| 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)
| |
| 14 | g.28768721G>A | CA389477273 | FOXG1 | c.1442G>A (p.Gly481Glu)
| ClinVar dbSNP |
| 14 | g.28768721G>C | CA389477274 | FOXG1 | c.1442G>C (p.Gly481Ala)
| |
| 14 | g.28768721G>T | CA389477275 | FOXG1 | c.1442G>T (p.Gly481Val)
| gnomAD v4 |
| 14 | g.28768722G>A | CA486098781 | FOXG1 | c.1443G>A (p.Gly481=)
| ClinVar dbSNP gnomAD v4 |
| 14 | g.28768722G>C | CA486098784 | FOXG1 | c.1443G>C (p.Gly481=)
| |
| 14 | g.28768722G= | CA2126000524 | FOXG1 | c.1443G= (p.Gly481=)
| |
| 14 | g.28768722G>T | CA486098782 | FOXG1 | c.1443G>T (p.Gly481=)
| |
| 14 | g.28768722_28768725delinsGTCT | CA2126000523 | FOXG1 | c.1443_1446delinsGTCT (p.Gly481=)
| |
| 14 | g.28768723T>A | CA389477278 | FOXG1 | c.1444T>A (p.Ser482Thr)
| |
| 14 | g.28768723T>C | CA389477276 | FOXG1 | c.1444T>C (p.Ser482Pro)
| |
| 14 | g.28768723T>G | CA389477277 | FOXG1 | c.1444T>G (p.Ser482Ala)
| dbSNP |
| 14 | g.28768723T= | CA2126000525 | FOXG1 | c.1444T= (p.Ser482=)
| |
| 14 | g.28768728_28768730del | CA7140695 | FOXG1 | c.1449_1451del (p.Ser484del)
| dbSNP ExAC |
| 14 | g.28768724C>A | CA389477279 | FOXG1 | c.1445C>A (p.Ser482Tyr)
| |
| 14 | g.28768724C>G | CA389477280 | FOXG1 | c.1445C>G (p.Ser482Cys)
| |
| 14 | g.28768724C>T | CA389477281 | FOXG1 | c.1445C>T (p.Ser482Phe)
| |
| 14 | g.28768725T>A | CA486098791 | FOXG1 | c.1446T>A (p.Ser482=)
| |
| 14 | g.28768725T>C | CA486098787 | FOXG1 | c.1446T>C (p.Ser482=)
| gnomAD v4 |
| 14 | g.28768725T>G | CA486098790 | FOXG1 | c.1446T>G (p.Ser482=)
| |
| 14 | g.28768726T>A | CA389477282 | FOXG1 | c.1447T>A (p.Ser483Thr)
| |
| 14 | g.28768726T>C | CA389477283 | FOXG1 | c.1447T>C (p.Ser483Pro)
| |
| 14 | g.28768726T>G | CA389477284 | FOXG1 | c.1447T>G (p.Ser483Ala)
| |
| 14 | g.28768727C>A | CA389477285 | FOXG1 | c.1448C>A (p.Ser483Tyr)
| |
| 14 | g.28768727C= | CA2126000526 | FOXG1 | c.1448C= (p.Ser483=)
| |
| 14 | g.28768727C>G | CA389477286 | FOXG1 | c.1448C>G (p.Ser483Cys)
| |
| 14 | g.28768727C>T | CA389477287 | FOXG1 | c.1448C>T (p.Ser483Phe)
| dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.28768728T>A | CA258396606 | FOXG1 | c.1449T>A (p.Ser483=)
| dbSNP |
| 14 | g.28768728T>C | CA7140696 | FOXG1 | c.1449T>C (p.Ser483=)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.28768728T>G | CA7140697 | FOXG1 | c.1449T>G (p.Ser483=)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
| 14 | g.28768728T= | CA2126000527 | FOXG1 | c.1449T= (p.Ser483=)
| |
| 14 | g.28768729T>A | CA389477288 | FOXG1 | c.1450T>A (p.Ser484Thr)
| |
| 14 | g.28768729T>C | CA389477290 | FOXG1 | c.1450T>C (p.Ser484Pro)
| |
| 14 | g.28768729T>G | CA389477289 | FOXG1 | c.1450T>G (p.Ser484Ala)
| |
| 14 | g.28768730C>A | CA389477291 | FOXG1 | c.1451C>A (p.Ser484Tyr)
| |
| 14 | g.28768730C>G | CA389477292 | FOXG1 | c.1451C>G (p.Ser484Cys)
| |
| 14 | g.28768730C>T | CA389477293 | FOXG1 | c.1451C>T (p.Ser484Phe)
| COSMIC |
| 14 | g.28768731C>A | CA486098796 | FOXG1 | c.1452C>A (p.Ser484=)
| |
| 14 | g.28768731C= | CA2126000528 | FOXG1 | c.1452C= (p.Ser484=)
| |
| 14 | g.28768731C>G | CA486098800 | FOXG1 | c.1452C>G (p.Ser484=)
| |
| 14 | g.28768731C>T | CA486098802 | FOXG1 | c.1452C>T (p.Ser484=)
| dbSNP gnomAD v4 |
| 14 | g.28768732A>C | CA389477294 | FOXG1 | c.1453A>C (p.Asn485His)
| |
| 14 | g.28768732A>G | CA389477295 | FOXG1 | c.1453A>G (p.Asn485Asp)
| |
| 14 | g.28768732A>T | CA389477296 | FOXG1 | c.1453A>T (p.Asn485Tyr)
| |
| 14 | g.28768733A>C | CA389477299 | FOXG1 | c.1454A>C (p.Asn485Thr)
| |
| 14 | g.28768733A>G | CA389477297 | FOXG1 | c.1454A>G (p.Asn485Ser)
| gnomAD v4 |
| 14 | g.28768733A>T | CA389477298 | FOXG1 | c.1454A>T (p.Asn485Ile)
| |
| 14 | g.28768734C>A | CA389477300 | FOXG1 | c.1455C>A (p.Asn485Lys)
| |
| 14 | g.28768734C>G | CA389477301 | FOXG1 | c.1455C>G (p.Asn485Lys)
| |
| 14 | g.28768734C>T | CA486098807 | FOXG1 | c.1455C>T (p.Asn485=)
| |
| 14 | g.28768736del | CA2575498213 | FOXG1 | c.1457del (p.Pro486LeufsTer2)
| |
| 14 | g.28768735C>A | CA389477302 | FOXG1 | c.1456C>A (p.Pro486Thr)
| |
| 14 | g.28768735C= | CA2126000529 | FOXG1 | c.1456C= (p.Pro486=)
| |
| 14 | g.28768735C>G | CA389477303 | FOXG1 | c.1456C>G (p.Pro486Ala)
| |
| 14 | g.28768735C>T | CA389477304 | FOXG1 | c.1456C>T (p.Pro486Ser)
| ClinVar dbSNP gnomAD v4 |
| 14 | g.28768736C>A | CA389477305 | FOXG1 | c.1457C>A (p.Pro486His)
| dbSNP |
| 14 | g.28768736C>G | CA389477307 | FOXG1 | c.1457C>G (p.Pro486Arg)
| |
| 14 | g.28768736C>T | CA389477306 | FOXG1 | c.1457C>T (p.Pro486Leu)
| |
| 14 | g.28768737T>A | CA486098811 | FOXG1 | c.1458T>A (p.Pro486=)
| |
| 14 | g.28768737T>C | CA486098813 | FOXG1 | c.1458T>C (p.Pro486=)
| ClinVar dbSNP |
| 14 | g.28768737T>G | CA486098817 | FOXG1 | c.1458T>G (p.Pro486=)
| ClinVar gnomAD v4 |
| 14 | g.28768738T>A | CA389477308 | FOXG1 | c.1459T>A (p.Leu487Ile)
| |
| 14 | g.28768738T>C | CA486098818 | FOXG1 | c.1459T>C (p.Leu487=)
| |
| 14 | g.28768738T>G | CA389477309 | FOXG1 | c.1459T>G (p.Leu487Val)
| |
| 14 | g.28768739T>A | CA389477310 | FOXG1 | c.1460T>A (p.Leu487Ter)
| |
| 14 | g.28768739T>C | CA389477311 | FOXG1 | c.1460T>C (p.Leu487Ser)
| |
| 14 | g.28768739T>G | CA389477312 | FOXG1 | c.1460T>G (p.Leu487Ter)
| |
| 14 | g.28768740A>C | CA389477313 | FOXG1 | c.1461A>C (p.Leu487Phe)
| |
| 14 | g.28768740A>G | CA486098824 | FOXG1 | c.1461A>G (p.Leu487=)
| |
| 14 | g.28768740A>T | CA389477314 | FOXG1 | c.1461A>T (p.Leu487Phe)
| |
| 14 | g.28768741A>C | CA389477315 | FOXG1 | c.1462A>C (p.Ile488Leu)
| |
| 14 | g.28768741A>G | CA389477316 | FOXG1 | c.1462A>G (p.Ile488Val)
| |
| 14 | g.28768741A>T | CA389477317 | FOXG1 | c.1462A>T (p.Ile488Leu)
| |
| 14 | g.28768742T>A | CA389477320 | FOXG1 | c.1463T>A (p.Ile488Lys)
| |
| 14 | g.28768742T>C | CA389477319 | FOXG1 | c.1463T>C (p.Ile488Thr)
| |
| 14 | g.28768742T>G | CA389477318 | FOXG1 | c.1463T>G (p.Ile488Arg)
| |
| 14 | g.28768743A>C | CA486098833 | FOXG1 | c.1464A>C (p.Ile488=)
| gnomAD v4 |
| 14 | g.28768743A>G | CA389477321 | FOXG1 | c.1464A>G (p.Ile488Met)
| |
| 14 | g.28768743A>T | CA486098834 | FOXG1 | c.1464A>T (p.Ile488=)
| |
| 14 | g.28768744C>A | CA389477323 | FOXG1 | c.1465C>A (p.His489Asn)
| |
| 14 | g.28768744C>G | CA389477322 | FOXG1 | c.1465C>G (p.His489Asp)
| |
| 14 | g.28768744C>T | CA389477324 | FOXG1 | c.1465C>T (p.His489Tyr)
| ClinVar |
| 14 | g.28768745A>C | CA389477325 | FOXG1 | c.1466A>C (p.His489Pro)
| |
| 14 | g.28768745A>G | CA389477326 | FOXG1 | c.1466A>G (p.His489Arg)
| gnomAD v4 |
| 14 | g.28768745A>T | CA389477327 | FOXG1 | c.1466A>T (p.His489Leu)
| |
| 14 | g.28768746T>A | CA389477328 | FOXG1 | c.1467T>A (p.His489Gln)
| |
| 14 | g.28768746T>C | CA486098839 | FOXG1 | c.1467T>C (p.His489=)
| |
| 14 | g.28768746T>G | CA389477329 | FOXG1 | c.1467T>G (p.His489Gln)
| |
| 14 | g.28768747T>A | CA389477330 | FOXG1 | c.1468T>A (p.Ter490Lys)
| |
| 14 | g.28768747T>C | CA389477331 | FOXG1 | c.1468T>C (p.Ter490Gln)
| |
| 14 | g.28768747T>G | CA389477332 | FOXG1 | c.1468T>G (p.Ter490Glu)
| |
| 14 | g.28768748A>C | CA389477333 | FOXG1 | c.1469A>C (p.Ter490Ser)
| |
| 14 | g.28768748A>G | CA486098843 | FOXG1 | c.1469A>G (p.Ter490=)
| |
| 14 | g.28768748A>T | CA389477334 | FOXG1 | c.1469A>T (p.Ter490Leu)
| |
| 14 | g.28768749A>C | CA389477335 | FOXG1 | c.1470A>C (p.Ter490Tyr)
| |
| 14 | g.28768749A>G | CA486098846 | FOXG1 | c.1470A>G (p.Ter490=)
| |
| 14 | g.28768749A>T | CA389477336 | FOXG1 | c.1470A>T (p.Ter490Tyr)
| |
| 14 | g.28768751A= | CA2126000530 | FOXG1 | c.*2A= (n.*2A=)
| |
| 14 | g.28768751A>C | CA2624400664 | FOXG1 | c.*2A>C (n.*2A>C)
| gnomAD v4 |
| 14 | g.28768751A>G | CA2801003456 | FOXG1 | c.*2A>G (n.*2A>G)
| |
| 14 | g.28768751A>T | CA7140698 | FOXG1 | c.*2A>T (n.*2A>T)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.28768753C>A | CA961430555 | FOXG1 | c.*4C>A (n.*4C>A)
| dbSNP gnomAD v3 gnomAD v4 |
| 14 | g.28768753C= | CA2126000531 | FOXG1 | c.*4C= (n.*4C=)
| |
| 14 | g.28768753C>T | CA200490 | FOXG1 | c.*4C>T (n.*4C>T)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.28768755C>A | CA2801003461 | FOXG1 | c.*6C>A (n.*6C>A)
| |
| 14 | g.28768755C= | CA2126000532 | FOXG1 | c.*6C= (n.*6C=)
| |
| 14 | g.28768755C>G | CA655705517 | FOXG1 | c.*6C>G (n.*6C>G)
| dbSNP gnomAD v3 gnomAD v4 COSMIC |
| 14 | g.28768755C>T | CA2126000533 | FOXG1 | c.*6C>T (n.*6C>T)
| dbSNP |
| 14 | g.28768756T>C | CA7140699 | FOXG1 | c.*7T>C (n.*7T>C)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
| 14 | g.28768756T>G | CA655705536 | FOXG1 | c.*7T>G (n.*7T>G)
| COSMIC |
| 14 | g.28768756T= | CA2126000534 | FOXG1 | c.*7T= (n.*7T=)
| |
| 14 | g.28768757G= | CA2126000535 | FOXG1 | c.*8G= (n.*8G=)
| |
| 14 | g.28768757G>T | CA206900 | FOXG1 | c.*8G>T (n.*8G>T)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.28768758G>A | CA2575498214 | FOXG1 | c.*9G>A (n.*9G>A)
| gnomAD v4 |
| 14 | g.28768759G>A | CA961430572 | FOXG1 | c.*10G>A (n.*10G>A)
| dbSNP gnomAD v3 gnomAD v4 |
| 14 | g.28768759G= | CA2126000536 | FOXG1 | c.*10G= (n.*10G=)
| |
