UPDATE - Protein Allele ID & Protein Sequence HGVS Requests Partially Restored
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 9 | g.77794475C>A | CA373997655 | GNAQ | c.723G>T (p.Glu241Asp) c.549G>T (p.Glu183Asp) | |
| 9 | g.77794475C>G | CA373997656 | GNAQ | c.723G>C (p.Glu241Asp) c.549G>C (p.Glu183Asp) | dbSNP |
| 9 | g.77794475C>T | CA465578290 | GNAQ | c.723G>A (p.Glu241=) c.549G>A (p.Glu183=) | |
| 9 | g.77794476T>A | CA373997657 | GNAQ | c.722A>T (p.Glu241Val) c.548A>T (p.Glu183Val) | |
| 9 | g.77794476T>C | CA373997658 | GNAQ | c.722A>G (p.Glu241Gly) c.548A>G (p.Glu183Gly) | |
| 9 | g.77794476T>G | CA373997659 | GNAQ | c.722A>C (p.Glu241Ala) c.548A>C (p.Glu183Ala) | |
| 9 | g.77794477C>A | CA373997660 | GNAQ | c.721G>T (p.Glu241Ter) c.547G>T (p.Glu183Ter) | dbSNP |
| 9 | g.77794477C>G | CA373997661 | GNAQ | c.721G>C (p.Glu241Gln) c.547G>C (p.Glu183Gln) | dbSNP |
| 9 | g.77794477C>T | CA373997662 | GNAQ | c.721G>A (p.Glu241Lys) c.547G>A (p.Glu183Lys) | dbSNP |
| 9 | g.77794478del | CA2690385156 | GNAQ | c.721del (p.Glu241SerfsTer?) c.547del (p.Glu183SerfsTer?) | gnomAD v4 |
| 9 | g.77794478C>A | CA465578291 | GNAQ | c.720G>T (p.Val240=) c.546G>T (p.Val182=) | |
| 9 | g.77794478C>G | CA465578292 | GNAQ | c.720G>C (p.Val240=) c.546G>C (p.Val182=) | dbSNP |
| 9 | g.77794478C>T | CA465578293 | GNAQ | c.720G>A (p.Val240=) c.546G>A (p.Val182=) | dbSNP gnomAD v4 |
| 9 | g.77794479A>C | CA373997663 | GNAQ | c.719T>G (p.Val240Gly) c.545T>G (p.Val182Gly) | dbSNP |
| 9 | g.77794479A>G | CA373997664 | GNAQ | c.719T>C (p.Val240Ala) c.545T>C (p.Val182Ala) | gnomAD v4 |
| 9 | g.77794479A>T | CA373997665 | GNAQ | c.719T>A (p.Val240Glu) c.545T>A (p.Val182Glu) | dbSNP |
| 9 | g.77794480C>A | CA373997666 | GNAQ | c.718G>T (p.Val240Leu) c.544G>T (p.Val182Leu) | dbSNP gnomAD v4 |
| 9 | g.77794480C= | CA1857429363 | GNAQ | c.718G= (p.Val240=) c.544G= (p.Val182=) | |
| 9 | g.77794480C>G | CA373997667 | GNAQ | c.718G>C (p.Val240Leu) c.544G>C (p.Val182Leu) | dbSNP |
| 9 | g.77794480C>T | CA194717254 | GNAQ | c.718G>A (p.Val240Met) c.544G>A (p.Val182Met) | dbSNP gnomAD v3 gnomAD v4 |
| 9 | g.77794481G>A | CA194717255 | GNAQ | c.717C>T (p.Leu239=) c.543C>T (p.Leu181=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.77794481G>C | CA465578294 | GNAQ | c.717C>G (p.Leu239=) c.543C>G (p.Leu181=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.77794481G= | CA1857429368 | GNAQ | c.717C= (p.Leu239=) c.543C= (p.Leu181=) | |
| 9 | g.77794481G>T | CA465578295 | GNAQ | c.717C>A (p.Leu239=) c.543C>A (p.Leu181=) | dbSNP gnomAD v4 |
| 9 | g.77794483_77794484dup | CA2690385157 | GNAQ | c.716_717dup (p.Val240SerfsTer?) c.542_543dup (p.Val182SerfsTer?) | gnomAD v4 |
| 9 | g.77794482A>C | CA373997670 | GNAQ | c.716T>G (p.Leu239Arg) c.542T>G (p.Leu181Arg) | |
| 9 | g.77794482A>G | CA373997668 | GNAQ | c.716T>C (p.Leu239Pro) c.542T>C (p.Leu181Pro) | |
| 9 | g.77794482A>T | CA373997669 | GNAQ | c.716T>A (p.Leu239His) c.542T>A (p.Leu181His) | dbSNP |
| 9 | g.77794483G>A | CA373997671 | GNAQ | c.715C>T (p.Leu239Phe) c.541C>T (p.Leu181Phe) | dbSNP |
| 9 | g.77794483G>C | CA373997672 | GNAQ | c.715C>G (p.Leu239Val) c.541C>G (p.Leu181Val) | dbSNP |
| 9 | g.77794483G>T | CA373997673 | GNAQ | c.715C>A (p.Leu239Ile) c.541C>A (p.Leu181Ile) | dbSNP gnomAD v4 |
| 9 | g.77794484A>C | CA465578296 | GNAQ | c.714T>G (p.Val238=) c.540T>G (p.Val180=) | |
| 9 | g.77794484A>G | CA465578297 | GNAQ | c.714T>C (p.Val238=) c.540T>C (p.Val180=) | |
| 9 | g.77794484A>T | CA465578298 | GNAQ | c.714T>A (p.Val238=) c.540T>A (p.Val180=) | dbSNP |
| 9 | g.77794485A= | CA1857429373 | GNAQ | c.713T= (p.Val238=) c.539T= (p.Val180=) | |
| 9 | g.77794485A>C | CA373997674 | GNAQ | c.713T>G (p.Val238Gly) c.539T>G (p.Val180Gly) | |
| 9 | g.77794485A>G | CA373997675 | GNAQ | c.713T>C (p.Val238Ala) c.539T>C (p.Val180Ala) | dbSNP |
| 9 | g.77794485A>T | CA373997676 | GNAQ | c.713T>A (p.Val238Asp) c.539T>A (p.Val180Asp) | dbSNP |
| 9 | g.77794486C>A | CA373997677 | GNAQ | c.712G>T (p.Val238Phe) c.538G>T (p.Val180Phe) | |
| 9 | g.77794486C>G | CA373997678 | GNAQ | c.712G>C (p.Val238Leu) c.538G>C (p.Val180Leu) | |
| 9 | g.77794486C>T | CA373997679 | GNAQ | c.712G>A (p.Val238Ile) c.538G>A (p.Val180Ile) | dbSNP COSMIC |
| 9 | g.77794487T>A | CA373997680 | GNAQ | c.711A>T (p.Gln237His) c.537A>T (p.Gln179His) | dbSNP |
| 9 | g.77794487T>C | CA465578299 | GNAQ | c.711A>G (p.Gln237=) c.537A>G (p.Gln179=) | dbSNP gnomAD v4 |
| 9 | g.77794487T>G | CA373997681 | GNAQ | c.711A>C (p.Gln237His) c.537A>C (p.Gln179His) | |
| 9 | g.77794487T= | CA1857429375 | GNAQ | c.711A= (p.Gln237=) c.537A= (p.Gln179=) | |
| 9 | g.77794488T>A | CA373997684 | GNAQ | c.710A>T (p.Gln237Leu) c.536A>T (p.Gln179Leu) | dbSNP |
| 9 | g.77794488T>C | CA373997683 | GNAQ | c.710A>G (p.Gln237Arg) c.536A>G (p.Gln179Arg) | dbSNP |
| 9 | g.77794488T>G | CA373997682 | GNAQ | c.710A>C (p.Gln237Pro) c.536A>C (p.Gln179Pro) | |
| 9 | g.77794489G>A | CA373997685 | GNAQ | c.709C>T (p.Gln237Ter) c.535C>T (p.Gln179Ter) | dbSNP |
| 9 | g.77794489G>C | CA373997686 | GNAQ | c.709C>G (p.Gln237Glu) c.535C>G (p.Gln179Glu) | dbSNP |
| 9 | g.77794489G>T | CA373997687 | GNAQ | c.709C>A (p.Gln237Lys) c.535C>A (p.Gln179Lys) | dbSNP gnomAD v4 |
| 9 | g.77794490A= | CA1857429378 | GNAQ | c.708T= (p.Asp236=) c.534T= (p.Asp178=) | |
| 9 | g.77794490A>C | CA373997688 | GNAQ | c.708T>G (p.Asp236Glu) c.534T>G (p.Asp178Glu) | dbSNP gnomAD v4 |
| 9 | g.77794490A>G | CA465578300 | GNAQ | c.708T>C (p.Asp236=) c.534T>C (p.Asp178=) | |
| 9 | g.77794490A>T | CA373997689 | GNAQ | c.708T>A (p.Asp236Glu) c.534T>A (p.Asp178Glu) | dbSNP gnomAD v3 gnomAD v4 |
| 9 | g.77794491T>A | CA373997690 | GNAQ | c.707A>T (p.Asp236Val) c.533A>T (p.Asp178Val) | dbSNP |
| 9 | g.77794491T>C | CA373997691 | GNAQ | c.707A>G (p.Asp236Gly) c.533A>G (p.Asp178Gly) | |
| 9 | g.77794491T>G | CA373997692 | GNAQ | c.707A>C (p.Asp236Ala) c.533A>C (p.Asp178Ala) | |
| 9 | g.77794492C>A | CA373997693 | GNAQ | c.706G>T (p.Asp236Tyr) c.532G>T (p.Asp178Tyr) | |
| 9 | g.77794492C>G | CA373997694 | GNAQ | c.706G>C (p.Asp236His) c.532G>C (p.Asp178His) | dbSNP |
| 9 | g.77794492C>T | CA373997695 | GNAQ | c.706G>A (p.Asp236Asn) c.532G>A (p.Asp178Asn) | dbSNP |
| 9 | g.77794493A= | CA1857429381 | GNAQ | c.705T= (p.Tyr235=) c.531T= (p.Tyr177=) | |
| 9 | g.77794493A>C | CA373997696 | GNAQ | c.705T>G (p.Tyr235Ter) c.531T>G (p.Tyr177Ter) | |
| 9 | g.77794493A>G | CA465578301 | GNAQ | c.705T>C (p.Tyr235=) c.531T>C (p.Tyr177=) | ClinVar dbSNP |
| 9 | g.77794493A>T | CA373997697 | GNAQ | c.705T>A (p.Tyr235Ter) c.531T>A (p.Tyr177Ter) | dbSNP |
| 9 | g.77794494T>A | CA373997700 | GNAQ | c.704A>T (p.Tyr235Phe) c.530A>T (p.Tyr177Phe) | dbSNP |
| 9 | g.77794494T>C | CA373997698 | GNAQ | c.704A>G (p.Tyr235Cys) c.530A>G (p.Tyr177Cys) | dbSNP |
| 9 | g.77794494T>G | CA373997699 | GNAQ | c.704A>C (p.Tyr235Ser) c.530A>C (p.Tyr177Ser) | |
| 9 | g.77794495A>C | CA373997701 | GNAQ | c.703T>G (p.Tyr235Asp) c.529T>G (p.Tyr177Asp) | dbSNP |
| 9 | g.77794495A>G | CA373997702 | GNAQ | c.703T>C (p.Tyr235His) c.529T>C (p.Tyr177His) | dbSNP |
| 9 | g.77794495A>T | CA373997703 | GNAQ | c.703T>A (p.Tyr235Asn) c.529T>A (p.Tyr177Asn) | dbSNP |
| 9 | g.77794496T>A | CA373997704 | GNAQ | c.702A>T (p.Glu234Asp) c.528A>T (p.Glu176Asp) | |
| 9 | g.77794496T>C | CA5094586 | GNAQ | c.702A>G (p.Glu234=) c.528A>G (p.Glu176=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 9 | g.77794496T>G | CA373997705 | GNAQ | c.702A>C (p.Glu234Asp) c.528A>C (p.Glu176Asp) | |
| 9 | g.77794496T= | CA1857429386 | GNAQ | c.702A= (p.Glu234=) c.528A= (p.Glu176=) | |
| 9 | g.77794497T>A | CA373997706 | GNAQ | c.701A>T (p.Glu234Val) c.527A>T (p.Glu176Val) | |
| 9 | g.77794497T>C | CA373997707 | GNAQ | c.701A>G (p.Glu234Gly) c.527A>G (p.Glu176Gly) | |
| 9 | g.77794497T>G | CA373997708 | GNAQ | c.701A>C (p.Glu234Ala) c.527A>C (p.Glu176Ala) | |
| 9 | g.77794498C>A | CA373997709 | GNAQ | c.700G>T (p.Glu234Ter) c.526G>T (p.Glu176Ter) | dbSNP gnomAD v4 |
| 9 | g.77794498C>G | CA373997710 | GNAQ | c.700G>C (p.Glu234Gln) c.526G>C (p.Glu176Gln) | dbSNP |
| 9 | g.77794498C>T | CA373997711 | GNAQ | c.700G>A (p.Glu234Lys) c.526G>A (p.Glu176Lys) | dbSNP |
| 9 | g.77794499A>C | CA373997713 | GNAQ | c.699T>G (p.Ser233Arg) c.525T>G (p.Ser175Arg) | |
| 9 | g.77794499A>G | CA465578302 | GNAQ | c.699T>C (p.Ser233=) c.525T>C (p.Ser175=) | |
| 9 | g.77794499A>T | CA373997712 | GNAQ | c.699T>A (p.Ser233Arg) c.525T>A (p.Ser175Arg) | dbSNP |
| 9 | g.77794500C>A | CA373997714 | GNAQ | c.698G>T (p.Ser233Ile) c.524G>T (p.Ser175Ile) | |
| 9 | g.77794500C>G | CA373997716 | GNAQ | c.698G>C (p.Ser233Thr) c.524G>C (p.Ser175Thr) | dbSNP |
| 9 | g.77794500C>T | CA373997715 | GNAQ | c.698G>A (p.Ser233Asn) c.524G>A (p.Ser175Asn) | dbSNP |
| 9 | g.77794501T>A | CA373997717 | GNAQ | c.697A>T (p.Ser233Cys) c.523A>T (p.Ser175Cys) | dbSNP |
| 9 | g.77794501T>C | CA373997718 | GNAQ | c.697A>G (p.Ser233Gly) c.523A>G (p.Ser175Gly) | |
| 9 | g.77794501T>G | CA373997719 | GNAQ | c.697A>C (p.Ser233Arg) c.523A>C (p.Ser175Arg) | |
| 9 | g.77794502A>C | CA465578303 | GNAQ | c.696T>G (p.Leu232=) c.522T>G (p.Leu174=) | gnomAD v4 |
| 9 | g.77794502A>G | CA465578305 | GNAQ | c.696T>C (p.Leu232=) c.522T>C (p.Leu174=) | dbSNP |
| 9 | g.77794502A>T | CA465578304 | GNAQ | c.696T>A (p.Leu232=) c.522T>A (p.Leu174=) | dbSNP gnomAD v4 |
| 9 | g.77794503A>C | CA373997720 | GNAQ | c.695T>G (p.Leu232Arg) c.521T>G (p.Leu174Arg) | |
| 9 | g.77794503A>G | CA373997721 | GNAQ | c.695T>C (p.Leu232Pro) c.521T>C (p.Leu174Pro) | |
| 9 | g.77794503A>T | CA373997722 | GNAQ | c.695T>A (p.Leu232His) c.521T>A (p.Leu174His) | dbSNP |
| 9 | g.77794504G>A | CA373997723 | GNAQ | c.694C>T (p.Leu232Phe) c.520C>T (p.Leu174Phe) | dbSNP |
| 9 | g.77794504G>C | CA373997724 | GNAQ | c.694C>G (p.Leu232Val) c.520C>G (p.Leu174Val) | dbSNP |
| 9 | g.77794504G>T | CA373997725 | GNAQ | c.694C>A (p.Leu232Ile) c.520C>A (p.Leu174Ile) | dbSNP |
| 9 | g.77794505C>A | CA465578307 | GNAQ | c.693G>T (p.Ala231=) c.519G>T (p.Ala173=) | dbSNP |
| 9 | g.77794505C= | CA1857429391 | GNAQ | c.693G= (p.Ala231=) c.519G= (p.Ala173=) | |
| 9 | g.77794505C>G | CA465578306 | GNAQ | c.693G>C (p.Ala231=) c.519G>C (p.Ala173=) | dbSNP |
| 9 | g.77794505C>T | CA5094587 | GNAQ | c.693G>A (p.Ala231=) c.519G>A (p.Ala173=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 9 | g.77794506G>A | CA373997726 | GNAQ | c.692C>T (p.Ala231Val) c.518C>T (p.Ala173Val) | dbSNP gnomAD v4 |
| 9 | g.77794506G>C | CA373997727 | GNAQ | c.692C>G (p.Ala231Gly) c.518C>G (p.Ala173Gly) | dbSNP |
| 9 | g.77794506G= | CA1857429393 | GNAQ | c.692C= (p.Ala231=) c.518C= (p.Ala173=) | |
| 9 | g.77794506G>T | CA373997728 | GNAQ | c.692C>A (p.Ala231Glu) c.518C>A (p.Ala173Glu) | dbSNP gnomAD v4 |
| 9 | g.77794507C>A | CA373997729 | GNAQ | c.691G>T (p.Ala231Ser) c.517G>T (p.Ala173Ser) | dbSNP |
| 9 | g.77794507C>G | CA373997731 | GNAQ | c.691G>C (p.Ala231Pro) c.517G>C (p.Ala173Pro) | dbSNP |
| 9 | g.77794507C>T | CA373997730 | GNAQ | c.691G>A (p.Ala231Thr) c.517G>A (p.Ala173Thr) | dbSNP |
| 9 | g.77794508T>A | CA465578308 | GNAQ | c.690A>T (p.Val230=) c.516A>T (p.Val172=) | dbSNP |
| 9 | g.77794508T>C | CA465578310 | GNAQ | c.690A>G (p.Val230=) c.516A>G (p.Val172=) | dbSNP |
| 9 | g.77794508T>G | CA465578309 | GNAQ | c.690A>C (p.Val230=) c.516A>C (p.Val172=) | gnomAD v4 |
| 9 | g.77794509A>C | CA373997732 | GNAQ | c.689T>G (p.Val230Gly) c.515T>G (p.Val172Gly) | dbSNP |
| 9 | g.77794509A>G | CA373997733 | GNAQ | c.689T>C (p.Val230Ala) c.515T>C (p.Val172Ala) | |
| 9 | g.77794509A>T | CA373997734 | GNAQ | c.689T>A (p.Val230Glu) c.515T>A (p.Val172Glu) | dbSNP |
| 9 | g.77794510C>A | CA373997735 | GNAQ | c.688G>T (p.Val230Leu) c.514G>T (p.Val172Leu) | dbSNP |
| 9 | g.77794510C= | CA1857429398 | GNAQ | c.688G= (p.Val230=) c.514G= (p.Val172=) | |
| 9 | g.77794510C>G | CA373997736 | GNAQ | c.688G>C (p.Val230Leu) c.514G>C (p.Val172Leu) | dbSNP |
| 9 | g.77794510C>T | CA373997737 | GNAQ | c.688G>A (p.Val230Ile) c.514G>A (p.Val172Ile) | dbSNP |
| 9 | g.77794511T>A | CA5094589 | GNAQ | c.687A>T (p.Leu229=) c.513A>T (p.Leu171=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 9 | g.77794511T>C | CA5094588 | GNAQ | c.687A>G (p.Leu229=) c.513A>G (p.Leu171=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.77794511T>G | CA465578311 | GNAQ | c.687A>C (p.Leu229=) c.513A>C (p.Leu171=) | |
| 9 | g.77794511T= | CA1857429405 | GNAQ | c.687A= (p.Leu229=) c.513A= (p.Leu171=) | |
| 9 | g.77794512A>C | CA373997738 | GNAQ | c.686T>G (p.Leu229Arg) c.512T>G (p.Leu171Arg) | |
| 9 | g.77794512A>G | CA373997739 | GNAQ | c.686T>C (p.Leu229Pro) c.512T>C (p.Leu171Pro) | |
| 9 | g.77794512A>T | CA373997740 | GNAQ | c.686T>A (p.Leu229Gln) c.512T>A (p.Leu171Gln) | dbSNP |
| 9 | g.77794513G>A | CA465578312 | GNAQ | c.685C>T (p.Leu229=) c.511C>T (p.Leu171=) | dbSNP |
| 9 | g.77794513G>C | CA373997742 | GNAQ | c.685C>G (p.Leu229Val) c.511C>G (p.Leu171Val) | |
| 9 | g.77794513G>T | CA373997741 | GNAQ | c.685C>A (p.Leu229Ile) c.511C>A (p.Leu171Ile) | dbSNP |
| 9 | g.77794514A>C | CA373997743 | GNAQ | c.684T>G (p.Phe228Leu) c.510T>G (p.Phe170Leu) | |
| 9 | g.77794514A>G | CA465578313 | GNAQ | c.684T>C (p.Phe228=) c.510T>C (p.Phe170=) | |
| 9 | g.77794514A>T | CA373997744 | GNAQ | c.684T>A (p.Phe228Leu) c.510T>A (p.Phe170Leu) | |
| 9 | g.77794515A>C | CA373997745 | GNAQ | c.683T>G (p.Phe228Cys) c.509T>G (p.Phe170Cys) | COSMIC |
| 9 | g.77794515A>G | CA373997746 | GNAQ | c.683T>C (p.Phe228Ser) c.509T>C (p.Phe170Ser) | dbSNP |
| 9 | g.77794515A>T | CA373997747 | GNAQ | c.683T>A (p.Phe228Tyr) c.509T>A (p.Phe170Tyr) | |
| 9 | g.77794516A>C | CA373997750 | GNAQ | c.682T>G (p.Phe228Val) c.508T>G (p.Phe170Val) | dbSNP |
| 9 | g.77794516A>G | CA373997749 | GNAQ | c.682T>C (p.Phe228Leu) c.508T>C (p.Phe170Leu) | |
| 9 | g.77794516A>T | CA373997748 | GNAQ | c.682T>A (p.Phe228Ile) c.508T>A (p.Phe170Ile) | dbSNP |
| 9 | g.77794517C>A | CA373997751 | GNAQ | c.681G>T (p.Met227Ile) c.507G>T (p.Met169Ile) | dbSNP |
| 9 | g.77794517C>G | CA373997752 | GNAQ | c.681G>C (p.Met227Ile) c.507G>C (p.Met169Ile) | dbSNP |
| 9 | g.77794517C>T | CA373997753 | GNAQ | c.681G>A (p.Met227Ile) c.507G>A (p.Met169Ile) | dbSNP |
| 9 | g.77794518A>C | CA373997754 | GNAQ | c.680T>G (p.Met227Arg) c.506T>G (p.Met169Arg) | |
| 9 | g.77794518A>G | CA373997755 | GNAQ | c.680T>C (p.Met227Thr) c.506T>C (p.Met169Thr) | gnomAD v4 |
| 9 | g.77794518A>T | CA373997756 | GNAQ | c.680T>A (p.Met227Lys) c.506T>A (p.Met169Lys) | dbSNP |
| 9 | g.77794519T>A | CA373997759 | GNAQ | c.679A>T (p.Met227Leu) c.505A>T (p.Met169Leu) | dbSNP |
| 9 | g.77794519T>C | CA373997757 | GNAQ | c.679A>G (p.Met227Val) c.505A>G (p.Met169Val) | dbSNP |
| 9 | g.77794519T>G | CA373997758 | GNAQ | c.679A>C (p.Met227Leu) c.505A>C (p.Met169Leu) | |
| 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) |