Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.55181352C>ACA367578798EGFR,EGFR-AS1c.2184C>A (p.Cys728Ter)
c.692C>A
c.2343C>A (p.Cys781Ter)
c.*28+8424C>A (n.*28+8424C>A)
c.2208C>A (p.Cys736Ter)
n.1219G>T
c.1542C>A (p.Cys514Ter)
 dbSNP
7g.55181352C>GCA367578799EGFR,EGFR-AS1c.2184C>G (p.Cys728Trp)
c.692C>G
c.2343C>G (p.Cys781Trp)
c.*28+8424C>G (n.*28+8424C>G)
c.2208C>G (p.Cys736Trp)
n.1219G>C
c.1542C>G (p.Cys514Trp)
 dbSNP
7g.55181352C>TCA455165127EGFR,EGFR-AS1c.2184C>T (p.Cys728=)
c.692C>T
c.2343C>T (p.Cys781=)
c.*28+8424C>T (n.*28+8424C>T)
c.2208C>T (p.Cys736=)
n.1219G>A
c.1542C>T (p.Cys514=)
 dbSNP
7g.55181353C>ACA367578800EGFR,EGFR-AS1c.2185C>A (p.Leu729Ile)
c.693C>A
c.2344C>A (p.Leu782Ile)
c.*28+8425C>A (n.*28+8425C>A)
c.2209C>A (p.Leu737Ile)
n.1218G>T
c.1543C>A (p.Leu515Ile)
 dbSNP
7g.55181353C>GCA367578801EGFR,EGFR-AS1c.2185C>G (p.Leu729Val)
c.693C>G
c.2344C>G (p.Leu782Val)
c.*28+8425C>G (n.*28+8425C>G)
c.2209C>G (p.Leu737Val)
n.1218G>C
c.1543C>G (p.Leu515Val)
7g.55181353C>TCA367578802EGFR,EGFR-AS1c.2185C>T (p.Leu729Phe)
c.693C>T
c.2344C>T (p.Leu782Phe)
c.*28+8425C>T (n.*28+8425C>T)
c.2209C>T (p.Leu737Phe)
n.1218G>A
c.1543C>T (p.Leu515Phe)
 dbSNP
7g.55181353_55181354delinsAACA645561608EGFR,EGFR-AS1c.2185_2186delinsAA (p.Leu729Asn)
c.693_694delinsAA
c.2344_2345delinsAA (p.Leu782Asn)
c.*28+8425_*28+8426delinsAA (n.*28+8425_*28+8426delinsAA)
c.2209_2210delinsAA (p.Leu737Asn)
n.1217_1218delinsTT
c.1543_1544delinsAA (p.Leu515Asn)
 COSMIC
7g.55181354T>ACA367578805EGFR,EGFR-AS1c.2186T>A (p.Leu729His)
c.694T>A
c.2345T>A (p.Leu782His)
c.*28+8426T>A (n.*28+8426T>A)
c.2210T>A (p.Leu737His)
n.1217A>T
c.1544T>A (p.Leu515His)
7g.55181354T>CCA367578803EGFR,EGFR-AS1c.2186T>C (p.Leu729Pro)
c.694T>C
c.2345T>C (p.Leu782Pro)
c.*28+8426T>C (n.*28+8426T>C)
c.2210T>C (p.Leu737Pro)
n.1217A>G
c.1544T>C (p.Leu515Pro)
7g.55181354T>GCA367578804EGFR,EGFR-AS1c.2186T>G (p.Leu729Arg)
c.694T>G
c.2345T>G (p.Leu782Arg)
c.*28+8426T>G (n.*28+8426T>G)
c.2210T>G (p.Leu737Arg)
n.1217A>C
c.1544T>G (p.Leu515Arg)
7g.55181355C>ACA455165130EGFR,EGFR-AS1c.2187C>A (p.Leu729=)
c.695C>A
c.2346C>A (p.Leu782=)
c.*28+8427C>A (n.*28+8427C>A)
c.2211C>A (p.Leu737=)
n.1216G>T
c.1545C>A (p.Leu515=)
 dbSNP gnomAD v3 gnomAD v4
7g.55181355C=CA1708905395EGFR,EGFR-AS1c.2187C= (p.Leu729=)
c.695C=
c.2346C= (p.Leu782=)
c.*28+8427C= (n.*28+8427C=)
c.2211C= (p.Leu737=)
n.1216G=
c.1545C= (p.Leu515=)
7g.55181355C>GCA455165132EGFR,EGFR-AS1c.2187C>G (p.Leu729=)
c.695C>G
c.2346C>G (p.Leu782=)
c.*28+8427C>G (n.*28+8427C>G)
c.2211C>G (p.Leu737=)
n.1216G>C
c.1545C>G (p.Leu515=)
 dbSNP gnomAD v4
7g.55181355C>TCA455165133EGFR,EGFR-AS1c.2187C>T (p.Leu729=)
c.695C>T
c.2346C>T (p.Leu782=)
c.*28+8427C>T (n.*28+8427C>T)
c.2211C>T (p.Leu737=)
n.1216G>A
c.1545C>T (p.Leu515=)
 ClinVar dbSNP gnomAD v4
7g.55181356A>CCA367578806EGFR,EGFR-AS1c.2188A>C (p.Thr730Pro)
c.696A>C
c.2347A>C (p.Thr783Pro)
c.*28+8428A>C (n.*28+8428A>C)
c.2212A>C (p.Thr738Pro)
n.1215T>G
c.1546A>C (p.Thr516Pro)
 dbSNP
7g.55181356A>GCA367578807EGFR,EGFR-AS1c.2188A>G (p.Thr730Ala)
c.696A>G
c.2347A>G (p.Thr783Ala)
c.*28+8428A>G (n.*28+8428A>G)
c.2212A>G (p.Thr738Ala)
n.1215T>C
c.1546A>G (p.Thr516Ala)
 dbSNP
7g.55181356A>TCA367578808EGFR,EGFR-AS1c.2188A>T (p.Thr730Ser)
c.696A>T
c.2347A>T (p.Thr783Ser)
c.*28+8428A>T (n.*28+8428A>T)
c.2212A>T (p.Thr738Ser)
n.1215T>A
c.1546A>T (p.Thr516Ser)
 dbSNP
7g.55181357C>ACA367578809EGFR,EGFR-AS1c.2189C>A (p.Thr730Asn)
c.697C>A
c.2348C>A (p.Thr783Asn)
c.*28+8429C>A (n.*28+8429C>A)
c.2213C>A (p.Thr738Asn)
n.1214G>T
c.1547C>A (p.Thr516Asn)
 dbSNP
7g.55181357C>GCA367578810EGFR,EGFR-AS1c.2189C>G (p.Thr730Ser)
c.697C>G
c.2348C>G (p.Thr783Ser)
c.*28+8429C>G (n.*28+8429C>G)
c.2213C>G (p.Thr738Ser)
n.1214G>C
c.1547C>G (p.Thr516Ser)
 dbSNP
7g.55181357C>TCA367578811EGFR,EGFR-AS1c.2189C>T (p.Thr730Ile)
c.697C>T
c.2348C>T (p.Thr783Ile)
c.*28+8429C>T (n.*28+8429C>T)
c.2213C>T (p.Thr738Ile)
n.1214G>A
c.1547C>T (p.Thr516Ile)
 dbSNP COSMIC
7g.55181358C>ACA4266057EGFR,EGFR-AS1c.2190C>A (p.Thr730=)
c.698C>A
c.2349C>A (p.Thr783=)
c.*28+8430C>A (n.*28+8430C>A)
c.2214C>A (p.Thr738=)
n.1213G>T
c.1548C>A (p.Thr516=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
7g.55181358C=CA1708905403EGFR,EGFR-AS1c.2190C= (p.Thr730=)
c.698C=
c.2349C= (p.Thr783=)
c.*28+8430C= (n.*28+8430C=)
c.2214C= (p.Thr738=)
n.1213G=
c.1548C= (p.Thr516=)
7g.55181358C>GCA455165137EGFR,EGFR-AS1c.2190C>G (p.Thr730=)
c.698C>G
c.2349C>G (p.Thr783=)
c.*28+8430C>G (n.*28+8430C>G)
c.2214C>G (p.Thr738=)
n.1213G>C
c.1548C>G (p.Thr516=)
 dbSNP
7g.55181358C>TCA135890EGFR,EGFR-AS1c.2190C>T (p.Thr730=)
c.698C>T
c.2349C>T (p.Thr783=)
c.*28+8430C>T (n.*28+8430C>T)
c.2214C>T (p.Thr738=)
n.1213G>A
c.1548C>T (p.Thr516=)
 ClinVar dbSNP gnomAD v4
7g.55181359T>ACA367578812EGFR,EGFR-AS1c.2191T>A (p.Ser731Thr)
c.699T>A
c.2350T>A (p.Ser784Thr)
c.*28+8431T>A (n.*28+8431T>A)
c.2215T>A (p.Ser739Thr)
n.1212A>T
c.1549T>A (p.Ser517Thr)
7g.55181359T>CCA367578813EGFR,EGFR-AS1c.2191T>C (p.Ser731Pro)
c.699T>C
c.2350T>C (p.Ser784Pro)
c.*28+8431T>C (n.*28+8431T>C)
c.2215T>C (p.Ser739Pro)
n.1212A>G
c.1549T>C (p.Ser517Pro)
 dbSNP gnomAD v4 COSMIC
7g.55181359T>GCA367578814EGFR,EGFR-AS1c.2191T>G (p.Ser731Ala)
c.699T>G
c.2350T>G (p.Ser784Ala)
c.*28+8431T>G (n.*28+8431T>G)
c.2215T>G (p.Ser739Ala)
n.1212A>C
c.1549T>G (p.Ser517Ala)
7g.55181360C>ACA367578816EGFR,EGFR-AS1c.2192C>A (p.Ser731Tyr)
c.700C>A
c.2351C>A (p.Ser784Tyr)
c.*28+8432C>A (n.*28+8432C>A)
c.2216C>A (p.Ser739Tyr)
n.1211G>T
c.1550C>A (p.Ser517Tyr)
 dbSNP COSMIC
7g.55181360C=CA1708905409EGFR,EGFR-AS1c.2192C= (p.Ser731=)
c.700C=
c.2351C= (p.Ser784=)
c.*28+8432C= (n.*28+8432C=)
c.2216C= (p.Ser739=)
n.1211G=
c.1550C= (p.Ser517=)
7g.55181360C>GCA367578817EGFR,EGFR-AS1c.2192C>G (p.Ser731Cys)
c.700C>G
c.2351C>G (p.Ser784Cys)
c.*28+8432C>G (n.*28+8432C>G)
c.2216C>G (p.Ser739Cys)
n.1211G>C
c.1550C>G (p.Ser517Cys)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
7g.55181360C>TCA367578815EGFR,EGFR-AS1c.2192C>T (p.Ser731Phe)
c.700C>T
c.2351C>T (p.Ser784Phe)
c.*28+8432C>T (n.*28+8432C>T)
c.2216C>T (p.Ser739Phe)
n.1211G>A
c.1550C>T (p.Ser517Phe)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
7g.55181361C>ACA455165144EGFR,EGFR-AS1c.2193C>A (p.Ser731=)
c.701C>A
c.2352C>A (p.Ser784=)
c.*28+8433C>A (n.*28+8433C>A)
c.2217C>A (p.Ser739=)
n.1210G>T
c.1551C>A (p.Ser517=)
7g.55181361C>GCA455165145EGFR,EGFR-AS1c.2193C>G (p.Ser731=)
c.701C>G
c.2352C>G (p.Ser784=)
c.*28+8433C>G (n.*28+8433C>G)
c.2217C>G (p.Ser739=)
n.1210G>C
c.1551C>G (p.Ser517=)
 dbSNP
7g.55181361C>TCA455165146EGFR,EGFR-AS1c.2193C>T (p.Ser731=)
c.701C>T
c.2352C>T (p.Ser784=)
c.*28+8433C>T (n.*28+8433C>T)
c.2217C>T (p.Ser739=)
n.1210G>A
c.1551C>T (p.Ser517=)
 ClinVar dbSNP
7g.55181362A>CCA367578818EGFR,EGFR-AS1c.2194A>C (p.Thr732Pro)
c.702A>C
c.2353A>C (p.Thr785Pro)
c.*28+8434A>C (n.*28+8434A>C)
c.2218A>C (p.Thr740Pro)
n.1209T>G
c.1552A>C (p.Thr518Pro)
 dbSNP COSMIC
7g.55181362A>GCA367578819EGFR,EGFR-AS1c.2194A>G (p.Thr732Ala)
c.702A>G
c.2353A>G (p.Thr785Ala)
c.*28+8434A>G (n.*28+8434A>G)
c.2218A>G (p.Thr740Ala)
n.1209T>C
c.1552A>G (p.Thr518Ala)
 ClinVar dbSNP gnomAD v4 COSMIC
7g.55181362A>TCA367578820EGFR,EGFR-AS1c.2194A>T (p.Thr732Ser)
c.702A>T
c.2353A>T (p.Thr785Ser)
c.*28+8434A>T (n.*28+8434A>T)
c.2218A>T (p.Thr740Ser)
n.1209T>A
c.1552A>T (p.Thr518Ser)
7g.55181363C>ACA367578821EGFR,EGFR-AS1c.2195C>A (p.Thr732Asn)
c.703C>A
c.2354C>A (p.Thr785Asn)
c.*28+8435C>A (n.*28+8435C>A)
c.2219C>A (p.Thr740Asn)
n.1208G>T
c.1553C>A (p.Thr518Asn)
 dbSNP COSMIC
7g.55181363C>GCA367578822EGFR,EGFR-AS1c.2195C>G (p.Thr732Ser)
c.703C>G
c.2354C>G (p.Thr785Ser)
c.*28+8435C>G (n.*28+8435C>G)
c.2219C>G (p.Thr740Ser)
n.1208G>C
c.1553C>G (p.Thr518Ser)
 dbSNP
7g.55181363C>TCA367578823EGFR,EGFR-AS1c.2195C>T (p.Thr732Ile)
c.703C>T
c.2354C>T (p.Thr785Ile)
c.*28+8435C>T (n.*28+8435C>T)
c.2219C>T (p.Thr740Ile)
n.1208G>A
c.1553C>T (p.Thr518Ile)
 dbSNP COSMIC
7g.55181364C>ACA455165150EGFR,EGFR-AS1c.2196C>A (p.Thr732=)
c.704C>A
c.2355C>A (p.Thr785=)
c.*28+8436C>A (n.*28+8436C>A)
c.2220C>A (p.Thr740=)
n.1207G>T
c.1554C>A (p.Thr518=)
 dbSNP gnomAD v2 gnomAD v4
7g.55181364C=CA1708905414EGFR,EGFR-AS1c.2196C= (p.Thr732=)
c.704C=
c.2355C= (p.Thr785=)
c.*28+8436C= (n.*28+8436C=)
c.2220C= (p.Thr740=)
n.1207G=
c.1554C= (p.Thr518=)
7g.55181364C>GCA455165151EGFR,EGFR-AS1c.2196C>G (p.Thr732=)
c.704C>G
c.2355C>G (p.Thr785=)
c.*28+8436C>G (n.*28+8436C>G)
c.2220C>G (p.Thr740=)
n.1207G>C
c.1554C>G (p.Thr518=)
 ClinVar dbSNP gnomAD v2 gnomAD v4
7g.55181364C>TCA135893EGFR,EGFR-AS1c.2196C>T (p.Thr732=)
c.704C>T
c.2355C>T (p.Thr785=)
c.*28+8436C>T (n.*28+8436C>T)
c.2220C>T (p.Thr740=)
n.1207G>A
c.1554C>T (p.Thr518=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.55181365G>ACA4266058EGFR,EGFR-AS1c.2197G>A (p.Val733Met)
c.705G>A
c.2356G>A (p.Val786Met)
c.*28+8437G>A (n.*28+8437G>A)
c.2221G>A (p.Val741Met)
n.1206C>T
c.1555G>A (p.Val519Met)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
7g.55181365G>CCA367578825EGFR,EGFR-AS1c.2197G>C (p.Val733Leu)
c.705G>C
c.2356G>C (p.Val786Leu)
c.*28+8437G>C (n.*28+8437G>C)
c.2221G>C (p.Val741Leu)
n.1206C>G
c.1555G>C (p.Val519Leu)
 dbSNP gnomAD v2
7g.55181365G=CA1708905428EGFR,EGFR-AS1c.2197G= (p.Val733=)
c.705G=
c.2356G= (p.Val786=)
c.*28+8437G= (n.*28+8437G=)
c.2221G= (p.Val741=)
n.1206C=
c.1555G= (p.Val519=)
7g.55181365G>TCA367578824EGFR,EGFR-AS1c.2197G>T (p.Val733Leu)
c.705G>T
c.2356G>T (p.Val786Leu)
c.*28+8437G>T (n.*28+8437G>T)
c.2221G>T (p.Val741Leu)
n.1206C>A
c.1555G>T (p.Val519Leu)
7g.55181366T>ACA367578826EGFR,EGFR-AS1c.2198T>A (p.Val733Glu)
c.706T>A
c.2357T>A (p.Val786Glu)
c.*28+8438T>A (n.*28+8438T>A)
c.2222T>A (p.Val741Glu)
n.1205A>T
c.1556T>A (p.Val519Glu)
 ClinVar dbSNP gnomAD v4
7g.55181366T>CCA367578827EGFR,EGFR-AS1c.2198T>C (p.Val733Ala)
c.706T>C
c.2357T>C (p.Val786Ala)
c.*28+8438T>C (n.*28+8438T>C)
c.2222T>C (p.Val741Ala)
n.1205A>G
c.1556T>C (p.Val519Ala)
 gnomAD v4

Number of alleles fetched