Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
14 | g.28768618G>A | CA389477052 | FOXG1 | c.1339G>A (p.Ala447Thr) | |
14 | g.28768618G>C | CA389477053 | FOXG1 | c.1339G>C (p.Ala447Pro) | |
14 | g.28768618G>T | CA389477054 | FOXG1 | c.1339G>T (p.Ala447Ser) | |
14 | g.28768619C>A | CA389477055 | FOXG1 | c.1340C>A (p.Ala447Asp) | gnomAD v4 |
14 | g.28768619C>G | CA389477056 | FOXG1 | c.1340C>G (p.Ala447Gly) | |
14 | g.28768619C>T | CA389477057 | FOXG1 | c.1340C>T (p.Ala447Val) | |
14 | g.28768623dup | CA2573149905 | FOXG1 | c.1344dup (p.Ser449LeufsTer6) | ClinVar dbSNP |
14 | g.28768620C>A | CA486098736 | FOXG1 | c.1341C>A (p.Ala447=) | |
14 | g.28768620C= | CA2126000490 | FOXG1 | c.1341C= (p.Ala447=) | |
14 | g.28768620C>G | CA486098737 | FOXG1 | c.1341C>G (p.Ala447=) | |
14 | g.28768620C>T | CA7140683 | FOXG1 | c.1341C>T (p.Ala447=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.28768621C>A | CA389477060 | FOXG1 | c.1342C>A (p.Pro448Thr) | |
14 | g.28768621C>G | CA389477059 | FOXG1 | c.1342C>G (p.Pro448Ala) | COSMIC |
14 | g.28768621C>T | CA389477058 | FOXG1 | c.1342C>T (p.Pro448Ser) | |
14 | g.28768622C>A | CA389477061 | FOXG1 | c.1343C>A (p.Pro448His) | dbSNP gnomAD v3 gnomAD v4 |
14 | g.28768622C>G | CA389477062 | FOXG1 | c.1343C>G (p.Pro448Arg) | |
14 | g.28768622C>T | CA389477063 | FOXG1 | c.1343C>T (p.Pro448Leu) | gnomAD v4 |
14 | g.28768623C>A | CA486098738 | FOXG1 | c.1344C>A (p.Pro448=) | |
14 | g.28768623C= | CA2126000491 | FOXG1 | c.1344C= (p.Pro448=) | |
14 | g.28768623C>G | CA486098739 | FOXG1 | c.1344C>G (p.Pro448=) | |
14 | g.28768623C>T | CA486098740 | FOXG1 | c.1344C>T (p.Pro448=) | dbSNP gnomAD v4 COSMIC |
14 | g.28768624T>A | CA389477064 | FOXG1 | c.1345T>A (p.Ser449Thr) | |
14 | g.28768624T>C | CA389477065 | FOXG1 | c.1345T>C (p.Ser449Pro) | |
14 | g.28768624T>G | CA389477066 | FOXG1 | c.1345T>G (p.Ser449Ala) | |
14 | g.28768625C>A | CA389477067 | FOXG1 | c.1346C>A (p.Ser449Ter) | |
14 | g.28768625C>G | CA389477068 | FOXG1 | c.1346C>G (p.Ser449Trp) | |
14 | g.28768625C>T | CA389477069 | FOXG1 | c.1346C>T (p.Ser449Leu) | |
14 | g.28768626G>A | CA486098743 | FOXG1 | c.1347G>A (p.Ser449=) | ClinVar gnomAD v4 COSMIC |
14 | g.28768626G>C | CA486098746 | FOXG1 | c.1347G>C (p.Ser449=) | |
14 | g.28768626G>T | CA486098745 | FOXG1 | c.1347G>T (p.Ser449=) | |
14 | g.28768627A>C | CA258396603 | FOXG1 | c.1348A>C (p.Thr450Pro) | |
14 | g.28768627A>G | CA389477070 | FOXG1 | c.1348A>G (p.Thr450Ala) | |
14 | g.28768627A>T | CA389477071 | FOXG1 | c.1348A>T (p.Thr450Ser) | |
14 | g.28768628C>A | CA389477074 | FOXG1 | c.1349C>A (p.Thr450Asn) | |
14 | g.28768628C>G | CA389477073 | FOXG1 | c.1349C>G (p.Thr450Ser) | |
14 | g.28768628C>T | CA389477072 | FOXG1 | c.1349C>T (p.Thr450Ile) | |
14 | g.28768629C>A | CA486098754 | FOXG1 | c.1350C>A (p.Thr450=) | |
14 | g.28768629C>G | CA486098755 | FOXG1 | c.1350C>G (p.Thr450=) | |
14 | g.28768629C>T | CA486098756 | FOXG1 | c.1350C>T (p.Thr450=) | gnomAD v4 COSMIC |
14 | g.28768630C>A | CA389477075 | FOXG1 | c.1351C>A (p.Leu451Met) | |
14 | g.28768630C>G | CA389477076 | FOXG1 | c.1351C>G (p.Leu451Val) | |
14 | g.28768630C>T | CA486098757 | FOXG1 | c.1351C>T (p.Leu451=) | ClinVar |
14 | g.28768631T>A | CA389477077 | FOXG1 | c.1352T>A (p.Leu451Gln) | |
14 | g.28768631T>C | CA389477078 | FOXG1 | c.1352T>C (p.Leu451Pro) | |
14 | g.28768631T>G | CA389477079 | FOXG1 | c.1352T>G (p.Leu451Arg) | |
14 | g.28768632G>A | CA486098758 | FOXG1 | c.1353G>A (p.Leu451=) | dbSNP |
14 | g.28768632G>C | CA486098759 | FOXG1 | c.1353G>C (p.Leu451=) | |
14 | g.28768632G= | CA2126000492 | FOXG1 | c.1353G= (p.Leu451=) | |
14 | g.28768632G>T | CA486098760 | FOXG1 | c.1353G>T (p.Leu451=) | |
14 | g.28768633C>A | CA389477080 | FOXG1 | c.1354C>A (p.Pro452Thr) | COSMIC |