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.28767924_28767932delinsCCCTTACTA | CA2125999899 | FOXG1 | c.645_653delinsCCCTTACTA (p.Phe215=) | |
| 14 | g.28767927_28767934del | CA234033 | FOXG1 | c.648_655del (p.Tyr217ArgfsTer?) | ClinVar dbSNP |
| 14 | g.28767931T>A | CA389475573 | FOXG1 | c.652T>A (p.Tyr218Asn) | |
| 14 | g.28767931T>C | CA389475571 | FOXG1 | c.652T>C (p.Tyr218His) | |
| 14 | g.28767931T>G | CA389475572 | FOXG1 | c.652T>G (p.Tyr218Asp) | |
| 14 | g.28767932A= | CA2125999917 | FOXG1 | c.653A= (p.Tyr218=) | |
| 14 | g.28767932A>C | CA389475574 | FOXG1 | c.653A>C (p.Tyr218Ser) | |
| 14 | g.28767932A>G | CA389475575 | FOXG1 | c.653A>G (p.Tyr218Cys) | ClinVar dbSNP |
| 14 | g.28767932A>T | CA389475576 | FOXG1 | c.653A>T (p.Tyr218Phe) | |
| 14 | g.28767933C>A | CA389475577 | FOXG1 | c.654C>A (p.Tyr218Ter) | ClinVar dbSNP |
| 14 | g.28767933C>G | CA389475578 | FOXG1 | c.654C>G (p.Tyr218Ter) | |
| 14 | g.28767933C>T | CA486098559 | FOXG1 | c.654C>T (p.Tyr218=) | |
| 14 | g.28767934del | CA2801003776 | FOXG1 | c.655del (p.Arg219AlafsTer22) | |
| 14 | g.28767934C>A | CA389475579 | FOXG1 | c.655C>A (p.Arg219Ser) | |
| 14 | g.28767934C= | CA2125999921 | FOXG1 | c.655C= (p.Arg219=) | |
| 14 | g.28767934C>G | CA389475580 | FOXG1 | c.655C>G (p.Arg219Gly) | ClinVar dbSNP |
| 14 | g.28767934C>T | CA389475581 | FOXG1 | c.655C>T (p.Arg219Cys) | dbSNP gnomAD v4 COSMIC |
| 14 | g.28767935G>A | CA389475582 | FOXG1 | c.656G>A (p.Arg219His) | dbSNP |
| 14 | g.28767935G>C | CA389475583 | FOXG1 | c.656G>C (p.Arg219Pro) | dbSNP |
| 14 | g.28767935G= | CA2125999925 | FOXG1 | c.656G= (p.Arg219=) | |
| 14 | g.28767935G>T | CA389475584 | FOXG1 | c.656G>T (p.Arg219Leu) | |
| 14 | g.28767936C>A | CA486098567 | FOXG1 | c.657C>A (p.Arg219=) | |
| 14 | g.28767936C= | CA2125999930 | FOXG1 | c.657C= (p.Arg219=) | |
| 14 | g.28767936C>G | CA486098568 | FOXG1 | c.657C>G (p.Arg219=) | ClinVar dbSNP gnomAD v4 |
| 14 | g.28767936C>T | CA7140624 | FOXG1 | c.657C>T (p.Arg219=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.28767937G>A | CA389475585 | FOXG1 | c.658G>A (p.Glu220Lys) | |
| 14 | g.28767937G>C | CA389475587 | FOXG1 | c.658G>C (p.Glu220Gln) | |
| 14 | g.28767937G>T | CA389475586 | FOXG1 | c.658G>T (p.Glu220Ter) | |
| 14 | g.28767938A>C | CA389475588 | FOXG1 | c.659A>C (p.Glu220Ala) | |
| 14 | g.28767938A>G | CA389475589 | FOXG1 | c.659A>G (p.Glu220Gly) | |
| 14 | g.28767938A>T | CA389475590 | FOXG1 | c.659A>T (p.Glu220Val) | |
| 14 | g.28767939G>A | CA486098575 | FOXG1 | c.660G>A (p.Glu220=) | ClinVar dbSNP |
| 14 | g.28767939G>C | CA389475591 | FOXG1 | c.660G>C (p.Glu220Asp) | |
| 14 | g.28767939G= | CA2125999935 | FOXG1 | c.660G= (p.Glu220=) | |
| 14 | g.28767939G>T | CA389475592 | FOXG1 | c.660G>T (p.Glu220Asp) | dbSNP |
| 14 | g.28767940A>C | CA389475593 | FOXG1 | c.661A>C (p.Asn221His) | |
| 14 | g.28767940A>G | CA389475594 | FOXG1 | c.661A>G (p.Asn221Asp) | |
| 14 | g.28767940A>T | CA389475595 | FOXG1 | c.661A>T (p.Asn221Tyr) | |
| 14 | g.28767941A>C | CA389475596 | FOXG1 | c.662A>C (p.Asn221Thr) | |
| 14 | g.28767941A>G | CA389475597 | FOXG1 | c.662A>G (p.Asn221Ser) | gnomAD v4 |
| 14 | g.28767941A>T | CA389475598 | FOXG1 | c.662A>T (p.Asn221Ile) | |
| 14 | g.28767942C>A | CA389475599 | FOXG1 | c.663C>A (p.Asn221Lys) | |
| 14 | g.28767942C>G | CA389475600 | FOXG1 | c.663C>G (p.Asn221Lys) | |
| 14 | g.28767942C>T | CA486098582 | FOXG1 | c.663C>T (p.Asn221=) | |
| 14 | g.28767943A>C | CA389475601 | FOXG1 | c.664A>C (p.Lys222Gln) | |
| 14 | g.28767943A>G | CA389475603 | FOXG1 | c.664A>G (p.Lys222Glu) | |
| 14 | g.28767943A>T | CA389475602 | FOXG1 | c.664A>T (p.Lys222Ter) | |
| 14 | g.28767944A>C | CA389475604 | FOXG1 | c.665A>C (p.Lys222Thr) | |
| 14 | g.28767944A>G | CA389475605 | FOXG1 | c.665A>G (p.Lys222Arg) | |
| 14 | g.28767944A>T | CA389475606 | FOXG1 | c.665A>T (p.Lys222Met) | |
| 14 | g.28767945G>A | CA486098592 | FOXG1 | c.666G>A (p.Lys222=) | |
| 14 | g.28767945G>C | CA389475607 | FOXG1 | c.666G>C (p.Lys222Asn) | |
| 14 | g.28767945G>T | CA389475608 | FOXG1 | c.666G>T (p.Lys222Asn) | |
| 14 | g.28767946C>A | CA389475609 | FOXG1 | c.667C>A (p.Gln223Lys) | |
| 14 | g.28767946C= | CA2125999937 | FOXG1 | c.667C= (p.Gln223=) | |
| 14 | g.28767946C>G | CA389475610 | FOXG1 | c.667C>G (p.Gln223Glu) | |
| 14 | g.28767946C>T | CA314614 | FOXG1 | c.667C>T (p.Gln223Ter) | ClinVar dbSNP |
| 14 | g.28767947A>C | CA389475611 | FOXG1 | c.668A>C (p.Gln223Pro) | |
| 14 | g.28767947A>G | CA389475612 | FOXG1 | c.668A>G (p.Gln223Arg) | |
| 14 | g.28767947A>T | CA389475613 | FOXG1 | c.668A>T (p.Gln223Leu) | |
| 14 | g.28767948G>A | CA486098601 | FOXG1 | c.669G>A (p.Gln223=) | COSMIC |
| 14 | g.28767948G>C | CA389475614 | FOXG1 | c.669G>C (p.Gln223His) | |
| 14 | g.28767948G>T | CA389475615 | FOXG1 | c.669G>T (p.Gln223His) | |
| 14 | g.28767949G>A | CA234034 | FOXG1 | c.670G>A (p.Gly224Ser) | ClinVar dbSNP |
| 14 | g.28767949G>C | CA389475617 | FOXG1 | c.670G>C (p.Gly224Arg) | |
| 14 | g.28767949G= | CA2125999941 | FOXG1 | c.670G= (p.Gly224=) | |
| 14 | g.28767949G>T | CA389475616 | FOXG1 | c.670G>T (p.Gly224Cys) | |
| 14 | g.28767950G>A | CA314648 | FOXG1 | c.671G>A (p.Gly224Asp) | ClinVar dbSNP |
| 14 | g.28767950G>C | CA389475618 | FOXG1 | c.671G>C (p.Gly224Ala) | |
| 14 | g.28767950G= | CA2125999945 | FOXG1 | c.671G= (p.Gly224=) | |
| 14 | g.28767950G>T | CA389475619 | FOXG1 | c.671G>T (p.Gly224Val) | |
| 14 | g.28767951C>A | CA486098613 | FOXG1 | c.672C>A (p.Gly224=) | |
| 14 | g.28767951C= | CA2125999950 | FOXG1 | c.672C= (p.Gly224=) | |
| 14 | g.28767951C>G | CA172189 | FOXG1 | c.672C>G (p.Gly224=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 14 | g.28767951C>T | CA486098617 | FOXG1 | c.672C>T (p.Gly224=) | dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.28767952T>A | CA389475620 | FOXG1 | c.673T>A (p.Trp225Arg) | |
| 14 | g.28767952T>C | CA314650 | FOXG1 | c.673T>C (p.Trp225Arg) | dbSNP |
| 14 | g.28767952T>G | CA389475621 | FOXG1 | c.673T>G (p.Trp225Gly) | ClinVar |
| 14 | g.28767952T= | CA2125999952 | FOXG1 | c.673T= (p.Trp225=) | |
| 14 | g.28767953G>A | CA389475622 | FOXG1 | c.674G>A (p.Trp225Ter) | |
| 14 | g.28767953G>C | CA16621656 | FOXG1 | c.674G>C (p.Trp225Ser) | ClinVar dbSNP |
| 14 | g.28767953G= | CA2125999955 | FOXG1 | c.674G= (p.Trp225=) | |
| 14 | g.28767953G>T | CA389475623 | FOXG1 | c.674G>T (p.Trp225Leu) | |
| 14 | g.28767954G>A | CA314616 | FOXG1 | c.675G>A (p.Trp225Ter) | dbSNP |
| 14 | g.28767954G>C | CA389475625 | FOXG1 | c.675G>C (p.Trp225Cys) | |
| 14 | g.28767954G= | CA2125999957 | FOXG1 | c.675G= (p.Trp225=) | |
| 14 | g.28767954G>T | CA389475624 | FOXG1 | c.675G>T (p.Trp225Cys) | |
| 14 | g.28767955C>A | CA389475626 | FOXG1 | c.676C>A (p.Gln226Lys) | |
| 14 | g.28767955C= | CA2125999961 | FOXG1 | c.676C= (p.Gln226=) | |
| 14 | g.28767955C>G | CA389475627 | FOXG1 | c.676C>G (p.Gln226Glu) | ClinVar |
| 14 | g.28767955C>T | CA389475628 | FOXG1 | c.676C>T (p.Gln226Ter) | ClinVar dbSNP |
| 14 | g.28767956A>C | CA389475629 | FOXG1 | c.677A>C (p.Gln226Pro) | ClinVar |
| 14 | g.28767956A>G | CA389475630 | FOXG1 | c.677A>G (p.Gln226Arg) | |
| 14 | g.28767956A>T | CA389475631 | FOXG1 | c.677A>T (p.Gln226Leu) | |
| 14 | g.28767957G>A | CA486098636 | FOXG1 | c.678G>A (p.Gln226=) | |
| 14 | g.28767957G>C | CA389475632 | FOXG1 | c.678G>C (p.Gln226His) | |
| 14 | g.28767957G>T | CA389475633 | FOXG1 | c.678G>T (p.Gln226His) | |
| 14 | g.28767958A= | CA2125999967 | FOXG1 | c.679A= (p.Asn227=) | |
| 14 | g.28767958A>C | CA389475634 | FOXG1 | c.679A>C (p.Asn227His) | |
| 14 | g.28767958A>G | CA389475635 | FOXG1 | c.679A>G (p.Asn227Asp) | ClinVar dbSNP |
| 14 | g.28767958A>T | CA389475636 | FOXG1 | c.679A>T (p.Asn227Tyr) | |
| 14 | g.28767959A>C | CA389475638 | FOXG1 | c.680A>C (p.Asn227Thr) | |
| 14 | g.28767959A>G | CA389475639 | FOXG1 | c.680A>G (p.Asn227Ser) | ClinVar |
| 14 | g.28767959A>T | CA389475637 | FOXG1 | c.680A>T (p.Asn227Ile) | ClinVar |
| 14 | g.28767960C>A | CA389475640 | FOXG1 | c.681C>A (p.Asn227Lys) | |
| 14 | g.28767960C= | CA2125999970 | FOXG1 | c.681C= (p.Asn227=) | |
| 14 | g.28767960C>G | CA199447 | FOXG1 | c.681C>G (p.Asn227Lys) | ClinVar dbSNP |
| 14 | g.28767960C>T | CA486098659 | FOXG1 | c.681C>T (p.Asn227=) | ClinVar |
| 14 | g.28767961T>A | CA389475641 | FOXG1 | c.682T>A (p.Ser228Thr) | |
| 14 | g.28767961T>C | CA389475642 | FOXG1 | c.682T>C (p.Ser228Pro) | dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.28767961T>G | CA389475643 | FOXG1 | c.682T>G (p.Ser228Ala) | |
| 14 | g.28767961T= | CA2125999973 | FOXG1 | c.682T= (p.Ser228=) | |
| 14 | g.28767962C>A | CA389475644 | FOXG1 | c.683C>A (p.Ser228Tyr) | |
| 14 | g.28767962C>G | CA389475645 | FOXG1 | c.683C>G (p.Ser228Cys) | ClinVar |
| 14 | g.28767962C>T | CA389475646 | FOXG1 | c.683C>T (p.Ser228Phe) | |
| 14 | g.28767963C>A | CA486098680 | FOXG1 | c.684C>A (p.Ser228=) | gnomAD v3 gnomAD v4 |
| 14 | g.28767963C= | CA2125999976 | FOXG1 | c.684C= (p.Ser228=) | |
| 14 | g.28767963C>G | CA486098704 | FOXG1 | c.684C>G (p.Ser228=) | |
| 14 | g.28767963C>T | CA7140625 | FOXG1 | c.684C>T (p.Ser228=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 14 | g.28767964A= | CA2125999978 | FOXG1 | c.685A= (p.Ile229=) | |
| 14 | g.28767964A>C | CA16621657 | FOXG1 | c.685A>C (p.Ile229Leu) | ClinVar dbSNP |
| 14 | g.28767964A>G | CA389475647 | FOXG1 | c.685A>G (p.Ile229Val) | |
| 14 | g.28767964A>T | CA389475648 | FOXG1 | c.685A>T (p.Ile229Phe) | |
| 14 | g.28767964_28767965del | CA645570773 | FOXG1 | c.685_686del (p.Ile229ProfsTer?) | COSMIC |
| 14 | g.28767965T>A | CA314618 | FOXG1 | c.686T>A (p.Ile229Asn) | dbSNP |
| 14 | g.28767965T>C | CA258396578 | FOXG1 | c.686T>C (p.Ile229Thr) | dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.28767965T>G | CA389475649 | FOXG1 | c.686T>G (p.Ile229Ser) | |
| 14 | g.28767965T= | CA2125999981 | FOXG1 | c.686T= (p.Ile229=) | |
| 14 | g.28767965_28767966delinsAA | CA2499222615 | FOXG1 | c.686_687delinsAA (p.Ile229Lys) | ClinVar dbSNP |
| 14 | g.28767966C>A | CA486098718 | FOXG1 | c.687C>A (p.Ile229=) | |
| 14 | g.28767966C>G | CA389475650 | FOXG1 | c.687C>G (p.Ile229Met) | |
| 14 | g.28767966C>T | CA486098721 | FOXG1 | c.687C>T (p.Ile229=) | |
| 14 | g.28767967C>A | CA389475651 | FOXG1 | c.688C>A (p.Arg230Ser) | gnomAD v3 gnomAD v4 |
| 14 | g.28767967C= | CA2125999986 | FOXG1 | c.688C= (p.Arg230=) | |
| 14 | g.28767967C>G | CA389475652 | FOXG1 | c.688C>G (p.Arg230Gly) | COSMIC |
| 14 | g.28767967C>T | CA389475653 | FOXG1 | c.688C>T (p.Arg230Cys) | ClinVar dbSNP |
| 14 | g.28767968G>A | CA199440 | FOXG1 | c.689G>A (p.Arg230His) | ClinVar dbSNP COSMIC |
| 14 | g.28767968G>C | CA389475654 | FOXG1 | c.689G>C (p.Arg230Pro) | |
| 14 | g.28767968G= | CA2125999994 | FOXG1 | c.689G= (p.Arg230=) | |
| 14 | g.28767968G>T | CA10606123 | FOXG1 | c.689G>T (p.Arg230Leu) | ClinVar dbSNP |
| 14 | g.28767969C>A | CA486098726 | FOXG1 | c.690C>A (p.Arg230=) | |
| 14 | g.28767969C= | CA2126000003 | FOXG1 | c.690C= (p.Arg230=) | |
| 14 | g.28767969C>G | CA486098729 | FOXG1 | c.690C>G (p.Arg230=) | gnomAD v3 gnomAD v4 |
| 14 | g.28767969C>T | CA7140626 | FOXG1 | c.690C>T (p.Arg230=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 14 | g.28767969_28767976dup | CA2573149902 | FOXG1 | c.690_697dup (p.Leu233ProfsTer11) | ClinVar dbSNP |
| 14 | g.28767970C>A | CA389475655 | FOXG1 | c.691C>A (p.His231Asn) | |
| 14 | g.28767970C>G | CA389475656 | FOXG1 | c.691C>G (p.His231Asp) | |
| 14 | g.28767970C>T | CA389475657 | FOXG1 | c.691C>T (p.His231Tyr) | |
| 14 | g.28767971A>C | CA389475658 | FOXG1 | c.692A>C (p.His231Pro) | |
| 14 | g.28767971A>G | CA389475659 | FOXG1 | c.692A>G (p.His231Arg) | ClinVar dbSNP |
| 14 | g.28767971A>T | CA389475660 | FOXG1 | c.692A>T (p.His231Leu) | |
| 14 | g.28767972C>A | CA389475661 | FOXG1 | c.693C>A (p.His231Gln) | |
| 14 | g.28767972C>G | CA389475662 | FOXG1 | c.693C>G (p.His231Gln) | dbSNP |
| 14 | g.28767972C>T | CA486098734 | FOXG1 | c.693C>T (p.His231=) | |
| 14 | g.28767973A= | CA2126000009 | FOXG1 | c.694A= (p.Asn232=) | |
| 14 | g.28767973A>C | CA389475663 | FOXG1 | c.694A>C (p.Asn232His) | |
| 14 | g.28767973A>G | CA389475664 | FOXG1 | c.694A>G (p.Asn232Asp) | ClinVar dbSNP |
| 14 | g.28767973A>T | CA235903 | FOXG1 | c.694A>T (p.Asn232Tyr) | ClinVar dbSNP |
| 14 | g.28767974A>C | CA389475665 | FOXG1 | c.695A>C (p.Asn232Thr) | ClinVar |
| 14 | g.28767974A>G | CA389475667 | FOXG1 | c.695A>G (p.Asn232Ser) | ClinVar dbSNP |
| 14 | g.28767974A>T | CA389475666 | FOXG1 | c.695A>T (p.Asn232Ile) | |
| 14 | g.28767975T>A | CA389475668 | FOXG1 | c.696T>A (p.Asn232Lys) | |
| 14 | g.28767975T>C | CA486098741 | FOXG1 | c.696T>C (p.Asn232=) | ClinVar dbSNP gnomAD v2 COSMIC |
| 14 | g.28767975T>G | CA389475669 | FOXG1 | c.696T>G (p.Asn232Lys) | |
| 14 | g.28767975T= | CA2126000019 | FOXG1 | c.696T= (p.Asn232=) | |
| 14 | g.28767976C>A | CA389475670 | FOXG1 | c.697C>A (p.Leu233Met) | |
| 14 | g.28767976C>G | CA389475671 | FOXG1 | c.697C>G (p.Leu233Val) | |
| 14 | g.28767976C>T | CA486098744 | FOXG1 | c.697C>T (p.Leu233=) | gnomAD v4 |
| 14 | g.28767977T>A | CA389475672 | FOXG1 | c.698T>A (p.Leu233Gln) | |
| 14 | g.28767977T>C | CA389475673 | FOXG1 | c.698T>C (p.Leu233Pro) | |
| 14 | g.28767977T>G | CA389475674 | FOXG1 | c.698T>G (p.Leu233Arg) | |
| 14 | g.28767978G>A | CA486098747 | FOXG1 | c.699G>A (p.Leu233=) | gnomAD v4 |
| 14 | g.28767978G>C | CA486098752 | FOXG1 | c.699G>C (p.Leu233=) | ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC |
| 14 | g.28767978G>T | CA486098749 | FOXG1 | c.699G>T (p.Leu233=) | ClinVar dbSNP gnomAD v4 |
| 14 | g.28767979T>A | CA389475675 | FOXG1 | c.700T>A (p.Ser234Thr) | |
| 14 | g.28767979T>C | CA199442 | FOXG1 | c.700T>C (p.Ser234Pro) | ClinVar dbSNP COSMIC |
| 14 | g.28767979T>G | CA389475676 | FOXG1 | c.700T>G (p.Ser234Ala) | COSMIC |
| 14 | g.28767979T= | CA2126000025 | FOXG1 | c.700T= (p.Ser234=) | |
| 14 | g.28767979_28767980delinsTC | CA2126000028 | FOXG1 | c.700_701delinsTC (p.Ser234=) | |
| 14 | g.28767980C>A | CA389475678 | FOXG1 | c.701C>A (p.Ser234Tyr) | |
| 14 | g.28767980C= | CA2126000043 | FOXG1 | c.701C= (p.Ser234=) | |
| 14 | g.28767980C>G | CA389475677 | FOXG1 | c.701C>G (p.Ser234Cys) | |
| 14 | g.28767980C>T | CA314620 | FOXG1 | c.701C>T (p.Ser234Phe) | ClinVar dbSNP |
| 14 | g.28767982del | CA16619862 | FOXG1 | c.703del (p.Leu235SerfsTer6) | ClinVar dbSNP |
| 14 | g.28767981C>A | CA486098761 | FOXG1 | c.702C>A (p.Ser234=) | |
| 14 | g.28767981C>G | CA486098764 | FOXG1 | c.702C>G (p.Ser234=) | |
| 14 | g.28767981C>T | CA486098766 | FOXG1 | c.702C>T (p.Ser234=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 14 | g.28767982C>A | CA389475679 | FOXG1 | c.703C>A (p.Leu235Ile) | |
| 14 | g.28767982C= | CA2126000051 | FOXG1 | c.703C= (p.Leu235=) | |
| 14 | g.28767982C>G | CA389475680 | FOXG1 | c.703C>G (p.Leu235Val) | |
| 14 | g.28767982C>T | CA389475681 | FOXG1 | c.703C>T (p.Leu235Phe) | ClinVar dbSNP COSMIC |
| 14 | g.28767983T>A | CA389475682 | FOXG1 | c.704T>A (p.Leu235His) | |
| 14 | g.28767983T>C | CA389475683 | FOXG1 | c.704T>C (p.Leu235Pro) | |
| 14 | g.28767983T>G | CA389475684 | FOXG1 | c.704T>G (p.Leu235Arg) | |
| 14 | g.28767984C>A | CA486098770 | FOXG1 | c.705C>A (p.Leu235=) | gnomAD v3 gnomAD v4 |
| 14 | g.28767984C>G | CA486098773 | FOXG1 | c.705C>G (p.Leu235=) | |
| 14 | g.28767984C>T | CA486098772 | FOXG1 | c.705C>T (p.Leu235=) | |
| 14 | g.28767987_28767989del | CA2582341746 | FOXG1 | c.708_710del (p.Asn236del) | ClinVar |
| 14 | g.28767985A>C | CA389475685 | FOXG1 | c.706A>C (p.Asn236His) | |
| 14 | g.28767985A>G | CA389475686 | FOXG1 | c.706A>G (p.Asn236Asp) | ClinVar |
| 14 | g.28767985A>T | CA389475687 | FOXG1 | c.706A>T (p.Asn236Tyr) | |
| 14 | g.28767986A>C | CA389475688 | FOXG1 | c.707A>C (p.Asn236Thr) | |
| 14 | g.28767986A>G | CA389475689 | FOXG1 | c.707A>G (p.Asn236Ser) | gnomAD v4 |
| 14 | g.28767986A>T | CA389475690 | FOXG1 | c.707A>T (p.Asn236Ile) | |
| 14 | g.28767987C>A | CA314622 | FOXG1 | c.708C>A (p.Asn236Lys) | ClinVar dbSNP |
| 14 | g.28767987C= | CA2126000057 | FOXG1 | c.708C= (p.Asn236=) | |
| 14 | g.28767987C>G | CA389475691 | FOXG1 | c.708C>G (p.Asn236Lys) | |
| 14 | g.28767987C>T | CA486098779 | FOXG1 | c.708C>T (p.Asn236=) | ClinVar dbSNP gnomAD v4 |
| 14 | g.28767988A>C | CA389475692 | FOXG1 | c.709A>C (p.Lys237Gln) | |
| 14 | g.28767988A>G | CA389475693 | FOXG1 | c.709A>G (p.Lys237Glu) | |
| 14 | g.28767988A>T | CA389475694 | FOXG1 | c.709A>T (p.Lys237Ter) | |
| 14 | g.28767989A>C | CA389475695 | FOXG1 | c.710A>C (p.Lys237Thr) | |
| 14 | g.28767989A>G | CA389475696 | FOXG1 | c.710A>G (p.Lys237Arg) | |
| 14 | g.28767989A>T | CA389475697 | FOXG1 | c.710A>T (p.Lys237Met) | |
| 14 | g.28767989_28767990insCACCAAACACACCCAACACA | CA2801003336 | FOXG1 | c.710_711insCACCAAACACACCCAACACA (p.Lys237AsnfsTer11) | |
| 14 | g.28767990G>A | CA486098785 | FOXG1 | c.711G>A (p.Lys237=) | |
| 14 | g.28767990G>C | CA389475698 | FOXG1 | c.711G>C (p.Lys237Asn) | |
| 14 | g.28767990G>T | CA389475699 | FOXG1 | c.711G>T (p.Lys237Asn) | |
| 14 | g.28767991T>A | CA389475700 | FOXG1 | c.712T>A (p.Cys238Ser) | gnomAD v3 gnomAD v4 COSMIC |
| 14 | g.28767991T>C | CA389475701 | FOXG1 | c.712T>C (p.Cys238Arg) | |
| 14 | g.28767991T>G | CA389475702 | FOXG1 | c.712T>G (p.Cys238Gly) | |
| 14 | g.28767992G>A | CA389475703 | FOXG1 | c.713G>A (p.Cys238Tyr) | ClinVar dbSNP |
| 14 | g.28767992G>C | CA389475704 | FOXG1 | c.713G>C (p.Cys238Ser) | |
| 14 | g.28767992G= | CA2126000061 | FOXG1 | c.713G= (p.Cys238=) | |
| 14 | g.28767992G>T | CA389475705 | FOXG1 | c.713G>T (p.Cys238Phe) | gnomAD v3 gnomAD v4 |
| 14 | g.28767993C>A | CA389475706 | FOXG1 | c.714C>A (p.Cys238Ter) | |
| 14 | g.28767993C>G | CA389475707 | FOXG1 | c.714C>G (p.Cys238Trp) | |
| 14 | g.28767993C>T | CA486098799 | FOXG1 | c.714C>T (p.Cys238=) | ClinVar |
| 14 | g.28767994T>A | CA389475708 | FOXG1 | c.715T>A (p.Phe239Ile) | |
| 14 | g.28767994T>C | CA389475709 | FOXG1 | c.715T>C (p.Phe239Leu) | |
| 14 | g.28767994T>G | CA389475710 | FOXG1 | c.715T>G (p.Phe239Val) | |
| 14 | g.28767995T>A | CA389475711 | FOXG1 | c.716T>A (p.Phe239Tyr) | |
| 14 | g.28767995T>C | CA389475712 | FOXG1 | c.716T>C (p.Phe239Ser) | |
| 14 | g.28767995T>G | CA389475713 | FOXG1 | c.716T>G (p.Phe239Cys) | |
| 14 | g.28767996C>A | CA389475714 | FOXG1 | c.717C>A (p.Phe239Leu) | |
| 14 | g.28767996C= | CA2126000065 | FOXG1 | c.717C= (p.Phe239=) | |
| 14 | g.28767996C>G | CA389475715 | FOXG1 | c.717C>G (p.Phe239Leu) | ClinVar dbSNP |
| 14 | g.28767996C>T | CA486098815 | FOXG1 | c.717C>T (p.Phe239=) | ClinVar COSMIC |
| 14 | g.28767997G>A | CA389475716 | FOXG1 | c.718G>A (p.Val240Met) | |
| 14 | g.28767997G>C | CA389475717 | FOXG1 | c.718G>C (p.Val240Leu) | |
| 14 | g.28767997G>T | CA389475718 | FOXG1 | c.718G>T (p.Val240Leu) | |
| 14 | g.28767998T>A | CA389475720 | FOXG1 | c.719T>A (p.Val240Glu) | |
| 14 | g.28767998T>C | CA389475719 | FOXG1 | c.719T>C (p.Val240Ala) | |
| 14 | g.28767998T>G | CA16619863 | FOXG1 | c.719T>G (p.Val240Gly) | ClinVar dbSNP |
| 14 | g.28767998T= | CA2126000070 | FOXG1 | c.719T= (p.Val240=) | |
| 14 | g.28767999G>A | CA486098828 | FOXG1 | c.720G>A (p.Val240=) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.28767999G>C | CA486098831 | FOXG1 | c.720G>C (p.Val240=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 14 | g.28767999G= | CA2126000073 | FOXG1 | c.720G= (p.Val240=) | |
| 14 | g.28767999G>T | CA486098829 | FOXG1 | c.720G>T (p.Val240=) | |
| 14 | g.28768000A= | CA2126000076 | FOXG1 | c.721A= (p.Lys241=) | |
| 14 | g.28768000A>C | CA389475721 | FOXG1 | c.721A>C (p.Lys241Gln) | |
| 14 | g.28768000A>G | CA314652 | FOXG1 | c.721A>G (p.Lys241Glu) | dbSNP |
| 14 | g.28768000A>T | CA389475722 | FOXG1 | c.721A>T (p.Lys241Ter) | |
| 14 | g.28768001A>C | CA389475723 | FOXG1 | c.722A>C (p.Lys241Thr) | |
| 14 | g.28768001A>G | CA389475724 | FOXG1 | c.722A>G (p.Lys241Arg) | |
| 14 | g.28768001A>T | CA389475725 | FOXG1 | c.722A>T (p.Lys241Met) | |
| 14 | g.28768002G>A | CA486098835 | FOXG1 | c.723G>A (p.Lys241=) | |
| 14 | g.28768002G>C | CA389475726 | FOXG1 | c.723G>C (p.Lys241Asn) | |
| 14 | g.28768002G>T | CA389475727 | FOXG1 | c.723G>T (p.Lys241Asn) | |
| 14 | g.28768003G>A | CA389475728 | FOXG1 | c.724G>A (p.Val242Met) | COSMIC |
| 14 | g.28768003G>C | CA389475729 | FOXG1 | c.724G>C (p.Val242Leu) | |
| 14 | g.28768003G>T | CA389475730 | FOXG1 | c.724G>T (p.Val242Leu) | |
| 14 | g.28768004_28768010dup | CA2580088018 | FOXG1 | c.725_731dup (p.His245AlafsTer?) | ClinVar |
| 14 | g.28768004T>A | CA389475731 | FOXG1 | c.725T>A (p.Val242Glu) | |
| 14 | g.28768004T>C | CA389475732 | FOXG1 | c.725T>C (p.Val242Ala) | |
| 14 | g.28768004T>G | CA389475733 | FOXG1 | c.725T>G (p.Val242Gly) | |
| 14 | g.28768005G>A | CA486098844 | FOXG1 | c.726G>A (p.Val242=) | gnomAD v4 COSMIC |
| 14 | g.28768005G>C | CA486098848 | FOXG1 | c.726G>C (p.Val242=) | |
| 14 | g.28768005G>T | CA486098845 | FOXG1 | c.726G>T (p.Val242=) | |
| 14 | g.28768006C>A | CA389475736 | FOXG1 | c.727C>A (p.Pro243Thr) | |
| 14 | g.28768006C>G | CA389475734 | FOXG1 | c.727C>G (p.Pro243Ala) | |
| 14 | g.28768006C>T | CA389475735 | FOXG1 | c.727C>T (p.Pro243Ser) | gnomAD v4 COSMIC |
| 14 | g.28768007C>A | CA389475737 | FOXG1 | c.728C>A (p.Pro243Gln) | |
| 14 | g.28768007C= | CA2126000078 | FOXG1 | c.728C= (p.Pro243=) | |
| 14 | g.28768007C>G | CA389475738 | FOXG1 | c.728C>G (p.Pro243Arg) | dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.28768007C>T | CA389475740 | FOXG1 | c.728C>T (p.Pro243Leu) | COSMIC |
| 14 | g.28768008G>A | CA486098849 | FOXG1 | c.729G>A (p.Pro243=) | ClinVar dbSNP COSMIC |
| 14 | g.28768008G>C | CA7140627 | FOXG1 | c.729G>C (p.Pro243=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 14 | g.28768008G= | CA2126000084 | FOXG1 | c.729G= (p.Pro243=) | |
| 14 | g.28768008G>T | CA486098850 | FOXG1 | c.729G>T (p.Pro243=) | |
| 14 | g.28768009C>A | CA389475741 | FOXG1 | c.730C>A (p.Arg244Ser) | gnomAD v3 gnomAD v4 |
| 14 | g.28768009C= | CA2126000087 | FOXG1 | c.730C= (p.Arg244=) | |
| 14 | g.28768009C>G | CA389475742 | FOXG1 | c.730C>G (p.Arg244Gly) | |
| 14 | g.28768009C>T | CA199444 | FOXG1 | c.730C>T (p.Arg244Cys) | ClinVar dbSNP COSMIC |
| 14 | g.28768010G>A | CA16619864 | FOXG1 | c.731G>A (p.Arg244His) | ClinVar dbSNP |
| 14 | g.28768010G>C | CA389475743 | FOXG1 | c.731G>C (p.Arg244Pro) | |
| 14 | g.28768010G= | CA2126000094 | FOXG1 | c.731G= (p.Arg244=) | |
| 14 | g.28768010G>T | CA314654 | FOXG1 | c.731G>T (p.Arg244Leu) | dbSNP |
| 14 | g.28768010_28768020delinsGCCACTACGAC | CA2126000099 | FOXG1 | c.731_741delinsGCCACTACGAC (p.Arg244=) | |
| 14 | g.28768011C>A | CA486098855 | FOXG1 | c.732C>A (p.Arg244=) | COSMIC |
| 14 | g.28768011C>G | CA486098856 | FOXG1 | c.732C>G (p.Arg244=) | gnomAD v3 gnomAD v4 |
| 14 | g.28768011C>T | CA486098857 | FOXG1 | c.732C>T (p.Arg244=) | |
| 14 | g.28768011_28768020del | CA658798196 | FOXG1 | c.732_741del (p.His245ThrfsTer?) | ClinVar dbSNP |
| 14 | g.28768012C>A | CA389475745 | FOXG1 | c.733C>A (p.His245Asn) | COSMIC |
| 14 | g.28768012C>G | CA389475746 | FOXG1 | c.733C>G (p.His245Asp) | |
| 14 | g.28768012C>T | CA389475744 | FOXG1 | c.733C>T (p.His245Tyr) | COSMIC |
| 14 | g.28768013A>C | CA389475747 | FOXG1 | c.734A>C (p.His245Pro) | |
| 14 | g.28768013A>G | CA389475748 | FOXG1 | c.734A>G (p.His245Arg) | COSMIC |
| 14 | g.28768013A>T | CA389475749 | FOXG1 | c.734A>T (p.His245Leu) | |
| 14 | g.28768014del | CA2573053897 | FOXG1 | c.735del (p.Tyr246ThrfsTer?) | ClinVar dbSNP |
| 14 | g.28768014C>A | CA389475750 | FOXG1 | c.735C>A (p.His245Gln) | |
| 14 | g.28768014C= | CA2126000113 | FOXG1 | c.735C= (p.His245=) | |
| 14 | g.28768014C>G | CA389475751 | FOXG1 | c.735C>G (p.His245Gln) | |
| 14 | g.28768014C>T | CA486098861 | FOXG1 | c.735C>T (p.His245=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 14 | g.28768015T>A | CA389475752 | FOXG1 | c.736T>A (p.Tyr246Asn) | dbSNP |
| 14 | g.28768015T>C | CA389475753 | FOXG1 | c.736T>C (p.Tyr246His) | |
| 14 | g.28768015T>G | CA389475754 | FOXG1 | c.736T>G (p.Tyr246Asp) | |
| 14 | g.28768016A>C | CA389475755 | FOXG1 | c.737A>C (p.Tyr246Ser) | |
| 14 | g.28768016A>G | CA389475756 | FOXG1 | c.737A>G (p.Tyr246Cys) | |
| 14 | g.28768016A>T | CA389475757 | FOXG1 | c.737A>T (p.Tyr246Phe) | COSMIC |
| 14 | g.28768017C>A | CA389475758 | FOXG1 | c.738C>A (p.Tyr246Ter) | |
| 14 | g.28768017C= | CA2126000122 | FOXG1 | c.738C= (p.Tyr246=) | |
| 14 | g.28768017C>G | CA389475759 | FOXG1 | c.738C>G (p.Tyr246Ter) | ClinVar dbSNP |
| 14 | g.28768017C>T | CA486098863 | FOXG1 | c.738C>T (p.Tyr246=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.28768018G>A | CA389475762 | FOXG1 | c.739G>A (p.Asp247Asn) | gnomAD v4 COSMIC |
| 14 | g.28768018G>C | CA389475761 | FOXG1 | c.739G>C (p.Asp247His) | |
| 14 | g.28768018G>T | CA389475760 | FOXG1 | c.739G>T (p.Asp247Tyr) | |
| 14 | g.28768019A>C | CA389475763 | FOXG1 | c.740A>C (p.Asp247Ala) | |
| 14 | g.28768019A>G | CA389475764 | FOXG1 | c.740A>G (p.Asp247Gly) | |
| 14 | g.28768019A>T | CA389475765 | FOXG1 | c.740A>T (p.Asp247Val) | |
| 14 | g.28768020C>A | CA389475766 | FOXG1 | c.741C>A (p.Asp247Glu) | |
| 14 | g.28768020C>G | CA389475767 | FOXG1 | c.741C>G (p.Asp247Glu) | |
| 14 | g.28768020C>T | CA486098867 | FOXG1 | c.741C>T (p.Asp247=) | |
| 14 | g.28768021G>A | CA389475768 | FOXG1 | c.742G>A (p.Asp248Asn) | COSMIC |
| 14 | g.28768021G>C | CA389475769 | FOXG1 | c.742G>C (p.Asp248His) | gnomAD v4 |
| 14 | g.28768021G>T | CA389475770 | FOXG1 | c.742G>T (p.Asp248Tyr) | |
| 14 | g.28768022A>C | CA389475771 | FOXG1 | c.743A>C (p.Asp248Ala) | |
| 14 | g.28768022A>G | CA389475772 | FOXG1 | c.743A>G (p.Asp248Gly) | |
| 14 | g.28768022A>T | CA389475773 | FOXG1 | c.743A>T (p.Asp248Val) | |
| 14 | g.28768023C>A | CA389475774 | FOXG1 | c.744C>A (p.Asp248Glu) | |
| 14 | g.28768023C>G | CA389475775 | FOXG1 | c.744C>G (p.Asp248Glu) | |
| 14 | g.28768023C>T | CA486098871 | FOXG1 | c.744C>T (p.Asp248=) | gnomAD v4 |
| 14 | g.28768024C>A | CA389475777 | FOXG1 | c.745C>A (p.Pro249Thr) | COSMIC |
| 14 | g.28768024C>G | CA389475778 | FOXG1 | c.745C>G (p.Pro249Ala) | |
| 14 | g.28768024C>T | CA389475776 | FOXG1 | c.745C>T (p.Pro249Ser) | |
| 14 | g.28768025C>A | CA389475780 | FOXG1 | c.746C>A (p.Pro249Gln) | |
| 14 | g.28768025C>G | CA389475779 | FOXG1 | c.746C>G (p.Pro249Arg) | |
| 14 | g.28768025C>T | CA389475781 | FOXG1 | c.746C>T (p.Pro249Leu) | |
| 14 | g.28768026G>A | CA486098872 | FOXG1 | c.747G>A (p.Pro249=) | gnomAD v4 |
| 14 | g.28768026G>C | CA486098874 | FOXG1 | c.747G>C (p.Pro249=) | gnomAD v3 gnomAD v4 |
| 14 | g.28768026G>T | CA486098875 | FOXG1 | c.747G>T (p.Pro249=) | COSMIC |
| 14 | g.28768027G>A | CA389475782 | FOXG1 | c.748G>A (p.Gly250Ser) | ClinVar |
| 14 | g.28768027G>C | CA389475784 | FOXG1 | c.748G>C (p.Gly250Arg) | ClinVar dbSNP |
| 14 | g.28768027G>T | CA389475783 | FOXG1 | c.748G>T (p.Gly250Cys) | |
| 14 | g.28768028G>A | CA389475785 | FOXG1 | c.749G>A (p.Gly250Asp) | ClinVar dbSNP |
| 14 | g.28768028G>C | CA389475786 | FOXG1 | c.749G>C (p.Gly250Ala) | |
| 14 | g.28768028G= | CA2126000128 | FOXG1 | c.749G= (p.Gly250=) | |
| 14 | g.28768028G>T | CA389475787 | FOXG1 | c.749G>T (p.Gly250Val) | |
| 14 | g.28768029C>A | CA486098876 | FOXG1 | c.750C>A (p.Gly250=) | |
| 14 | g.28768029C= | CA2126000134 | FOXG1 | c.750C= (p.Gly250=) | |
| 14 | g.28768029C>G | CA486098878 | FOXG1 | c.750C>G (p.Gly250=) | gnomAD v4 |
| 14 | g.28768029C>T | CA7140628 | FOXG1 | c.750C>T (p.Gly250=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.28768030A>C | CA389475788 | FOXG1 | c.751A>C (p.Lys251Gln) | |
| 14 | g.28768030A>G | CA389475789 | FOXG1 | c.751A>G (p.Lys251Glu) | |
| 14 | g.28768030A>T | CA389475790 | FOXG1 | c.751A>T (p.Lys251Ter) | |
| 14 | g.28768031A>C | CA389475791 | FOXG1 | c.752A>C (p.Lys251Thr) | |
| 14 | g.28768031A>G | CA389475792 | FOXG1 | c.752A>G (p.Lys251Arg) | |
| 14 | g.28768031A>T | CA389475793 | FOXG1 | c.752A>T (p.Lys251Met) |