UPDATE - Protein Allele ID & Protein Sequence HGVS Requests Partially Restored
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 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 |
| 14 | g.28768633C= | CA2126000493 | FOXG1 | c.1354C= (p.Pro452=) | |
| 14 | g.28768633C>G | CA389477081 | FOXG1 | c.1354C>G (p.Pro452Ala) | dbSNP gnomAD v3 gnomAD v4 |
| 14 | g.28768633C>T | CA389477082 | FOXG1 | c.1354C>T (p.Pro452Ser) | gnomAD v4 |
| 14 | g.28768634C>A | CA389477083 | FOXG1 | c.1355C>A (p.Pro452His) | |
| 14 | g.28768634C>G | CA389477084 | FOXG1 | c.1355C>G (p.Pro452Arg) | |
| 14 | g.28768634C>T | CA389477085 | FOXG1 | c.1355C>T (p.Pro452Leu) | |
| 14 | g.28768635C>A | CA486098768 | FOXG1 | c.1356C>A (p.Pro452=) | |
| 14 | g.28768635C= | CA2126000494 | FOXG1 | c.1356C= (p.Pro452=) | |
| 14 | g.28768635C>G | CA486098769 | FOXG1 | c.1356C>G (p.Pro452=) | gnomAD v4 |
| 14 | g.28768635C>T | CA7140684 | FOXG1 | c.1356C>T (p.Pro452=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 14 | g.28768636T>A | CA389477088 | FOXG1 | c.1357T>A (p.Cys453Ser) | |
| 14 | g.28768636T>C | CA389477087 | FOXG1 | c.1357T>C (p.Cys453Arg) | |
| 14 | g.28768636T>G | CA389477086 | FOXG1 | c.1357T>G (p.Cys453Gly) | |
| 14 | g.28768638_28768639del | CA2697553888 | FOXG1 | c.1359_1360del (p.Cys453Ter) | ClinVar |
| 14 | g.28768637G>A | CA389477089 | FOXG1 | c.1358G>A (p.Cys453Tyr) | |
| 14 | g.28768637G>C | CA389477091 | FOXG1 | c.1358G>C (p.Cys453Ser) | |
| 14 | g.28768637G>T | CA389477090 | FOXG1 | c.1358G>T (p.Cys453Phe) | |
| 14 | g.28768638T>A | CA389477092 | FOXG1 | c.1359T>A (p.Cys453Ter) | |
| 14 | g.28768638T>C | CA486098777 | FOXG1 | c.1359T>C (p.Cys453=) | |
| 14 | g.28768638T>G | CA389477093 | FOXG1 | c.1359T>G (p.Cys453Trp) | |
| 14 | g.28768639G>A | CA389477094 | FOXG1 | c.1360G>A (p.Glu454Lys) | |
| 14 | g.28768639G>C | CA389477095 | FOXG1 | c.1360G>C (p.Glu454Gln) | |
| 14 | g.28768639G>T | CA389477096 | FOXG1 | c.1360G>T (p.Glu454Ter) | |
| 14 | g.28768640A>C | CA389477097 | FOXG1 | c.1361A>C (p.Glu454Ala) | |
| 14 | g.28768640A>G | CA389477098 | FOXG1 | c.1361A>G (p.Glu454Gly) | |
| 14 | g.28768640A>T | CA389477099 | FOXG1 | c.1361A>T (p.Glu454Val) | |
| 14 | g.28768641G>A | CA486098780 | FOXG1 | c.1362G>A (p.Glu454=) | gnomAD v4 |
| 14 | g.28768641G>C | CA389477100 | FOXG1 | c.1362G>C (p.Glu454Asp) | |
| 14 | g.28768641G>T | CA389477101 | FOXG1 | c.1362G>T (p.Glu454Asp) | |
| 14 | g.28768642T>A | CA389477102 | FOXG1 | c.1363T>A (p.Ser455Thr) | |
| 14 | g.28768642T>C | CA389477103 | FOXG1 | c.1363T>C (p.Ser455Pro) | |
| 14 | g.28768642T>G | CA389477104 | FOXG1 | c.1363T>G (p.Ser455Ala) | |
| 14 | g.28768643C>A | CA389477107 | FOXG1 | c.1364C>A (p.Ser455Tyr) | |
| 14 | g.28768643C>G | CA389477105 | FOXG1 | c.1364C>G (p.Ser455Cys) | |
| 14 | g.28768643C>T | CA389477106 | FOXG1 | c.1364C>T (p.Ser455Phe) | |
| 14 | g.28768645_28768654del | CA2580617980 | FOXG1 | c.1366_1375del (p.Arg457CysfsTer28) | ClinVar |
| 14 | g.28768644T>A | CA486098786 | FOXG1 | c.1365T>A (p.Ser455=) | |
| 14 | g.28768644T>C | CA7140685 | FOXG1 | c.1365T>C (p.Ser455=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.28768644T>G | CA486098788 | FOXG1 | c.1365T>G (p.Ser455=) | |
| 14 | g.28768644T= | CA2126000495 | FOXG1 | c.1365T= (p.Ser455=) | |
| 14 | g.28768645T>A | CA389477108 | FOXG1 | c.1366T>A (p.Leu456Ile) | |
| 14 | g.28768645T>C | CA258396604 | FOXG1 | c.1366T>C (p.Leu456=) | dbSNP |
| 14 | g.28768645T>G | CA389477109 | FOXG1 | c.1366T>G (p.Leu456Val) | |
| 14 | g.28768645T= | CA2126000496 | FOXG1 | c.1366T= (p.Leu456=) | |
| 14 | g.28768646T>A | CA389477110 | FOXG1 | c.1367T>A (p.Leu456Ter) | |
| 14 | g.28768646T>C | CA389477111 | FOXG1 | c.1367T>C (p.Leu456Ser) | |
| 14 | g.28768646T>G | CA389477112 | FOXG1 | c.1367T>G (p.Leu456Ter) | |
| 14 | g.28768647A>C | CA389477113 | FOXG1 | c.1368A>C (p.Leu456Phe) | |
| 14 | g.28768647A>G | CA486098795 | FOXG1 | c.1368A>G (p.Leu456=) | |
| 14 | g.28768647A>T | CA389477114 | FOXG1 | c.1368A>T (p.Leu456Phe) | |
| 14 | g.28768648del | CA645570800 | FOXG1 | c.1369del (p.Arg457AspfsTer?) | COSMIC |
| 14 | g.28768648A>C | CA486098798 | FOXG1 | c.1369A>C (p.Arg457=) | |
| 14 | g.28768648A>G | CA389477115 | FOXG1 | c.1369A>G (p.Arg457Gly) | |
| 14 | g.28768648A>T | CA389477116 | FOXG1 | c.1369A>T (p.Arg457Ter) | |
| 14 | g.28768649G>A | CA389477118 | FOXG1 | c.1370G>A (p.Arg457Lys) | |
| 14 | g.28768649G>C | CA389477119 | FOXG1 | c.1370G>C (p.Arg457Thr) | |
| 14 | g.28768649G>T | CA389477117 | FOXG1 | c.1370G>T (p.Arg457Ile) | COSMIC |
| 14 | g.28768650A>C | CA389477120 | FOXG1 | c.1371A>C (p.Arg457Ser) | |
| 14 | g.28768650A>G | CA486098803 | FOXG1 | c.1371A>G (p.Arg457=) | |
| 14 | g.28768650A>T | CA389477121 | FOXG1 | c.1371A>T (p.Arg457Ser) | |
| 14 | g.28768651C>A | CA389477122 | FOXG1 | c.1372C>A (p.Pro458Thr) | ClinVar dbSNP gnomAD v4 |
| 14 | g.28768651C= | CA2126000497 | FOXG1 | c.1372C= (p.Pro458=) | |
| 14 | g.28768651C>G | CA389477123 | FOXG1 | c.1372C>G (p.Pro458Ala) | |
| 14 | g.28768651C>T | CA389477124 | FOXG1 | c.1372C>T (p.Pro458Ser) | gnomAD v4 |
| 14 | g.28768652C>A | CA389477125 | FOXG1 | c.1373C>A (p.Pro458His) | |
| 14 | g.28768652C= | CA2126000498 | FOXG1 | c.1373C= (p.Pro458=) | |
| 14 | g.28768652C>G | CA7140686 | FOXG1 | c.1373C>G (p.Pro458Arg) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 14 | g.28768652C>T | CA389477126 | FOXG1 | c.1373C>T (p.Pro458Leu) | |
| 14 | g.28768653C>A | CA486098812 | FOXG1 | c.1374C>A (p.Pro458=) | COSMIC |
| 14 | g.28768653C= | CA2126000499 | FOXG1 | c.1374C= (p.Pro458=) | |
| 14 | g.28768653C>G | CA486098814 | FOXG1 | c.1374C>G (p.Pro458=) | |
| 14 | g.28768653C>T | CA486098816 | FOXG1 | c.1374C>T (p.Pro458=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.28768654T>A | CA389477127 | FOXG1 | c.1375T>A (p.Ser459Thr) | |
| 14 | g.28768654T>C | CA389477128 | FOXG1 | c.1375T>C (p.Ser459Pro) | gnomAD v4 |
| 14 | g.28768654T>G | CA314633 | FOXG1 | c.1375T>G (p.Ser459Ala) | ClinVar dbSNP |
| 14 | g.28768654T= | CA2126000500 | FOXG1 | c.1375T= (p.Ser459=) | |
| 14 | g.28768655C>A | CA389477131 | FOXG1 | c.1376C>A (p.Ser459Tyr) | |
| 14 | g.28768655C= | CA2126000501 | FOXG1 | c.1376C= (p.Ser459=) | |
| 14 | g.28768655C>G | CA389477130 | FOXG1 | c.1376C>G (p.Ser459Cys) | ClinVar dbSNP |
| 14 | g.28768655C>T | CA389477129 | FOXG1 | c.1376C>T (p.Ser459Phe) | |
| 14 | g.28768656T>A | CA486098825 | FOXG1 | c.1377T>A (p.Ser459=) | |
| 14 | g.28768656T>C | CA486098826 | FOXG1 | c.1377T>C (p.Ser459=) | |
| 14 | g.28768656T>G | CA486098827 | FOXG1 | c.1377T>G (p.Ser459=) | |
| 14 | g.28768657T>A | CA389477132 | FOXG1 | c.1378T>A (p.Leu460Met) | |
| 14 | g.28768657T>C | CA486098830 | FOXG1 | c.1378T>C (p.Leu460=) | gnomAD v4 |
| 14 | g.28768657T>G | CA389477133 | FOXG1 | c.1378T>G (p.Leu460Val) | COSMIC |
| 14 | g.28768658T>A | CA389477134 | FOXG1 | c.1379T>A (p.Leu460Ter) | |
| 14 | g.28768658T>C | CA389477135 | FOXG1 | c.1379T>C (p.Leu460Ser) | |
| 14 | g.28768658T>G | CA389477136 | FOXG1 | c.1379T>G (p.Leu460Trp) | |
| 14 | g.28768659G>A | CA486098832 | FOXG1 | c.1380G>A (p.Leu460=) | |
| 14 | g.28768659G>C | CA389477137 | FOXG1 | c.1380G>C (p.Leu460Phe) | COSMIC |
| 14 | g.28768659G>T | CA389477138 | FOXG1 | c.1380G>T (p.Leu460Phe) | |
| 14 | g.28768660C>A | CA389477139 | FOXG1 | c.1381C>A (p.Pro461Thr) | |
| 14 | g.28768660C= | CA2126000502 | FOXG1 | c.1381C= (p.Pro461=) | |
| 14 | g.28768660C>G | CA389477140 | FOXG1 | c.1381C>G (p.Pro461Ala) | ClinVar dbSNP gnomAD v4 |
| 14 | g.28768660C>T | CA389477141 | FOXG1 | c.1381C>T (p.Pro461Ser) | |
| 14 | g.28768661C>A | CA389477142 | FOXG1 | c.1382C>A (p.Pro461Gln) | |
| 14 | g.28768661C>G | CA389477143 | FOXG1 | c.1382C>G (p.Pro461Arg) | |
| 14 | g.28768661C>T | CA389477144 | FOXG1 | c.1382C>T (p.Pro461Leu) | |
| 14 | g.28768662A= | CA2126000503 | FOXG1 | c.1383A= (p.Pro461=) | |
| 14 | g.28768662A>C | CA486098836 | FOXG1 | c.1383A>C (p.Pro461=) | |
| 14 | g.28768662A>G | CA486098837 | FOXG1 | c.1383A>G (p.Pro461=) | dbSNP |
| 14 | g.28768662A>T | CA486098838 | FOXG1 | c.1383A>T (p.Pro461=) | |
| 14 | g.28768663A= | CA2126000504 | FOXG1 | c.1384A= (p.Ser462=) | |
| 14 | g.28768663A>C | CA389477146 | FOXG1 | c.1384A>C (p.Ser462Arg) | |
| 14 | g.28768663A>G | CA208363 | FOXG1 | c.1384A>G (p.Ser462Gly) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.28768663A>T | CA389477145 | FOXG1 | c.1384A>T (p.Ser462Cys) | |
| 14 | g.28768664G>A | CA389477149 | FOXG1 | c.1385G>A (p.Ser462Asn) | gnomAD v4 |
| 14 | g.28768664G>C | CA389477147 | FOXG1 | c.1385G>C (p.Ser462Thr) | |
| 14 | g.28768664G>T | CA389477148 | FOXG1 | c.1385G>T (p.Ser462Ile) | COSMIC |
| 14 | g.28768665T>A | CA389477150 | FOXG1 | c.1386T>A (p.Ser462Arg) | |
| 14 | g.28768665T>C | CA486098847 | FOXG1 | c.1386T>C (p.Ser462=) | |
| 14 | g.28768665T>G | CA389477151 | FOXG1 | c.1386T>G (p.Ser462Arg) | |
| 14 | g.28768666T>A | CA389477152 | FOXG1 | c.1387T>A (p.Phe463Ile) | |
| 14 | g.28768666T>C | CA389477153 | FOXG1 | c.1387T>C (p.Phe463Leu) | |
| 14 | g.28768666T>G | CA389477154 | FOXG1 | c.1387T>G (p.Phe463Val) | |
| 14 | g.28768667T>A | CA389477155 | FOXG1 | c.1388T>A (p.Phe463Tyr) | |
| 14 | g.28768667T>C | CA389477156 | FOXG1 | c.1388T>C (p.Phe463Ser) | |
| 14 | g.28768667T>G | CA389477157 | FOXG1 | c.1388T>G (p.Phe463Cys) | |
| 14 | g.28768668T>A | CA389477158 | FOXG1 | c.1389T>A (p.Phe463Leu) | |
| 14 | g.28768668T>C | CA486098602 | FOXG1 | c.1389T>C (p.Phe463=) | gnomAD v4 |
| 14 | g.28768668T>G | CA389477159 | FOXG1 | c.1389T>G (p.Phe463Leu) | |
| 14 | g.28768669A= | CA2126000505 | FOXG1 | c.1390A= (p.Thr464=) | |
| 14 | g.28768669A>C | CA389477162 | FOXG1 | c.1390A>C (p.Thr464Pro) | |
| 14 | g.28768669A>G | CA389477161 | FOXG1 | c.1390A>G (p.Thr464Ala) | ClinVar dbSNP gnomAD v4 |
| 14 | g.28768669A>T | CA389477160 | FOXG1 | c.1390A>T (p.Thr464Ser) | |
| 14 | g.28768670C>A | CA389477163 | FOXG1 | c.1391C>A (p.Thr464Lys) | |
| 14 | g.28768670C= | CA2126000506 | FOXG1 | c.1391C= (p.Thr464=) | |
| 14 | g.28768670C>G | CA389477164 | FOXG1 | c.1391C>G (p.Thr464Arg) | |
| 14 | g.28768670C>T | CA389477165 | FOXG1 | c.1391C>T (p.Thr464Met) | dbSNP gnomAD v2 COSMIC |
| 14 | g.28768671G>A | CA486098604 | FOXG1 | c.1392G>A (p.Thr464=) | |
| 14 | g.28768671G>C | CA7140687 | FOXG1 | c.1392G>C (p.Thr464=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 14 | g.28768671G= | CA2126000507 | FOXG1 | c.1392G= (p.Thr464=) | |
| 14 | g.28768671G>T | CA486098607 | FOXG1 | c.1392G>T (p.Thr464=) | |
| 14 | g.28768672A>C | CA389477166 | FOXG1 | c.1393A>C (p.Thr465Pro) | |
| 14 | g.28768672A>G | CA389477167 | FOXG1 | c.1393A>G (p.Thr465Ala) | |
| 14 | g.28768672A>T | CA389477168 | FOXG1 | c.1393A>T (p.Thr465Ser) | |
| 14 | g.28768673C>A | CA389477169 | FOXG1 | c.1394C>A (p.Thr465Lys) | |
| 14 | g.28768673C>G | CA389477170 | FOXG1 | c.1394C>G (p.Thr465Arg) | |
| 14 | g.28768673C>T | CA389477171 | FOXG1 | c.1394C>T (p.Thr465Met) | COSMIC |
| 14 | g.28768673_28768685delinsCGGGACTGTCTGG | CA2126000508 | FOXG1 | c.1394_1406delinsCGGGACTGTCTGG (p.Thr465=) | |
| 14 | g.28768674G>A | CA7140688 | FOXG1 | c.1395G>A (p.Thr465=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
| 14 | g.28768674G>C | CA7140689 | FOXG1 | c.1395G>C (p.Thr465=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.28768674G= | CA2126000509 | FOXG1 | c.1395G= (p.Thr465=) | |
| 14 | g.28768674G>T | CA486098612 | FOXG1 | c.1395G>T (p.Thr465=) | |
| 14 | g.28768685_28768696del | CA613324876 | FOXG1 | c.1406_1417del (p.Gly469_Ser472del) | dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.28768675G>A | CA389477174 | FOXG1 | c.1396G>A (p.Gly466Arg) | |
| 14 | g.28768675G>C | CA389477173 | FOXG1 | c.1396G>C (p.Gly466Arg) | |
| 14 | g.28768675G>T | CA389477172 | FOXG1 | c.1396G>T (p.Gly466Ter) | |
| 14 | g.28768676G>A | CA389477175 | FOXG1 | c.1397G>A (p.Gly466Glu) | ClinVar dbSNP |
| 14 | g.28768676G>C | CA389477176 | FOXG1 | c.1397G>C (p.Gly466Ala) | |
| 14 | g.28768676G= | CA2126000510 | FOXG1 | c.1397G= (p.Gly466=) | |
| 14 | g.28768676G>T | CA389477177 | FOXG1 | c.1397G>T (p.Gly466Val) | |
| 14 | g.28768677A>C | CA486098625 | FOXG1 | c.1398A>C (p.Gly466=) | |
| 14 | g.28768677A>G | CA486098627 | FOXG1 | c.1398A>G (p.Gly466=) | |
| 14 | g.28768677A>T | CA486098630 | FOXG1 | c.1398A>T (p.Gly466=) | |
| 14 | g.28768677_28768681delinsACTGT | CA2126000511 | FOXG1 | c.1398_1402delinsACTGT (p.Gly466=) | |
| 14 | g.28768678C>A | CA389477178 | FOXG1 | c.1399C>A (p.Leu467Met) | |
| 14 | g.28768678C= | CA2126000512 | FOXG1 | c.1399C= (p.Leu467=) | |
| 14 | g.28768678C>G | CA389477179 | FOXG1 | c.1399C>G (p.Leu467Val) | |
| 14 | g.28768678C>T | CA314596 | FOXG1 | c.1399C>T (p.Leu467=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.28768681_28768684del | CA314657 | FOXG1 | c.1402_1405del (p.Ser468GlyfsTer19) | ClinVar dbSNP |
| 14 | g.28768679T>A | CA389477181 | FOXG1 | c.1400T>A (p.Leu467Gln) | |
| 14 | g.28768679T>C | CA7140690 | FOXG1 | c.1400T>C (p.Leu467Pro) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 14 | g.28768679T>G | CA389477180 | FOXG1 | c.1400T>G (p.Leu467Arg) | |
| 14 | g.28768679T= | CA2126000513 | FOXG1 | c.1400T= (p.Leu467=) | |
| 14 | g.28768680G>A | CA486098634 | FOXG1 | c.1401G>A (p.Leu467=) | |
| 14 | g.28768680G>C | CA7140691 | FOXG1 | c.1401G>C (p.Leu467=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 14 | g.28768680G= | CA2126000514 | FOXG1 | c.1401G= (p.Leu467=) | |
| 14 | g.28768680G>T | CA486098635 | FOXG1 | c.1401G>T (p.Leu467=) | |
| 14 | g.28768681del | CA2695219199 | FOXG1 | c.1402del (p.Ser468LeufsTer20) | |
| 14 | g.28768681T>A | CA389477182 | FOXG1 | c.1402T>A (p.Ser468Thr) | |
| 14 | g.28768681T>C | CA389477183 | FOXG1 | c.1402T>C (p.Ser468Pro) | gnomAD v4 |
| 14 | g.28768681T>G | CA389477184 | FOXG1 | c.1402T>G (p.Ser468Ala) | |
| 14 | g.28768682del | CA2695219200 | FOXG1 | c.1403del (p.Ser468LeufsTer20) | |
| 14 | g.28768682C>A | CA389477185 | FOXG1 | c.1403C>A (p.Ser468Tyr) | |
| 14 | g.28768682C>G | CA389477187 | FOXG1 | c.1403C>G (p.Ser468Cys) | |
| 14 | g.28768682C>T | CA389477186 | FOXG1 | c.1403C>T (p.Ser468Phe) | |
| 14 | g.28768683T>A | CA486098643 | FOXG1 | c.1404T>A (p.Ser468=) | |
| 14 | g.28768683T>C | CA486098644 | FOXG1 | c.1404T>C (p.Ser468=) | dbSNP COSMIC |
| 14 | g.28768683T>G | CA486098648 | FOXG1 | c.1404T>G (p.Ser468=) | |
| 14 | g.28768684G>A | CA389477188 | FOXG1 | c.1405G>A (p.Gly469Arg) | |
| 14 | g.28768684G>C | CA389477189 | FOXG1 | c.1405G>C (p.Gly469Arg) | |
| 14 | g.28768684G>T | CA389477190 | FOXG1 | c.1405G>T (p.Gly469Trp) | COSMIC |
| 14 | g.28768685G>A | CA389477191 | FOXG1 | c.1406G>A (p.Gly469Glu) | |
| 14 | g.28768685G>C | CA258396605 | FOXG1 | c.1406G>C (p.Gly469Ala) | dbSNP |
| 14 | g.28768685G= | CA2126000515 | FOXG1 | c.1406G= (p.Gly469=) | |
| 14 | g.28768685G>T | CA389477192 | FOXG1 | c.1406G>T (p.Gly469Val) | ClinVar gnomAD v4 |
| 14 | g.28768686G>A | CA486098652 | FOXG1 | c.1407G>A (p.Gly469=) | |
| 14 | g.28768686G>C | CA486098656 | FOXG1 | c.1407G>C (p.Gly469=) | |
| 14 | g.28768686G>T | CA486098655 | FOXG1 | c.1407G>T (p.Gly469=) | |
| 14 | g.28768687G>A | CA389477193 | FOXG1 | c.1408G>A (p.Gly470Arg) | |
| 14 | g.28768687G>C | CA389477194 | FOXG1 | c.1408G>C (p.Gly470Arg) | |
| 14 | g.28768687G>T | CA389477195 | FOXG1 | c.1408G>T (p.Gly470Ter) | |
| 14 | g.28768688G>A | CA389477196 | FOXG1 | c.1409G>A (p.Gly470Glu) | |
| 14 | g.28768688G>C | CA389477197 | FOXG1 | c.1409G>C (p.Gly470Ala) | |
| 14 | g.28768688G>T | CA389477198 | FOXG1 | c.1409G>T (p.Gly470Val) | ClinVar |
| 14 | g.28768689del | CA2499222617 | FOXG1 | c.1410del (p.Leu471CysfsTer17) | ClinVar dbSNP |
| 14 | g.28768689A= | CA2126000516 | FOXG1 | c.1410A= (p.Gly470=) | |
| 14 | g.28768689A>C | CA486098657 | FOXG1 | c.1410A>C (p.Gly470=) | |
| 14 | g.28768689A>G | CA486098658 | FOXG1 | c.1410A>G (p.Gly470=) | dbSNP |
| 14 | g.28768689A>T | CA486098660 | FOXG1 | c.1410A>T (p.Gly470=) | |
| 14 | g.28768689_28768693delinsACTGT | CA2126000517 | FOXG1 | c.1410_1414delinsACTGT (p.Gly470=) | |
| 14 | g.28768691_28768706del | CA2697553889 | FOXG1 | c.1412_1427del (p.Leu471HisfsTer12) | ClinVar |
| 14 | g.28768690C>A | CA389477199 | FOXG1 | c.1411C>A (p.Leu471Met) | |
| 14 | g.28768690C= | CA2126000518 | FOXG1 | c.1411C= (p.Leu471=) | |
| 14 | g.28768690C>G | CA389477200 | FOXG1 | c.1411C>G (p.Leu471Val) | |
| 14 | g.28768690C>T | CA7140692 | FOXG1 | c.1411C>T (p.Leu471=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 14 | g.28768693_28768696del | CA916083366 | FOXG1 | c.1414_1417del (p.Ser472IlefsTer15) | ClinVar dbSNP |
| 14 | g.28768691T>A | CA389477202 | FOXG1 | c.1412T>A (p.Leu471Gln) | |
| 14 | g.28768691T>C | CA389477201 | FOXG1 | c.1412T>C (p.Leu471Pro) | |
| 14 | g.28768691T>G | CA389477203 | FOXG1 | c.1412T>G (p.Leu471Arg) | |
| 14 | g.28768692G>A | CA486098672 | FOXG1 | c.1413G>A (p.Leu471=) | |
| 14 | g.28768692G>C | CA486098674 | FOXG1 | c.1413G>C (p.Leu471=) | gnomAD v4 |
| 14 | g.28768692G>T | CA486098675 | FOXG1 | c.1413G>T (p.Leu471=) | |
| 14 | g.28768693T>A | CA389477204 | FOXG1 | c.1414T>A (p.Ser472Thr) | ClinVar |
| 14 | g.28768693T>C | CA7140693 | FOXG1 | c.1414T>C (p.Ser472Pro) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 14 | g.28768693T>G | CA389477205 | FOXG1 | c.1414T>G (p.Ser472Ala) | |
| 14 | g.28768693T= | CA2126000519 | FOXG1 | c.1414T= (p.Ser472=) | |
| 14 | g.28768694_28768695del | CA2579988445 | FOXG1 | c.1415_1416del (p.Ser472Ter) | gnomAD v4 |
| 14 | g.28768694C>A | CA389477206 | FOXG1 | c.1415C>A (p.Ser472Tyr) | |
| 14 | g.28768694C>G | CA389477207 | FOXG1 | c.1415C>G (p.Ser472Cys) | |
| 14 | g.28768694C>T | CA389477208 | FOXG1 | c.1415C>T (p.Ser472Phe) | |
| 14 | g.28768695T>A | CA486098685 | FOXG1 | c.1416T>A (p.Ser472=) | |
| 14 | g.28768695T>C | CA486098684 | FOXG1 | c.1416T>C (p.Ser472=) | |
| 14 | g.28768695T>G | CA486098682 | FOXG1 | c.1416T>G (p.Ser472=) | |
| 14 | g.28768696G>A | CA389477209 | FOXG1 | c.1417G>A (p.Asp473Asn) | |
| 14 | g.28768696G>C | CA389477210 | FOXG1 | c.1417G>C (p.Asp473His) | |
| 14 | g.28768696G>T | CA389477211 | FOXG1 | c.1417G>T (p.Asp473Tyr) | |
| 14 | g.28768697A>C | CA389477212 | FOXG1 | c.1418A>C (p.Asp473Ala) | |
| 14 | g.28768697A>G | CA389477213 | FOXG1 | c.1418A>G (p.Asp473Gly) | |
| 14 | g.28768697A>T | CA389477214 | FOXG1 | c.1418A>T (p.Asp473Val) | |
| 14 | g.28768698T>A | CA389477215 | FOXG1 | c.1419T>A (p.Asp473Glu) | |
| 14 | g.28768698T>C | CA486098693 | FOXG1 | c.1419T>C (p.Asp473=) | |
| 14 | g.28768698T>G | CA389477216 | FOXG1 | c.1419T>G (p.Asp473Glu) | |
| 14 | g.28768699T>A | CA389477219 | FOXG1 | c.1420T>A (p.Tyr474Asn) | |
| 14 | g.28768699T>C | CA389477217 | FOXG1 | c.1420T>C (p.Tyr474His) | |
| 14 | g.28768699T>G | CA389477218 | FOXG1 | c.1420T>G (p.Tyr474Asp) | |
| 14 | g.28768700A>C | CA389477220 | FOXG1 | c.1421A>C (p.Tyr474Ser) | |
| 14 | g.28768700A>G | CA389477221 | FOXG1 | c.1421A>G (p.Tyr474Cys) | |
| 14 | g.28768700A>T | CA389477222 | FOXG1 | c.1421A>T (p.Tyr474Phe) | |
| 14 | g.28768701T>A | CA389477223 | FOXG1 | c.1422T>A (p.Tyr474Ter) | |
| 14 | g.28768701T>C | CA486098699 | FOXG1 | c.1422T>C (p.Tyr474=) | gnomAD v4 |
| 14 | g.28768701T>G | CA389477224 | FOXG1 | c.1422T>G (p.Tyr474Ter) | |
| 14 | g.28768702T>A | CA389477225 | FOXG1 | c.1423T>A (p.Phe475Ile) | |
| 14 | g.28768702T>C | CA389477226 | FOXG1 | c.1423T>C (p.Phe475Leu) | |
| 14 | g.28768702T>G | CA389477227 | FOXG1 | c.1423T>G (p.Phe475Val) | |
| 14 | g.28768703T>A | CA389477228 | FOXG1 | c.1424T>A (p.Phe475Tyr) | |
| 14 | g.28768703T>C | CA389477229 | FOXG1 | c.1424T>C (p.Phe475Ser) | |
| 14 | g.28768703T>G | CA389477230 | FOXG1 | c.1424T>G (p.Phe475Cys) | |
| 14 | g.28768704C>A | CA389477232 | FOXG1 | c.1425C>A (p.Phe475Leu) | |
| 14 | g.28768704C= | CA2126000520 | FOXG1 | c.1425C= (p.Phe475=) | |
| 14 | g.28768704C>G | CA389477231 | FOXG1 | c.1425C>G (p.Phe475Leu) | dbSNP gnomAD v3 gnomAD v4 |
| 14 | g.28768704C>T | CA486098712 | FOXG1 | c.1425C>T (p.Phe475=) | ClinVar |
| 14 | g.28768705A>C | CA389477233 | FOXG1 | c.1426A>C (p.Thr476Pro) | |
| 14 | g.28768705A>G | CA389477234 | FOXG1 | c.1426A>G (p.Thr476Ala) | ClinVar |
| 14 | g.28768705A>T | CA389477235 | FOXG1 | c.1426A>T (p.Thr476Ser) | |
| 14 | g.28768706C>A | CA389477236 | FOXG1 | c.1427C>A (p.Thr476Lys) | |
| 14 | g.28768706C>G | CA389477237 | FOXG1 | c.1427C>G (p.Thr476Arg) | |
| 14 | g.28768706C>T | CA389477238 | FOXG1 | c.1427C>T (p.Thr476Ile) | gnomAD v4 |
| 14 | g.28768707A= | CA2126000521 | FOXG1 | c.1428A= (p.Thr476=) | |
| 14 | g.28768707A>C | CA486098724 | FOXG1 | c.1428A>C (p.Thr476=) | |
| 14 | g.28768707A>G | CA486098725 | FOXG1 | c.1428A>G (p.Thr476=) | gnomAD v4 |
| 14 | g.28768707A>T | CA7140694 | FOXG1 | c.1428A>T (p.Thr476=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 14 | g.28768708C>A | CA389477239 | FOXG1 | c.1429C>A (p.His477Asn) | |
| 14 | g.28768708C>G | CA389477240 | FOXG1 | c.1429C>G (p.His477Asp) | |
| 14 | g.28768708C>T | CA389477241 | FOXG1 | c.1429C>T (p.His477Tyr) | |
| 14 | g.28768709A>C | CA389477242 | FOXG1 | c.1430A>C (p.His477Pro) | |
| 14 | g.28768709A>G | CA389477243 | FOXG1 | c.1430A>G (p.His477Arg) | |
| 14 | g.28768709A>T | CA389477244 | FOXG1 | c.1430A>T (p.His477Leu) | |
| 14 | g.28768710T>A | CA389477246 | FOXG1 | c.1431T>A (p.His477Gln) | |
| 14 | g.28768710T>C | CA486098751 | FOXG1 | c.1431T>C (p.His477=) | |
| 14 | g.28768710T>G | CA389477245 | FOXG1 | c.1431T>G (p.His477Gln) | |
| 14 | g.28768711C>A | CA389477247 | FOXG1 | c.1432C>A (p.Gln478Lys) | |
| 14 | g.28768711C>G | CA389477248 | FOXG1 | c.1432C>G (p.Gln478Glu) | |
| 14 | g.28768711C>T | CA389477249 | FOXG1 | c.1432C>T (p.Gln478Ter) | |
| 14 | g.28768712A>C | CA389477250 | FOXG1 | c.1433A>C (p.Gln478Pro) | |
| 14 | g.28768712A>G | CA389477251 | FOXG1 | c.1433A>G (p.Gln478Arg) | |
| 14 | g.28768712A>T | CA389477252 | FOXG1 | c.1433A>T (p.Gln478Leu) | |
| 14 | g.28768713A>C | CA389477253 | FOXG1 | c.1434A>C (p.Gln478His) | |
| 14 | g.28768713A>G | CA486098762 | FOXG1 | c.1434A>G (p.Gln478=) | ClinVar gnomAD v4 |
| 14 | g.28768713A>T | CA389477254 | FOXG1 | c.1434A>T (p.Gln478His) | |
| 14 | g.28768714A>C | CA389477255 | FOXG1 | c.1435A>C (p.Asn479His) | |
| 14 | g.28768714A>G | CA389477256 | FOXG1 | c.1435A>G (p.Asn479Asp) | |
| 14 | g.28768714A>T | CA389477257 | FOXG1 | c.1435A>T (p.Asn479Tyr) | gnomAD v4 |
| 14 | g.28768715A>C | CA389477258 | FOXG1 | c.1436A>C (p.Asn479Thr) | |
| 14 | g.28768715A>G | CA389477259 | FOXG1 | c.1436A>G (p.Asn479Ser) | |
| 14 | g.28768715A>T | CA389477260 | FOXG1 | c.1436A>T (p.Asn479Ile) | |
| 14 | g.28768716T>A | CA389477262 | FOXG1 | c.1437T>A (p.Asn479Lys) | |
| 14 | g.28768716T>C | CA486098771 | FOXG1 | c.1437T>C (p.Asn479=) | |
| 14 | g.28768716T>G | CA389477261 | FOXG1 | c.1437T>G (p.Asn479Lys) | |
| 14 | g.28768717C>A | CA389477263 | FOXG1 | c.1438C>A (p.Gln480Lys) | |
| 14 | g.28768717C>G | CA389477264 | FOXG1 | c.1438C>G (p.Gln480Glu) | |
| 14 | g.28768717C>T | CA389477265 | FOXG1 | c.1438C>T (p.Gln480Ter) | |
| 14 | g.28768718A= | CA2126000522 | FOXG1 | c.1439A= (p.Gln480=) | |
| 14 | g.28768718A>C | CA389477266 | FOXG1 | c.1439A>C (p.Gln480Pro) | ClinVar |
| 14 | g.28768718A>G | CA314635 | FOXG1 | c.1439A>G (p.Gln480Arg) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 14 | g.28768718A>T | CA389477267 | FOXG1 | c.1439A>T (p.Gln480Leu) | |
| 14 | g.28768719G>A | CA486098778 | FOXG1 | c.1440G>A (p.Gln480=) | |
| 14 | g.28768719G>C | CA389477269 | FOXG1 | c.1440G>C (p.Gln480His) | |
| 14 | g.28768719G>T | CA389477268 | FOXG1 | c.1440G>T (p.Gln480His) | |
| 14 | g.28768720G>A | CA389477270 | FOXG1 | c.1441G>A (p.Gly481Arg) | ClinVar |
| 14 | g.28768720G>C | CA389477271 | FOXG1 | c.1441G>C (p.Gly481Arg) | |
| 14 | g.28768720G>T | CA389477272 | FOXG1 | c.1441G>T (p.Gly481Trp) |