Chr Mutation (hg38) CAid Gene Transcript Linkouts
13g.113149097C>ACA485424070F10c.1047C>A (p.Ala349=)
c.*38C>A (n.*38C>A)
c.915C>A (p.Ala305=)
gnomAD v4
13g.113149097C=CA2120140166F10c.1047C= (p.Ala349=)
c.*38C= (n.*38C=)
c.915C= (p.Ala305=)
13g.113149097C>GCA485424071F10c.1047C>G (p.Ala349=)
c.*38C>G (n.*38C>G)
c.915C>G (p.Ala305=)
gnomAD v4
13g.113149097C>TCA256478678F10c.1047C>T (p.Ala349=)
c.*38C>T (n.*38C>T)
c.915C>T (p.Ala305=)
dbSNP gnomAD v3 gnomAD v4
13g.113149098delCA2623809576F10c.1048del (p.Glu350SerfsTer4)
c.*39del (n.*39del)
c.916del (p.Glu306SerfsTer4)
gnomAD v4
13g.113149098G>ACA256478679F10c.1048G>A (p.Glu350Lys)
c.*39G>A (n.*39G>A)
c.916G>A (p.Glu306Lys)
dbSNP gnomAD v3 gnomAD v4
13g.113149098G>CCA388792770F10c.1048G>C (p.Glu350Gln)
c.*39G>C (n.*39G>C)
c.916G>C (p.Glu306Gln)
13g.113149098G=CA2120140169F10c.1048G= (p.Glu350=)
c.*39G= (n.*39G=)
c.916G= (p.Glu306=)
13g.113149098G>TCA388792773F10c.1048G>T (p.Glu350Ter)
c.*39G>T (n.*39G>T)
c.916G>T (p.Glu306Ter)
13g.113149099A>CCA388792775F10c.1049A>C (p.Glu350Ala)
c.*40A>C (n.*40A>C)
c.917A>C (p.Glu306Ala)
13g.113149099A>GCA388792778F10c.1049A>G (p.Glu350Gly)
c.*40A>G (n.*40A>G)
c.917A>G (p.Glu306Gly)
13g.113149099A>TCA388792780F10c.1049A>T (p.Glu350Val)
c.*40A>T (n.*40A>T)
c.917A>T (p.Glu306Val)
13g.113149100G>ACA7060675F10c.1050G>A (p.Glu350=)
c.*41G>A (n.*41G>A)
c.918G>A (p.Glu306=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.113149100G>CCA388792783F10c.1050G>C (p.Glu350Asp)
c.*41G>C (n.*41G>C)
c.918G>C (p.Glu306Asp)
13g.113149100G=CA2120140171F10c.1050G= (p.Glu350=)
c.*41G= (n.*41G=)
c.918G= (p.Glu306=)
13g.113149100G>TCA388792785F10c.1050G>T (p.Glu350Asp)
c.*41G>T (n.*41G>T)
c.918G>T (p.Glu306Asp)
13g.113149101T>ACA388792788F10c.1051T>A (p.Ser351Thr)
c.*42T>A (n.*42T>A)
c.919T>A (p.Ser307Thr)
13g.113149101T>CCA388792789F10c.1051T>C (p.Ser351Pro)
c.*42T>C (n.*42T>C)
c.919T>C (p.Ser307Pro)
gnomAD v4
13g.113149101T>GCA388792792F10c.1051T>G (p.Ser351Ala)
c.*42T>G (n.*42T>G)
c.919T>G (p.Ser307Ala)
13g.113149102C>ACA388792794F10c.1052C>A (p.Ser351Tyr)
c.*43C>A (n.*43C>A)
c.920C>A (p.Ser307Tyr)
13g.113149102C>GCA388792799F10c.1052C>G (p.Ser351Cys)
c.*43C>G (n.*43C>G)
c.920C>G (p.Ser307Cys)
13g.113149102C>TCA388792796F10c.1052C>T (p.Ser351Phe)
c.*43C>T (n.*43C>T)
c.920C>T (p.Ser307Phe)
13g.113149103C>ACA485424072F10c.1053C>A (p.Ser351=)
c.*44C>A (n.*44C>A)
c.921C>A (p.Ser307=)
COSMIC
13g.113149103C>GCA485424073F10c.1053C>G (p.Ser351=)
c.*44C>G (n.*44C>G)
c.921C>G (p.Ser307=)
13g.113149103C>TCA485424074F10c.1053C>T (p.Ser351=)
c.*44C>T (n.*44C>T)
c.921C>T (p.Ser307=)
gnomAD v4
13g.113149104A>CCA388792801F10c.1054A>C (p.Thr352Pro)
c.*45A>C (n.*45A>C)
c.922A>C (p.Thr308Pro)
13g.113149104A>GCA388792802F10c.1054A>G (p.Thr352Ala)
c.*45A>G (n.*45A>G)
c.922A>G (p.Thr308Ala)
13g.113149104A>TCA388792805F10c.1054A>T (p.Thr352Ser)
c.*45A>T (n.*45A>T)
c.922A>T (p.Thr308Ser)
13g.113149105C>ACA388792808F10c.1055C>A (p.Thr352Lys)
c.*46C>A (n.*46C>A)
c.923C>A (p.Thr308Lys)
13g.113149105C=CA2120140173F10c.1055C= (p.Thr352=)
c.*46C= (n.*46C=)
c.923C= (p.Thr308=)
13g.113149105C>GCA388792809F10c.1055C>G (p.Thr352Arg)
c.*46C>G (n.*46C>G)
c.923C>G (p.Thr308Arg)
13g.113149105C>TCA388792810F10c.1055C>T (p.Thr352Met)
c.*46C>T (n.*46C>T)
c.923C>T (p.Thr308Met)
dbSNP gnomAD v2 gnomAD v4
13g.113149106G>ACA7060676F10c.1056G>A (p.Thr352=)
c.*47G>A (n.*47G>A)
c.924G>A (p.Thr308=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.113149106G>CCA485424075F10c.1056G>C (p.Thr352=)
c.*47G>C (n.*47G>C)
c.924G>C (p.Thr308=)
13g.113149106G=CA2120140175F10c.1056G= (p.Thr352=)
c.*47G= (n.*47G=)
c.924G= (p.Thr308=)
13g.113149106G>TCA485424076F10c.1056G>T (p.Thr352=)
c.*47G>T (n.*47G>T)
c.924G>T (p.Thr308=)
dbSNP gnomAD v3 gnomAD v4
13g.113149107C>ACA388792813F10c.1057C>A (p.Leu353Met)
c.*48C>A (n.*48C>A)
c.925C>A (p.Leu309Met)
13g.113149107C>GCA388792816F10c.1057C>G (p.Leu353Val)
c.*48C>G (n.*48C>G)
c.925C>G (p.Leu309Val)
13g.113149107C>TCA485424077F10c.1057C>T (p.Leu353=)
c.*48C>T (n.*48C>T)
c.925C>T (p.Leu309=)
13g.113149107_113149108delinsCTCA2120140177F10c.1057_1058delinsCT (p.Leu353=)
c.*48_*49delinsCT (n.*48_*49delinsCT)
c.925_926delinsCT (p.Leu309=)
13g.113149108delCA7060677F10c.1058del (p.Leu353ArgfsTer2)
c.*49del (n.*49del)
c.926del (p.Leu309ArgfsTer2)
dbSNP ExAC gnomAD v2 gnomAD v4
13g.113149108T>ACA388792818F10c.1058T>A (p.Leu353Gln)
c.*49T>A (n.*49T>A)
c.926T>A (p.Leu309Gln)
13g.113149108T>CCA388792820F10c.1058T>C (p.Leu353Pro)
c.*49T>C (n.*49T>C)
c.926T>C (p.Leu309Pro)
gnomAD v4
13g.113149108T>GCA388792823F10c.1058T>G (p.Leu353Arg)
c.*49T>G (n.*49T>G)
c.926T>G (p.Leu309Arg)
13g.113149109G>ACA485424078F10c.1059G>A (p.Leu353=)
c.*50G>A (n.*50G>A)
c.927G>A (p.Leu309=)
13g.113149109G>CCA256478684F10c.1059G>C (p.Leu353=)
c.*50G>C (n.*50G>C)
c.927G>C (p.Leu309=)
dbSNP gnomAD v4
13g.113149109G=CA2120140179F10c.1059G= (p.Leu353=)
c.*50G= (n.*50G=)
c.927G= (p.Leu309=)
13g.113149109G>TCA485424079F10c.1059G>T (p.Leu353=)
c.*50G>T (n.*50G>T)
c.927G>T (p.Leu309=)
13g.113149110A>CCA388792830F10c.1060A>C (p.Met354Leu)
c.*51A>C (n.*51A>C)
c.928A>C (p.Met310Leu)
13g.113149110A>GCA388792827F10c.1060A>G (p.Met354Val)
c.*51A>G (n.*51A>G)
c.928A>G (p.Met310Val)

Number of alleles fetched