G>C | CA381663633 | FGF3 | c.539C>G (p.Pro180Arg) n.386C>G | |
11 | g.69810486G= | CA1980742048 | FGF3 | c.539C= (p.Pro180=) n.386C= | |
11 | g.69810486G>T | CA6157042 | FGF3 | c.539C>A (p.Pro180His) n.386C>A | dbSNP ExAC gnomAD v2 gnomAD v4 |
11 | g.69810487G>A | CA381663635 | FGF3 | c.538C>T (p.Pro180Ser) n.385C>T | |
11 | g.69810487G>C | CA381663636 | FGF3 | c.538C>G (p.Pro180Ala) n.385C>G | |
11 | g.69810487G= | CA1980742049 | FGF3 | c.538C= (p.Pro180=) n.385C= | |
11 | g.69810487G>T | CA381663634 | FGF3 | c.538C>A (p.Pro180Thr) n.385C>A | dbSNP gnomAD v2 gnomAD v4 |
11 | g.69810488C>A | CA475468047 | FGF3 | c.537G>T (p.Leu179=) n.384G>T | |
11 | g.69810488C>G | CA475468048 | FGF3 | c.537G>C (p.Leu179=) n.384G>C | dbSNP |
11 | g.69810488C>T | CA475468046 | FGF3 | c.537G>A (p.Leu179=) n.384G>A | dbSNP gnomAD v4 |
11 | g.69810489A>C | CA381663637 | FGF3 | c.536T>G (p.Leu179Arg) n.383T>G | |
11 | g.69810489A>G | CA381663638 | FGF3 | c.536T>C (p.Leu179Pro) n.383T>C | |
11 | g.69810489A>T | CA381663639 | FGF3 | c.536T>A (p.Leu179Gln) n.383T>A | gnomAD v4 |
11 | g.69810490G>A | CA475468049 | FGF3 | c.535C>T (p.Leu179=) n.382C>T | |
11 | g.69810490G>C | CA381663640 | FGF3 | c.535C>G (p.Leu179Val) n.382C>G | |
11 | g.69810490G>T | CA381663641 | FGF3 | c.535C>A (p.Leu179Met) n.382C>A | gnomAD v4 |
11 | g.69810491G>A | CA475468050 | FGF3 | c.534C>T (p.Phe178=) n.381C>T | dbSNP gnomAD v3 gnomAD v4 COSMIC |
11 | g.69810491G>C | CA6157043 | FGF3 | c.534C>G (p.Phe178Leu) n.381C>G | dbSNP ExAC gnomAD v2 gnomAD v4 |
11 | g.69810491G= | CA1980742050 | FGF3 | c.534C= (p.Phe178=) n.381C= | |
11 | g.69810491G>T | CA381663642 | FGF3 | c.534C>A (p.Phe178Leu) n.381C>A | |
11 | g.69810492A>C | CA381663643 | FGF3 | c.533T>G (p.Phe178Cys) n.380T>G | |
11 | g.69810492A>G | CA381663644 | FGF3 | c.533T>C (p.Phe178Ser) n.380T>C | |
11 | g.69810492A>T | CA381663645 | FGF3 | c.533T>A (p.Phe178Tyr) n.380T>A | |
11 | g.69810493A>C | CA381663646 | FGF3 | c.532T>G (p.Phe178Val) n.379T>G | |
11 | g.69810493A>G | CA381663647 | FGF3 | c.532T>C (p.Phe178Leu) n.379T>C | |
11 | g.69810493A>T | CA381663648 | FGF3 | c.532T>A (p.Phe178Ile) n.379T>A | |
11 | g.69810494C>A | CA475468051 | FGF3 | c.531G>T (p.Leu177=) n.378G>T | |
11 | g.69810494C>G | CA475468053 | FGF3 | c.531G>C (p.Leu177=) n.378G>C | gnomAD v4 |
11 | g.69810494C>T | CA475468052 | FGF3 | c.531G>A (p.Leu177=) n.378G>A | |
11 | g.69810495A>C | CA381663649 | FGF3 | c.530T>G (p.Leu177Arg) n.377T>G | |
11 | g.69810495A>G | CA381663651 | FGF3 | c.530T>C (p.Leu177Pro) n.377T>C | |
11 | g.69810495A>T | CA381663650 | FGF3 | c.530T>A (p.Leu177Gln) n.377T>A | |
11 | g.69810496G>A | CA475468054 | FGF3 | c.529C>T (p.Leu177=) n.376C>T | |
11 | g.69810496G>C | CA381663652 | FGF3 | c.529C>G (p.Leu177Val) n.376C>G | |
11 | g.69810496G>T | CA381663653 | FGF3 | c.529C>A (p.Leu177Met) n.376C>A | |
11 | g.69810496_69810499delinsGGGA | CA1980742051 | FGF3 | c.526_529delinsTCCC (p.Ser176=) n.373_376delinsTCCC | |
11 | g.69810497G>A | CA475468055 | FGF3 | c.528C>T (p.Ser176=) n.375C>T | |
11 | g.69810497G>C | CA475468056 | FGF3 | c.528C>G (p.Ser176=) n.375C>G | |
11 | g.69810497G= | CA1980742053 | FGF3 | c.528C= (p.Ser176=) n.375C= | |
11 | g.69810497G>T | CA475468057 | FGF3 | c.528C>A (p.Ser176=) n.375C>A | dbSNP gnomAD v2 |
11 | g.69810500_69810502del | CA1980742052 | FGF3 | c.526_528del (p.Ser176del) n.373_375del | dbSNP |
11 | g.69810498G>A | CA381663654 | FGF3 | c.527C>T (p.Ser176Phe) n.374C>T | gnomAD v4 COSMIC |
11 | g.69810498G>C | CA381663655 | FGF3 | c.527C>G (p.Ser176Cys) n.374C>G | |
11 | g.69810498G>T | CA381663656 | FGF3 | c.527C>A (p.Ser176Tyr) n.374C>A | dbSNP |
11 | g.69810499A>C | CA381663657 | FGF3 | c.526T>G (p.Ser176Ala) n.373T>G | |
11 | g.69810499A>G | CA381663658 | FGF3 | c.526T>C (p.Ser176Pro) n.373T>C | |
11 | g.69810499A>T | CA381663659 | FGF3 | c.526T>A (p.Ser176Thr) n.373T>A | |
11 | g.69810500G>A | CA475468058 | FGF3 | c.525C>T (p.Ser175=) n.372C>T | dbSNP |
11 | g.69810500G>C | CA475468059 | FGF3 | c.525C>G (p.Ser175=) n.372C>G | |
11 | g.69810500G>T | CA475468060 | FGF3 | c.525C>A (p.Ser175=) n.372C>A | |
11 | g.69810501G>A | CA381663660 | FGF3 | c.524C>T (p.Ser175Phe) n.371C>T | gnomAD v4 |
11 | g.69810501G>C | CA381663661 | FGF3 | c.524C>G (p.Ser175Cys) n.371C>G | dbSNP |
11 | g.69810501G>T | CA381663662 | FGF3 | c.524C>A (p.Ser175Tyr) n.371C>A | |
11 | g.69810502A>C | CA381663663 | FGF3 | c.523T>G (p.Ser175Ala) n.370T>G | |
11 | g.69810502A>G | CA381663664 | FGF3 | c.523T>C (p.Ser175Pro) n.370T>C | |
11 | g.69810502A>T | CA381663665 | FGF3 | c.523T>A (p.Ser175Thr) n.370T>A | ClinVar dbSNP |
11 | g.69810503C>A | CA6157044 | FGF3 | c.522G>T (p.Lys174Asn) n.369G>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
11 | g.69810503C= | CA1980742054 | FGF3 | c.522G= (p.Lys174=) n.369G= | |
11 | g.69810503C>G | CA381663666 | FGF3 | c.522G>C (p.Lys174Asn) n.369G>C | dbSNP gnomAD v4 |
11 | g.69810503C>T | CA475468061 | FGF3 | c.522G>A (p.Lys174=) n.369G>A | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.69810504T>A | CA381663667 | FGF3 | c.521A>T (p.Lys174Met) n.368A>T | |
11 | g.69810504T>C | CA381663668 | FGF3 | c.521A>G (p.Lys174Arg) n.368A>G | |
11 | g.69810504T>G | CA381663669 | FGF3 | c.521A>C (p.Lys174Thr) n.368A>C | |
11 | g.69810505T>A | CA381663670 | FGF3 | c.520A>T (p.Lys174Ter) n.367A>T | |
11 | g.69810505T>C | CA381663671 | FGF3 | c.520A>G (p.Lys174Glu) n.367A>G | COSMIC |
11 | g.69810505T>G | CA381663672 | FGF3 | c.520A>C (p.Lys174Gln) n.367A>C | |
11 | g.69810505_69810506delinsTC | CA1980742055 | FGF3 | c.519_520delinsGA (p.Gln173=) n.366_367delinsGA | |
11 | g.69810506del | CA679738694 | FGF3 | c.519del (p.Lys174SerfsTer?) n.366del | dbSNP gnomAD v4 |
11 | g.69810506C>A | CA381663674 | FGF3 | c.519G>T (p.Gln173His) n.366G>T | gnomAD v4 |
11 | g.69810506C>G | CA381663673 | FGF3 | c.519G>C (p.Gln173His) n.366G>C | |
11 | g.69810506C>T | CA475468062 | FGF3 | c.519G>A (p.Gln173=) n.366G>A | |
11 | g.69810507T>A | CA223497103 | FGF3 | c.518A>T (p.Gln173Leu) n.365A>T | dbSNP |
11 | g.69810507T>C | CA381663675 | FGF3 | c.518A>G (p.Gln173Arg) n.365A>G | gnomAD v4 |
11 | g.69810507T>G | CA381663676 | FGF3 | c.518A>C (p.Gln173Pro) n.365A>C | gnomAD v4 |
11 | g.69810507T= | CA1980742056 | FGF3 | c.518A= (p.Gln173=) n.365A= | |
11 | g.69810511_69810512del | CA2614796971 | FGF3 | c.517_518del (p.Gln173GlufsTer?) n.364_365del | gnomAD v4 |
11 | g.69810508G>A | CA381663677 | FGF3 | c.517C>T (p.Gln173Ter) n.364C>T | gnomAD v4 |
11 | g.69810508G>C | CA381663678 | FGF3 | c.517C>G (p.Gln173Glu) n.364C>G | |
11 | g.69810508G>T | CA381663679 | FGF3 | c.517C>A (p.Gln173Lys) n.364C>A | |
11 | g.69810509T>A | CA475468063 | FGF3 | c.516A>T (p.Thr172=) n.363A>T | gnomAD v4 |
11 | g.69810509T>C | CA475468064 | FGF3 | c.516A>G (p.Thr172=) n.363A>G | |
11 | g.69810509T>G | CA475468065 | FGF3 | c.516A>C (p.Thr172=) n.363A>C | |
11 | g.69810510G>A | CA381663680 | FGF3 | c.515C>T (p.Thr172Ile) n.362C>T | |
11 | g.69810510G>C | CA381663682 | FGF3 | c.515C>G (p.Thr172Arg) n.362C>G | |
11 | g.69810510G>T | CA381663681 | FGF3 | c.515C>A (p.Thr172Lys) n.362C>A | |
11 | g.69810511T>A | CA381663683 | FGF3 | c.514A>T (p.Thr172Ser) n.361A>T | |
11 | g.69810511T>C | CA381663684 | FGF3 | c.514A>G (p.Thr172Ala) n.361A>G | |
11 | g.69810511T>G | CA381663685 | FGF3 | c.514A>C (p.Thr172Pro) n.361A>C | |
11 | g.69810512G>A | CA475468066 | FGF3 | c.513C>T (p.Arg171=) n.360C>T | dbSNP gnomAD v2 |
11 | g.69810512G>C | CA475468067 | FGF3 | c.513C>G (p.Arg171=) n.360C>G | |
11 | g.69810512G= | CA1980742057 | FGF3 | c.513C= (p.Arg171=) n.360C= | |
11 | g.69810512G>T | CA475468068 | FGF3 | c.513C>A (p.Arg171=) n.360C>A | |
11 | g.69810513C>A | CA381663686 | FGF3 | c.512G>T (p.Arg171Leu) n.359G>T | |
11 | g.69810513C= | CA1980742058 | FGF3 | c.512G= (p.Arg171=) n.359G= | |
11 | g.69810513C>G | CA381663687 | FGF3 | c.512G>C (p.Arg171Pro) n.359G>C | |
11 | g.69810513C>T | CA6157045 | FGF3 | c.512G>A (p.Arg171His) n.359G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.69810514G>A | CA381663688 | FGF3 | c.511C>T (p.Arg171Cys) n.358C>T | dbSNP gnomAD v2 gnomAD v4 |
11 | g.69810514G>C | CA381663689 | FGF3 | c.511C>G (p.Arg171Gly) n.358C>G | gnomAD v4 |
11 | g.69810514G= | CA1980742059 | FGF3 | c.511C= (p.Arg171=) n.358C= | |
11 | g.69810514G>T | CA381663690 | FGF3 | c.511C>A (p.Arg171Ser) n.358C>A | dbSNP |
11 | g.69810515G>A | CA475468069 | FGF3 | c.510C>T (p.Arg170=) n.357C>T | COSMIC |
11 | g.69810515G>C | CA475468070 | FGF3 | c.510C>G (p.Arg170=) n.357C>G | gnomAD v4 |
11 | g.69810515G= | CA1980742060 | FGF3 | c.510C= (p.Arg170=) n.357C= | |
11 | g.69810515G>T | CA6157046 | FGF3 | c.510C>A (p.Arg170=) n.357C>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.69810516C>A | CA6157048 | FGF3 | c.509G>T (p.Arg170Leu) n.356G>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.69810516C= | CA1980742061 | FGF3 | c.509G= (p.Arg170=) n.356G= | |
11 | g.69810516C>G | CA381663691 | FGF3 | c.509G>C (p.Arg170Pro) n.356G>C | |
11 | g.69810516C>T | CA6157047 | FGF3 | c.509G>A (p.Arg170His) n.356G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
11 | g.69810517G>A | CA6157049 | FGF3 | c.508C>T (p.Arg170Cys) n.355C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.69810517G>C | CA381663693 | FGF3 | c.508C>G (p.Arg170Gly) n.355C>G | dbSNP |
11 | g.69810517G= | CA1980742062 | FGF3 | c.508C= (p.Arg170=) n.355C= | |
11 | g.69810517G>T | CA381663692 | FGF3 | c.508C>A (p.Arg170Ser) n.355C>A | dbSNP |
11 | g.69810519del | CA2614797007 | FGF3 | c.508del (p.Arg170AlafsTer?) n.355del | gnomAD v4 |
11 | g.69810518G>A | CA475468071 | FGF3 | c.507C>T (p.Thr169=) n.354C>T | dbSNP |
11 | g.69810518G>C | CA475468072 | FGF3 | c.507C>G (p.Thr169=) n.354C>G | ClinVar |
11 | g.69810518G>T | CA475468073 | FGF3 | c.507C>A (p.Thr169=) n.354C>A | |
11 | g.69810519G>A | CA381663694 | FGF3 | c.506C>T (p.Thr169Ile) n.353C>T | gnomAD v4 |
11 | g.69810519G>C | CA381663695 | FGF3 | c.506C>G (p.Thr169Ser) n.353C>G | |
11 | g.69810519G>T | CA381663696 | FGF3 | c.506C>A (p.Thr169Asn) n.353C>A | |
11 | g.69810520T>A | CA381663697 | FGF3 | c.505A>T (p.Thr169Ser) n.352A>T | dbSNP |
11 | g.69810520T>C | CA381663698 | FGF3 | c.505A>G (p.Thr169Ala) n.352A>G | dbSNP gnomAD v4 COSMIC |
11 | g.69810520T>G | CA6157050 | FGF3 | c.505A>C (p.Thr169Pro) n.352A>C | dbSNP ExAC gnomAD v2 gnomAD v4 |
11 | g.69810520T= | CA1980742063 | FGF3 | c.505A= (p.Thr169=) n.352A= | |
11 | g.69810521C>A | CA381663699 | FGF3 | c.504G>T (p.Lys168Asn) n.351G>T | |
11 | g.69810521C= | CA1980742064 | FGF3 | c.504G= (p.Lys168=) n.351G= | |
11 | g.69810521C>G | CA381663700 | FGF3 | c.504G>C (p.Lys168Asn) n.351G>C | |
11 | g.69810521C>T | CA475468074 | FGF3 | c.504G>A (p.Lys168=) n.351G>A | dbSNP gnomAD v2 gnomAD v4 |
11 | g.69810522T>A | CA381663701 | FGF3 | c.503A>T (p.Lys168Met) n.350A>T | |
11 | g.69810522T>C | CA381663702 | FGF3 | c.503A>G (p.Lys168Arg) n.350A>G | dbSNP gnomAD v2 |
11 | g.69810522T>G | CA381663703 | FGF3 | c.503A>C (p.Lys168Thr) n.350A>C | |
11 | g.69810522T= | CA1980742065 | FGF3 | c.503A= (p.Lys168=) n.350A= | |
11 | g.69810523T>A | CA381663705 | FGF3 | c.502A>T (p.Lys168Ter) n.349A>T | |
11 | g.69810523T>C | CA381663706 | FGF3 | c.502A>G (p.Lys168Glu) n.349A>G | dbSNP |
11 | g.69810523T>G | CA381663704 | FGF3 | c.502A>C (p.Lys168Gln) n.349A>C | |
11 | g.69810524G>A | CA475468075 | FGF3 | c.501C>T (p.Phe167=) n.348C>T | |
11 | g.69810524G>C | CA381663708 | FGF3 | c.501C>G (p.Phe167Leu) n.348C>G | dbSNP |
11 | g.69810524G= | CA1980742066 | FGF3 | c.501C= (p.Phe167=) n.348C= | |
11 | g.69810524G>T | CA381663707 | FGF3 | c.501C>A (p.Phe167Leu) n.348C>A | dbSNP gnomAD v4 |
11 | g.69810525A>C | CA381663710 | FGF3 | c.500T>G (p.Phe167Cys) n.347T>G | |
11 | g.69810525A>G | CA381663709 | FGF3 | c.500T>C (p.Phe167Ser) n.347T>C | |
11 | g.69810525A>T | CA381663711 | FGF3 | c.500T>A (p.Phe167Tyr) n.347T>A | |
11 | g.69810526A>C | CA381663712 | FGF3 | c.499T>G (p.Phe167Val) n.346T>G | |
11 | g.69810526A>G | CA381663713 | FGF3 | c.499T>C (p.Phe167Leu) n.346T>C | dbSNP |
11 | g.69810526A>T | CA381663714 | FGF3 | c.499T>A (p.Phe167Ile) n.346T>A | dbSNP |
11 | g.69810527G>A | CA6157051 | FGF3 | c.498C>T (p.Gly166=) n.345C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.69810527G>C | CA475468076 | FGF3 | c.498C>G (p.Gly166=) n.345C>G | |
11 | g.69810527G= | CA1980742067 | FGF3 | c.498C= (p.Gly166=) n.345C= | |
11 | g.69810527G>T | CA475468077 | FGF3 | c.498C>A (p.Gly166=) n.345C>A | |
11 | g.69810528C>A | CA381663715 | FGF3 | c.497G>T (p.Gly166Val) n.344G>T | |
11 | g.69810528C>G | CA381663716 | FGF3 | c.497G>C (p.Gly166Ala) n.344G>C | |
11 | g.69810528C>T | CA381663717 | FGF3 | c.497G>A (p.Gly166Asp) n.344G>A | dbSNP gnomAD v4 |
11 | g.69810531dup | CA2614797057 | FGF3 | c.497dup (p.Phe167LeufsTer?) n.344dup | gnomAD v4 |
11 | g.69810529C>A | CA381663718 | FGF3 | c.496G>T (p.Gly166Cys) n.343G>T | |
11 | g.69810529C= | CA1980742068 | FGF3 | c.496G= (p.Gly166=) n.343G= | |
11 | g.69810529C>G | CA381663719 | FGF3 | c.496G>C (p.Gly166Arg) n.343G>C | |
11 | g.69810529C>T | CA381663720 | FGF3 | c.496G>A (p.Gly166Ser) n.343G>A | dbSNP gnomAD v3 gnomAD v4 |
11 | g.69810530C>A | CA381663721 | FGF3 | c.495G>T (p.Arg165Ser) n.342G>T | |
11 | g.69810530C= | CA1980742069 | FGF3 | c.495G= (p.Arg165=) n.342G= | |
11 | g.69810530C>G | CA381663722 | FGF3 | c.495G>C (p.Arg165Ser) n.342G>C | |
11 | g.69810530C>T | CA6157052 | FGF3 | c.495G>A (p.Arg165=) n.342G>A | dbSNP ExAC gnomAD v2 gnomAD v4 |
11 | g.69810531C>A | CA381663725 | FGF3 | c.494G>T (p.Arg165Met) n.341G>T | |
11 | g.69810531C>G | CA381663723 | FGF3 | c.494G>C (p.Arg165Thr) n.341G>C | |
11 | g.69810531C>T | CA381663724 | FGF3 | c.494G>A (p.Arg165Lys) n.341G>A | gnomAD v4 |
11 | g.69810532T>A | CA381663726 | FGF3 | c.493A>T (p.Arg165Trp) n.340A>T | |
11 | g.69810532T>C | CA381663727 | FGF3 | c.493A>G (p.Arg165Gly) n.340A>G | gnomAD v4 |
11 | g.69810532T>G | CA475468078 | FGF3 | c.493A>C (p.Arg165=) n.340A>C | |
11 | g.69810533G>A | CA475468079 | FGF3 | c.492C>T (p.Arg164=) n.339C>T | gnomAD v4 |
11 | g.69810533G>C | CA475468081 | FGF3 | c.492C>G (p.Arg164=) n.339C>G | gnomAD v4 |
11 | g.69810533G>T | CA475468080 | FGF3 | c.492C>A (p.Arg164=) n.339C>A | |
11 | g.69810534C>A | CA381663728 | FGF3 | c.491G>T (p.Arg164Leu) n.338G>T | |
11 | g.69810534C= | CA1980742070 | FGF3 | c.491G= (p.Arg164=) n.338G= | |
11 | g.69810534C>G | CA381663729 | FGF3 | c.491G>C (p.Arg164Pro) n.338G>C | |
11 | g.69810534C>T | CA6157053 | FGF3 | c.491G>A (p.Arg164His) n.338G>A | dbSNP ExAC gnomAD v2 gnomAD v4 |
11 | g.69810535G>A | CA381663730 | FGF3 | c.490C>T (p.Arg164Cys) n.337C>T | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.69810535G>C | CA381663731 | FGF3 | c.490C>G (p.Arg164Gly) n.337C>G | gnomAD v4 |
11 | g.69810535G= | CA1980742071 | FGF3 | c.490C= (p.Arg164=) n.337C= | |
11 | g.69810535G>T | CA381663732 | FGF3 | c.490C>A (p.Arg164Ser) n.337C>A | |
11 | g.69810536G>A | CA475468082 | FGF3 | c.489C>T (p.Pro163=) n.336C>T | gnomAD v4 |
11 | g.69810536G>C | CA475468083 | FGF3 | c.489C>G (p.Pro163=) n.336C>G | |
11 | g.69810536G>T | CA475468084 | FGF3 | c.489C>A (p.Pro163=) n.336C>A | |
11 | g.69810537G>A | CA381663733 | FGF3 | c.488C>T (p.Pro163Leu) n.335C>T | |
11 | g.69810537G>C | CA381663734 | FGF3 | c.488C>G (p.Pro163Arg) n.335C>G | |
11 | g.69810537G>T | CA381663735 | FGF3 | c.488C>A (p.Pro163His) n.335C>A | gnomAD v4 |
11 | g.69810538G>A | CA381663738 | FGF3 | c.487C>T (p.Pro163Ser) n.334C>T | dbSNP |
11 | g.69810538G>C | CA381663737 | FGF3 | c.487C>G (p.Pro163Ala) n.334C>G | dbSNP |
11 | g.69810538G>T | CA381663736 | FGF3 | c.487C>A (p.Pro163Thr) n.334C>A | |
11 | g.69810539C>A | CA475468085 | FGF3 | c.486G>T (p.Arg162=) n.333G>T | |
11 | g.69810539C= | CA1980742072 | FGF3 | c.486G= (p.Arg162=) n.333G= | |
11 | g.69810539C>G | CA475468086 | FGF3 | c.486G>C (p.Arg162=) n.333G>C | |
11 | g.69810539C>T | CA223497123 | FGF3 | c.486G>A (p.Arg162=) n.333G>A | dbSNP gnomAD v4 |
11 | g.69810540C>A | CA6157054 | FGF3 | c.485G>T (p.Arg162Leu) n.332G>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
11 | g.69810540C= | CA1980742073 | FGF3 | c.485G= (p.Arg162=) n.332G= | |
11 | g.69810540C>G | CA381663739 | FGF3 | c.485G>C (p.Arg162Pro) n.332G>C | |
11 | g.69810540C>T | CA381663740 | FGF3 | c.485G>A (p.Arg162Gln) n.332G>A | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.69810541G>A | CA381663741 | FGF3 | c.484C>T (p.Arg162Trp) n.331C>T | dbSNP gnomAD v4 |
11 | g.69810541G>C | CA381663742 | FGF3 | c.484C>G (p.Arg162Gly) n.331C>G | dbSNP gnomAD v3 gnomAD v4 |
11 | g.69810541G= | CA1980742074 | FGF3 | c.484C= (p.Arg162=) n.331C= | |
11 | g.69810541G>T | CA6157055 | FGF3 | c.484C>A (p.Arg162=) n.331C>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.69810542G>A | CA475468089 | FGF3 | c.483C>T (p.Gly161=) n.330C>T | dbSNP gnomAD v4 |
11 | g.69810542G>C | CA475468088 | FGF3 | c.483C>G (p.Gly161=) n.330C>G | |
11 | g.69810542G>T | CA475468087 | FGF3 | c.483C>A (p.Gly161=) n.330C>A | |
11 | g.69810543C>A | CA381663743 | FGF3 | c.482G>T (p.Gly161Val) n.329G>T | |
11 | g.69810543C>G | CA381663744 | FGF3 | c.482G>C (p.Gly161Ala) n.329G>C | |
11 | g.69810543C>T | CA381663745 | FGF3 | c.482G>A (p.Gly161Asp) n.329G>A | |
11 | g.69810544C>A | CA381663746 | FGF3 | c.481G>T (p.Gly161Cys) n.328G>T | |
11 | g.69810544C>G | CA381663747 | FGF3 | c.481G>C (p.Gly161Arg) n.328G>C | |
11 | g.69810544C>T | CA381663748 | FGF3 | c.481G>A (p.Gly161Ser) n.328G>A | |
11 | g.69810545C>A | CA381663750 | FGF3 | c.480G>T (p.Lys160Asn) n.327G>T | |
11 | g.69810545C= | CA1980742075 | FGF3 | c.480G= (p.Lys160=) n.327G= | |
11 | g.69810545C>G | CA381663749 | FGF3 | c.480G>C (p.Lys160Asn) n.327G>C | |
11 | g.69810545C>T | CA6157056 | FGF3 | c.480G>A (p.Lys160=) n.327G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
11 | g.69810546T>A | CA381663751 | FGF3 | c.479A>T (p.Lys160Met) n.326A>T | dbSNP |
11 | g.69810546T>C | CA381663752 | FGF3 | c.479A>G (p.Lys160Arg) n.326A>G | dbSNP |
11 | g.69810546T>G | CA381663753 | FGF3 | c.479A>C (p.Lys160Thr) n.326A>C | |
11 | g.69810547T>A | CA381663754 | FGF3 | c.478A>T (p.Lys160Ter) n.325A>T | |
11 | g.69810547T>C | CA381663755 | FGF3 | c.478A>G (p.Lys160Glu) n.325A>G | |
11 | g.69810547T>G | CA381663756 | FGF3 | c.478A>C (p.Lys160Gln) n.325A>C | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.69810547T= | CA1980742076 | FGF3 | c.478A= (p.Lys160=) n.325A= | |
11 | g.69810548G>A | CA475468090 | FGF3 | c.477C>T (p.Gly159=) n.324C>T | dbSNP gnomAD v2 gnomAD v4 |
11 | g.69810548G>C | CA475468091 | FGF3 | c.477C>G (p.Gly159=) n.324C>G | |
11 | g.69810548G= | CA1980742077 | FGF3 | c.477C= (p.Gly159=) n.324C= | |
11 | g.69810548G>T | CA475468092 | FGF3 | c.477C>A (p.Gly159=) n.324C>A | |
11 | g.69810549C>A | CA381663757 | FGF3 | c.476G>T (p.Gly159Val) n.323G>T | |
11 | g.69810549C= | CA1980742078 | FGF3 | c.476G= (p.Gly159=) n.323G= | |
11 | g.69810549C>G | CA381663758 | FGF3 | c.476G>C (p.Gly159Ala) n.323G>C | |
11 | g.69810549C>T | CA381663759 | FGF3 | c.476G>A (p.Gly159Asp) n.323G>A | dbSNP gnomAD v2 gnomAD v4 |
11 | g.69810550C>A | CA381663760 | FGF3 | c.475G>T (p.Gly159Cys) n.322G>T | |
11 | g.69810550C= | CA1980742079 | FGF3 | c.475G= (p.Gly159=) n.322G= | |
11 | g.69810550C>G | CA381663761 | FGF3 | c.475G>C (p.Gly159Arg) n.322G>C | dbSNP gnomAD v2 gnomAD v4 |
11 | g.69810550C>T | CA223497154 | FGF3 | c.475G>A (p.Gly159Ser) n.322G>A | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.69810551G>A | CA475468093 | FGF3 | c.474C>T (p.Asn158=) n.321C>T | dbSNP gnomAD v4 COSMIC |
11 | g.69810551G>C | CA381663763 | FGF3 | c.474C>G (p.Asn158Lys) n.321C>G | |
11 | g.69810551G= | CA1980742080 | FGF3 | c.474C= (p.Asn158=) n.321C= | |
11 | g.69810551G>T | CA381663762 | FGF3 | c.474C>A (p.Asn158Lys) n.321C>A | gnomAD v4 |
11 | g.69810552T>A | CA381663764 | FGF3 | c.473A>T (p.Asn158Ile) n.320A>T | dbSNP |
11 | g.69810552T>C | CA381663765 | FGF3 | c.473A>G (p.Asn158Ser) n.320A>G | dbSNP gnomAD v3 gnomAD v4 |
11 | g.69810552T>G | CA381663766 | FGF3 | c.473A>C (p.Asn158Thr) n.320A>C | |
11 | g.69810552T= | CA1980742081 | FGF3 | c.473A= (p.Asn158=) n.320A= | |
11 | g.69810553T>A | CA381663767 | FGF3 | c.472A>T (p.Asn158Tyr) n.319A>T | |
11 | g.69810553T>C | CA381663768 | FGF3 | c.472A>G (p.Asn158Asp) n.319A>G | dbSNP |
11 | g.69810553T>G | CA381663769 | FGF3 | c.472A>C (p.Asn158His) n.319A>C | |
11 | g.69810554C>A | CA475468094 | FGF3 | c.471G>T (p.Val157=) n.318G>T | |
11 | g.69810554C= | CA1980742082 | FGF3 | c.471G= (p.Val157=) n.318G= | |
11 | g.69810554C>G | CA475468095 | FGF3 | c.471G>C (p.Val157=) n.318G>C | |
11 | g.69810554C>T | CA475468096 | FGF3 | c.471G>A (p.Val157=) n.318G>A | dbSNP gnomAD v2 gnomAD v4 |
11 | g.69810556_69810557del | CA2614797122 | FGF3 | c.470_471del (p.Val157GlufsTer?) n.317_318del | gnomAD v4 |
11 | g.69810555A>C | CA381663772 | FGF3 | c.470T>G (p.Val157Gly) n.317T>G | |
11 | g.69810555A>G | CA381663771 | FGF3 | c.470T>C (p.Val157Ala) n.317T>C | gnomAD v4 |
11 | g.69810555A>T | CA381663770 | FGF3 | c.470T>A (p.Val157Glu) n.317T>A | |
11 | g.69810556C>A | CA381663773 | FGF3 | c.469G>T (p.Val157Leu) n.316G>T | |
11 | g.69810556C>G | CA381663774 | FGF3 | c.469G>C (p.Val157Leu) n.316G>C | |
11 | g.69810556C>T | CA381663775 | FGF3 | c.469G>A (p.Val157Met) n.316G>A | |
11 | g.69810557A= | CA1980742083 | FGF3 | c.468T= (p.Ser156=) n.315T= | |
11 | g.69810557A>C | CA6157057 | FGF3 | c.468T>G (p.Ser156=) n.315T>G | dbSNP ExAC gnomAD v2 gnomAD v4 |
11 | g.69810557A>G | CA475468097 | FGF3 | c.468T>C (p.Ser156=) n.315T>C | |
11 | g.69810557A>T | CA475468098 | FGF3 | c.468T>A (p.Ser156=) n.315T>A | |
11 | g.69810558G>A | CA381663776 | FGF3 | c.467C>T (p.Ser156Phe) n.314C>T | |
11 | g.69810558G>C | CA381663777 | FGF3 | c.467C>G (p.Ser156Cys) n.314C>G | dbSNP gnomAD v4 |
11 | g.69810558G= | CA1980742084 | FGF3 | c.467C= (p.Ser156=) n.314C= | |
11 | g.69810558G>T | CA381663778 | FGF3 | c.467C>A (p.Ser156Tyr) n.314C>A | |
11 | g.69810559A= | CA1980742085 | FGF3 | c.466T= (p.Ser156=) n.313T= | |
11 | g.69810559A>C | CA381663779 | FGF3 | c.466T>G (p.Ser156Ala) n.313T>G | |
11 | g.69810559A>G | CA341306 | FGF3 | c.466T>C (p.Ser156Pro) n.313T>C | ClinVar dbSNP ExAC |
11 | g.69810559A>T | CA381663780 | FGF3 | c.466T>A (p.Ser156Thr) n.313T>A |