| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 14 | g.28768339C>A | CA389476452 | FOXG1 | c.1060C>A (p.His354Asn) | |
| 14 | g.28768339C>G | CA389476453 | FOXG1 | c.1060C>G (p.His354Asp) | |
| 14 | g.28768339C>T | CA389476454 | FOXG1 | c.1060C>T (p.His354Tyr) | |
| 14 | g.28768340A>C | CA389476455 | FOXG1 | c.1061A>C (p.His354Pro) | gnomAD v4 |
| 14 | g.28768340A>G | CA389476456 | FOXG1 | c.1061A>G (p.His354Arg) | |
| 14 | g.28768340A>T | CA389476457 | FOXG1 | c.1061A>T (p.His354Leu) | |
| 14 | g.28768340_28768341delinsAC | CA2126000377 | FOXG1 | c.1061_1062delinsAC (p.His354=) | |
| 14 | g.28768341del | CA1139663430 | FOXG1 | c.1062del (p.Ser355ProfsTer8) | ClinVar dbSNP |
| 14 | g.28768341C>A | CA389476459 | FOXG1 | c.1062C>A (p.His354Gln) | |
| 14 | g.28768341C= | CA2126000378 | FOXG1 | c.1062C= (p.His354=) | |
| 14 | g.28768341C>G | CA389476458 | FOXG1 | c.1062C>G (p.His354Gln) | |
| 14 | g.28768341C>T | CA258396592 | FOXG1 | c.1062C>T (p.His354=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 14 | g.28768342T>A | CA389476460 | FOXG1 | c.1063T>A (p.Ser355Thr) | |
| 14 | g.28768342T>C | CA389476462 | FOXG1 | c.1063T>C (p.Ser355Pro) | |
| 14 | g.28768342T>G | CA389476461 | FOXG1 | c.1063T>G (p.Ser355Ala) | |
| 14 | g.28768343C>A | CA389476463 | FOXG1 | c.1064C>A (p.Ser355Tyr) | |
| 14 | g.28768343C>G | CA389476464 | FOXG1 | c.1064C>G (p.Ser355Cys) | |
| 14 | g.28768343C>T | CA389476465 | FOXG1 | c.1064C>T (p.Ser355Phe) | |
| 14 | g.28768343_28768346delinsCCTT | CA2126000379 | FOXG1 | c.1064_1067delinsCCTT (p.Ser355=) | |
| 14 | g.28768344C>A | CA486098510 | FOXG1 | c.1065C>A (p.Ser355=) | |
| 14 | g.28768344C= | CA2126000382 | FOXG1 | c.1065C= (p.Ser355=) | |
| 14 | g.28768344C>G | CA486098511 | FOXG1 | c.1065C>G (p.Ser355=) | ClinVar dbSNP gnomAD v4 |
| 14 | g.28768344C>T | CA486098512 | FOXG1 | c.1065C>T (p.Ser355=) | ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC |
| 14 | g.28768344_28768345delinsCT | CA2126000381 | FOXG1 | c.1065_1066delinsCT (p.Ser355=) | |
| 14 | g.28768346_28768348del | CA2126000380 | FOXG1 | c.1067_1069del (p.Phe356del) | dbSNP gnomAD v4 |
| 14 | g.28768345T>A | CA389476466 | FOXG1 | c.1066T>A (p.Phe356Ile) | |
| 14 | g.28768345T>C | CA389476467 | FOXG1 | c.1066T>C (p.Phe356Leu) | |
| 14 | g.28768345T>G | CA389476468 | FOXG1 | c.1066T>G (p.Phe356Val) | |
| 14 | g.28768346del | CA658798200 | FOXG1 | c.1067del (p.Phe356SerfsTer7) | ClinVar dbSNP |
| 14 | g.28768346T>A | CA389476469 | FOXG1 | c.1067T>A (p.Phe356Tyr) | |
| 14 | g.28768346T>C | CA389476470 | FOXG1 | c.1067T>C (p.Phe356Ser) | |
| 14 | g.28768346T>G | CA389476471 | FOXG1 | c.1067T>G (p.Phe356Cys) | |
| 14 | g.28768347C>A | CA389476472 | FOXG1 | c.1068C>A (p.Phe356Leu) | |
| 14 | g.28768347C>G | CA389476473 | FOXG1 | c.1068C>G (p.Phe356Leu) | |
| 14 | g.28768347C>T | CA486098518 | FOXG1 | c.1068C>T (p.Phe356=) | |
| 14 | g.28768348_28768350del | CA2624400221 | FOXG1 | c.1069_1071del (p.Ser357del) | gnomAD v4 |
| 14 | g.28768348T>A | CA389476476 | FOXG1 | c.1069T>A (p.Ser357Thr) | |
| 14 | g.28768348T>C | CA389476475 | FOXG1 | c.1069T>C (p.Ser357Pro) | |
| 14 | g.28768348T>G | CA389476474 | FOXG1 | c.1069T>G (p.Ser357Ala) | |
| 14 | g.28768349C>A | CA389476477 | FOXG1 | c.1070C>A (p.Ser357Tyr) | |
| 14 | g.28768349C>G | CA389476478 | FOXG1 | c.1070C>G (p.Ser357Cys) | |
| 14 | g.28768349C>T | CA389476479 | FOXG1 | c.1070C>T (p.Ser357Phe) | |
| 14 | g.28768351_28768353del | CA2624400222 | FOXG1 | c.1072_1074del (p.Thr358del) | gnomAD v4 |
| 14 | g.28768350C>A | CA486098524 | FOXG1 | c.1071C>A (p.Ser357=) | COSMIC |
| 14 | g.28768350C= | CA2126000383 | FOXG1 | c.1071C= (p.Ser357=) | |
| 14 | g.28768350C>G | CA486098525 | FOXG1 | c.1071C>G (p.Ser357=) | |
| 14 | g.28768350C>T | CA7140654 | FOXG1 | c.1071C>T (p.Ser357=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.28768351A>C | CA389476480 | FOXG1 | c.1072A>C (p.Thr358Pro) | |
| 14 | g.28768351A>G | CA389476481 | FOXG1 | c.1072A>G (p.Thr358Ala) | |
| 14 | g.28768351A>T | CA389476482 | FOXG1 | c.1072A>T (p.Thr358Ser) |