14 | g.28767906G>A | CA486098490 | FOXG1 | c.627G>A (p.Glu209=)
| gnomAD v4 |
14 | g.28767906G>C | CA389475511 | FOXG1 | c.627G>C (p.Glu209Asp)
| |
14 | g.28767906G>T | CA389475512 | FOXG1 | c.627G>T (p.Glu209Asp)
| |
14 | g.28767907T>A | CA389475513 | FOXG1 | c.628T>A (p.Phe210Ile)
| |
14 | g.28767907T>C | CA389475514 | FOXG1 | c.628T>C (p.Phe210Leu)
| COSMIC |
14 | g.28767907T>G | CA389475515 | FOXG1 | c.628T>G (p.Phe210Val)
| |
14 | g.28767908T>A | CA389475516 | FOXG1 | c.629T>A (p.Phe210Tyr)
| |
14 | g.28767908T>C | CA389475517 | FOXG1 | c.629T>C (p.Phe210Ser)
| |
14 | g.28767908T>G | CA389475518 | FOXG1 | c.629T>G (p.Phe210Cys)
| |
14 | g.28767909C>A | CA389475519 | FOXG1 | c.630C>A (p.Phe210Leu)
| |
14 | g.28767909C>G | CA389475520 | FOXG1 | c.630C>G (p.Phe210Leu)
| |
14 | g.28767909C>T | CA486098501 | FOXG1 | c.630C>T (p.Phe210=)
| gnomAD v4 |
14 | g.28767910A>C | CA389475522 | FOXG1 | c.631A>C (p.Ile211Leu)
| |
14 | g.28767910A>G | CA389475523 | FOXG1 | c.631A>G (p.Ile211Val)
| |
14 | g.28767910A>T | CA389475521 | FOXG1 | c.631A>T (p.Ile211Phe)
| gnomAD v3 gnomAD v4 |
14 | g.28767911T>A | CA389475524 | FOXG1 | c.632T>A (p.Ile211Asn)
| ClinVar dbSNP |
14 | g.28767911T>C | CA389475525 | FOXG1 | c.632T>C (p.Ile211Thr)
| ClinVar dbSNP gnomAD v4 COSMIC |
14 | g.28767911T>G | CA389475526 | FOXG1 | c.632T>G (p.Ile211Ser)
| |
14 | g.28767911T= | CA2125999874 | FOXG1 | c.632T= (p.Ile211=)
| |
14 | g.28767912del | CA2830782521 | FOXG1 | c.633del (p.Met212Ter)
| |
14 | g.28767912C>A | CA486098505 | FOXG1 | c.633C>A (p.Ile211=)
| |
14 | g.28767912C>G | CA389475527 | FOXG1 | c.633C>G (p.Ile211Met)
| |
14 | g.28767912C>T | CA486098507 | FOXG1 | c.633C>T (p.Ile211=)
| gnomAD v4 |
14 | g.28767913del | CA2573053896 | FOXG1 | c.634del (p.Met212Ter)
| ClinVar dbSNP |
14 | g.28767913A>C | CA389475528 | FOXG1 | c.634A>C (p.Met212Leu)
| |
14 | g.28767913A>G | CA389475529 | FOXG1 | c.634A>G (p.Met212Val)
| |
14 | g.28767913A>T | CA389475530 | FOXG1 | c.634A>T (p.Met212Leu)
| |
14 | g.28767914_28767919del | CA2580088013 | FOXG1 | c.635_640del (p.Met212_Lys213del)
| ClinVar |
14 | g.28767914T>A | CA389475531 | FOXG1 | c.635T>A (p.Met212Lys)
| |
14 | g.28767914T>C | CA389475532 | FOXG1 | c.635T>C (p.Met212Thr)
| ClinVar dbSNP |
14 | g.28767914T>G | CA389475533 | FOXG1 | c.635T>G (p.Met212Arg)
| |
14 | g.28767915G>A | CA389475534 | FOXG1 | c.636G>A (p.Met212Ile)
| |
14 | g.28767915G>C | CA389475535 | FOXG1 | c.636G>C (p.Met212Ile)
| |
14 | g.28767915G>T | CA389475536 | FOXG1 | c.636G>T (p.Met212Ile)
| |
14 | g.28767916A>C | CA389475539 | FOXG1 | c.637A>C (p.Lys213Gln)
| |
14 | g.28767916A>G | CA389475538 | FOXG1 | c.637A>G (p.Lys213Glu)
| |
14 | g.28767916A>T | CA389475537 | FOXG1 | c.637A>T (p.Lys213Ter)
| ClinVar |
14 | g.28767917A>C | CA389475540 | FOXG1 | c.638A>C (p.Lys213Thr)
| |
14 | g.28767917A>G | CA389475541 | FOXG1 | c.638A>G (p.Lys213Arg)
| gnomAD v4 |
14 | g.28767917A>T | CA389475542 | FOXG1 | c.638A>T (p.Lys213Met)
| gnomAD v3 gnomAD v4 |
14 | g.28767918G>A | CA486098517 | FOXG1 | c.639G>A (p.Lys213=)
| ClinVar dbSNP COSMIC |
14 | g.28767918G>C | CA389475543 | FOXG1 | c.639G>C (p.Lys213Asn)
| |
14 | g.28767918G= | CA2125999880 | FOXG1 | c.639G= (p.Lys213=)
| |
14 | g.28767918G>T | CA389475544 | FOXG1 | c.639G>T (p.Lys213Asn)
| |
14 | g.28767919A>C | CA389475545 | FOXG1 | c.640A>C (p.Asn214His)
| |
14 | g.28767919A>G | CA389475546 | FOXG1 | c.640A>G (p.Asn214Asp)
| |
14 | g.28767919A>T | CA389475547 | FOXG1 | c.640A>T (p.Asn214Tyr)
| |
14 | g.28767920A>C | CA389475548 | FOXG1 | c.641A>C (p.Asn214Thr)
| |
14 | g.28767920A>G | CA389475549 | FOXG1 | c.641A>G (p.Asn214Ser)
| |
14 | g.28767920A>T | CA389475550 | FOXG1 | c.641A>T (p.Asn214Ile)
| |
14 | g.28767921C>A | CA389475551 | FOXG1 | c.642C>A (p.Asn214Lys)
| |
14 | g.28767921C= | CA2125999884 | FOXG1 | c.642C= (p.Asn214=)
| |
14 | g.28767921C>G | CA389475552 | FOXG1 | c.642C>G (p.Asn214Lys)
| |
14 | g.28767921C>T | CA486098521 | FOXG1 | c.642C>T (p.Asn214=)
| ClinVar dbSNP |
14 | g.28767922T>A | CA389475554 | FOXG1 | c.643T>A (p.Phe215Ile)
| ClinVar |
14 | g.28767922T>C | CA123554 | FOXG1 | c.643T>C (p.Phe215Leu)
| ClinVar dbSNP |
14 | g.28767922T>G | CA389475553 | FOXG1 | c.643T>G (p.Phe215Val)
| |
14 | g.28767922T= | CA2125999890 | FOXG1 | c.643T= (p.Phe215=)
| |
14 | g.28767923T>A | CA389475555 | FOXG1 | c.644T>A (p.Phe215Tyr)
| |
14 | g.28767923T>C | CA389475556 | FOXG1 | c.644T>C (p.Phe215Ser)
| |
14 | g.28767923T>G | CA389475557 | FOXG1 | c.644T>G (p.Phe215Cys)
| |
14 | g.28767923_28767924delinsCT | CA207940 | FOXG1 | c.644_645delinsCT (p.Phe215Ser)
| ClinVar dbSNP |
14 | g.28767923_28767924delinsTC | CA2125999895 | FOXG1 | c.644_645delinsTC (p.Phe215=)
| |
14 | g.28767924C>A | CA389475558 | FOXG1 | c.645C>A (p.Phe215Leu)
| ClinVar dbSNP |
14 | g.28767924C= | CA2125999900 | FOXG1 | c.645C= (p.Phe215=)
| |
14 | g.28767924C>G | CA16042954 | FOXG1 | c.645C>G (p.Phe215Leu)
| ClinVar dbSNP |
14 | g.28767924C>T | CA486098527 | FOXG1 | c.645C>T (p.Phe215=)
| ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.28767926del | CA2695219194 | FOXG1 | c.647del (p.Pro216LeufsTer25)
| |
14 | g.28767924_28767932delinsCCCTTACTA | CA2125999899 | FOXG1 | c.645_653delinsCCCTTACTA (p.Phe215=)
| |
14 | g.28767925C>A | CA389475560 | FOXG1 | c.646C>A (p.Pro216Thr)
| |
14 | g.28767925C= | CA2125999907 | FOXG1 | c.646C= (p.Pro216=)
| |
14 | g.28767925C>G | CA389475559 | FOXG1 | c.646C>G (p.Pro216Ala)
| |
14 | g.28767925C>T | CA7140623 | FOXG1 | c.646C>T (p.Pro216Ser)
| dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.28767927_28767934del | CA234033 | FOXG1 | c.648_655del (p.Tyr217ArgfsTer?)
| ClinVar dbSNP |
14 | g.28767926C>A | CA389475561 | FOXG1 | c.647C>A (p.Pro216His)
| |
14 | g.28767926C>G | CA389475562 | FOXG1 | c.647C>G (p.Pro216Arg)
| |
14 | g.28767926C>T | CA389475563 | FOXG1 | c.647C>T (p.Pro216Leu)
| |
14 | g.28767927T>A | CA486098538 | FOXG1 | c.648T>A (p.Pro216=)
| ClinVar dbSNP gnomAD v4 |
14 | g.28767927T>C | CA486098539 | FOXG1 | c.648T>C (p.Pro216=)
| dbSNP |
14 | g.28767927T>G | CA486098543 | FOXG1 | c.648T>G (p.Pro216=)
| |
14 | g.28767927_28767928insAT | CA2579988444 | FOXG1 | c.648_649insAT (p.Tyr217IlefsTer25)
| |
14 | g.28767928T>A | CA389475566 | FOXG1 | c.649T>A (p.Tyr217Asn)
| |
14 | g.28767928T>C | CA389475564 | FOXG1 | c.649T>C (p.Tyr217His)
| |
14 | g.28767928T>G | CA389475565 | FOXG1 | c.649T>G (p.Tyr217Asp)
| |
14 | g.28767929A>C | CA389475567 | FOXG1 | c.650A>C (p.Tyr217Ser)
| |
14 | g.28767929A>G | CA389475568 | FOXG1 | c.650A>G (p.Tyr217Cys)
| |
14 | g.28767929A>T | CA389475569 | FOXG1 | c.650A>T (p.Tyr217Phe)
| |
14 | g.28767930C>A | CA389475570 | FOXG1 | c.651C>A (p.Tyr217Ter)
| |
14 | g.28767930C= | CA2125999910 | FOXG1 | c.651C= (p.Tyr217=)
| |
14 | g.28767930C>G | CA314612 | FOXG1 | c.651C>G (p.Tyr217Ter)
| ClinVar dbSNP |
14 | g.28767930C>T | CA486098546 | FOXG1 | c.651C>T (p.Tyr217=)
| 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.28767998_28767999del | CA2840770143 | FOXG1 | c.719_720del (p.Val240GlufsTer?)
| |
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 |