Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
14 | g.28768065_28768070delinsCGACGT | CA2126000221 | FOXG1 | c.786_791delinsCGACGT (p.Asp262=) | |
14 | g.28768067_28768071del | CA199445 | FOXG1 | c.788_792del (p.Asp263ValfsTer?) | ClinVar dbSNP |
14 | g.28768067A>C | CA389475874 | FOXG1 | c.788A>C (p.Asp263Ala) | |
14 | g.28768067A>G | CA389475875 | FOXG1 | c.788A>G (p.Asp263Gly) | COSMIC |
14 | g.28768067A>T | CA389475876 | FOXG1 | c.788A>T (p.Asp263Val) | |
14 | g.28768068C>A | CA389475877 | FOXG1 | c.789C>A (p.Asp263Glu) | |
14 | g.28768068C= | CA2126000231 | FOXG1 | c.789C= (p.Asp263=) | |
14 | g.28768068C>G | CA389475878 | FOXG1 | c.789C>G (p.Asp263Glu) | gnomAD v4 |
14 | g.28768068C>T | CA258396580 | FOXG1 | c.789C>T (p.Asp263=) | dbSNP |
14 | g.28768069G>A | CA389475879 | FOXG1 | c.790G>A (p.Val264Met) | gnomAD v4 |
14 | g.28768069G>C | CA389475881 | FOXG1 | c.790G>C (p.Val264Leu) | |
14 | g.28768069G>T | CA389475880 | FOXG1 | c.790G>T (p.Val264Leu) | |
14 | g.28768070T>A | CA389475882 | FOXG1 | c.791T>A (p.Val264Glu) | |
14 | g.28768070T>C | CA389475883 | FOXG1 | c.791T>C (p.Val264Ala) | ClinVar dbSNP |
14 | g.28768070T>G | CA389475884 | FOXG1 | c.791T>G (p.Val264Gly) | ClinVar |
14 | g.28768070T= | CA2126000237 | FOXG1 | c.791T= (p.Val264=) | |
14 | g.28768071G>A | CA486098931 | FOXG1 | c.792G>A (p.Val264=) | gnomAD v4 |
14 | g.28768071G>C | CA486098933 | FOXG1 | c.792G>C (p.Val264=) | |
14 | g.28768071G>T | CA486098935 | FOXG1 | c.792G>T (p.Val264=) | |
14 | g.28768072T>A | CA389475885 | FOXG1 | c.793T>A (p.Phe265Ile) | |
14 | g.28768072T>C | CA389475886 | FOXG1 | c.793T>C (p.Phe265Leu) | |
14 | g.28768072T>G | CA389475887 | FOXG1 | c.793T>G (p.Phe265Val) | |
14 | g.28768072_28768087del | CA2573149903 | FOXG1 | c.793_808del (p.Phe265ArgfsTer?) | ClinVar dbSNP |
14 | g.28768073T>A | CA389475888 | FOXG1 | c.794T>A (p.Phe265Tyr) | |
14 | g.28768073T>C | CA389475889 | FOXG1 | c.794T>C (p.Phe265Ser) | |
14 | g.28768073T>G | CA389475890 | FOXG1 | c.794T>G (p.Phe265Cys) | |
14 | g.28768074C>A | CA389475891 | FOXG1 | c.795C>A (p.Phe265Leu) | COSMIC |
14 | g.28768074C= | CA2126000248 | FOXG1 | c.795C= (p.Phe265=) | |
14 | g.28768074C>G | CA389475892 | FOXG1 | c.795C>G (p.Phe265Leu) | |
14 | g.28768074C>T | CA486098942 | FOXG1 | c.795C>T (p.Phe265=) | dbSNP |
14 | g.28768075A>C | CA389475895 | FOXG1 | c.796A>C (p.Ile266Leu) | |
14 | g.28768075A>G | CA389475894 | FOXG1 | c.796A>G (p.Ile266Val) | gnomAD v4 |
14 | g.28768075A>T | CA389475893 | FOXG1 | c.796A>T (p.Ile266Phe) | |
14 | g.28768076T>A | CA10603236 | FOXG1 | c.797T>A (p.Ile266Asn) | ClinVar dbSNP |
14 | g.28768076T>C | CA389475897 | FOXG1 | c.797T>C (p.Ile266Thr) | ClinVar |
14 | g.28768076T>G | CA389475896 | FOXG1 | c.797T>G (p.Ile266Ser) | ClinVar dbSNP |
14 | g.28768076T= | CA2126000254 | FOXG1 | c.797T= (p.Ile266=) | |
14 | g.28768077C>A | CA486098943 | FOXG1 | c.798C>A (p.Ile266=) | |
14 | g.28768077C= | CA2126000262 | FOXG1 | c.798C= (p.Ile266=) | |
14 | g.28768077C>G | CA389475898 | FOXG1 | c.798C>G (p.Ile266Met) | |
14 | g.28768077C>T | CA7140630 | FOXG1 | c.798C>T (p.Ile266=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
14 | g.28768081_28768083del | CA2739277845 | FOXG1 | c.802_804del (p.Gly268del) | ClinVar |
14 | g.28768078G>A | CA172199 | FOXG1 | c.799G>A (p.Gly267Ser) | ClinVar dbSNP |
14 | g.28768078G>C | CA389475899 | FOXG1 | c.799G>C (p.Gly267Arg) | |
14 | g.28768078G= | CA2126000267 | FOXG1 | c.799G= (p.Gly267=) | |
14 | g.28768078G>T | CA389475900 | FOXG1 | c.799G>T (p.Gly267Cys) | |
14 | g.28768079G>A | CA389475901 | FOXG1 | c.800G>A (p.Gly267Asp) | ClinVar |
14 | g.28768079G>C | CA389475902 | FOXG1 | c.800G>C (p.Gly267Ala) | |
14 | g.28768079G>T | CA389475903 | FOXG1 | c.800G>T (p.Gly267Val) | |
14 | g.28768080C>A | CA486098949 | FOXG1 | c.801C>A (p.Gly267=) | ClinVar dbSNP gnomAD v2 gnomAD v4 |