Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
1 | g.110061450A>C | CA419396914 | ALX3,STRIP1 | c.708T>G (p.Thr236=) c.279T>G (p.Thr93=) n.4213+6648A>C | |
1 | g.110061450A>G | CA419396915 | ALX3,STRIP1 | c.708T>C (p.Thr236=) c.279T>C (p.Thr93=) n.4213+6648A>G | gnomAD v4 |
1 | g.110061450A>T | CA419396916 | ALX3,STRIP1 | c.708T>A (p.Thr236=) c.279T>A (p.Thr93=) n.4213+6648A>T | |
1 | g.110061451del | CA419396917 | ALX3,STRIP1 | c.707del (p.Thr236MetfsTer?) c.278del (p.Thr93MetfsTer?) n.4213+6649del | COSMIC |
1 | g.110061451G>A | CA341581837 | ALX3,STRIP1 | c.707C>T (p.Thr236Ile) c.278C>T (p.Thr93Ile) n.4213+6649G>A | |
1 | g.110061451G>C | CA341581838 | ALX3,STRIP1 | c.707C>G (p.Thr236Ser) c.278C>G (p.Thr93Ser) n.4213+6649G>C | |
1 | g.110061451G= | CA1188347333 | ALX3,STRIP1 | c.707C= (p.Thr236=) c.278C= (p.Thr93=) n.4213+6649G= | |
1 | g.110061451G>T | CA341581840 | ALX3,STRIP1 | c.707C>A (p.Thr236Asn) c.278C>A (p.Thr93Asn) n.4213+6649G>T | dbSNP |
1 | g.110061452T>A | CA341581846 | ALX3,STRIP1 | c.706A>T (p.Thr236Ser) c.277A>T (p.Thr93Ser) n.4213+6650T>A | |
1 | g.110061452T>C | CA341581844 | ALX3,STRIP1 | c.706A>G (p.Thr236Ala) c.277A>G (p.Thr93Ala) n.4213+6650T>C | |
1 | g.110061452T>G | CA341581842 | ALX3,STRIP1 | c.706A>C (p.Thr236Pro) c.277A>C (p.Thr93Pro) n.4213+6650T>G | |
1 | g.110061453A>C | CA419396918 | ALX3,STRIP1 | c.705T>G (p.Arg235=) c.276T>G (p.Arg92=) n.4213+6651A>C | |
1 | g.110061453A>G | CA419396919 | ALX3,STRIP1 | c.705T>C (p.Arg235=) c.276T>C (p.Arg92=) n.4213+6651A>G | dbSNP gnomAD v4 |
1 | g.110061453A>T | CA419396920 | ALX3,STRIP1 | c.705T>A (p.Arg235=) c.276T>A (p.Arg92=) n.4213+6651A>T | |
1 | g.110061454C>A | CA341581848 | ALX3,STRIP1 | c.704G>T (p.Arg235Leu) c.275G>T (p.Arg92Leu) n.4213+6652C>A | |
1 | g.110061454C= | CA1143372488 | ALX3,STRIP1 | c.704G= (p.Arg235=) c.275G= (p.Arg92=) n.4213+6652C= | |
1 | g.110061454C>G | CA341581850 | ALX3,STRIP1 | c.704G>C (p.Arg235Pro) c.275G>C (p.Arg92Pro) n.4213+6652C>G | dbSNP |
1 | g.110061454C>T | CA997520 | ALX3,STRIP1 | c.704G>A (p.Arg235His) c.275G>A (p.Arg92His) n.4213+6652C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
1 | g.110061455G>A | CA997521 | ALX3,STRIP1 | c.703C>T (p.Arg235Cys) c.274C>T (p.Arg92Cys) n.4213+6653G>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.110061455G>C | CA997522 | ALX3,STRIP1 | c.703C>G (p.Arg235Gly) c.274C>G (p.Arg92Gly) n.4213+6653G>C | dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.110061455G= | CA1142059432 | ALX3,STRIP1 | c.703C= (p.Arg235=) c.274C= (p.Arg92=) n.4213+6653G= | |
1 | g.110061455G>T | CA341581854 | ALX3,STRIP1 | c.703C>A (p.Arg235Ser) c.274C>A (p.Arg92Ser) n.4213+6653G>T | |
1 | g.110061456G>A | CA419396921 | ALX3,STRIP1 | c.702C>T (p.Pro234=) c.273C>T (p.Pro91=) n.4213+6654G>A | |
1 | g.110061456G>C | CA419396922 | ALX3,STRIP1 | c.702C>G (p.Pro234=) c.273C>G (p.Pro91=) n.4213+6654G>C | dbSNP |
1 | g.110061456G= | CA1188347334 | ALX3,STRIP1 | c.702C= (p.Pro234=) c.273C= (p.Pro91=) n.4213+6654G= | |
1 | g.110061456G>T | CA997523 | ALX3,STRIP1 | c.702C>A (p.Pro234=) c.273C>A (p.Pro91=) n.4213+6654G>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.110061457G>A | CA341581857 | ALX3,STRIP1 | c.701C>T (p.Pro234Leu) c.272C>T (p.Pro91Leu) n.4213+6655G>A | dbSNP gnomAD v4 |
1 | g.110061457G>C | CA341581859 | ALX3,STRIP1 | c.701C>G (p.Pro234Arg) c.272C>G (p.Pro91Arg) n.4213+6655G>C | dbSNP gnomAD v3 gnomAD v4 |
1 | g.110061457G= | CA1188347335 | ALX3,STRIP1 | c.701C= (p.Pro234=) c.272C= (p.Pro91=) n.4213+6655G= | |
1 | g.110061457G>T | CA341581860 | ALX3,STRIP1 | c.701C>A (p.Pro234His) c.272C>A (p.Pro91His) n.4213+6655G>T | |
1 | g.110061458G>A | CA341581862 | ALX3,STRIP1 | c.700C>T (p.Pro234Ser) c.271C>T (p.Pro91Ser) n.4213+6656G>A | gnomAD v4 |
1 | g.110061458G>C | CA28737114 | ALX3,STRIP1 | c.700C>G (p.Pro234Ala) c.271C>G (p.Pro91Ala) n.4213+6656G>C | dbSNP |
1 | g.110061458G= | CA1140429967 | ALX3,STRIP1 | c.700C= (p.Pro234=) c.271C= (p.Pro91=) n.4213+6656G= | |
1 | g.110061458G>T | CA341581865 | ALX3,STRIP1 | c.700C>A (p.Pro234Thr) c.271C>A (p.Pro91Thr) n.4213+6656G>T | |
1 | g.110061459C>A | CA997524 | ALX3,STRIP1 | c.699G>T (p.Leu233=) c.270G>T (p.Leu90=) n.4213+6657C>A | dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.110061459C= | CA1188347336 | ALX3,STRIP1 | c.699G= (p.Leu233=) c.270G= (p.Leu90=) n.4213+6657C= | |
1 | g.110061459C>G | CA419396923 | ALX3,STRIP1 | c.699G>C (p.Leu233=) c.270G>C (p.Leu90=) n.4213+6657C>G | gnomAD v4 |
1 | g.110061459C>T | CA419396924 | ALX3,STRIP1 | c.699G>A (p.Leu233=) c.270G>A (p.Leu90=) n.4213+6657C>T | |
1 | g.110061460A>C | CA341581871 | ALX3,STRIP1 | c.698T>G (p.Leu233Arg) c.269T>G (p.Leu90Arg) n.4213+6658A>C | |
1 | g.110061460A>G | CA341581868 | ALX3,STRIP1 | c.698T>C (p.Leu233Pro) c.269T>C (p.Leu90Pro) n.4213+6658A>G | |
1 | g.110061460A>T | CA341581869 | ALX3,STRIP1 | c.698T>A (p.Leu233Gln) c.269T>A (p.Leu90Gln) n.4213+6658A>T | |
1 | g.110061461G>A | CA419396925 | ALX3,STRIP1 | c.697C>T (p.Leu233=) c.268C>T (p.Leu90=) n.4213+6659G>A | |
1 | g.110061461G>C | CA341581873 | ALX3,STRIP1 | c.697C>G (p.Leu233Val) c.268C>G (p.Leu90Val) n.4213+6659G>C | |
1 | g.110061461G>T | CA341581875 | ALX3,STRIP1 | c.697C>A (p.Leu233Met) c.268C>A (p.Leu90Met) n.4213+6659G>T | |
1 | g.110061462C>A | CA419396926 | ALX3,STRIP1 | c.696G>T (p.Val232=) c.267G>T (p.Val89=) n.4213+6660C>A | |
1 | g.110061462C= | CA1149037145 | ALX3,STRIP1 | c.696G= (p.Val232=) c.267G= (p.Val89=) n.4213+6660C= | |
1 | g.110061462C>G | CA997525 | ALX3,STRIP1 | c.696G>C (p.Val232=) c.267G>C (p.Val89=) n.4213+6660C>G | dbSNP ExAC |
1 | g.110061462C>T | CA997526 | ALX3,STRIP1 | c.696G>A (p.Val232=) c.267G>A (p.Val89=) n.4213+6660C>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.110061463A>C | CA341581879 | ALX3,STRIP1 | c.695T>G (p.Val232Gly) c.266T>G (p.Val89Gly) n.4213+6661A>C | |
1 | g.110061463A>G | CA341581881 | ALX3,STRIP1 | c.695T>C (p.Val232Ala) c.266T>C (p.Val89Ala) n.4213+6661A>G |