| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 17 | g.80108501T>A | CA401364928 | GAA | c.1088T>A (p.Met363Lys) | |
| 17 | g.80108501T>C | CA401364929 | GAA | c.1088T>C (p.Met363Thr) | |
| 17 | g.80108501T>G | CA8815165 | GAA | c.1088T>G (p.Met363Arg) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 17 | g.80108501T= | CA2277812785 | GAA | c.1088T= (p.Met363=) | |
| 17 | g.80108502G>A | CA401364932 | GAA | c.1089G>A (p.Met363Ile) | ClinVar |
| 17 | g.80108502G>C | CA401364930 | GAA | c.1089G>C (p.Met363Ile) | |
| 17 | g.80108502G>T | CA401364931 | GAA | c.1089G>T (p.Met363Ile) | gnomAD v4 |
| 17 | g.80108503C>A | CA401364933 | GAA | c.1090C>A (p.Pro364Thr) | |
| 17 | g.80108503C= | CA2277812786 | GAA | c.1090C= (p.Pro364=) | |
| 17 | g.80108503C>G | CA401364934 | GAA | c.1090C>G (p.Pro364Ala) | |
| 17 | g.80108503C>T | CA401364935 | GAA | c.1090C>T (p.Pro364Ser) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 17 | g.80108504del | CA2573154955 | GAA | c.1091del (p.Pro364ArgfsTer28) | ClinVar dbSNP |
| 17 | g.80108504C>A | CA401364936 | GAA | c.1091C>A (p.Pro364Gln) | gnomAD v4 |
| 17 | g.80108504C= | CA2277812787 | GAA | c.1091C= (p.Pro364=) | |
| 17 | g.80108504C>G | CA401364937 | GAA | c.1091C>G (p.Pro364Arg) | |
| 17 | g.80108504C>T | CA8815166 | GAA | c.1091C>T (p.Pro364Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 17 | g.80108505G>A | CA8815167 | GAA | c.1092G>A (p.Pro364=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 17 | g.80108505G>C | CA502402377 | GAA | c.1092G>C (p.Pro364=) | ClinVar gnomAD v4 |
| 17 | g.80108505G= | CA2277812788 | GAA | c.1092G= (p.Pro364=) | |
| 17 | g.80108505G>T | CA502402378 | GAA | c.1092G>T (p.Pro364=) | gnomAD v4 |
| 17 | g.80108506C>A | CA401364938 | GAA | c.1093C>A (p.Pro365Thr) | |
| 17 | g.80108506C= | CA2277812789 | GAA | c.1093C= (p.Pro365=) | |
| 17 | g.80108506C>G | CA401364939 | GAA | c.1093C>G (p.Pro365Ala) | |
| 17 | g.80108506C>T | CA8815168 | GAA | c.1093C>T (p.Pro365Ser) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 17 | g.80108507C>A | CA401364940 | GAA | c.1094C>A (p.Pro365Gln) | |
| 17 | g.80108507C>G | CA401364941 | GAA | c.1094C>G (p.Pro365Arg) | |
| 17 | g.80108507C>T | CA401364942 | GAA | c.1094C>T (p.Pro365Leu) | gnomAD v4 |
| 17 | g.80108508A= | CA2277812790 | GAA | c.1095A= (p.Pro365=) | |
| 17 | g.80108508A>C | CA502402379 | GAA | c.1095A>C (p.Pro365=) | ClinVar dbSNP gnomAD v4 |
| 17 | g.80108508A>G | CA502402380 | GAA | c.1095A>G (p.Pro365=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 17 | g.80108508A>T | CA502402381 | GAA | c.1095A>T (p.Pro365=) | |
| 17 | g.80108509T>A | CA401364943 | GAA | c.1096T>A (p.Tyr366Asn) | |
| 17 | g.80108509T>C | CA8815169 | GAA | c.1096T>C (p.Tyr366His) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 17 | g.80108509T>G | CA401364944 | GAA | c.1096T>G (p.Tyr366Asp) | |
| 17 | g.80108509T= | CA2277812791 | GAA | c.1096T= (p.Tyr366=) | |
| 17 | g.80108510A>C | CA401364945 | GAA | c.1097A>C (p.Tyr366Ser) | ClinVar dbSNP |
| 17 | g.80108510A>G | CA401364946 | GAA | c.1097A>G (p.Tyr366Cys) | gnomAD v4 |
| 17 | g.80108510A>T | CA401364947 | GAA | c.1097A>T (p.Tyr366Phe) | COSMIC |
| 17 | g.80108511C>A | CA401364948 | GAA | c.1098C>A (p.Tyr366Ter) | |
| 17 | g.80108511C>G | CA401364949 | GAA | c.1098C>G (p.Tyr366Ter) | |
| 17 | g.80108511C>T | CA502402382 | GAA | c.1098C>T (p.Tyr366=) | ClinVar dbSNP gnomAD v4 |
| 17 | g.80108511_80108512delinsCT | CA2277812792 | GAA | c.1098_1099delinsCT (p.Tyr366=) | |
| 17 | g.80108512del | CA16041888 | GAA | c.1099del (p.Trp367GlyfsTer25) | ClinVar dbSNP |
| 17 | g.80108512T>A | CA401364950 | GAA | c.1099T>A (p.Trp367Arg) | |
| 17 | g.80108512T>C | CA401364951 | GAA | c.1099T>C (p.Trp367Arg) | ClinVar dbSNP gnomAD v4 |
| 17 | g.80108512T>G | CA401364952 | GAA | c.1099T>G (p.Trp367Gly) | |
| 17 | g.80108512T= | CA2277812793 | GAA | c.1099T= (p.Trp367=) | |
| 17 | g.80108513G>A | CA401364953 | GAA | c.1100G>A (p.Trp367Ter) | ClinVar dbSNP gnomAD v2 |
| 17 | g.80108513G>C | CA401364954 | GAA | c.1100G>C (p.Trp367Ser) | |
| 17 | g.80108513G= | CA2277812794 | GAA | c.1100G= (p.Trp367=) |