Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
14 | g.28768357A>C | CA389476493 | FOXG1 | c.1078A>C (p.Asn360His) | |
14 | g.28768357A>G | CA389476492 | FOXG1 | c.1078A>G (p.Asn360Asp) | |
14 | g.28768357A>T | CA389476494 | FOXG1 | c.1078A>T (p.Asn360Tyr) | |
14 | g.28768358A>C | CA389476495 | FOXG1 | c.1079A>C (p.Asn360Thr) | |
14 | g.28768358A>G | CA389476497 | FOXG1 | c.1079A>G (p.Asn360Ser) | |
14 | g.28768358A>T | CA389476496 | FOXG1 | c.1079A>T (p.Asn360Ile) | |
14 | g.28768359C>A | CA389476498 | FOXG1 | c.1080C>A (p.Asn360Lys) | gnomAD v4 COSMIC |
14 | g.28768359C= | CA2126000385 | FOXG1 | c.1080C= (p.Asn360=) | |
14 | g.28768359C>G | CA389476499 | FOXG1 | c.1080C>G (p.Asn360Lys) | |
14 | g.28768359C>T | CA486098547 | FOXG1 | c.1080C>T (p.Asn360=) | gnomAD v4 COSMIC |
14 | g.28768360G>A | CA389476500 | FOXG1 | c.1081G>A (p.Gly361Ser) | ClinVar dbSNP COSMIC |
14 | g.28768360G>C | CA389476501 | FOXG1 | c.1081G>C (p.Gly361Arg) | |
14 | g.28768360G= | CA2126000386 | FOXG1 | c.1081G= (p.Gly361=) | |
14 | g.28768360G>T | CA389476502 | FOXG1 | c.1081G>T (p.Gly361Cys) | |
14 | g.28768361dup | CA658770581 | FOXG1 | c.1082dup (p.Leu362ProfsTer?) | ClinVar dbSNP |
14 | g.28768361G>A | CA389476503 | FOXG1 | c.1082G>A (p.Gly361Asp) | |
14 | g.28768361G>C | CA389476504 | FOXG1 | c.1082G>C (p.Gly361Ala) | |
14 | g.28768361G>T | CA389476505 | FOXG1 | c.1082G>T (p.Gly361Val) | |
14 | g.28768362C>A | CA486098557 | FOXG1 | c.1083C>A (p.Gly361=) | |
14 | g.28768362C>G | CA486098556 | FOXG1 | c.1083C>G (p.Gly361=) | COSMIC |
14 | g.28768362C>T | CA486098555 | FOXG1 | c.1083C>T (p.Gly361=) | gnomAD v4 |
14 | g.28768363C>A | CA389476506 | FOXG1 | c.1084C>A (p.Leu362Met) | |
14 | g.28768363C= | CA2126000387 | FOXG1 | c.1084C= (p.Leu362=) | |
14 | g.28768363C>G | CA389476507 | FOXG1 | c.1084C>G (p.Leu362Val) | |
14 | g.28768363C>T | CA486098558 | FOXG1 | c.1084C>T (p.Leu362=) | ClinVar dbSNP |
14 | g.28768364T>A | CA389476508 | FOXG1 | c.1085T>A (p.Leu362Gln) | |
14 | g.28768364T>C | CA389476509 | FOXG1 | c.1085T>C (p.Leu362Pro) | |
14 | g.28768364T>G | CA389476510 | FOXG1 | c.1085T>G (p.Leu362Arg) | |
14 | g.28768365G>A | CA172173 | FOXG1 | c.1086G>A (p.Leu362=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.28768365G>C | CA486098570 | FOXG1 | c.1086G>C (p.Leu362=) | gnomAD v4 |
14 | g.28768365G= | CA2126000388 | FOXG1 | c.1086G= (p.Leu362=) | |
14 | g.28768365G>T | CA486098566 | FOXG1 | c.1086G>T (p.Leu362=) | |
14 | g.28768366A>C | CA389476511 | FOXG1 | c.1087A>C (p.Ser363Arg) | |
14 | g.28768366A>G | CA389476512 | FOXG1 | c.1087A>G (p.Ser363Gly) | |
14 | g.28768366A>T | CA389476513 | FOXG1 | c.1087A>T (p.Ser363Cys) | |
14 | g.28768367G>A | CA389476514 | FOXG1 | c.1088G>A (p.Ser363Asn) | |
14 | g.28768367G>C | CA389476515 | FOXG1 | c.1088G>C (p.Ser363Thr) | gnomAD v4 |
14 | g.28768367G>T | CA389476516 | FOXG1 | c.1088G>T (p.Ser363Ile) | |
14 | g.28768368C>A | CA389476517 | FOXG1 | c.1089C>A (p.Ser363Arg) | |
14 | g.28768368C= | CA2126000389 | FOXG1 | c.1089C= (p.Ser363=) | |
14 | g.28768368C>G | CA389476518 | FOXG1 | c.1089C>G (p.Ser363Arg) | |
14 | g.28768368C>T | CA486098574 | FOXG1 | c.1089C>T (p.Ser363=) | dbSNP gnomAD v2 COSMIC |
14 | g.28768369G>A | CA389476519 | FOXG1 | c.1090G>A (p.Val364Met) | |
14 | g.28768369G>C | CA389476520 | FOXG1 | c.1090G>C (p.Val364Leu) | |
14 | g.28768369G>T | CA389476521 | FOXG1 | c.1090G>T (p.Val364Leu) | |
14 | g.28768370T>A | CA389476522 | FOXG1 | c.1091T>A (p.Val364Glu) | |
14 | g.28768370T>C | CA389476523 | FOXG1 | c.1091T>C (p.Val364Ala) | |
14 | g.28768370T>G | CA389476524 | FOXG1 | c.1091T>G (p.Val364Gly) | |
14 | g.28768371G>A | CA486098577 | FOXG1 | c.1092G>A (p.Val364=) | |
14 | g.28768371G>C | CA258396593 | FOXG1 | c.1092G>C (p.Val364=) | ClinVar dbSNP gnomAD v4 |