| 14 | g.28768520C>A | CA389476834 | FOXG1 | c.1241C>A (p.Thr414Asn)
| dbSNP |
| 14 | g.28768520C= | CA2126000448 | FOXG1 | c.1241C= (p.Thr414=)
| |
| 14 | g.28768520C>G | CA389476835 | FOXG1 | c.1241C>G (p.Thr414Ser)
| |
| 14 | g.28768520C>T | CA389476836 | FOXG1 | c.1241C>T (p.Thr414Ile)
| |
| 14 | g.28768521C>A | CA486098491 | FOXG1 | c.1242C>A (p.Thr414=)
| |
| 14 | g.28768521C= | CA2126000449 | FOXG1 | c.1242C= (p.Thr414=)
| |
| 14 | g.28768521C>G | CA486098493 | FOXG1 | c.1242C>G (p.Thr414=)
| |
| 14 | g.28768521C>T | CA7140673 | FOXG1 | c.1242C>T (p.Thr414=)
| dbSNP ExAC gnomAD v2 |
| 14 | g.28768522A= | CA2126000450 | FOXG1 | c.1243A= (p.Ser415=)
| |
| 14 | g.28768522A>C | CA389476837 | FOXG1 | c.1243A>C (p.Ser415Arg)
| |
| 14 | g.28768522A>G | CA389476838 | FOXG1 | c.1243A>G (p.Ser415Gly)
| ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.28768522A>T | CA389476839 | FOXG1 | c.1243A>T (p.Ser415Cys)
| |
| 14 | g.28768523G>A | CA389476840 | FOXG1 | c.1244G>A (p.Ser415Asn)
| dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 14 | g.28768523G>C | CA389476841 | FOXG1 | c.1244G>C (p.Ser415Thr)
| |
| 14 | g.28768523G= | CA2126000451 | FOXG1 | c.1244G= (p.Ser415=)
| |
| 14 | g.28768523G>T | CA389476842 | FOXG1 | c.1244G>T (p.Ser415Ile)
| |
| 14 | g.28768523_28768524del | CA2739277848 | FOXG1 | c.1244_1245del (p.Ser415IlefsTer?)
| ClinVar |
| 14 | g.28768524T>A | CA389476844 | FOXG1 | c.1245T>A (p.Ser415Arg)
| |
| 14 | g.28768524T>C | CA486098500 | FOXG1 | c.1245T>C (p.Ser415=)
| |
| 14 | g.28768524T>G | CA389476843 | FOXG1 | c.1245T>G (p.Ser415Arg)
| |
| 14 | g.28768525T>A | CA389476845 | FOXG1 | c.1246T>A (p.Tyr416Asn)
| |
| 14 | g.28768525T>C | CA389476847 | FOXG1 | c.1246T>C (p.Tyr416His)
| |
| 14 | g.28768525T>G | CA389476846 | FOXG1 | c.1246T>G (p.Tyr416Asp)
| |
| 14 | g.28768526A>C | CA389476848 | FOXG1 | c.1247A>C (p.Tyr416Ser)
| ClinVar |
| 14 | g.28768526A>G | CA389476849 | FOXG1 | c.1247A>G (p.Tyr416Cys)
| |
| 14 | g.28768526A>T | CA389476850 | FOXG1 | c.1247A>T (p.Tyr416Phe)
| |
| 14 | g.28768527C>A | CA389476851 | FOXG1 | c.1248C>A (p.Tyr416Ter)
| |
| 14 | g.28768527C= | CA2126000452 | FOXG1 | c.1248C= (p.Tyr416=)
| |
| 14 | g.28768527C>G | CA199429 | FOXG1 | c.1248C>G (p.Tyr416Ter)
| ClinVar dbSNP |
| 14 | g.28768527C>T | CA486098503 | FOXG1 | c.1248C>T (p.Tyr416=)
| dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.28768528T>A | CA389476852 | FOXG1 | c.1249T>A (p.Phe417Ile)
| |
| 14 | g.28768528T>C | CA7140674 | FOXG1 | c.1249T>C (p.Phe417Leu)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
| 14 | g.28768528T>G | CA389476853 | FOXG1 | c.1249T>G (p.Phe417Val)
| |
| 14 | g.28768528T= | CA2126000453 | FOXG1 | c.1249T= (p.Phe417=)
| |
| 14 | g.28768529T>A | CA389476854 | FOXG1 | c.1250T>A (p.Phe417Tyr)
| |
| 14 | g.28768529T>C | CA389476855 | FOXG1 | c.1250T>C (p.Phe417Ser)
| |
| 14 | g.28768529T>G | CA389476856 | FOXG1 | c.1250T>G (p.Phe417Cys)
| |
| 14 | g.28768530T>A | CA389476857 | FOXG1 | c.1251T>A (p.Phe417Leu)
| |
| 14 | g.28768530T>C | CA486098506 | FOXG1 | c.1251T>C (p.Phe417=)
| |
| 14 | g.28768530T>G | CA389476858 | FOXG1 | c.1251T>G (p.Phe417Leu)
| |
| 14 | g.28768531T>A | CA389476861 | FOXG1 | c.1252T>A (p.Phe418Ile)
| |
| 14 | g.28768531T>C | CA389476859 | FOXG1 | c.1252T>C (p.Phe418Leu)
| |
| 14 | g.28768531T>G | CA389476860 | FOXG1 | c.1252T>G (p.Phe418Val)
| |
| 14 | g.28768532T>A | CA389476862 | FOXG1 | c.1253T>A (p.Phe418Tyr)
| |
| 14 | g.28768532T>C | CA389476863 | FOXG1 | c.1253T>C (p.Phe418Ser)
| dbSNP |
| 14 | g.28768532T>G | CA389476864 | FOXG1 | c.1253T>G (p.Phe418Cys)
| |
| 14 | g.28768532T= | CA2126000454 | FOXG1 | c.1253T= (p.Phe418=)
| |
| 14 | g.28768534_28768553dup | CA2697553887 | FOXG1 | c.1255_1274dup (p.Met426ProfsTer8)
| ClinVar |
| 14 | g.28768533C>A | CA389476865 | FOXG1 | c.1254C>A (p.Phe418Leu)
| ClinVar dbSNP |
| 14 | g.28768533C= | CA2126000455 | FOXG1 | c.1254C= (p.Phe418=)
| |
| 14 | g.28768533C>G | CA389476866 | FOXG1 | c.1254C>G (p.Phe418Leu)
| |
| 14 | g.28768533C>T | CA7140675 | FOXG1 | c.1254C>T (p.Phe418=)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 14 | g.28768537del | CA645570799 | FOXG1 | c.1258del (p.His420ThrfsTer7)
| COSMIC |
| 14 | g.28768534C>A | CA389476867 | FOXG1 | c.1255C>A (p.Pro419Thr)
| |
| 14 | g.28768534C>G | CA389476868 | FOXG1 | c.1255C>G (p.Pro419Ala)
| |
| 14 | g.28768534C>T | CA389476869 | FOXG1 | c.1255C>T (p.Pro419Ser)
| ClinVar dbSNP |
| 14 | g.28768535C>A | CA389476870 | FOXG1 | c.1256C>A (p.Pro419His)
| |
| 14 | g.28768535C= | CA2126000456 | FOXG1 | c.1256C= (p.Pro419=)
| |
| 14 | g.28768535C>G | CA389476871 | FOXG1 | c.1256C>G (p.Pro419Arg)
| |
| 14 | g.28768535C>T | CA389476872 | FOXG1 | c.1256C>T (p.Pro419Leu)
| ClinVar dbSNP |
| 14 | g.28768536C>A | CA486098513 | FOXG1 | c.1257C>A (p.Pro419=)
| |
| 14 | g.28768536C>G | CA486098516 | FOXG1 | c.1257C>G (p.Pro419=)
| |
| 14 | g.28768536C>T | CA486098514 | FOXG1 | c.1257C>T (p.Pro419=)
| ClinVar gnomAD v4 |
| 14 | g.28768537C>A | CA389476873 | FOXG1 | c.1258C>A (p.His420Asn)
| |
| 14 | g.28768537C>G | CA389476875 | FOXG1 | c.1258C>G (p.His420Asp)
| |
| 14 | g.28768537C>T | CA389476874 | FOXG1 | c.1258C>T (p.His420Tyr)
| |
| 14 | g.28768538A>C | CA389476876 | FOXG1 | c.1259A>C (p.His420Pro)
| |
| 14 | g.28768538A>G | CA389476877 | FOXG1 | c.1259A>G (p.His420Arg)
| |
| 14 | g.28768538A>T | CA389476878 | FOXG1 | c.1259A>T (p.His420Leu)
| |
| 14 | g.28768539C>A | CA389476879 | FOXG1 | c.1260C>A (p.His420Gln)
| |
| 14 | g.28768539C= | CA2126000457 | FOXG1 | c.1260C= (p.His420=)
| |
| 14 | g.28768539C>G | CA389476880 | FOXG1 | c.1260C>G (p.His420Gln)
| gnomAD v4 |
| 14 | g.28768539C>T | CA486098523 | FOXG1 | c.1260C>T (p.His420=)
| dbSNP gnomAD v4 |
| 14 | g.28768540G>A | CA389476881 | FOXG1 | c.1261G>A (p.Val421Ile)
| gnomAD v4 |
| 14 | g.28768540G>C | CA389476882 | FOXG1 | c.1261G>C (p.Val421Leu)
| dbSNP |
| 14 | g.28768540G= | CA2126000458 | FOXG1 | c.1261G= (p.Val421=)
| |
| 14 | g.28768540G>T | CA389476883 | FOXG1 | c.1261G>T (p.Val421Phe)
| |
| 14 | g.28768541T>A | CA389476884 | FOXG1 | c.1262T>A (p.Val421Asp)
| |
| 14 | g.28768541T>C | CA389476885 | FOXG1 | c.1262T>C (p.Val421Ala)
| |
| 14 | g.28768541T>G | CA389476886 | FOXG1 | c.1262T>G (p.Val421Gly)
| |
| 14 | g.28768542C>A | CA486098526 | FOXG1 | c.1263C>A (p.Val421=)
| |
| 14 | g.28768542C= | CA2126000459 | FOXG1 | c.1263C= (p.Val421=)
| |
| 14 | g.28768542C>G | CA7140676 | FOXG1 | c.1263C>G (p.Val421=)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.28768542C>T | CA486098529 | FOXG1 | c.1263C>T (p.Val421=)
| COSMIC |
| 14 | g.28768544del | CA2801003439 | FOXG1 | c.1265del (p.Pro422ArgfsTer5)
| |
| 14 | g.28768543C>A | CA389476889 | FOXG1 | c.1264C>A (p.Pro422Thr)
| |
| 14 | g.28768543C>G | CA389476887 | FOXG1 | c.1264C>G (p.Pro422Ala)
| |
| 14 | g.28768543C>T | CA389476888 | FOXG1 | c.1264C>T (p.Pro422Ser)
| COSMIC |
| 14 | g.28768544C>A | CA389476890 | FOXG1 | c.1265C>A (p.Pro422Gln)
| |
| 14 | g.28768544C>G | CA389476891 | FOXG1 | c.1265C>G (p.Pro422Arg)
| |
| 14 | g.28768544C>T | CA389476892 | FOXG1 | c.1265C>T (p.Pro422Leu)
| gnomAD v4 COSMIC |
| 14 | g.28768545G>A | CA486098534 | FOXG1 | c.1266G>A (p.Pro422=)
| dbSNP COSMIC |
| 14 | g.28768545G>C | CA486098536 | FOXG1 | c.1266G>C (p.Pro422=)
| |
| 14 | g.28768545G= | CA2126000460 | FOXG1 | c.1266G= (p.Pro422=)
| |
| 14 | g.28768545G>T | CA486098537 | FOXG1 | c.1266G>T (p.Pro422=)
| gnomAD v4 |
| 14 | g.28768546C>A | CA389476893 | FOXG1 | c.1267C>A (p.His423Asn)
| |
| 14 | g.28768546C>G | CA389476894 | FOXG1 | c.1267C>G (p.His423Asp)
| |
| 14 | g.28768546C>T | CA389476895 | FOXG1 | c.1267C>T (p.His423Tyr)
| |
| 14 | g.28768547A= | CA2126000461 | FOXG1 | c.1268A= (p.His423=)
| |
| 14 | g.28768547A>C | CA389476896 | FOXG1 | c.1268A>C (p.His423Pro)
| |
| 14 | g.28768547A>G | CA389476897 | FOXG1 | c.1268A>G (p.His423Arg)
| dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.28768547A>T | CA389476898 | FOXG1 | c.1268A>T (p.His423Leu)
| |
| 14 | g.28768548C>A | CA389476899 | FOXG1 | c.1269C>A (p.His423Gln)
| |
| 14 | g.28768548C>G | CA389476900 | FOXG1 | c.1269C>G (p.His423Gln)
| |
| 14 | g.28768548C>T | CA486098548 | FOXG1 | c.1269C>T (p.His423=)
| |
| 14 | g.28768549C>A | CA389476902 | FOXG1 | c.1270C>A (p.Pro424Thr)
| |
| 14 | g.28768549C= | CA2126000462 | FOXG1 | c.1270C= (p.Pro424=)
| |
| 14 | g.28768549C>G | CA389476903 | FOXG1 | c.1270C>G (p.Pro424Ala)
| dbSNP gnomAD v4 |
| 14 | g.28768549C>T | CA389476901 | FOXG1 | c.1270C>T (p.Pro424Ser)
| gnomAD v4 |
| 14 | g.28768550C>A | CA389476906 | FOXG1 | c.1271C>A (p.Pro424Gln)
| dbSNP |
| 14 | g.28768550C>G | CA389476904 | FOXG1 | c.1271C>G (p.Pro424Arg)
| |
| 14 | g.28768550C>T | CA389476905 | FOXG1 | c.1271C>T (p.Pro424Leu)
| |
| 14 | g.28768551G>A | CA7140677 | FOXG1 | c.1272G>A (p.Pro424=)
| dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
| 14 | g.28768551G>C | CA486098552 | FOXG1 | c.1272G>C (p.Pro424=)
| |
| 14 | g.28768551G= | CA2126000463 | FOXG1 | c.1272G= (p.Pro424=)
| |
| 14 | g.28768551G>T | CA486098551 | FOXG1 | c.1272G>T (p.Pro424=)
| |
| 14 | g.28768552T>A | CA389476907 | FOXG1 | c.1273T>A (p.Ser425Thr)
| |
| 14 | g.28768552T>C | CA314592 | FOXG1 | c.1273T>C (p.Ser425Pro)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.28768552T>G | CA389476908 | FOXG1 | c.1273T>G (p.Ser425Ala)
| |
| 14 | g.28768552T= | CA2126000464 | FOXG1 | c.1273T= (p.Ser425=)
| |
| 14 | g.28768553C>A | CA389476909 | FOXG1 | c.1274C>A (p.Ser425Ter)
| |
| 14 | g.28768553C>G | CA389476910 | FOXG1 | c.1274C>G (p.Ser425Ter)
| |
| 14 | g.28768553C>T | CA389476911 | FOXG1 | c.1274C>T (p.Ser425Leu)
| |
| 14 | g.28768554A= | CA2126000465 | FOXG1 | c.1275A= (p.Ser425=)
| |
| 14 | g.28768554A>C | CA486098563 | FOXG1 | c.1275A>C (p.Ser425=)
| |
| 14 | g.28768554A>G | CA258396599 | FOXG1 | c.1275A>G (p.Ser425=)
| dbSNP |
| 14 | g.28768554A>T | CA486098564 | FOXG1 | c.1275A>T (p.Ser425=)
| |
| 14 | g.28768555A= | CA2126000466 | FOXG1 | c.1276A= (p.Met426=)
| |
| 14 | g.28768555A>C | CA389476912 | FOXG1 | c.1276A>C (p.Met426Leu)
| |
| 14 | g.28768555A>G | CA389476913 | FOXG1 | c.1276A>G (p.Met426Val)
| ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.28768555A>T | CA389476914 | FOXG1 | c.1276A>T (p.Met426Leu)
| |
| 14 | g.28768556T>A | CA389476917 | FOXG1 | c.1277T>A (p.Met426Lys)
| |
| 14 | g.28768556T>C | CA389476915 | FOXG1 | c.1277T>C (p.Met426Thr)
| |
| 14 | g.28768556T>G | CA389476916 | FOXG1 | c.1277T>G (p.Met426Arg)
| |
| 14 | g.28768557G>A | CA314594 | FOXG1 | c.1278G>A (p.Met426Ile)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.28768557G>C | CA389476918 | FOXG1 | c.1278G>C (p.Met426Ile)
| |
| 14 | g.28768557G= | CA2126000467 | FOXG1 | c.1278G= (p.Met426=)
| |
| 14 | g.28768557G>T | CA389476919 | FOXG1 | c.1278G>T (p.Met426Ile)
| COSMIC |
| 14 | g.28768558A>C | CA389476920 | FOXG1 | c.1279A>C (p.Thr427Pro)
| |
| 14 | g.28768558A>G | CA389476921 | FOXG1 | c.1279A>G (p.Thr427Ala)
| |
| 14 | g.28768558A>T | CA389476922 | FOXG1 | c.1279A>T (p.Thr427Ser)
| |
| 14 | g.28768559C>A | CA389476923 | FOXG1 | c.1280C>A (p.Thr427Asn)
| |
| 14 | g.28768559C>G | CA389476924 | FOXG1 | c.1280C>G (p.Thr427Ser)
| |
| 14 | g.28768559C>T | CA389476925 | FOXG1 | c.1280C>T (p.Thr427Ile)
| gnomAD v4 |
| 14 | g.28768560T>A | CA486098578 | FOXG1 | c.1281T>A (p.Thr427=)
| |
| 14 | g.28768560T>C | CA486098579 | FOXG1 | c.1281T>C (p.Thr427=)
| |
| 14 | g.28768560T>G | CA486098581 | FOXG1 | c.1281T>G (p.Thr427=)
| |
| 14 | g.28768561T>A | CA389476926 | FOXG1 | c.1282T>A (p.Ser428Thr)
| gnomAD v4 |
| 14 | g.28768561T>C | CA389476927 | FOXG1 | c.1282T>C (p.Ser428Pro)
| |
| 14 | g.28768561T>G | CA389476928 | FOXG1 | c.1282T>G (p.Ser428Ala)
| |
| 14 | g.28768562C>A | CA389476930 | FOXG1 | c.1283C>A (p.Ser428Ter)
| |
| 14 | g.28768562C>G | CA389476931 | FOXG1 | c.1283C>G (p.Ser428Trp)
| |
| 14 | g.28768562C>T | CA389476929 | FOXG1 | c.1283C>T (p.Ser428Leu)
| |
| 14 | g.28768563G>A | CA486098585 | FOXG1 | c.1284G>A (p.Ser428=)
| dbSNP gnomAD v4 COSMIC |
| 14 | g.28768563G>C | CA258396600 | FOXG1 | c.1284G>C (p.Ser428=)
| dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.28768563G= | CA2126000468 | FOXG1 | c.1284G= (p.Ser428=)
| |
| 14 | g.28768563G>T | CA486098584 | FOXG1 | c.1284G>T (p.Ser428=)
| dbSNP |
| 14 | g.28768564C>A | CA389476932 | FOXG1 | c.1285C>A (p.Gln429Lys)
| |
| 14 | g.28768564C>G | CA389476933 | FOXG1 | c.1285C>G (p.Gln429Glu)
| |
| 14 | g.28768564C>T | CA389476934 | FOXG1 | c.1285C>T (p.Gln429Ter)
| |
| 14 | g.28768565A>C | CA389476935 | FOXG1 | c.1286A>C (p.Gln429Pro)
| |
| 14 | g.28768565A>G | CA389476936 | FOXG1 | c.1286A>G (p.Gln429Arg)
| |
| 14 | g.28768565A>T | CA389476937 | FOXG1 | c.1286A>T (p.Gln429Leu)
| |
| 14 | g.28768566G>A | CA486098593 | FOXG1 | c.1287G>A (p.Gln429=)
| gnomAD v4 COSMIC |
| 14 | g.28768566G>C | CA389476938 | FOXG1 | c.1287G>C (p.Gln429His)
| |
| 14 | g.28768566G>T | CA389476939 | FOXG1 | c.1287G>T (p.Gln429His)
| |
| 14 | g.28768567A= | CA2126000469 | FOXG1 | c.1288A= (p.Ser430=)
| |
| 14 | g.28768567A>C | CA389476940 | FOXG1 | c.1288A>C (p.Ser430Arg)
| |
| 14 | g.28768567A>G | CA389476941 | FOXG1 | c.1288A>G (p.Ser430Gly)
| ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.28768567A>T | CA389476942 | FOXG1 | c.1288A>T (p.Ser430Cys)
| |
| 14 | g.28768568G>A | CA389476943 | FOXG1 | c.1289G>A (p.Ser430Asn)
| |
| 14 | g.28768568G>C | CA389476944 | FOXG1 | c.1289G>C (p.Ser430Thr)
| gnomAD v4 COSMIC |
| 14 | g.28768568G>T | CA389476945 | FOXG1 | c.1289G>T (p.Ser430Ile)
| COSMIC |
| 14 | g.28768569C>A | CA389476947 | FOXG1 | c.1290C>A (p.Ser430Arg)
| gnomAD v4 |
| 14 | g.28768569C= | CA2126000470 | FOXG1 | c.1290C= (p.Ser430=)
| |
| 14 | g.28768569C>G | CA389476946 | FOXG1 | c.1290C>G (p.Ser430Arg)
| |
| 14 | g.28768569C>T | CA486098600 | FOXG1 | c.1290C>T (p.Ser430=)
| dbSNP |
| 14 | g.28768570del | CA2624400475 | FOXG1 | c.1291del (p.Ser431AlafsTer4)
| gnomAD v4 |
| 14 | g.28768570A>C | CA389476948 | FOXG1 | c.1291A>C (p.Ser431Arg)
| |
| 14 | g.28768570A>G | CA389476949 | FOXG1 | c.1291A>G (p.Ser431Gly)
| |
| 14 | g.28768570A>T | CA389476950 | FOXG1 | c.1291A>T (p.Ser431Cys)
| |
| 14 | g.28768571G>A | CA389476951 | FOXG1 | c.1292G>A (p.Ser431Asn)
| gnomAD v4 |
| 14 | g.28768571G>C | CA389476952 | FOXG1 | c.1292G>C (p.Ser431Thr)
| dbSNP |
| 14 | g.28768571G= | CA2126000471 | FOXG1 | c.1292G= (p.Ser431=)
| |
| 14 | g.28768571G>T | CA389476953 | FOXG1 | c.1292G>T (p.Ser431Ile)
| |
| 14 | g.28768572C>A | CA389476955 | FOXG1 | c.1293C>A (p.Ser431Arg)
| |
| 14 | g.28768572C>G | CA389476954 | FOXG1 | c.1293C>G (p.Ser431Arg)
| |
| 14 | g.28768572C>T | CA486098608 | FOXG1 | c.1293C>T (p.Ser431=)
| |
| 14 | g.28768572_28768574del | CA2624400481 | FOXG1 | c.1293_1295del (p.Ser431_Thr432delinsArg)
| gnomAD v4 |
| 14 | g.28768573A>C | CA389476956 | FOXG1 | c.1294A>C (p.Thr432Pro)
| |
| 14 | g.28768573A>G | CA389476957 | FOXG1 | c.1294A>G (p.Thr432Ala)
| |
| 14 | g.28768573A>T | CA389476958 | FOXG1 | c.1294A>T (p.Thr432Ser)
| |
| 14 | g.28768574del | CA486098616 | FOXG1 | c.1295del (p.Thr432SerfsTer3)
| COSMIC |
| 14 | g.28768574C>A | CA389476959 | FOXG1 | c.1295C>A (p.Thr432Lys)
| |
| 14 | g.28768574C= | CA2126000472 | FOXG1 | c.1295C= (p.Thr432=)
| |
| 14 | g.28768574C>G | CA389476960 | FOXG1 | c.1295C>G (p.Thr432Arg)
| |
| 14 | g.28768574C>T | CA258396601 | FOXG1 | c.1295C>T (p.Thr432Met)
| dbSNP gnomAD v3 gnomAD v4 |
| 14 | g.28768575G>A | CA7140678 | FOXG1 | c.1296G>A (p.Thr432=)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
| 14 | g.28768575G>C | CA486098620 | FOXG1 | c.1296G>C (p.Thr432=)
| gnomAD v4 |
| 14 | g.28768575G= | CA2126000473 | FOXG1 | c.1296G= (p.Thr432=)
| |
| 14 | g.28768575G>T | CA486098622 | FOXG1 | c.1296G>T (p.Thr432=)
| |
| 14 | g.28768576T>A | CA389476962 | FOXG1 | c.1297T>A (p.Ser433Thr)
| ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 14 | g.28768576T>C | CA389476963 | FOXG1 | c.1297T>C (p.Ser433Pro)
| |
| 14 | g.28768576T>G | CA389476961 | FOXG1 | c.1297T>G (p.Ser433Ala)
| |
| 14 | g.28768576T= | CA2126000474 | FOXG1 | c.1297T= (p.Ser433=)
| |
| 14 | g.28768577C>A | CA389476964 | FOXG1 | c.1298C>A (p.Ser433Tyr)
| |
| 14 | g.28768577C>G | CA389476966 | FOXG1 | c.1298C>G (p.Ser433Cys)
| |
| 14 | g.28768577C>T | CA389476965 | FOXG1 | c.1298C>T (p.Ser433Phe)
| |
| 14 | g.28768578C>A | CA486098626 | FOXG1 | c.1299C>A (p.Ser433=)
| COSMIC |
| 14 | g.28768578C>G | CA486098628 | FOXG1 | c.1299C>G (p.Ser433=)
| |
| 14 | g.28768578C>T | CA486098629 | FOXG1 | c.1299C>T (p.Ser433=)
| |
| 14 | g.28768579A= | CA2126000475 | FOXG1 | c.1300A= (p.Met434=)
| |
| 14 | g.28768579A>C | CA389476967 | FOXG1 | c.1300A>C (p.Met434Leu)
| |
| 14 | g.28768579A>G | CA389476969 | FOXG1 | c.1300A>G (p.Met434Val)
| dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.28768579A>T | CA389476968 | FOXG1 | c.1300A>T (p.Met434Leu)
| gnomAD v4 |
| 14 | g.28768580T>A | CA389476970 | FOXG1 | c.1301T>A (p.Met434Lys)
| |
| 14 | g.28768580T>C | CA389476972 | FOXG1 | c.1301T>C (p.Met434Thr)
| gnomAD v4 |
| 14 | g.28768580T>G | CA389476971 | FOXG1 | c.1301T>G (p.Met434Arg)
| |
| 14 | g.28768581G>A | CA389476973 | FOXG1 | c.1302G>A (p.Met434Ile)
| |
| 14 | g.28768581G>C | CA389476975 | FOXG1 | c.1302G>C (p.Met434Ile)
| |
| 14 | g.28768581G>T | CA389476974 | FOXG1 | c.1302G>T (p.Met434Ile)
| |
| 14 | g.28768582A>C | CA389476976 | FOXG1 | c.1303A>C (p.Ser435Arg)
| |
| 14 | g.28768582A>G | CA389476977 | FOXG1 | c.1303A>G (p.Ser435Gly)
| |
| 14 | g.28768582A>T | CA389476978 | FOXG1 | c.1303A>T (p.Ser435Cys)
| |
| 14 | g.28768583G>A | CA389476979 | FOXG1 | c.1304G>A (p.Ser435Asn)
| dbSNP gnomAD v4 |
| 14 | g.28768583G>C | CA389476980 | FOXG1 | c.1304G>C (p.Ser435Thr)
| |
| 14 | g.28768583G= | CA2126000476 | FOXG1 | c.1304G= (p.Ser435=)
| |
| 14 | g.28768583G>T | CA389476981 | FOXG1 | c.1304G>T (p.Ser435Ile)
| |
| 14 | g.28768584C>A | CA389476982 | FOXG1 | c.1305C>A (p.Ser435Arg)
| COSMIC |
| 14 | g.28768584C>G | CA389476983 | FOXG1 | c.1305C>G (p.Ser435Arg)
| |
| 14 | g.28768584C>T | CA486098632 | FOXG1 | c.1305C>T (p.Ser435=)
| gnomAD v4 |
| 14 | g.28768585G>A | CA389476984 | FOXG1 | c.1306G>A (p.Ala436Thr)
| dbSNP gnomAD v2 COSMIC |
| 14 | g.28768585G>C | CA389476985 | FOXG1 | c.1306G>C (p.Ala436Pro)
| |
| 14 | g.28768585G= | CA2126000477 | FOXG1 | c.1306G= (p.Ala436=)
| |
| 14 | g.28768585G>T | CA389476986 | FOXG1 | c.1306G>T (p.Ala436Ser)
| |
| 14 | g.28768586C>A | CA389476987 | FOXG1 | c.1307C>A (p.Ala436Asp)
| |
| 14 | g.28768586C>G | CA389476988 | FOXG1 | c.1307C>G (p.Ala436Gly)
| |
| 14 | g.28768586C>T | CA389476989 | FOXG1 | c.1307C>T (p.Ala436Val)
| |
| 14 | g.28768587C>A | CA486098639 | FOXG1 | c.1308C>A (p.Ala436=)
| |
| 14 | g.28768587C>G | CA486098640 | FOXG1 | c.1308C>G (p.Ala436=)
| gnomAD v4 |
| 14 | g.28768587C>T | CA486098641 | FOXG1 | c.1308C>T (p.Ala436=)
| |
| 14 | g.28768588A>C | CA486098642 | FOXG1 | c.1309A>C (p.Arg437=)
| COSMIC |
| 14 | g.28768588A>G | CA389476990 | FOXG1 | c.1309A>G (p.Arg437Gly)
| gnomAD v4 |
| 14 | g.28768588A>T | CA389476991 | FOXG1 | c.1309A>T (p.Arg437Trp)
| |
| 14 | g.28768589G>A | CA389476992 | FOXG1 | c.1310G>A (p.Arg437Lys)
| |
| 14 | g.28768589G>C | CA389476993 | FOXG1 | c.1310G>C (p.Arg437Thr)
| gnomAD v4 |
| 14 | g.28768589G>T | CA389476994 | FOXG1 | c.1310G>T (p.Arg437Met)
| |
| 14 | g.28768590G>A | CA7140679 | FOXG1 | c.1311G>A (p.Arg437=)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.28768590G>C | CA389476995 | FOXG1 | c.1311G>C (p.Arg437Ser)
| |
| 14 | g.28768590G= | CA2126000478 | FOXG1 | c.1311G= (p.Arg437=)
| |
| 14 | g.28768590G>T | CA389476996 | FOXG1 | c.1311G>T (p.Arg437Ser)
| COSMIC |
| 14 | g.28768591G>A | CA389476997 | FOXG1 | c.1312G>A (p.Ala438Thr)
| |
| 14 | g.28768591G>C | CA389476998 | FOXG1 | c.1312G>C (p.Ala438Pro)
| |
| 14 | g.28768591G>T | CA389476999 | FOXG1 | c.1312G>T (p.Ala438Ser)
| |
| 14 | g.28768592C>A | CA389477000 | FOXG1 | c.1313C>A (p.Ala438Asp)
| |
| 14 | g.28768592C= | CA2126000479 | FOXG1 | c.1313C= (p.Ala438=)
| |
| 14 | g.28768592C>G | CA389477001 | FOXG1 | c.1313C>G (p.Ala438Gly)
| |
| 14 | g.28768592C>T | CA7140680 | FOXG1 | c.1313C>T (p.Ala438Val)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.28768593C>A | CA486098650 | FOXG1 | c.1314C>A (p.Ala438=)
| |
| 14 | g.28768593C= | CA2126000480 | FOXG1 | c.1314C= (p.Ala438=)
| |
| 14 | g.28768593C>G | CA486098651 | FOXG1 | c.1314C>G (p.Ala438=)
| gnomAD v4 |
| 14 | g.28768593C>T | CA486098653 | FOXG1 | c.1314C>T (p.Ala438=)
| dbSNP gnomAD v2 gnomAD v4 COSMIC |
| 14 | g.28768594G>A | CA389477002 | FOXG1 | c.1315G>A (p.Ala439Thr)
| COSMIC |
| 14 | g.28768594G>C | CA389477004 | FOXG1 | c.1315G>C (p.Ala439Pro)
| |
| 14 | g.28768594G>T | CA389477003 | FOXG1 | c.1315G>T (p.Ala439Ser)
| |
| 14 | g.28768595C>A | CA389477006 | FOXG1 | c.1316C>A (p.Ala439Glu)
| |
| 14 | g.28768595C= | CA2126000481 | FOXG1 | c.1316C= (p.Ala439=)
| |
| 14 | g.28768595C>G | CA389477007 | FOXG1 | c.1316C>G (p.Ala439Gly)
| |
| 14 | g.28768595C>T | CA7140681 | FOXG1 | c.1316C>T (p.Ala439Val)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 14 | g.28768596G>A | CA486098665 | FOXG1 | c.1317G>A (p.Ala439=)
| gnomAD v4 COSMIC |
| 14 | g.28768596G>C | CA486098667 | FOXG1 | c.1317G>C (p.Ala439=)
| |
| 14 | g.28768596G>T | CA486098666 | FOXG1 | c.1317G>T (p.Ala439=)
| |
| 14 | g.28768596_28768599delinsGTCC | CA2126000482 | FOXG1 | c.1317_1320delinsGTCC (p.Ala439=)
| |
| 14 | g.28768597T>A | CA389477008 | FOXG1 | c.1318T>A (p.Ser440Thr)
| |
| 14 | g.28768597T>C | CA389477009 | FOXG1 | c.1318T>C (p.Ser440Pro)
| |
| 14 | g.28768597T>G | CA389477010 | FOXG1 | c.1318T>G (p.Ser440Ala)
| |
| 14 | g.28768603_28768605del | CA613324890 | FOXG1 | c.1324_1326del (p.Ser442del)
| dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.28768598C>A | CA389477011 | FOXG1 | c.1319C>A (p.Ser440Tyr)
| |
| 14 | g.28768598C>G | CA389477012 | FOXG1 | c.1319C>G (p.Ser440Cys)
| |
| 14 | g.28768598C>T | CA389477013 | FOXG1 | c.1319C>T (p.Ser440Phe)
| |
| 14 | g.28768599C>A | CA486098673 | FOXG1 | c.1320C>A (p.Ser440=)
| |
| 14 | g.28768599C= | CA2126000483 | FOXG1 | c.1320C= (p.Ser440=)
| |
| 14 | g.28768599C>G | CA16607645 | FOXG1 | c.1320C>G (p.Ser440=)
| ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 14 | g.28768599C>T | CA486098679 | FOXG1 | c.1320C>T (p.Ser440=)
| |
| 14 | g.28768600T>A | CA389477014 | FOXG1 | c.1321T>A (p.Ser441Thr)
| |
| 14 | g.28768600T>C | CA389477015 | FOXG1 | c.1321T>C (p.Ser441Pro)
| |
| 14 | g.28768600T>G | CA389477016 | FOXG1 | c.1321T>G (p.Ser441Ala)
| |
| 14 | g.28768601C>A | CA389477019 | FOXG1 | c.1322C>A (p.Ser441Tyr)
| |
| 14 | g.28768601C= | CA2126000484 | FOXG1 | c.1322C= (p.Ser441=)
| |
| 14 | g.28768601C>G | CA389477017 | FOXG1 | c.1322C>G (p.Ser441Cys)
| |
| 14 | g.28768601C>T | CA389477018 | FOXG1 | c.1322C>T (p.Ser441Phe)
| dbSNP |
| 14 | g.28768602C>A | CA486098689 | FOXG1 | c.1323C>A (p.Ser441=)
| |
| 14 | g.28768602C= | CA2126000485 | FOXG1 | c.1323C= (p.Ser441=)
| |
| 14 | g.28768602C>G | CA486098691 | FOXG1 | c.1323C>G (p.Ser441=)
| |
| 14 | g.28768602C>T | CA290951 | FOXG1 | c.1323C>T (p.Ser441=)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.28768603T>A | CA389477020 | FOXG1 | c.1324T>A (p.Ser442Thr)
| |
| 14 | g.28768603T>C | CA389477021 | FOXG1 | c.1324T>C (p.Ser442Pro)
| |
| 14 | g.28768603T>G | CA389477022 | FOXG1 | c.1324T>G (p.Ser442Ala)
| ClinVar gnomAD v4 |
| 14 | g.28768604C>A | CA389477023 | FOXG1 | c.1325C>A (p.Ser442Tyr)
| COSMIC |
| 14 | g.28768604C>G | CA389477024 | FOXG1 | c.1325C>G (p.Ser442Cys)
| gnomAD v4 |
| 14 | g.28768604C>T | CA389477025 | FOXG1 | c.1325C>T (p.Ser442Phe)
| |
| 14 | g.28768605C>A | CA486098698 | FOXG1 | c.1326C>A (p.Ser442=)
| |
| 14 | g.28768605C>G | CA486098697 | FOXG1 | c.1326C>G (p.Ser442=)
| gnomAD v4 |
| 14 | g.28768605C>T | CA486098696 | FOXG1 | c.1326C>T (p.Ser442=)
| COSMIC |
| 14 | g.28768606A>C | CA389477026 | FOXG1 | c.1327A>C (p.Thr443Pro)
| |
| 14 | g.28768606A>G | CA389477027 | FOXG1 | c.1327A>G (p.Thr443Ala)
| |
| 14 | g.28768606A>T | CA389477028 | FOXG1 | c.1327A>T (p.Thr443Ser)
| |
| 14 | g.28768607C>A | CA389477031 | FOXG1 | c.1328C>A (p.Thr443Lys)
| |
| 14 | g.28768607C>G | CA389477030 | FOXG1 | c.1328C>G (p.Thr443Arg)
| |
| 14 | g.28768607C>T | CA389477029 | FOXG1 | c.1328C>T (p.Thr443Met)
| COSMIC |
| 14 | g.28768608G>A | CA486098706 | FOXG1 | c.1329G>A (p.Thr443=)
| COSMIC |
| 14 | g.28768608G>C | CA486098707 | FOXG1 | c.1329G>C (p.Thr443=)
| |
| 14 | g.28768608G= | CA2126000486 | FOXG1 | c.1329G= (p.Thr443=)
| |
| 14 | g.28768608G>T | CA7140682 | FOXG1 | c.1329G>T (p.Thr443=)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 14 | g.28768609T>A | CA389477034 | FOXG1 | c.1330T>A (p.Ser444Thr)
| |
| 14 | g.28768609T>C | CA389477032 | FOXG1 | c.1330T>C (p.Ser444Pro)
| |
| 14 | g.28768609T>G | CA389477033 | FOXG1 | c.1330T>G (p.Ser444Ala)
| |
| 14 | g.28768610C>A | CA389477035 | FOXG1 | c.1331C>A (p.Ser444Ter)
| |
| 14 | g.28768610C>G | CA389477036 | FOXG1 | c.1331C>G (p.Ser444Trp)
| |
| 14 | g.28768610C>T | CA389477037 | FOXG1 | c.1331C>T (p.Ser444Leu)
| gnomAD v4 |
| 14 | g.28768611G>A | CA486098715 | FOXG1 | c.1332G>A (p.Ser444=)
| gnomAD v4 |
| 14 | g.28768611G>C | CA486098716 | FOXG1 | c.1332G>C (p.Ser444=)
| |
| 14 | g.28768611G= | CA2126000487 | FOXG1 | c.1332G= (p.Ser444=)
| |
| 14 | g.28768611G>T | CA258396602 | FOXG1 | c.1332G>T (p.Ser444=)
| ClinVar dbSNP |
| 14 | g.28768612C>A | CA389477038 | FOXG1 | c.1333C>A (p.Pro445Thr)
| |
| 14 | g.28768612C>G | CA389477039 | FOXG1 | c.1333C>G (p.Pro445Ala)
| |
| 14 | g.28768612C>T | CA389477040 | FOXG1 | c.1333C>T (p.Pro445Ser)
| COSMIC |
| 14 | g.28768613C>A | CA389477041 | FOXG1 | c.1334C>A (p.Pro445Gln)
| |
| 14 | g.28768613C>G | CA389477042 | FOXG1 | c.1334C>G (p.Pro445Arg)
| |
| 14 | g.28768613C>T | CA389477043 | FOXG1 | c.1334C>T (p.Pro445Leu)
| |
| 14 | g.28768614G>A | CA486098728 | FOXG1 | c.1335G>A (p.Pro445=)
| gnomAD v4 COSMIC |
| 14 | g.28768614G>C | CA486098730 | FOXG1 | c.1335G>C (p.Pro445=)
| |
| 14 | g.28768614G= | CA2126000488 | FOXG1 | c.1335G= (p.Pro445=)
| |
| 14 | g.28768614G>T | CA486098731 | FOXG1 | c.1335G>T (p.Pro445=)
| dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.28768615C>A | CA389477046 | FOXG1 | c.1336C>A (p.Gln446Lys)
| |
| 14 | g.28768615C>G | CA389477045 | FOXG1 | c.1336C>G (p.Gln446Glu)
| |
| 14 | g.28768615C>T | CA389477044 | FOXG1 | c.1336C>T (p.Gln446Ter)
| |
| 14 | g.28768616A= | CA2126000489 | FOXG1 | c.1337A= (p.Gln446=)
| |
| 14 | g.28768616A>C | CA389477047 | FOXG1 | c.1337A>C (p.Gln446Pro)
| |
| 14 | g.28768616A>G | CA389477048 | FOXG1 | c.1337A>G (p.Gln446Arg)
| ClinVar gnomAD v4 |
| 14 | g.28768616A>T | CA389477049 | FOXG1 | c.1337A>T (p.Gln446Leu)
| ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.28768617G>A | CA486098733 | FOXG1 | c.1338G>A (p.Gln446=)
| |
| 14 | g.28768617G>C | CA389477050 | FOXG1 | c.1338G>C (p.Gln446His)
| |
| 14 | g.28768617G>T | CA389477051 | FOXG1 | c.1338G>T (p.Gln446His)
| |
| 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 |
