Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
11 | g.44275372T>A | CA473833854 | ALX4 | c.753A>T (p.Thr251=) c.231A>T (p.Thr77=) | |
11 | g.44275372T>C | CA473833855 | ALX4 | c.753A>G (p.Thr251=) c.231A>G (p.Thr77=) | |
11 | g.44275372T>G | CA473833856 | ALX4 | c.753A>C (p.Thr251=) c.231A>C (p.Thr77=) | |
11 | g.44275373G>A | CA380182182 | ALX4 | c.752C>T (p.Thr251Ile) c.230C>T (p.Thr77Ile) | |
11 | g.44275373G>C | CA380182181 | ALX4 | c.752C>G (p.Thr251Arg) c.230C>G (p.Thr77Arg) | |
11 | g.44275373G>T | CA380182180 | ALX4 | c.752C>A (p.Thr251Lys) c.230C>A (p.Thr77Lys) | |
11 | g.44275374T>A | CA380182183 | ALX4 | c.751A>T (p.Thr251Ser) c.229A>T (p.Thr77Ser) | |
11 | g.44275374T>C | CA380182184 | ALX4 | c.751A>G (p.Thr251Ala) c.229A>G (p.Thr77Ala) | |
11 | g.44275374T>G | CA380182185 | ALX4 | c.751A>C (p.Thr251Pro) c.229A>C (p.Thr77Pro) | |
11 | g.44275375C>A | CA221497431 | ALX4 | c.750G>T (p.Arg250Ser) c.228G>T (p.Arg76Ser) | dbSNP |
11 | g.44275375C= | CA1967928908 | ALX4 | c.750G= (p.Arg250=) c.228G= (p.Arg76=) | |
11 | g.44275375C>G | CA380182186 | ALX4 | c.750G>C (p.Arg250Ser) c.228G>C (p.Arg76Ser) | |
11 | g.44275375C>T | CA473833857 | ALX4 | c.750G>A (p.Arg250=) c.228G>A (p.Arg76=) | dbSNP gnomAD v3 gnomAD v4 |
11 | g.44275376C>A | CA380182187 | ALX4 | c.749G>T (p.Arg250Met) c.227G>T (p.Arg76Met) | |
11 | g.44275376C= | CA1967928915 | ALX4 | c.749G= (p.Arg250=) c.227G= (p.Arg76=) | |
11 | g.44275376C>G | CA221497437 | ALX4 | c.749G>C (p.Arg250Thr) c.227G>C (p.Arg76Thr) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.44275376C>T | CA380182188 | ALX4 | c.749G>A (p.Arg250Lys) c.227G>A (p.Arg76Lys) | dbSNP |
11 | g.44275377T>A | CA380182189 | ALX4 | c.748A>T (p.Arg250Trp) c.226A>T (p.Arg76Trp) | |
11 | g.44275377T>C | CA380182190 | ALX4 | c.748A>G (p.Arg250Gly) c.226A>G (p.Arg76Gly) | |
11 | g.44275377T>G | CA473833860 | ALX4 | c.748A>C (p.Arg250=) c.226A>C (p.Arg76=) | |
11 | g.44275378C>A | CA380182191 | ALX4 | c.747G>T (p.Met249Ile) c.225G>T (p.Met75Ile) | |
11 | g.44275378C>G | CA380182192 | ALX4 | c.747G>C (p.Met249Ile) c.225G>C (p.Met75Ile) | |
11 | g.44275378C>T | CA380182193 | ALX4 | c.747G>A (p.Met249Ile) c.225G>A (p.Met75Ile) | |
11 | g.44275379A= | CA1967928919 | ALX4 | c.746T= (p.Met249=) c.224T= (p.Met75=) | |
11 | g.44275379A>C | CA380182195 | ALX4 | c.746T>G (p.Met249Arg) c.224T>G (p.Met75Arg) | |
11 | g.44275379A>G | CA5955665 | ALX4 | c.746T>C (p.Met249Thr) c.224T>C (p.Met75Thr) | dbSNP ExAC gnomAD v2 gnomAD v4 |
11 | g.44275379A>T | CA380182194 | ALX4 | c.746T>A (p.Met249Lys) c.224T>A (p.Met75Lys) | |
11 | g.44275380T>A | CA380182196 | ALX4 | c.745A>T (p.Met249Leu) c.223A>T (p.Met75Leu) | gnomAD v4 |
11 | g.44275380T>C | CA380182198 | ALX4 | c.745A>G (p.Met249Val) c.223A>G (p.Met75Val) | |
11 | g.44275380T>G | CA380182197 | ALX4 | c.745A>C (p.Met249Leu) c.223A>C (p.Met75Leu) | |
11 | g.44275381G>A | CA473833864 | ALX4 | c.744C>T (p.Ala248=) c.222C>T (p.Ala74=) | |
11 | g.44275381G>C | CA473833866 | ALX4 | c.744C>G (p.Ala248=) c.222C>G (p.Ala74=) | gnomAD v4 |
11 | g.44275381G>T | CA473833865 | ALX4 | c.744C>A (p.Ala248=) c.222C>A (p.Ala74=) | |
11 | g.44275382G>A | CA380182199 | ALX4 | c.743C>T (p.Ala248Val) c.221C>T (p.Ala74Val) | |
11 | g.44275382G>C | CA380182201 | ALX4 | c.743C>G (p.Ala248Gly) c.221C>G (p.Ala74Gly) | |
11 | g.44275382G>T | CA380182200 | ALX4 | c.743C>A (p.Ala248Asp) c.221C>A (p.Ala74Asp) | |
11 | g.44275383C>A | CA380182202 | ALX4 | c.742G>T (p.Ala248Ser) c.220G>T (p.Ala74Ser) | |
11 | g.44275383C>G | CA380182203 | ALX4 | c.742G>C (p.Ala248Pro) c.220G>C (p.Ala74Pro) | |
11 | g.44275383C>T | CA380182204 | ALX4 | c.742G>A (p.Ala248Thr) c.220G>A (p.Ala74Thr) | |
11 | g.44275384C>A | CA473833870 | ALX4 | c.741G>T (p.Leu247=) c.219G>T (p.Leu73=) | |
11 | g.44275384C= | CA1967928921 | ALX4 | c.741G= (p.Leu247=) c.219G= (p.Leu73=) | |
11 | g.44275384C>G | CA5955666 | ALX4 | c.741G>C (p.Leu247=) c.219G>C (p.Leu73=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.44275384C>T | CA473833871 | ALX4 | c.741G>A (p.Leu247=) c.219G>A (p.Leu73=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.44275385A>C | CA380182205 | ALX4 | c.740T>G (p.Leu247Arg) c.218T>G (p.Leu73Arg) | |
11 | g.44275385A>G | CA380182206 | ALX4 | c.740T>C (p.Leu247Pro) c.218T>C (p.Leu73Pro) | |
11 | g.44275385A>T | CA380182207 | ALX4 | c.740T>A (p.Leu247Gln) c.218T>A (p.Leu73Gln) | |
11 | g.44275386G>A | CA473833873 | ALX4 | c.739C>T (p.Leu247=) c.217C>T (p.Leu73=) | gnomAD v4 |
11 | g.44275386G>C | CA380182208 | ALX4 | c.739C>G (p.Leu247Val) c.217C>G (p.Leu73Val) | |
11 | g.44275386G= | CA1967928927 | ALX4 | c.739C= (p.Leu247=) c.217C= (p.Leu73=) | |
11 | g.44275386G>T | CA5955667 | ALX4 | c.739C>A (p.Leu247Met) c.217C>A (p.Leu73Met) | dbSNP ExAC gnomAD v2 gnomAD v4 |