Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
9 | g.77794520G>A | CA465578314 | GNAQ | c.678C>T (p.Ile226=) c.504C>T (p.Ile168=) | dbSNP |
9 | g.77794520G>C | CA373997760 | GNAQ | c.678C>G (p.Ile226Met) c.504C>G (p.Ile168Met) | dbSNP |
9 | g.77794520G>T | CA465578315 | GNAQ | c.678C>A (p.Ile226=) c.504C>A (p.Ile168=) | dbSNP gnomAD v4 |
9 | g.77794521A>C | CA373997761 | GNAQ | c.677T>G (p.Ile226Ser) c.503T>G (p.Ile168Ser) | |
9 | g.77794521A>G | CA373997762 | GNAQ | c.677T>C (p.Ile226Thr) c.503T>C (p.Ile168Thr) | dbSNP gnomAD v4 |
9 | g.77794521A>T | CA373997763 | GNAQ | c.677T>A (p.Ile226Asn) c.503T>A (p.Ile168Asn) | dbSNP |
9 | g.77794522T>A | CA373997764 | GNAQ | c.676A>T (p.Ile226Phe) c.502A>T (p.Ile168Phe) | dbSNP |
9 | g.77794522T>C | CA194717256 | GNAQ | c.676A>G (p.Ile226Val) c.502A>G (p.Ile168Val) | dbSNP gnomAD v4 COSMIC |
9 | g.77794522T>G | CA373997765 | GNAQ | c.676A>C (p.Ile226Leu) c.502A>C (p.Ile168Leu) | gnomAD v4 |
9 | g.77794522T= | CA1857429407 | GNAQ | c.676A= (p.Ile226=) c.502A= (p.Ile168=) | |
9 | g.77794523A>C | CA465578317 | GNAQ | c.675T>G (p.Ser225=) c.501T>G (p.Ser167=) | |
9 | g.77794523A>G | CA465578318 | GNAQ | c.675T>C (p.Ser225=) c.501T>C (p.Ser167=) | dbSNP |
9 | g.77794523A>T | CA465578316 | GNAQ | c.675T>A (p.Ser225=) c.501T>A (p.Ser167=) | dbSNP |
9 | g.77794524G>A | CA373997766 | GNAQ | c.674C>T (p.Ser225Phe) c.500C>T (p.Ser167Phe) | dbSNP |
9 | g.77794524G>C | CA373997767 | GNAQ | c.674C>G (p.Ser225Cys) c.500C>G (p.Ser167Cys) | dbSNP |
9 | g.77794524G>T | CA373997768 | GNAQ | c.674C>A (p.Ser225Tyr) c.500C>A (p.Ser167Tyr) | dbSNP gnomAD v4 |
9 | g.77794525A>C | CA373997769 | GNAQ | c.673T>G (p.Ser225Ala) c.499T>G (p.Ser167Ala) | |
9 | g.77794525A>G | CA373997770 | GNAQ | c.673T>C (p.Ser225Pro) c.499T>C (p.Ser167Pro) | gnomAD v4 COSMIC |
9 | g.77794525A>T | CA373997771 | GNAQ | c.673T>A (p.Ser225Thr) c.499T>A (p.Ser167Thr) | dbSNP |
9 | g.77794526G>A | CA465578319 | GNAQ | c.672C>T (p.Thr224=) c.498C>T (p.Thr166=) | dbSNP |
9 | g.77794526G>C | CA465578320 | GNAQ | c.672C>G (p.Thr224=) c.498C>G (p.Thr166=) | |
9 | g.77794526G>T | CA465578321 | GNAQ | c.672C>A (p.Thr224=) c.498C>A (p.Thr166=) | dbSNP |
9 | g.77794527G>A | CA373997774 | GNAQ | c.671C>T (p.Thr224Ile) c.497C>T (p.Thr166Ile) | dbSNP |
9 | g.77794527G>C | CA373997772 | GNAQ | c.671C>G (p.Thr224Ser) c.497C>G (p.Thr166Ser) | dbSNP |
9 | g.77794527G>T | CA373997773 | GNAQ | c.671C>A (p.Thr224Asn) c.497C>A (p.Thr166Asn) | dbSNP COSMIC |
9 | g.77794528T>A | CA373997775 | GNAQ | c.670A>T (p.Thr224Ser) c.496A>T (p.Thr166Ser) | dbSNP |
9 | g.77794528T>C | CA373997776 | GNAQ | c.670A>G (p.Thr224Ala) c.496A>G (p.Thr166Ala) | |
9 | g.77794528T>G | CA373997777 | GNAQ | c.670A>C (p.Thr224Pro) c.496A>C (p.Thr166Pro) | dbSNP |
9 | g.77794529G>A | CA465578324 | GNAQ | c.669C>T (p.Val223=) c.495C>T (p.Val165=) | dbSNP |
9 | g.77794529G>C | CA465578323 | GNAQ | c.669C>G (p.Val223=) c.495C>G (p.Val165=) | dbSNP |
9 | g.77794529G>T | CA465578322 | GNAQ | c.669C>A (p.Val223=) c.495C>A (p.Val165=) | gnomAD v4 |
9 | g.77794530A>C | CA373997778 | GNAQ | c.668T>G (p.Val223Gly) c.494T>G (p.Val165Gly) | |
9 | g.77794530A>G | CA373997779 | GNAQ | c.668T>C (p.Val223Ala) c.494T>C (p.Val165Ala) | dbSNP |
9 | g.77794530A>T | CA373997780 | GNAQ | c.668T>A (p.Val223Asp) c.494T>A (p.Val165Asp) | dbSNP |
9 | g.77794531C>A | CA373997783 | GNAQ | c.667G>T (p.Val223Phe) c.493G>T (p.Val165Phe) | dbSNP |
9 | g.77794531C>G | CA373997782 | GNAQ | c.667G>C (p.Val223Leu) c.493G>C (p.Val165Leu) | dbSNP |
9 | g.77794531C>T | CA373997781 | GNAQ | c.667G>A (p.Val223Ile) c.493G>A (p.Val165Ile) | dbSNP gnomAD v4 |
9 | g.77794532A= | CA1857429411 | GNAQ | c.666T= (p.Asn222=) c.492T= (p.Asn164=) | |
9 | g.77794532A>C | CA373997784 | GNAQ | c.666T>G (p.Asn222Lys) c.492T>G (p.Asn164Lys) | |
9 | g.77794532A>G | CA5094590 | GNAQ | c.666T>C (p.Asn222=) c.492T>C (p.Asn164=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.77794532A>T | CA373997785 | GNAQ | c.666T>A (p.Asn222Lys) c.492T>A (p.Asn164Lys) | |
9 | g.77794533T>A | CA373997786 | GNAQ | c.665A>T (p.Asn222Ile) c.491A>T (p.Asn164Ile) | dbSNP |
9 | g.77794533T>C | CA373997787 | GNAQ | c.665A>G (p.Asn222Ser) c.491A>G (p.Asn164Ser) | dbSNP gnomAD v4 |
9 | g.77794533T>G | CA373997788 | GNAQ | c.665A>C (p.Asn222Thr) c.491A>C (p.Asn164Thr) | |
9 | g.77794533T= | CA1857429413 | GNAQ | c.665A= (p.Asn222=) c.491A= (p.Asn164=) | |
9 | g.77794534T>A | CA373997791 | GNAQ | c.664A>T (p.Asn222Tyr) c.490A>T (p.Asn164Tyr) | dbSNP |
9 | g.77794534T>C | CA373997789 | GNAQ | c.664A>G (p.Asn222Asp) c.490A>G (p.Asn164Asp) | |
9 | g.77794534T>G | CA373997790 | GNAQ | c.664A>C (p.Asn222His) c.490A>C (p.Asn164His) | |
9 | g.77794535T>A | CA373997792 | GNAQ | c.663A>T (p.Glu221Asp) c.489A>T (p.Glu163Asp) | |
9 | g.77794535T>C | CA465578325 | GNAQ | c.663A>G (p.Glu221=) c.489A>G (p.Glu163=) | dbSNP |
9 | g.77794535T>G | CA373997793 | GNAQ | c.663A>C (p.Glu221Asp) c.489A>C (p.Glu163Asp) | |
9 | g.77794536T>A | CA373997794 | GNAQ | c.662A>T (p.Glu221Val) c.488A>T (p.Glu163Val) | |
9 | g.77794536T>C | CA373997795 | GNAQ | c.662A>G (p.Glu221Gly) c.488A>G (p.Glu163Gly) | |
9 | g.77794536T>G | CA373997796 | GNAQ | c.662A>C (p.Glu221Ala) c.488A>C (p.Glu163Ala) | |
9 | g.77794537C>A | CA373997797 | GNAQ | c.661G>T (p.Glu221Ter) c.487G>T (p.Glu163Ter) | |
9 | g.77794537C>G | CA373997798 | GNAQ | c.661G>C (p.Glu221Gln) c.487G>C (p.Glu163Gln) | dbSNP |
9 | g.77794537C>T | CA373997799 | GNAQ | c.661G>A (p.Glu221Lys) c.487G>A (p.Glu163Lys) | dbSNP |
9 | g.77794538A>C | CA373997800 | GNAQ | c.660T>G (p.Phe220Leu) c.486T>G (p.Phe162Leu) | gnomAD v4 |
9 | g.77794538A>G | CA465578326 | GNAQ | c.660T>C (p.Phe220=) c.486T>C (p.Phe162=) | |
9 | g.77794538A>T | CA373997801 | GNAQ | c.660T>A (p.Phe220Leu) c.486T>A (p.Phe162Leu) | dbSNP |
9 | g.77794539A>C | CA373997802 | GNAQ | c.659T>G (p.Phe220Cys) c.485T>G (p.Phe162Cys) | |
9 | g.77794539A>G | CA373997803 | GNAQ | c.659T>C (p.Phe220Ser) c.485T>C (p.Phe162Ser) | |
9 | g.77794539A>T | CA373997804 | GNAQ | c.659T>A (p.Phe220Tyr) c.485T>A (p.Phe162Tyr) | dbSNP |
9 | g.77794540A>C | CA373997805 | GNAQ | c.658T>G (p.Phe220Val) c.484T>G (p.Phe162Val) | |
9 | g.77794540A>G | CA373997807 | GNAQ | c.658T>C (p.Phe220Leu) c.484T>C (p.Phe162Leu) | |
9 | g.77794540A>T | CA373997806 | GNAQ | c.658T>A (p.Phe220Ile) c.484T>A (p.Phe162Ile) | dbSNP |
9 | g.77794541G>A | CA5094591 | GNAQ | c.657C>T (p.Cys219=) c.483C>T (p.Cys161=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.77794541G>C | CA373997808 | GNAQ | c.657C>G (p.Cys219Trp) c.483C>G (p.Cys161Trp) | dbSNP |
9 | g.77794541G= | CA1857429416 | GNAQ | c.657C= (p.Cys219=) c.483C= (p.Cys161=) | |
9 | g.77794541G>T | CA373997809 | GNAQ | c.657C>A (p.Cys219Ter) c.483C>A (p.Cys161Ter) | dbSNP gnomAD v4 |
9 | g.77794542C>A | CA373997810 | GNAQ | c.656G>T (p.Cys219Phe) c.482G>T (p.Cys161Phe) | dbSNP |
9 | g.77794542C>G | CA373997811 | GNAQ | c.656G>C (p.Cys219Ser) c.482G>C (p.Cys161Ser) | dbSNP |
9 | g.77794542C>T | CA373997812 | GNAQ | c.656G>A (p.Cys219Tyr) c.482G>A (p.Cys161Tyr) | dbSNP gnomAD v4 |
9 | g.77794543A>C | CA373997815 | GNAQ | c.655T>G (p.Cys219Gly) c.481T>G (p.Cys161Gly) | |
9 | g.77794543A>G | CA373997813 | GNAQ | c.655T>C (p.Cys219Arg) c.481T>C (p.Cys161Arg) | |
9 | g.77794543A>T | CA373997814 | GNAQ | c.655T>A (p.Cys219Ser) c.481T>A (p.Cys161Ser) | dbSNP |
9 | g.77794544G>A | CA465578327 | GNAQ | c.654C>T (p.His218=) c.480C>T (p.His160=) | dbSNP gnomAD v4 |
9 | g.77794544G>C | CA373997816 | GNAQ | c.654C>G (p.His218Gln) c.480C>G (p.His160Gln) | |
9 | g.77794544G= | CA1857429420 | GNAQ | c.654C= (p.His218=) c.480C= (p.His160=) | |
9 | g.77794544G>T | CA373997817 | GNAQ | c.654C>A (p.His218Gln) c.480C>A (p.His160Gln) | dbSNP |
9 | g.77794545T>A | CA373997818 | GNAQ | c.653A>T (p.His218Leu) c.479A>T (p.His160Leu) | dbSNP |
9 | g.77794545T>C | CA373997819 | GNAQ | c.653A>G (p.His218Arg) c.479A>G (p.His160Arg) | |
9 | g.77794545T>G | CA373997820 | GNAQ | c.653A>C (p.His218Pro) c.479A>C (p.His160Pro) | |
9 | g.77794546G>A | CA373997821 | GNAQ | c.652C>T (p.His218Tyr) c.478C>T (p.His160Tyr) | dbSNP |
9 | g.77794546G>C | CA373997823 | GNAQ | c.652C>G (p.His218Asp) c.478C>G (p.His160Asp) | dbSNP |
9 | g.77794546G>T | CA373997822 | GNAQ | c.652C>A (p.His218Asn) c.478C>A (p.His160Asn) | dbSNP |
9 | g.77794547T>A | CA465578328 | GNAQ | c.651A>T (p.Ile217=) c.477A>T (p.Ile159=) | dbSNP |
9 | g.77794547T>C | CA373997824 | GNAQ | c.651A>G (p.Ile217Met) c.477A>G (p.Ile159Met) | |
9 | g.77794547T>G | CA465578329 | GNAQ | c.651A>C (p.Ile217=) c.477A>C (p.Ile159=) | |
9 | g.77794547T= | CA1857429422 | GNAQ | c.651A= (p.Ile217=) c.477A= (p.Ile159=) | |
9 | g.77794548A>C | CA373997825 | GNAQ | c.650T>G (p.Ile217Arg) c.476T>G (p.Ile159Arg) | |
9 | g.77794548A>G | CA373997826 | GNAQ | c.650T>C (p.Ile217Thr) c.476T>C (p.Ile159Thr) | |
9 | g.77794548A>T | CA373997827 | GNAQ | c.650T>A (p.Ile217Lys) c.476T>A (p.Ile159Lys) | |
9 | g.77794549T>A | CA373997828 | GNAQ | c.649A>T (p.Ile217Leu) c.475A>T (p.Ile159Leu) | |
9 | g.77794549T>C | CA373997829 | GNAQ | c.649A>G (p.Ile217Val) c.475A>G (p.Ile159Val) | gnomAD v4 |
9 | g.77794549T>G | CA373997830 | GNAQ | c.649A>C (p.Ile217Leu) c.475A>C (p.Ile159Leu) | |
9 | g.77794550C>A | CA373997831 | GNAQ | c.648G>T (p.Trp216Cys) c.474G>T (p.Trp158Cys) | dbSNP |
9 | g.77794550C>G | CA373997832 | GNAQ | c.648G>C (p.Trp216Cys) c.474G>C (p.Trp158Cys) | dbSNP |
9 | g.77794550C>T | CA373997833 | GNAQ | c.648G>A (p.Trp216Ter) c.474G>A (p.Trp158Ter) | dbSNP |
9 | g.77794551del | CA2719856287 | GNAQ | c.648del (p.Trp216Ter) c.474del (p.Trp158Ter) | dbSNP |
9 | g.77794551C>A | CA373997834 | GNAQ | c.647G>T (p.Trp216Leu) c.473G>T (p.Trp158Leu) | dbSNP |
9 | g.77794551C>G | CA373997836 | GNAQ | c.647G>C (p.Trp216Ser) c.473G>C (p.Trp158Ser) | dbSNP |
9 | g.77794551C>T | CA373997835 | GNAQ | c.647G>A (p.Trp216Ter) c.473G>A (p.Trp158Ter) | dbSNP |
9 | g.77794552A>C | CA373997837 | GNAQ | c.646T>G (p.Trp216Gly) c.472T>G (p.Trp158Gly) | |
9 | g.77794552A>G | CA373997839 | GNAQ | c.646T>C (p.Trp216Arg) c.472T>C (p.Trp158Arg) | |
9 | g.77794552A>T | CA373997838 | GNAQ | c.646T>A (p.Trp216Arg) c.472T>A (p.Trp158Arg) | |
9 | g.77794553T>A | CA373997840 | GNAQ | c.645A>T (p.Lys215Asn) c.471A>T (p.Lys157Asn) | dbSNP |
9 | g.77794553T>C | CA5094592 | GNAQ | c.645A>G (p.Lys215=) c.471A>G (p.Lys157=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
9 | g.77794553T>G | CA373997841 | GNAQ | c.645A>C (p.Lys215Asn) c.471A>C (p.Lys157Asn) | |
9 | g.77794553T= | CA1857429425 | GNAQ | c.645A= (p.Lys215=) c.471A= (p.Lys157=) | |
9 | g.77794556del | CA645561180 | GNAQ | c.645del (p.Lys215AsnfsTer15) c.471del (p.Lys157AsnfsTer15) | COSMIC |
9 | g.77794554T>A | CA373997842 | GNAQ | c.644A>T (p.Lys215Ile) c.470A>T (p.Lys157Ile) | dbSNP |
9 | g.77794554T>C | CA373997844 | GNAQ | c.644A>G (p.Lys215Arg) c.470A>G (p.Lys157Arg) | |
9 | g.77794554T>G | CA373997843 | GNAQ | c.644A>C (p.Lys215Thr) c.470A>C (p.Lys157Thr) | |
9 | g.77794555T>A | CA373997845 | GNAQ | c.643A>T (p.Lys215Ter) c.469A>T (p.Lys157Ter) | |
9 | g.77794555T>C | CA373997846 | GNAQ | c.643A>G (p.Lys215Glu) c.469A>G (p.Lys157Glu) | |
9 | g.77794555T>G | CA373997847 | GNAQ | c.643A>C (p.Lys215Gln) c.469A>C (p.Lys157Gln) | |
9 | g.77794556T>A | CA373997848 | GNAQ | c.642A>T (p.Arg214Ser) c.468A>T (p.Arg156Ser) | dbSNP |
9 | g.77794556T>C | CA465578330 | GNAQ | c.642A>G (p.Arg214=) c.468A>G (p.Arg156=) | |
9 | g.77794556T>G | CA373997849 | GNAQ | c.642A>C (p.Arg214Ser) c.468A>C (p.Arg156Ser) | |
9 | g.77794557C>A | CA373997850 | GNAQ | c.641G>T (p.Arg214Ile) c.467G>T (p.Arg156Ile) | |
9 | g.77794557C>G | CA373997851 | GNAQ | c.641G>C (p.Arg214Thr) c.467G>C (p.Arg156Thr) | dbSNP |
9 | g.77794557C>T | CA373997852 | GNAQ | c.641G>A (p.Arg214Lys) c.467G>A (p.Arg156Lys) | dbSNP |
9 | g.77794558T>A | CA373997853 | GNAQ | c.640A>T (p.Arg214Ter) c.466A>T (p.Arg156Ter) | |
9 | g.77794558T>C | CA373997854 | GNAQ | c.640A>G (p.Arg214Gly) c.466A>G (p.Arg156Gly) | |
9 | g.77794558T>G | CA465578331 | GNAQ | c.640A>C (p.Arg214=) c.466A>C (p.Arg156=) | |
9 | g.77794559T>A | CA373997855 | GNAQ | c.639A>T (p.Arg213Ser) c.465A>T (p.Arg155Ser) | dbSNP |
9 | g.77794559T>C | CA465578332 | GNAQ | c.639A>G (p.Arg213=) c.465A>G (p.Arg155=) | |
9 | g.77794559T>G | CA373997856 | GNAQ | c.639A>C (p.Arg213Ser) c.465A>C (p.Arg155Ser) | |
9 | g.77794560C>A | CA373997859 | GNAQ | c.638G>T (p.Arg213Ile) c.464G>T (p.Arg155Ile) | dbSNP |
9 | g.77794560C>G | CA373997857 | GNAQ | c.638G>C (p.Arg213Thr) c.464G>C (p.Arg155Thr) | dbSNP |
9 | g.77794560C>T | CA373997858 | GNAQ | c.638G>A (p.Arg213Lys) c.464G>A (p.Arg155Lys) | dbSNP |
9 | g.77794561T>A | CA373997860 | GNAQ | c.637A>T (p.Arg213Ter) c.463A>T (p.Arg155Ter) | dbSNP |
9 | g.77794561T>C | CA373997861 | GNAQ | c.637A>G (p.Arg213Gly) c.463A>G (p.Arg155Gly) | |
9 | g.77794561T>G | CA465578333 | GNAQ | c.637A>C (p.Arg213=) c.463A>C (p.Arg155=) | |
9 | g.77794562C>A | CA373997862 | GNAQ | c.636G>T (p.Glu212Asp) c.462G>T (p.Glu154Asp) | |
9 | g.77794562C>G | CA373997863 | GNAQ | c.636G>C (p.Glu212Asp) c.462G>C (p.Glu154Asp) | |
9 | g.77794562C>T | CA465578334 | GNAQ | c.636G>A (p.Glu212=) c.462G>A (p.Glu154=) | gnomAD v4 |
9 | g.77794563T>A | CA373997864 | GNAQ | c.635A>T (p.Glu212Val) c.461A>T (p.Glu154Val) | dbSNP |
9 | g.77794563T>C | CA373997865 | GNAQ | c.635A>G (p.Glu212Gly) c.461A>G (p.Glu154Gly) | |
9 | g.77794563T>G | CA373997866 | GNAQ | c.635A>C (p.Glu212Ala) c.461A>C (p.Glu154Ala) | |
9 | g.77794564C>A | CA373997867 | GNAQ | c.634G>T (p.Glu212Ter) c.460G>T (p.Glu154Ter) | dbSNP |
9 | g.77794564C>G | CA373997868 | GNAQ | c.634G>C (p.Glu212Gln) c.460G>C (p.Glu154Gln) | dbSNP |
9 | g.77794564C>T | CA373997869 | GNAQ | c.634G>A (p.Glu212Lys) c.460G>A (p.Glu154Lys) | dbSNP |
9 | g.77794565T>A | CA465578335 | GNAQ | c.633A>T (p.Ser211=) c.459A>T (p.Ser153=) | |
9 | g.77794565T>C | CA465578336 | GNAQ | c.633A>G (p.Ser211=) c.459A>G (p.Ser153=) | dbSNP gnomAD v4 |
9 | g.77794565T>G | CA465578337 | GNAQ | c.633A>C (p.Ser211=) c.459A>C (p.Ser153=) | |
9 | g.77794566G>A | CA373997872 | GNAQ | c.632C>T (p.Ser211Leu) c.458C>T (p.Ser153Leu) | dbSNP COSMIC |
9 | g.77794566G>C | CA373997871 | GNAQ | c.632C>G (p.Ser211Ter) c.458C>G (p.Ser153Ter) | dbSNP |
9 | g.77794566G>T | CA373997870 | GNAQ | c.632C>A (p.Ser211Ter) c.458C>A (p.Ser153Ter) | gnomAD v4 |
9 | g.77794567A>C | CA373997873 | GNAQ | c.631T>G (p.Ser211Ala) c.457T>G (p.Ser153Ala) | dbSNP |
9 | g.77794567A>G | CA373997874 | GNAQ | c.631T>C (p.Ser211Pro) c.457T>C (p.Ser153Pro) | |
9 | g.77794567A>T | CA373997875 | GNAQ | c.631T>A (p.Ser211Thr) c.457T>A (p.Ser153Thr) | dbSNP |
9 | g.77794568C>A | CA373997876 | GNAQ | c.630G>T (p.Arg210Ser) c.456G>T (p.Arg152Ser) | |
9 | g.77794568C= | CA1857429429 | GNAQ | c.630G= (p.Arg210=) c.456G= (p.Arg152=) | |
9 | g.77794568C>G | CA373997877 | GNAQ | c.630G>C (p.Arg210Ser) c.456G>C (p.Arg152Ser) | |
9 | g.77794568C>T | CA194717257 | GNAQ | c.630G>A (p.Arg210=) c.456G>A (p.Arg152=) | dbSNP gnomAD v4 |
9 | g.77794569C>A | CA373997878 | GNAQ | c.629G>T (p.Arg210Met) c.455G>T (p.Arg152Met) | |
9 | g.77794569C>G | CA373997879 | GNAQ | c.629G>C (p.Arg210Thr) c.455G>C (p.Arg152Thr) | |
9 | g.77794569C>T | CA373997880 | GNAQ | c.629G>A (p.Arg210Lys) c.455G>A (p.Arg152Lys) | dbSNP gnomAD v3 gnomAD v4 COSMIC |
9 | g.77794570T>A | CA373997881 | GNAQ | c.628A>T (p.Arg210Trp) c.454A>T (p.Arg152Trp) | dbSNP |
9 | g.77794570T>C | CA373997882 | GNAQ | c.628A>G (p.Arg210Gly) c.454A>G (p.Arg152Gly) | dbSNP gnomAD v4 |
9 | g.77794570T>G | CA465578338 | GNAQ | c.628A>C (p.Arg210=) c.454A>C (p.Arg152=) | dbSNP gnomAD v4 |
9 | g.77794571T>A | CA373997883 | GNAQ | c.627A>T (p.Gln209His) c.453A>T (p.Gln151His) | ClinVar dbSNP COSMIC |
9 | g.77794571T>C | CA465578339 | GNAQ | c.627A>G (p.Gln209=) c.453A>G (p.Gln151=) | dbSNP gnomAD v4 |
9 | g.77794571T>G | CA373997884 | GNAQ | c.627A>C (p.Gln209His) c.453A>C (p.Gln151His) | ClinVar dbSNP COSMIC |
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 |
9 | g.77794585C>T | CA373997912 | GNAQ | c.613G>A (p.Asp205Asn) c.439G>A (p.Asp147Asn) | dbSNP |
9 | g.77794586G>A | CA5094594 | GNAQ | c.612C>T (p.Val204=) c.438C>T (p.Val146=) | dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
9 | g.77794586G>C | CA465578349 | GNAQ | c.612C>G (p.Val204=) c.438C>G (p.Val146=) | dbSNP |
9 | g.77794586G= | CA1857429464 | GNAQ | c.612C= (p.Val204=) c.438C= (p.Val146=) | |
9 | g.77794586G>T | CA465578350 | GNAQ | c.612C>A (p.Val204=) c.438C>A (p.Val146=) | dbSNP gnomAD v4 |
9 | g.77794587A>C | CA373997914 | GNAQ | c.611T>G (p.Val204Gly) c.437T>G (p.Val146Gly) | |
9 | g.77794587A>G | CA373997915 | GNAQ | c.611T>C (p.Val204Ala) c.437T>C (p.Val146Ala) | gnomAD v4 |
9 | g.77794587A>T | CA373997916 | GNAQ | c.611T>A (p.Val204Asp) c.437T>A (p.Val146Asp) | |
9 | g.77794588C>A | CA373997917 | GNAQ | c.610G>T (p.Val204Phe) c.436G>T (p.Val146Phe) | dbSNP |
9 | g.77794588C>G | CA373997918 | GNAQ | c.610G>C (p.Val204Leu) c.436G>C (p.Val146Leu) | dbSNP |
9 | g.77794588C>T | CA373997919 | GNAQ | c.610G>A (p.Val204Ile) c.436G>A (p.Val146Ile) | dbSNP |
9 | g.77794589del | CA2719858479 | GNAQ | c.610del (p.Val204SerfsTer3) c.436del (p.Val146SerfsTer3) | dbSNP |
9 | g.77794589C>A | CA373997920 | GNAQ | c.609G>T (p.Met203Ile) c.435G>T (p.Met145Ile) | dbSNP gnomAD v4 |
9 | g.77794589C>G | CA373997921 | GNAQ | c.609G>C (p.Met203Ile) c.435G>C (p.Met145Ile) | |
9 | g.77794589C>T | CA373997922 | GNAQ | c.609G>A (p.Met203Ile) c.435G>A (p.Met145Ile) | |
9 | g.77794590A= | CA1857429468 | GNAQ | c.608T= (p.Met203=) c.434T= (p.Met145=) | |
9 | g.77794590A>C | CA373997924 | GNAQ | c.608T>G (p.Met203Arg) c.434T>G (p.Met145Arg) | dbSNP |
9 | g.77794590A>G | CA373997925 | GNAQ | c.608T>C (p.Met203Thr) c.434T>C (p.Met145Thr) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.77794590A>T | CA373997923 | GNAQ | c.608T>A (p.Met203Lys) c.434T>A (p.Met145Lys) | dbSNP |
9 | g.77794591T>A | CA373997926 | GNAQ | c.607A>T (p.Met203Leu) c.433A>T (p.Met145Leu) | dbSNP |
9 | g.77794591T>C | CA373997927 | GNAQ | c.607A>G (p.Met203Val) c.433A>G (p.Met145Val) | dbSNP |
9 | g.77794591T>G | CA373997928 | GNAQ | c.607A>C (p.Met203Leu) c.433A>C (p.Met145Leu) | |
9 | g.77794591T= | CA1857429472 | GNAQ | c.607A= (p.Met203=) c.433A= (p.Met145=) | |
9 | g.77794592T>A | CA373997929 | GNAQ | c.606A>T (p.Arg202Ser) c.432A>T (p.Arg144Ser) | dbSNP |
9 | g.77794592T>C | CA465578354 | GNAQ | c.606A>G (p.Arg202=) c.432A>G (p.Arg144=) | |
9 | g.77794592T>G | CA373997930 | GNAQ | c.606A>C (p.Arg202Ser) c.432A>C (p.Arg144Ser) | |
9 | g.77794593C>A | CA373997931 | GNAQ | c.606-1G>T (n.606-1G>T) c.432-1G>T (n.432-1G>T) | dbSNP |
9 | g.77794593C>G | CA373997932 | GNAQ | c.606-1G>C (n.606-1G>C) c.432-1G>C (n.432-1G>C) | dbSNP |
9 | g.77794593C>T | CA373997933 | GNAQ | c.606-1G>A (n.606-1G>A) c.432-1G>A (n.432-1G>A) | dbSNP gnomAD v4 |
9 | g.77794594T>A | CA373997934 | GNAQ | c.606-2A>T (n.606-2A>T) c.432-2A>T (n.432-2A>T) | dbSNP |
9 | g.77794594T>C | CA373997935 | GNAQ | c.606-2A>G (n.606-2A>G) c.432-2A>G (n.432-2A>G) | dbSNP |
9 | g.77794594T>G | CA373997936 | GNAQ | c.606-2A>C (n.606-2A>C) c.432-2A>C (n.432-2A>C) | |
9 | g.77794595G>A | CA2690385159 | GNAQ | c.606-3C>T (n.606-3C>T) c.432-3C>T (n.432-3C>T) | dbSNP gnomAD v4 |
9 | g.77794595G>C | CA2719858703 | GNAQ | c.606-3C>G (n.606-3C>G) c.432-3C>G (n.432-3C>G) | dbSNP |
9 | g.77794595G>T | CA2690385160 | GNAQ | c.606-3C>A (n.606-3C>A) c.432-3C>A (n.432-3C>A) | dbSNP gnomAD v4 |
9 | g.77794596C>A | CA1125711858 | GNAQ | c.606-4G>T (n.606-4G>T) c.432-4G>T (n.432-4G>T) | dbSNP gnomAD v3 gnomAD v4 |
9 | g.77794596C= | CA1857429474 | GNAQ | c.606-4G= (n.606-4G=) c.432-4G= (n.432-4G=) | |
9 | g.77794596C>G | CA2719690288 | GNAQ | c.606-4G>C (n.606-4G>C) c.432-4G>C (n.432-4G>C) | dbSNP |
9 | g.77794596C>T | CA2579361430 | GNAQ | c.606-4G>A (n.606-4G>A) c.432-4G>A (n.432-4G>A) | dbSNP |
9 | g.77794597A>G | CA2690385161 | GNAQ | c.606-5T>C (n.606-5T>C) c.432-5T>C (n.432-5T>C) | dbSNP gnomAD v4 |
9 | g.77794597A>T | CA2719858738 | GNAQ | c.606-5T>A (n.606-5T>A) c.432-5T>A (n.432-5T>A) | dbSNP |
9 | g.77794598A>G | CA2719858750 | GNAQ | c.606-6T>C (n.606-6T>C) c.432-6T>C (n.432-6T>C) | dbSNP |
9 | g.77794598A>T | CA2719858749 | GNAQ | c.606-6T>A (n.606-6T>A) c.432-6T>A (n.432-6T>A) | dbSNP |
9 | g.77794599G>A | CA2690385162 | GNAQ | c.606-7C>T (n.606-7C>T) c.432-7C>T (n.432-7C>T) | gnomAD v4 |
9 | g.77794599G>C | CA2719858753 | GNAQ | c.606-7C>G (n.606-7C>G) c.432-7C>G (n.432-7C>G) | dbSNP |
9 | g.77794599G>T | CA2690385163 | GNAQ | c.606-7C>A (n.606-7C>A) c.432-7C>A (n.432-7C>A) | gnomAD v4 |
9 | g.77794600G>T | CA2690385164 | GNAQ | c.606-8C>A (n.606-8C>A) c.432-8C>A (n.432-8C>A) | gnomAD v4 |
9 | g.77794602T>A | CA2719858754 | GNAQ | c.606-10A>T (n.606-10A>T) c.432-10A>T (n.432-10A>T) | dbSNP |
9 | g.77794602T>C | CA2690385165 | GNAQ | c.606-10A>G (n.606-10A>G) c.432-10A>G (n.432-10A>G) | gnomAD v4 |
9 | g.77794603A>T | CA2719858857 | GNAQ | c.606-11T>A (n.606-11T>A) c.432-11T>A (n.432-11T>A) | dbSNP |
9 | g.77794604A>C | CA2719858859 | GNAQ | c.606-12T>G (n.606-12T>G) c.432-12T>G (n.432-12T>G) | dbSNP |
9 | g.77794604A>G | CA2719858861 | GNAQ | c.606-12T>C (n.606-12T>C) c.432-12T>C (n.432-12T>C) | dbSNP |
9 | g.77794604A>T | CA2719858860 | GNAQ | c.606-12T>A (n.606-12T>A) c.432-12T>A (n.432-12T>A) | dbSNP |
9 | g.77794605C>A | CA2719641694 | GNAQ | c.606-13G>T (n.606-13G>T) c.432-13G>T (n.432-13G>T) | dbSNP |
9 | g.77794605C= | CA1857429476 | GNAQ | c.606-13G= (n.606-13G=) c.432-13G= (n.432-13G=) | |
9 | g.77794605C>G | CA2719641695 | GNAQ | c.606-13G>C (n.606-13G>C) c.432-13G>C (n.432-13G>C) | dbSNP |
9 | g.77794605C>T | CA867169464 | GNAQ | c.606-13G>A (n.606-13G>A) c.432-13G>A (n.432-13G>A) | dbSNP gnomAD v3 gnomAD v4 |
9 | g.77794606A>G | CA2690385166 | GNAQ | c.606-14T>C (n.606-14T>C) c.432-14T>C (n.432-14T>C) | gnomAD v4 |
9 | g.77794607A= | CA1857429477 | GNAQ | c.606-15T= (n.606-15T=) c.432-15T= (n.432-15T=) | |
9 | g.77794607A>G | CA5094595 | GNAQ | c.606-15T>C (n.606-15T>C) c.432-15T>C (n.432-15T>C) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.77794608T>C | CA2690385167 | GNAQ | c.606-16A>G (n.606-16A>G) c.432-16A>G (n.432-16A>G) | gnomAD v4 |
9 | g.77794609A= | CA1857429479 | GNAQ | c.606-17T= (n.606-17T=) c.432-17T= (n.432-17T=) | |
9 | g.77794609A>C | CA2719624083 | GNAQ | c.606-17T>G (n.606-17T>G) c.432-17T>G (n.432-17T>G) | dbSNP |
9 | g.77794609A>G | CA867169468 | GNAQ | c.606-17T>C (n.606-17T>C) c.432-17T>C (n.432-17T>C) | dbSNP gnomAD v4 |
9 | g.77794609A>T | CA2719624086 | GNAQ | c.606-17T>A (n.606-17T>A) c.432-17T>A (n.432-17T>A) | dbSNP |
9 | g.77794610C>A | CA2690385168 | GNAQ | c.606-18G>T (n.606-18G>T) c.432-18G>T (n.432-18G>T) | dbSNP gnomAD v4 |
9 | g.77794610C>G | CA2719858938 | GNAQ | c.606-18G>C (n.606-18G>C) c.432-18G>C (n.432-18G>C) | dbSNP |
9 | g.77794610C>T | CA2690385169 | GNAQ | c.606-18G>A (n.606-18G>A) c.432-18G>A (n.432-18G>A) | gnomAD v4 |
9 | g.77794611T>A | CA2690385170 | GNAQ | c.606-19A>T (n.606-19A>T) c.432-19A>T (n.432-19A>T) | gnomAD v4 |
9 | g.77794611T>C | CA2690385171 | GNAQ | c.606-19A>G (n.606-19A>G) c.432-19A>G (n.432-19A>G) | gnomAD v4 |
9 | g.77794611T>G | CA5094596 | GNAQ | c.606-19A>C (n.606-19A>C) c.432-19A>C (n.432-19A>C) | dbSNP ExAC gnomAD v2 gnomAD v4 |
9 | g.77794611T= | CA1857429481 | GNAQ | c.606-19A= (n.606-19A=) c.432-19A= (n.432-19A=) | |
9 | g.77794612C>A | CA2690385172 | GNAQ | c.606-20G>T (n.606-20G>T) c.432-20G>T (n.432-20G>T) | dbSNP gnomAD v4 |
9 | g.77794612C= | CA1857429486 | GNAQ | c.606-20G= (n.606-20G=) c.432-20G= (n.432-20G=) | |
9 | g.77794612C>G | CA2719594395 | GNAQ | c.606-20G>C (n.606-20G>C) c.432-20G>C (n.432-20G>C) | dbSNP |
9 | g.77794612C>T | CA5094597 | GNAQ | c.606-20G>A (n.606-20G>A) c.432-20G>A (n.432-20G>A) | dbSNP ExAC gnomAD v2 gnomAD v4 |
9 | g.77794613A= | CA1857429488 | GNAQ | c.606-21T= (n.606-21T=) c.432-21T= (n.432-21T=) | |
9 | g.77794613A>G | CA5094598 | GNAQ | c.606-21T>C (n.606-21T>C) c.432-21T>C (n.432-21T>C) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.77794613A>T | CA2719592172 | GNAQ | c.606-21T>A (n.606-21T>A) c.432-21T>A (n.432-21T>A) | dbSNP |
9 | g.77794614T>A | CA2719858969 | GNAQ | c.606-22A>T (n.606-22A>T) c.432-22A>T (n.432-22A>T) | dbSNP |
9 | g.77794614T>C | CA2690385173 | GNAQ | c.606-22A>G (n.606-22A>G) c.432-22A>G (n.432-22A>G) | dbSNP gnomAD v4 |
9 | g.77794615A= | CA1857429490 | GNAQ | c.606-23T= (n.606-23T=) c.432-23T= (n.432-23T=) | |
9 | g.77794615A>G | CA5094599 | GNAQ | c.606-23T>C (n.606-23T>C) c.432-23T>C (n.432-23T>C) | dbSNP ExAC gnomAD v2 gnomAD v4 |
9 | g.77794616T>A | CA2719859161 | GNAQ | c.606-24A>T (n.606-24A>T) c.432-24A>T (n.432-24A>T) | dbSNP |
9 | g.77794617T>A | CA2719690289 | GNAQ | c.606-25A>T (n.606-25A>T) c.432-25A>T (n.432-25A>T) | dbSNP |
9 | g.77794617T>C | CA1125711864 | GNAQ | c.606-25A>G (n.606-25A>G) c.432-25A>G (n.432-25A>G) | dbSNP gnomAD v3 gnomAD v4 |
9 | g.77794617T= | CA1857429492 | GNAQ | c.606-25A= (n.606-25A=) c.432-25A= (n.432-25A=) | |
9 | g.77794618A>G | CA2690385174 | GNAQ | c.606-26T>C (n.606-26T>C) c.432-26T>C (n.432-26T>C) | dbSNP gnomAD v4 |
9 | g.77794618A>T | CA2690385175 | GNAQ | c.606-26T>A (n.606-26T>A) c.432-26T>A (n.432-26T>A) | gnomAD v4 |
9 | g.77794619A>T | CA2690385176 | GNAQ | c.606-27T>A (n.606-27T>A) c.432-27T>A (n.432-27T>A) | gnomAD v4 |
9 | g.77794620T>A | CA2719637638 | GNAQ | c.606-28A>T (n.606-28A>T) c.432-28A>T (n.432-28A>T) | dbSNP |
9 | g.77794620T>C | CA588764524 | GNAQ | c.606-28A>G (n.606-28A>G) c.432-28A>G (n.432-28A>G) | dbSNP gnomAD v2 gnomAD v4 |
9 | g.77794620T= | CA1857429494 | GNAQ | c.606-28A= (n.606-28A=) c.432-28A= (n.432-28A=) |