| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 9 | g.77794571_77794573delinsATA | CA645561181 | GNAQ | c.625_627delinsTAT (p.Gln209Tyr) c.451_453delinsTAT (p.Gln151Tyr) | dbSNP COSMIC |
| 9 | g.77794572T>A | CA16602434 | GNAQ | c.626A>T (p.Gln209Leu) c.452A>T (p.Gln151Leu) | ClinVar dbSNP COSMIC |
| 9 | g.77794572T>C | CA16602435 | GNAQ | c.626A>G (p.Gln209Arg) c.452A>G (p.Gln151Arg) | ClinVar dbSNP COSMIC |
| 9 | g.77794572T>G | CA16602436 | GNAQ | c.626A>C (p.Gln209Pro) c.452A>C (p.Gln151Pro) | ClinVar dbSNP COSMIC |
| 9 | g.77794572T= | CA1857429449 | GNAQ | c.626A= (p.Gln209=) c.452A= (p.Gln151=) | |
| 9 | g.77794572_77794573delinsAA | CA16602757 | GNAQ | c.625_626delinsTT (p.Gln209Leu) c.451_452delinsTT (p.Gln151Leu) | ClinVar dbSNP COSMIC |
| 9 | g.77794572_77794573delinsTG | CA1857429443 | GNAQ | c.625_626delinsCA (p.Gln209=) c.451_452delinsCA (p.Gln151=) | |
| 9 | g.77794573G>A | CA373997885 | GNAQ | c.625C>T (p.Gln209Ter) c.451C>T (p.Gln151Ter) | |
| 9 | g.77794573G>C | CA373997886 | GNAQ | c.625C>G (p.Gln209Glu) c.451C>G (p.Gln151Glu) | |
| 9 | g.77794573G>T | CA373997887 | GNAQ | c.625C>A (p.Gln209Lys) c.451C>A (p.Gln151Lys) | dbSNP gnomAD v4 COSMIC |
| 9 | g.77794574G>A | CA465578342 | GNAQ | c.624C>T (p.Gly208=) c.450C>T (p.Gly150=) | gnomAD v4 |
| 9 | g.77794574G>C | CA465578341 | GNAQ | c.624C>G (p.Gly208=) c.450C>G (p.Gly150=) | gnomAD v4 |
| 9 | g.77794574G>T | CA465578340 | GNAQ | c.624C>A (p.Gly208=) c.450C>A (p.Gly150=) | |
| 9 | g.77794575C>A | CA373997888 | GNAQ | c.623G>T (p.Gly208Val) c.449G>T (p.Gly150Val) | dbSNP |
| 9 | g.77794575C>G | CA373997889 | GNAQ | c.623G>C (p.Gly208Ala) c.449G>C (p.Gly150Ala) | dbSNP |
| 9 | g.77794575C>T | CA373997890 | GNAQ | c.623G>A (p.Gly208Asp) c.449G>A (p.Gly150Asp) | dbSNP gnomAD v4 |
| 9 | g.77794579dup | CA2690385158 | GNAQ | c.623dup (p.Gln209ProfsTer13) c.449dup (p.Gln151ProfsTer13) | gnomAD v4 |
| 9 | g.77794579del | CA2580652612 | GNAQ | c.623del (p.Gly208AlafsTer22) c.449del (p.Gly150AlafsTer22) | |
| 9 | g.77794576C>A | CA373997891 | GNAQ | c.622G>T (p.Gly208Cys) c.448G>T (p.Gly150Cys) | dbSNP |
| 9 | g.77794576C>G | CA373997892 | GNAQ | c.622G>C (p.Gly208Arg) c.448G>C (p.Gly150Arg) | dbSNP |
| 9 | g.77794576C>T | CA373997893 | GNAQ | c.622G>A (p.Gly208Ser) c.448G>A (p.Gly150Ser) | dbSNP |
| 9 | g.77794577C>A | CA465578343 | GNAQ | c.621G>T (p.Gly207=) c.447G>T (p.Gly149=) | dbSNP |
| 9 | g.77794577C= | CA1857429454 | GNAQ | c.621G= (p.Gly207=) c.447G= (p.Gly149=) | |
| 9 | g.77794577C>G | CA465578344 | GNAQ | c.621G>C (p.Gly207=) c.447G>C (p.Gly149=) | dbSNP gnomAD v4 |
| 9 | g.77794577C>T | CA5094593 | GNAQ | c.621G>A (p.Gly207=) c.447G>A (p.Gly149=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.77794578C>A | CA373997896 | GNAQ | c.620G>T (p.Gly207Val) c.446G>T (p.Gly149Val) | dbSNP |
| 9 | g.77794578C>G | CA373997895 | GNAQ | c.620G>C (p.Gly207Ala) c.446G>C (p.Gly149Ala) | dbSNP |
| 9 | g.77794578C>T | CA373997894 | GNAQ | c.620G>A (p.Gly207Glu) c.446G>A (p.Gly149Glu) | dbSNP COSMIC |
| 9 | g.77794579C>A | CA373997897 | GNAQ | c.619G>T (p.Gly207Trp) c.445G>T (p.Gly149Trp) | dbSNP |
| 9 | g.77794579C>G | CA373997899 | GNAQ | c.619G>C (p.Gly207Arg) c.445G>C (p.Gly149Arg) | |
| 9 | g.77794579C>T | CA373997898 | GNAQ | c.619G>A (p.Gly207Arg) c.445G>A (p.Gly149Arg) | COSMIC |
| 9 | g.77794580T>A | CA465578345 | GNAQ | c.618A>T (p.Val206=) c.444A>T (p.Val148=) | dbSNP |
| 9 | g.77794580T>C | CA465578346 | GNAQ | c.618A>G (p.Val206=) c.444A>G (p.Val148=) | dbSNP gnomAD v4 |
| 9 | g.77794580T>G | CA465578347 | GNAQ | c.618A>C (p.Val206=) c.444A>C (p.Val148=) | gnomAD v4 |
| 9 | g.77794581A>C | CA373997900 | GNAQ | c.617T>G (p.Val206Gly) c.443T>G (p.Val148Gly) | dbSNP |
| 9 | g.77794581A>G | CA373997901 | GNAQ | c.617T>C (p.Val206Ala) c.443T>C (p.Val148Ala) | |
| 9 | g.77794581A>T | CA373997902 | GNAQ | c.617T>A (p.Val206Glu) c.443T>A (p.Val148Glu) | dbSNP |
| 9 | g.77794582C>A | CA373997903 | GNAQ | c.616G>T (p.Val206Leu) c.442G>T (p.Val148Leu) | |
| 9 | g.77794582C= | CA1857429457 | GNAQ | c.616G= (p.Val206=) c.442G= (p.Val148=) | |
| 9 | g.77794582C>G | CA373997904 | GNAQ | c.616G>C (p.Val206Leu) c.442G>C (p.Val148Leu) | dbSNP |
| 9 | g.77794582C>T | CA373997905 | GNAQ | c.616G>A (p.Val206Ile) c.442G>A (p.Val148Ile) | dbSNP gnomAD v4 COSMIC |
| 9 | g.77794583A= | CA1857429462 | GNAQ | c.615T= (p.Asp205=) c.441T= (p.Asp147=) | |
| 9 | g.77794583A>C | CA373997906 | GNAQ | c.615T>G (p.Asp205Glu) c.441T>G (p.Asp147Glu) | dbSNP |
| 9 | g.77794583A>G | CA465578348 | GNAQ | c.615T>C (p.Asp205=) c.441T>C (p.Asp147=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.77794583A>T | CA373997907 | GNAQ | c.615T>A (p.Asp205Glu) c.441T>A (p.Asp147Glu) | dbSNP |
| 9 | g.77794584T>A | CA373997908 | GNAQ | c.614A>T (p.Asp205Val) c.440A>T (p.Asp147Val) | dbSNP |
| 9 | g.77794584T>C | CA373997909 | GNAQ | c.614A>G (p.Asp205Gly) c.440A>G (p.Asp147Gly) | |
| 9 | g.77794584T>G | CA373997910 | GNAQ | c.614A>C (p.Asp205Ala) c.440A>C (p.Asp147Ala) | |
| 9 | g.77794585C>A | CA373997913 | GNAQ | c.613G>T (p.Asp205Tyr) c.439G>T (p.Asp147Tyr) | dbSNP |
| 9 | g.77794585C>G | CA373997911 | GNAQ | c.613G>C (p.Asp205His) c.439G>C (p.Asp147His) | dbSNP |