Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
13 | g.113149097C>A | CA485424070 | F10 | c.1047C>A (p.Ala349=) c.*38C>A (n.*38C>A) c.915C>A (p.Ala305=) | gnomAD v4 |
13 | g.113149097C= | CA2120140166 | F10 | c.1047C= (p.Ala349=) c.*38C= (n.*38C=) c.915C= (p.Ala305=) | |
13 | g.113149097C>G | CA485424071 | F10 | c.1047C>G (p.Ala349=) c.*38C>G (n.*38C>G) c.915C>G (p.Ala305=) | gnomAD v4 |
13 | g.113149097C>T | CA256478678 | F10 | c.1047C>T (p.Ala349=) c.*38C>T (n.*38C>T) c.915C>T (p.Ala305=) | dbSNP gnomAD v3 gnomAD v4 |
13 | g.113149098del | CA2623809576 | F10 | c.1048del (p.Glu350SerfsTer4) c.*39del (n.*39del) c.916del (p.Glu306SerfsTer4) | gnomAD v4 |
13 | g.113149098G>A | CA256478679 | F10 | c.1048G>A (p.Glu350Lys) c.*39G>A (n.*39G>A) c.916G>A (p.Glu306Lys) | dbSNP gnomAD v3 gnomAD v4 |
13 | g.113149098G>C | CA388792770 | F10 | c.1048G>C (p.Glu350Gln) c.*39G>C (n.*39G>C) c.916G>C (p.Glu306Gln) | |
13 | g.113149098G= | CA2120140169 | F10 | c.1048G= (p.Glu350=) c.*39G= (n.*39G=) c.916G= (p.Glu306=) | |
13 | g.113149098G>T | CA388792773 | F10 | c.1048G>T (p.Glu350Ter) c.*39G>T (n.*39G>T) c.916G>T (p.Glu306Ter) | |
13 | g.113149099A>C | CA388792775 | F10 | c.1049A>C (p.Glu350Ala) c.*40A>C (n.*40A>C) c.917A>C (p.Glu306Ala) | |
13 | g.113149099A>G | CA388792778 | F10 | c.1049A>G (p.Glu350Gly) c.*40A>G (n.*40A>G) c.917A>G (p.Glu306Gly) | |
13 | g.113149099A>T | CA388792780 | F10 | c.1049A>T (p.Glu350Val) c.*40A>T (n.*40A>T) c.917A>T (p.Glu306Val) | |
13 | g.113149100G>A | CA7060675 | F10 | c.1050G>A (p.Glu350=) c.*41G>A (n.*41G>A) c.918G>A (p.Glu306=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
13 | g.113149100G>C | CA388792783 | F10 | c.1050G>C (p.Glu350Asp) c.*41G>C (n.*41G>C) c.918G>C (p.Glu306Asp) | |
13 | g.113149100G= | CA2120140171 | F10 | c.1050G= (p.Glu350=) c.*41G= (n.*41G=) c.918G= (p.Glu306=) | |
13 | g.113149100G>T | CA388792785 | F10 | c.1050G>T (p.Glu350Asp) c.*41G>T (n.*41G>T) c.918G>T (p.Glu306Asp) | |
13 | g.113149101T>A | CA388792788 | F10 | c.1051T>A (p.Ser351Thr) c.*42T>A (n.*42T>A) c.919T>A (p.Ser307Thr) | |
13 | g.113149101T>C | CA388792789 | F10 | c.1051T>C (p.Ser351Pro) c.*42T>C (n.*42T>C) c.919T>C (p.Ser307Pro) | gnomAD v4 |
13 | g.113149101T>G | CA388792792 | F10 | c.1051T>G (p.Ser351Ala) c.*42T>G (n.*42T>G) c.919T>G (p.Ser307Ala) | |
13 | g.113149102C>A | CA388792794 | F10 | c.1052C>A (p.Ser351Tyr) c.*43C>A (n.*43C>A) c.920C>A (p.Ser307Tyr) | |
13 | g.113149102C>G | CA388792799 | F10 | c.1052C>G (p.Ser351Cys) c.*43C>G (n.*43C>G) c.920C>G (p.Ser307Cys) | |
13 | g.113149102C>T | CA388792796 | F10 | c.1052C>T (p.Ser351Phe) c.*43C>T (n.*43C>T) c.920C>T (p.Ser307Phe) | |
13 | g.113149103C>A | CA485424072 | F10 | c.1053C>A (p.Ser351=) c.*44C>A (n.*44C>A) c.921C>A (p.Ser307=) | COSMIC |
13 | g.113149103C>G | CA485424073 | F10 | c.1053C>G (p.Ser351=) c.*44C>G (n.*44C>G) c.921C>G (p.Ser307=) | |
13 | g.113149103C>T | CA485424074 | F10 | c.1053C>T (p.Ser351=) c.*44C>T (n.*44C>T) c.921C>T (p.Ser307=) | gnomAD v4 |
13 | g.113149104A>C | CA388792801 | F10 | c.1054A>C (p.Thr352Pro) c.*45A>C (n.*45A>C) c.922A>C (p.Thr308Pro) | |
13 | g.113149104A>G | CA388792802 | F10 | c.1054A>G (p.Thr352Ala) c.*45A>G (n.*45A>G) c.922A>G (p.Thr308Ala) | |
13 | g.113149104A>T | CA388792805 | F10 | c.1054A>T (p.Thr352Ser) c.*45A>T (n.*45A>T) c.922A>T (p.Thr308Ser) | |
13 | g.113149105C>A | CA388792808 | F10 | c.1055C>A (p.Thr352Lys) c.*46C>A (n.*46C>A) c.923C>A (p.Thr308Lys) | |
13 | g.113149105C= | CA2120140173 | F10 | c.1055C= (p.Thr352=) c.*46C= (n.*46C=) c.923C= (p.Thr308=) | |
13 | g.113149105C>G | CA388792809 | F10 | c.1055C>G (p.Thr352Arg) c.*46C>G (n.*46C>G) c.923C>G (p.Thr308Arg) | |
13 | g.113149105C>T | CA388792810 | F10 | c.1055C>T (p.Thr352Met) c.*46C>T (n.*46C>T) c.923C>T (p.Thr308Met) | dbSNP gnomAD v2 gnomAD v4 |
13 | g.113149106G>A | CA7060676 | F10 | c.1056G>A (p.Thr352=) c.*47G>A (n.*47G>A) c.924G>A (p.Thr308=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
13 | g.113149106G>C | CA485424075 | F10 | c.1056G>C (p.Thr352=) c.*47G>C (n.*47G>C) c.924G>C (p.Thr308=) | |
13 | g.113149106G= | CA2120140175 | F10 | c.1056G= (p.Thr352=) c.*47G= (n.*47G=) c.924G= (p.Thr308=) | |
13 | g.113149106G>T | CA485424076 | F10 | c.1056G>T (p.Thr352=) c.*47G>T (n.*47G>T) c.924G>T (p.Thr308=) | dbSNP gnomAD v3 gnomAD v4 |
13 | g.113149107C>A | CA388792813 | F10 | c.1057C>A (p.Leu353Met) c.*48C>A (n.*48C>A) c.925C>A (p.Leu309Met) | |
13 | g.113149107C>G | CA388792816 | F10 | c.1057C>G (p.Leu353Val) c.*48C>G (n.*48C>G) c.925C>G (p.Leu309Val) | |
13 | g.113149107C>T | CA485424077 | F10 | c.1057C>T (p.Leu353=) c.*48C>T (n.*48C>T) c.925C>T (p.Leu309=) | |
13 | g.113149107_113149108delinsCT | CA2120140177 | F10 | c.1057_1058delinsCT (p.Leu353=) c.*48_*49delinsCT (n.*48_*49delinsCT) c.925_926delinsCT (p.Leu309=) | |
13 | g.113149108del | CA7060677 | F10 | c.1058del (p.Leu353ArgfsTer2) c.*49del (n.*49del) c.926del (p.Leu309ArgfsTer2) | dbSNP ExAC gnomAD v2 gnomAD v4 |
13 | g.113149108T>A | CA388792818 | F10 | c.1058T>A (p.Leu353Gln) c.*49T>A (n.*49T>A) c.926T>A (p.Leu309Gln) | |
13 | g.113149108T>C | CA388792820 | F10 | c.1058T>C (p.Leu353Pro) c.*49T>C (n.*49T>C) c.926T>C (p.Leu309Pro) | gnomAD v4 |
13 | g.113149108T>G | CA388792823 | F10 | c.1058T>G (p.Leu353Arg) c.*49T>G (n.*49T>G) c.926T>G (p.Leu309Arg) | |
13 | g.113149109G>A | CA485424078 | F10 | c.1059G>A (p.Leu353=) c.*50G>A (n.*50G>A) c.927G>A (p.Leu309=) | |
13 | g.113149109G>C | CA256478684 | F10 | c.1059G>C (p.Leu353=) c.*50G>C (n.*50G>C) c.927G>C (p.Leu309=) | dbSNP gnomAD v4 |
13 | g.113149109G= | CA2120140179 | F10 | c.1059G= (p.Leu353=) c.*50G= (n.*50G=) c.927G= (p.Leu309=) | |
13 | g.113149109G>T | CA485424079 | F10 | c.1059G>T (p.Leu353=) c.*50G>T (n.*50G>T) c.927G>T (p.Leu309=) | |
13 | g.113149110A>C | CA388792830 | F10 | c.1060A>C (p.Met354Leu) c.*51A>C (n.*51A>C) c.928A>C (p.Met310Leu) | |
13 | g.113149110A>G | CA388792827 | F10 | c.1060A>G (p.Met354Val) c.*51A>G (n.*51A>G) c.928A>G (p.Met310Val) |