Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
14 | g.28768117T>A | CA389475974 | FOXG1 | c.838T>A (p.Ser280Thr) | |
14 | g.28768117T>C | CA389475975 | FOXG1 | c.838T>C (p.Ser280Pro) | |
14 | g.28768117T>G | CA389475976 | FOXG1 | c.838T>G (p.Ser280Ala) | |
14 | g.28768118C>A | CA389475977 | FOXG1 | c.839C>A (p.Ser280Ter) | COSMIC |
14 | g.28768118C= | CA2126000287 | FOXG1 | c.839C= (p.Ser280=) | |
14 | g.28768118C>G | CA389475978 | FOXG1 | c.839C>G (p.Ser280Trp) | gnomAD v4 |
14 | g.28768118C>T | CA258396581 | FOXG1 | c.839C>T (p.Ser280Leu) | dbSNP |
14 | g.28768119G>A | CA486099056 | FOXG1 | c.840G>A (p.Ser280=) | gnomAD v4 |
14 | g.28768119G>C | CA486099057 | FOXG1 | c.840G>C (p.Ser280=) | |
14 | g.28768119G= | CA2126000288 | FOXG1 | c.840G= (p.Ser280=) | |
14 | g.28768119G>T | CA486099058 | FOXG1 | c.840G>T (p.Ser280=) | dbSNP gnomAD v2 gnomAD v4 |
14 | g.28768120del | CA2580088020 | FOXG1 | c.841del (p.Arg281GlyfsTer?) | ClinVar |
14 | g.28768120C>A | CA486099062 | FOXG1 | c.841C>A (p.Arg281=) | |
14 | g.28768120C>G | CA389475980 | FOXG1 | c.841C>G (p.Arg281Gly) | |
14 | g.28768120C>T | CA389475979 | FOXG1 | c.841C>T (p.Arg281Trp) | COSMIC |
14 | g.28768121G>A | CA389475981 | FOXG1 | c.842G>A (p.Arg281Gln) | |
14 | g.28768121G>C | CA389475982 | FOXG1 | c.842G>C (p.Arg281Pro) | dbSNP COSMIC |
14 | g.28768121G= | CA2126000289 | FOXG1 | c.842G= (p.Arg281=) | |
14 | g.28768121G>T | CA389475983 | FOXG1 | c.842G>T (p.Arg281Leu) | |
14 | g.28768123dup | CA2573053898 | FOXG1 | c.844dup (p.Ala282GlyfsTer?) | ClinVar dbSNP |
14 | g.28768122G>A | CA7140634 | FOXG1 | c.843G>A (p.Arg281=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.28768122G>C | CA486099066 | FOXG1 | c.843G>C (p.Arg281=) | |
14 | g.28768122G= | CA2126000290 | FOXG1 | c.843G= (p.Arg281=) | |
14 | g.28768122G>T | CA486099067 | FOXG1 | c.843G>T (p.Arg281=) | COSMIC |
14 | g.28768123G>A | CA314626 | FOXG1 | c.844G>A (p.Ala282Thr) | ClinVar dbSNP gnomAD v4 |
14 | g.28768123G>C | CA389475984 | FOXG1 | c.844G>C (p.Ala282Pro) | |
14 | g.28768123G= | CA2126000291 | FOXG1 | c.844G= (p.Ala282=) | |
14 | g.28768123G>T | CA389475985 | FOXG1 | c.844G>T (p.Ala282Ser) | dbSNP gnomAD v2 gnomAD v4 |
14 | g.28768124C>A | CA389475986 | FOXG1 | c.845C>A (p.Ala282Asp) | |
14 | g.28768124C>G | CA389475987 | FOXG1 | c.845C>G (p.Ala282Gly) | |
14 | g.28768124C>T | CA389475988 | FOXG1 | c.845C>T (p.Ala282Val) | COSMIC |
14 | g.28768125C>A | CA486099070 | FOXG1 | c.846C>A (p.Ala282=) | gnomAD v4 |
14 | g.28768125C>G | CA486099071 | FOXG1 | c.846C>G (p.Ala282=) | |
14 | g.28768125C>T | CA486099069 | FOXG1 | c.846C>T (p.Ala282=) | |
14 | g.28768126A>C | CA389475989 | FOXG1 | c.847A>C (p.Lys283Gln) | |
14 | g.28768126A>G | CA389475990 | FOXG1 | c.847A>G (p.Lys283Glu) | |
14 | g.28768126A>T | CA389475991 | FOXG1 | c.847A>T (p.Lys283Ter) | ClinVar |
14 | g.28768126_28768127insGACC | CA961450741 | FOXG1 | c.847_848insGACC (p.Lys283ArgfsTer?) | gnomAD v3 gnomAD v4 |
14 | g.28768127A>C | CA389475993 | FOXG1 | c.848A>C (p.Lys283Thr) | |
14 | g.28768127A>G | CA389475994 | FOXG1 | c.848A>G (p.Lys283Arg) | COSMIC |
14 | g.28768127A>T | CA389475992 | FOXG1 | c.848A>T (p.Lys283Met) | |
14 | g.28768128G>A | CA486099072 | FOXG1 | c.849G>A (p.Lys283=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
14 | g.28768128G>C | CA389475995 | FOXG1 | c.849G>C (p.Lys283Asn) | |
14 | g.28768128G= | CA2126000292 | FOXG1 | c.849G= (p.Lys283=) | |
14 | g.28768128G>T | CA389475996 | FOXG1 | c.849G>T (p.Lys283Asn) | |
14 | g.28768129C>A | CA389475997 | FOXG1 | c.850C>A (p.Leu284Met) | |
14 | g.28768129C= | CA2126000293 | FOXG1 | c.850C= (p.Leu284=) | |
14 | g.28768129C>G | CA389475998 | FOXG1 | c.850C>G (p.Leu284Val) | |
14 | g.28768129C>T | CA258396582 | FOXG1 | c.850C>T (p.Leu284=) | dbSNP gnomAD v4 |
14 | g.28768130T>A | CA389475999 | FOXG1 | c.851T>A (p.Leu284Gln) |