Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
14 | g.28768110C>A | CA486099033 | FOXG1 | c.831C>A (p.Ser277=) | |
14 | g.28768110C>G | CA486099035 | FOXG1 | c.831C>G (p.Ser277=) | |
14 | g.28768110C>T | CA486099034 | FOXG1 | c.831C>T (p.Ser277=) | |
14 | g.28768111A>C | CA389475962 | FOXG1 | c.832A>C (p.Thr278Pro) | |
14 | g.28768111A>G | CA389475963 | FOXG1 | c.832A>G (p.Thr278Ala) | COSMIC |
14 | g.28768111A>T | CA389475964 | FOXG1 | c.832A>T (p.Thr278Ser) | |
14 | g.28768112C>A | CA389475965 | FOXG1 | c.833C>A (p.Thr278Asn) | |
14 | g.28768112C>G | CA389475966 | FOXG1 | c.833C>G (p.Thr278Ser) | |
14 | g.28768112C>T | CA389475967 | FOXG1 | c.833C>T (p.Thr278Ile) | gnomAD v4 |
14 | g.28768113C>A | CA486099042 | FOXG1 | c.834C>A (p.Thr278=) | |
14 | g.28768113C= | CA2126000285 | FOXG1 | c.834C= (p.Thr278=) | |
14 | g.28768113C>G | CA486099043 | FOXG1 | c.834C>G (p.Thr278=) | |
14 | g.28768113C>T | CA7140632 | FOXG1 | c.834C>T (p.Thr278=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
14 | g.28768114A>C | CA389475968 | FOXG1 | c.835A>C (p.Thr279Pro) | |
14 | g.28768114A>G | CA389475969 | FOXG1 | c.835A>G (p.Thr279Ala) | |
14 | g.28768114A>T | CA389475970 | FOXG1 | c.835A>T (p.Thr279Ser) | |
14 | g.28768115C>A | CA389475971 | FOXG1 | c.836C>A (p.Thr279Asn) | ClinVar gnomAD v4 COSMIC |
14 | g.28768115C>G | CA389475972 | FOXG1 | c.836C>G (p.Thr279Ser) | |
14 | g.28768115C>T | CA389475973 | FOXG1 | c.836C>T (p.Thr279Ile) | |
14 | g.28768116C>A | CA486099049 | FOXG1 | c.837C>A (p.Thr279=) | |
14 | g.28768116C= | CA2126000286 | FOXG1 | c.837C= (p.Thr279=) | |
14 | g.28768116C>G | CA486099051 | FOXG1 | c.837C>G (p.Thr279=) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
14 | g.28768116C>T | CA7140633 | FOXG1 | c.837C>T (p.Thr279=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
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=) |