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 |
|---|---|---|---|---|---|
| 5 | g.174729301G>A | CA3565226 | MSX2 | c.522G>A (p.Glu174=) c.*146G>A (n.*146G>A) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 5 | g.174729301G>C | CA362230050 | MSX2 | c.522G>C (p.Glu174Asp) c.*146G>C (n.*146G>C) | |
| 5 | g.174729301G= | CA1602356136 | MSX2 | c.522G= (p.Glu174=) c.*146G= (n.*146G=) | |
| 5 | g.174729301G>T | CA362230051 | MSX2 | c.522G>T (p.Glu174Asp) c.*146G>T (n.*146G>T) | |
| 5 | g.174729302T>A | CA362230052 | MSX2 | c.523T>A (p.Phe175Ile) c.*147T>A (n.*147T>A) | |
| 5 | g.174729302T>C | CA362230053 | MSX2 | c.523T>C (p.Phe175Leu) c.*147T>C (n.*147T>C) | gnomAD v4 |
| 5 | g.174729302T>G | CA362230054 | MSX2 | c.523T>G (p.Phe175Val) c.*147T>G (n.*147T>G) | |
| 5 | g.174729303T>A | CA362230056 | MSX2 | c.524T>A (p.Phe175Tyr) c.*148T>A (n.*148T>A) | |
| 5 | g.174729303T>C | CA362230057 | MSX2 | c.524T>C (p.Phe175Ser) c.*148T>C (n.*148T>C) | |
| 5 | g.174729303T>G | CA362230055 | MSX2 | c.524T>G (p.Phe175Cys) c.*148T>G (n.*148T>G) | |
| 5 | g.174729304C>A | CA362230058 | MSX2 | c.525C>A (p.Phe175Leu) c.*149C>A (n.*149C>A) | |
| 5 | g.174729304C>G | CA362230059 | MSX2 | c.525C>G (p.Phe175Leu) c.*149C>G (n.*149C>G) | |
| 5 | g.174729304C>T | CA447978852 | MSX2 | c.525C>T (p.Phe175=) c.*149C>T (n.*149C>T) | |
| 5 | g.174729305T>A | CA362230060 | MSX2 | c.526T>A (p.Ser176Thr) c.*150T>A (n.*150T>A) | |
| 5 | g.174729305T>C | CA362230061 | MSX2 | c.526T>C (p.Ser176Pro) c.*150T>C (n.*150T>C) | dbSNP gnomAD v3 gnomAD v4 |
| 5 | g.174729305T>G | CA362230062 | MSX2 | c.526T>G (p.Ser176Ala) c.*150T>G (n.*150T>G) | |
| 5 | g.174729305T= | CA1602356140 | MSX2 | c.526T= (p.Ser176=) c.*150T= (n.*150T=) | |
| 5 | g.174729306C>A | CA362230063 | MSX2 | c.527C>A (p.Ser176Tyr) c.*151C>A (n.*151C>A) | |
| 5 | g.174729306C= | CA1602356144 | MSX2 | c.527C= (p.Ser176=) c.*151C= (n.*151C=) | |
| 5 | g.174729306C>G | CA362230064 | MSX2 | c.527C>G (p.Ser176Cys) c.*151C>G (n.*151C>G) | |
| 5 | g.174729306C>T | CA362230065 | MSX2 | c.527C>T (p.Ser176Phe) c.*151C>T (n.*151C>T) | dbSNP gnomAD v3 gnomAD v4 |
| 5 | g.174729307C>A | CA447978855 | MSX2 | c.528C>A (p.Ser176=) c.*152C>A (n.*152C>A) | gnomAD v4 |
| 5 | g.174729307C>G | CA447978857 | MSX2 | c.528C>G (p.Ser176=) c.*152C>G (n.*152C>G) | |
| 5 | g.174729307C>T | CA447978853 | MSX2 | c.528C>T (p.Ser176=) c.*152C>T (n.*152C>T) | ClinVar gnomAD v4 |
| 5 | g.174729308A>C | CA362230066 | MSX2 | c.529A>C (p.Ser177Arg) c.*153A>C (n.*153A>C) | |
| 5 | g.174729308A>G | CA362230067 | MSX2 | c.529A>G (p.Ser177Gly) c.*153A>G (n.*153A>G) | |
| 5 | g.174729308A>T | CA362230068 | MSX2 | c.529A>T (p.Ser177Cys) c.*153A>T (n.*153A>T) | |
| 5 | g.174729309G>A | CA362230069 | MSX2 | c.530G>A (p.Ser177Asn) c.*154G>A (n.*154G>A) | ClinVar gnomAD v4 |
| 5 | g.174729309G>C | CA362230070 | MSX2 | c.530G>C (p.Ser177Thr) c.*154G>C (n.*154G>C) | |
| 5 | g.174729309G>T | CA362230071 | MSX2 | c.530G>T (p.Ser177Ile) c.*154G>T (n.*154G>T) | |
| 5 | g.174729310C>A | CA362230072 | MSX2 | c.531C>A (p.Ser177Arg) c.*155C>A (n.*155C>A) | |
| 5 | g.174729310C>G | CA362230073 | MSX2 | c.531C>G (p.Ser177Arg) c.*155C>G (n.*155C>G) | |
| 5 | g.174729310C>T | CA447978859 | MSX2 | c.531C>T (p.Ser177=) c.*155C>T (n.*155C>T) | |
| 5 | g.174729314_174729315del | CA2676572998 | MSX2 | c.535_536del (p.Leu179GlufsTer?) c.*159_*160del (n.*159_*160del) | gnomAD v4 |
| 5 | g.174729311T>A | CA362230074 | MSX2 | c.532T>A (p.Ser178Thr) c.*156T>A (n.*156T>A) | |
| 5 | g.174729311T>C | CA362230075 | MSX2 | c.532T>C (p.Ser178Pro) c.*156T>C (n.*156T>C) | |
| 5 | g.174729311T>G | CA362230076 | MSX2 | c.532T>G (p.Ser178Ala) c.*156T>G (n.*156T>G) | |
| 5 | g.174729312C>A | CA362230077 | MSX2 | c.533C>A (p.Ser178Tyr) c.*157C>A (n.*157C>A) | |
| 5 | g.174729312C>G | CA362230078 | MSX2 | c.533C>G (p.Ser178Cys) c.*157C>G (n.*157C>G) | |
| 5 | g.174729312C>T | CA362230079 | MSX2 | c.533C>T (p.Ser178Phe) c.*157C>T (n.*157C>T) | gnomAD v4 |
| 5 | g.174729313T>A | CA447978862 | MSX2 | c.534T>A (p.Ser178=) c.*158T>A (n.*158T>A) | |
| 5 | g.174729313T>C | CA447978863 | MSX2 | c.534T>C (p.Ser178=) c.*158T>C (n.*158T>C) | |
| 5 | g.174729313T>G | CA447978864 | MSX2 | c.534T>G (p.Ser178=) c.*158T>G (n.*158T>G) | |
| 5 | g.174729314C>A | CA362230080 | MSX2 | c.535C>A (p.Leu179Met) c.*159C>A (n.*159C>A) | |
| 5 | g.174729314C= | CA1602356152 | MSX2 | c.535C= (p.Leu179=) c.*159C= (n.*159C=) | |
| 5 | g.174729314C>G | CA362230081 | MSX2 | c.535C>G (p.Leu179Val) c.*159C>G (n.*159C>G) | |
| 5 | g.174729314C>T | CA447978866 | MSX2 | c.535C>T (p.Leu179=) c.*159C>T (n.*159C>T) | dbSNP gnomAD v4 |
| 5 | g.174729315T>A | CA362230082 | MSX2 | c.536T>A (p.Leu179Gln) c.*160T>A (n.*160T>A) | |
| 5 | g.174729315T>C | CA362230083 | MSX2 | c.536T>C (p.Leu179Pro) c.*160T>C (n.*160T>C) | |
| 5 | g.174729315T>G | CA362230084 | MSX2 | c.536T>G (p.Leu179Arg) c.*160T>G (n.*160T>G) | |
| 5 | g.174729316G>A | CA447978867 | MSX2 | c.537G>A (p.Leu179=) c.*161G>A (n.*161G>A) | |
| 5 | g.174729316G>C | CA447978868 | MSX2 | c.537G>C (p.Leu179=) c.*161G>C (n.*161G>C) | |
| 5 | g.174729316G>T | CA447978869 | MSX2 | c.537G>T (p.Leu179=) c.*161G>T (n.*161G>T) | |
| 5 | g.174729317A>C | CA362230085 | MSX2 | c.538A>C (p.Asn180His) c.*162A>C (n.*162A>C) | |
| 5 | g.174729317A>G | CA362230086 | MSX2 | c.538A>G (p.Asn180Asp) c.*162A>G (n.*162A>G) | |
| 5 | g.174729317A>T | CA362230087 | MSX2 | c.538A>T (p.Asn180Tyr) c.*162A>T (n.*162A>T) | |
| 5 | g.174729318A= | CA1602356159 | MSX2 | c.539A= (p.Asn180=) c.*163A= (n.*163A=) | |
| 5 | g.174729318A>C | CA362230089 | MSX2 | c.539A>C (p.Asn180Thr) c.*163A>C (n.*163A>C) | |
| 5 | g.174729318A>G | CA362230090 | MSX2 | c.539A>G (p.Asn180Ser) c.*163A>G (n.*163A>G) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 5 | g.174729318A>T | CA362230088 | MSX2 | c.539A>T (p.Asn180Ile) c.*163A>T (n.*163A>T) | |
| 5 | g.174729319C>A | CA362230091 | MSX2 | c.540C>A (p.Asn180Lys) c.*164C>A (n.*164C>A) | |
| 5 | g.174729319C= | CA1602356163 | MSX2 | c.540C= (p.Asn180=) c.*164C= (n.*164C=) | |
| 5 | g.174729319C>G | CA362230092 | MSX2 | c.540C>G (p.Asn180Lys) c.*164C>G (n.*164C>G) | |
| 5 | g.174729319C>T | CA447978873 | MSX2 | c.540C>T (p.Asn180=) c.*164C>T (n.*164C>T) | dbSNP gnomAD v2 gnomAD v4 |
| 5 | g.174729320C>A | CA362230093 | MSX2 | c.541C>A (p.Leu181Ile) c.*165C>A (n.*165C>A) | |
| 5 | g.174729320C>G | CA362230094 | MSX2 | c.541C>G (p.Leu181Val) c.*165C>G (n.*165C>G) | |
| 5 | g.174729320C>T | CA362230095 | MSX2 | c.541C>T (p.Leu181Phe) c.*165C>T (n.*165C>T) | |
| 5 | g.174729321T>A | CA362230096 | MSX2 | c.542T>A (p.Leu181His) c.*166T>A (n.*166T>A) | |
| 5 | g.174729321T>C | CA362230097 | MSX2 | c.542T>C (p.Leu181Pro) c.*166T>C (n.*166T>C) | |
| 5 | g.174729321T>G | CA362230098 | MSX2 | c.542T>G (p.Leu181Arg) c.*166T>G (n.*166T>G) | |
| 5 | g.174729322C>A | CA447978877 | MSX2 | c.543C>A (p.Leu181=) c.*167C>A (n.*167C>A) | |
| 5 | g.174729322C= | CA1602356165 | MSX2 | c.543C= (p.Leu181=) c.*167C= (n.*167C=) | |
| 5 | g.174729322C>G | CA447978878 | MSX2 | c.543C>G (p.Leu181=) c.*167C>G (n.*167C>G) | |
| 5 | g.174729322C>T | CA447978879 | MSX2 | c.543C>T (p.Leu181=) c.*167C>T (n.*167C>T) | dbSNP gnomAD v3 gnomAD v4 |
| 5 | g.174729323A= | CA1602356167 | MSX2 | c.544A= (p.Thr182=) c.*168A= (n.*168A=) | |
| 5 | g.174729323A>C | CA362230099 | MSX2 | c.544A>C (p.Thr182Pro) c.*168A>C (n.*168A>C) | |
| 5 | g.174729323A>G | CA362230100 | MSX2 | c.544A>G (p.Thr182Ala) c.*168A>G (n.*168A>G) | dbSNP gnomAD v2 COSMIC |
| 5 | g.174729323A>T | CA362230101 | MSX2 | c.544A>T (p.Thr182Ser) c.*168A>T (n.*168A>T) | |
| 5 | g.174729323_174729331delinsACAGAGACC | CA1602356168 | MSX2 | c.544_552delinsACAGAGACC (p.Thr182=) c.*168_*176delinsACAGAGACC (n.*168_*176delinsACAGAGACC) | |
| 5 | g.174729324C>A | CA362230102 | MSX2 | c.545C>A (p.Thr182Lys) c.*169C>A (n.*169C>A) | |
| 5 | g.174729324C>G | CA362230103 | MSX2 | c.545C>G (p.Thr182Arg) c.*169C>G (n.*169C>G) | |
| 5 | g.174729324C>T | CA362230104 | MSX2 | c.545C>T (p.Thr182Ile) c.*169C>T (n.*169C>T) | |
| 5 | g.174729327_174729334del | CA913189700 | MSX2 | c.548_555del (p.Glu183GlyfsTer?) c.*172_*179del (n.*172_*179del) | ClinVar dbSNP |
| 5 | g.174729325A>C | CA447978883 | MSX2 | c.546A>C (p.Thr182=) c.*170A>C (n.*170A>C) | |
| 5 | g.174729325A>G | CA447978884 | MSX2 | c.546A>G (p.Thr182=) c.*170A>G (n.*170A>G) | |
| 5 | g.174729325A>T | CA447978885 | MSX2 | c.546A>T (p.Thr182=) c.*170A>T (n.*170A>T) | |
| 5 | g.174729326G>A | CA362230107 | MSX2 | c.547G>A (p.Glu183Lys) c.*171G>A (n.*171G>A) | |
| 5 | g.174729326G>C | CA362230105 | MSX2 | c.547G>C (p.Glu183Gln) c.*171G>C (n.*171G>C) | |
| 5 | g.174729326G>T | CA362230106 | MSX2 | c.547G>T (p.Glu183Ter) c.*171G>T (n.*171G>T) | |
| 5 | g.174729327A>C | CA362230108 | MSX2 | c.548A>C (p.Glu183Ala) c.*172A>C (n.*172A>C) | |
| 5 | g.174729327A>G | CA362230109 | MSX2 | c.548A>G (p.Glu183Gly) c.*172A>G (n.*172A>G) | |
| 5 | g.174729327A>T | CA362230110 | MSX2 | c.548A>T (p.Glu183Val) c.*172A>T (n.*172A>T) | |
| 5 | g.174729328G>A | CA447978889 | MSX2 | c.549G>A (p.Glu183=) c.*173G>A (n.*173G>A) | gnomAD v4 |
| 5 | g.174729328G>C | CA362230111 | MSX2 | c.549G>C (p.Glu183Asp) c.*173G>C (n.*173G>C) | |
| 5 | g.174729328G>T | CA362230112 | MSX2 | c.549G>T (p.Glu183Asp) c.*173G>T (n.*173G>T) | |
| 5 | g.174729329A>C | CA362230113 | MSX2 | c.550A>C (p.Thr184Pro) c.*174A>C (n.*174A>C) | |
| 5 | g.174729329A>G | CA362230114 | MSX2 | c.550A>G (p.Thr184Ala) c.*174A>G (n.*174A>G) | |
| 5 | g.174729329A>T | CA362230115 | MSX2 | c.550A>T (p.Thr184Ser) c.*174A>T (n.*174A>T) | |
| 5 | g.174729330C>A | CA362230116 | MSX2 | c.551C>A (p.Thr184Asn) c.*175C>A (n.*175C>A) | |
| 5 | g.174729330C>G | CA362230117 | MSX2 | c.551C>G (p.Thr184Ser) c.*175C>G (n.*175C>G) | |
| 5 | g.174729330C>T | CA362230118 | MSX2 | c.551C>T (p.Thr184Ile) c.*175C>T (n.*175C>T) | |
| 5 | g.174729331C>A | CA447978892 | MSX2 | c.552C>A (p.Thr184=) c.*176C>A (n.*176C>A) | |
| 5 | g.174729331C= | CA1602356178 | MSX2 | c.552C= (p.Thr184=) c.*176C= (n.*176C=) | |
| 5 | g.174729331C>G | CA3565227 | MSX2 | c.552C>G (p.Thr184=) c.*176C>G (n.*176C>G) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 5 | g.174729331C>T | CA447978893 | MSX2 | c.552C>T (p.Thr184=) c.*176C>T (n.*176C>T) | |
| 5 | g.174729332C>A | CA362230121 | MSX2 | c.553C>A (p.Gln185Lys) c.*177C>A (n.*177C>A) | |
| 5 | g.174729332C>G | CA362230120 | MSX2 | c.553C>G (p.Gln185Glu) c.*177C>G (n.*177C>G) | |
| 5 | g.174729332C>T | CA362230119 | MSX2 | c.553C>T (p.Gln185Ter) c.*177C>T (n.*177C>T) | |
| 5 | g.174729333A>C | CA362230124 | MSX2 | c.554A>C (p.Gln185Pro) c.*178A>C (n.*178A>C) | |
| 5 | g.174729333A>G | CA362230122 | MSX2 | c.554A>G (p.Gln185Arg) c.*178A>G (n.*178A>G) | gnomAD v4 |
| 5 | g.174729333A>T | CA362230123 | MSX2 | c.554A>T (p.Gln185Leu) c.*178A>T (n.*178A>T) | |
| 5 | g.174729334G>A | CA3565228 | MSX2 | c.555G>A (p.Gln185=) c.*179G>A (n.*179G>A) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 5 | g.174729334G>C | CA362230125 | MSX2 | c.555G>C (p.Gln185His) c.*179G>C (n.*179G>C) | |
| 5 | g.174729334G= | CA1602356185 | MSX2 | c.555G= (p.Gln185=) c.*179G= (n.*179G=) | |
| 5 | g.174729334G>T | CA362230126 | MSX2 | c.555G>T (p.Gln185His) c.*179G>T (n.*179G>T) | |
| 5 | g.174729335G>A | CA362230129 | MSX2 | c.556G>A (p.Val186Ile) c.*180G>A (n.*180G>A) | |
| 5 | g.174729335G>C | CA362230128 | MSX2 | c.556G>C (p.Val186Leu) c.*180G>C (n.*180G>C) | |
| 5 | g.174729335G>T | CA362230127 | MSX2 | c.556G>T (p.Val186Phe) c.*180G>T (n.*180G>T) | |
| 5 | g.174729336T>A | CA362230130 | MSX2 | c.557T>A (p.Val186Asp) c.*181T>A (n.*181T>A) | gnomAD v4 |
| 5 | g.174729336T>C | CA362230131 | MSX2 | c.557T>C (p.Val186Ala) c.*181T>C (n.*181T>C) | |
| 5 | g.174729336T>G | CA362230132 | MSX2 | c.557T>G (p.Val186Gly) c.*181T>G (n.*181T>G) | |
| 5 | g.174729337C>A | CA447978897 | MSX2 | c.558C>A (p.Val186=) c.*182C>A (n.*182C>A) | COSMIC |
| 5 | g.174729337C>G | CA447978898 | MSX2 | c.558C>G (p.Val186=) c.*182C>G (n.*182C>G) | gnomAD v4 |
| 5 | g.174729337C>T | CA447978899 | MSX2 | c.558C>T (p.Val186=) c.*182C>T (n.*182C>T) | |
| 5 | g.174729338A>C | CA362230133 | MSX2 | c.559A>C (p.Lys187Gln) c.*183A>C (n.*183A>C) | |
| 5 | g.174729338A>G | CA362230134 | MSX2 | c.559A>G (p.Lys187Glu) c.*183A>G (n.*183A>G) | |
| 5 | g.174729338A>T | CA362230135 | MSX2 | c.559A>T (p.Lys187Ter) c.*183A>T (n.*183A>T) | |
| 5 | g.174729339A>C | CA362230136 | MSX2 | c.560A>C (p.Lys187Thr) c.*184A>C (n.*184A>C) | |
| 5 | g.174729339A>G | CA362230138 | MSX2 | c.560A>G (p.Lys187Arg) c.*184A>G (n.*184A>G) | |
| 5 | g.174729339A>T | CA362230137 | MSX2 | c.560A>T (p.Lys187Ile) c.*184A>T (n.*184A>T) | |
| 5 | g.174729340A>C | CA362230139 | MSX2 | c.561A>C (p.Lys187Asn) c.*185A>C (n.*185A>C) | |
| 5 | g.174729340A>G | CA447978903 | MSX2 | c.561A>G (p.Lys187=) c.*185A>G (n.*185A>G) | gnomAD v4 |
| 5 | g.174729340A>T | CA362230140 | MSX2 | c.561A>T (p.Lys187Asn) c.*185A>T (n.*185A>T) | |
| 5 | g.174729341A>C | CA362230141 | MSX2 | c.562A>C (p.Ile188Leu) c.*186A>C (n.*186A>C) | |
| 5 | g.174729341A>G | CA362230142 | MSX2 | c.562A>G (p.Ile188Val) c.*186A>G (n.*186A>G) | |
| 5 | g.174729341A>T | CA362230143 | MSX2 | c.562A>T (p.Ile188Phe) c.*186A>T (n.*186A>T) | |
| 5 | g.174729342T>A | CA362230144 | MSX2 | c.563T>A (p.Ile188Asn) c.*187T>A (n.*187T>A) | |
| 5 | g.174729342T>C | CA362230145 | MSX2 | c.563T>C (p.Ile188Thr) c.*187T>C (n.*187T>C) | |
| 5 | g.174729342T>G | CA362230146 | MSX2 | c.563T>G (p.Ile188Ser) c.*187T>G (n.*187T>G) | |
| 5 | g.174729343C>A | CA447978906 | MSX2 | c.564C>A (p.Ile188=) c.*188C>A (n.*188C>A) | |
| 5 | g.174729343C>G | CA362230147 | MSX2 | c.564C>G (p.Ile188Met) c.*188C>G (n.*188C>G) | |
| 5 | g.174729343C>T | CA447978908 | MSX2 | c.564C>T (p.Ile188=) c.*188C>T (n.*188C>T) | |
| 5 | g.174729344T>A | CA362230148 | MSX2 | c.565T>A (p.Trp189Arg) c.*189T>A (n.*189T>A) | |
| 5 | g.174729344T>C | CA362230149 | MSX2 | c.565T>C (p.Trp189Arg) c.*189T>C (n.*189T>C) | |
| 5 | g.174729344T>G | CA362230150 | MSX2 | c.565T>G (p.Trp189Gly) c.*189T>G (n.*189T>G) | |
| 5 | g.174729345G>A | CA362230151 | MSX2 | c.566G>A (p.Trp189Ter) c.*190G>A (n.*190G>A) | |
| 5 | g.174729345G>C | CA362230152 | MSX2 | c.566G>C (p.Trp189Ser) c.*190G>C (n.*190G>C) | |
| 5 | g.174729345G= | CA1602356189 | MSX2 | c.566G= (p.Trp189=) c.*190G= (n.*190G=) | |
| 5 | g.174729345G>T | CA132701453 | MSX2 | c.566G>T (p.Trp189Leu) c.*190G>T (n.*190G>T) | dbSNP |
| 5 | g.174729346G>A | CA362230153 | MSX2 | c.567G>A (p.Trp189Ter) c.*191G>A (n.*191G>A) | |
| 5 | g.174729346G>C | CA362230155 | MSX2 | c.567G>C (p.Trp189Cys) c.*191G>C (n.*191G>C) | |
| 5 | g.174729346G>T | CA362230154 | MSX2 | c.567G>T (p.Trp189Cys) c.*191G>T (n.*191G>T) | COSMIC |
| 5 | g.174729347T>A | CA362230156 | MSX2 | c.568T>A (p.Phe190Ile) c.*192T>A (n.*192T>A) | |
| 5 | g.174729347T>C | CA362230157 | MSX2 | c.568T>C (p.Phe190Leu) c.*192T>C (n.*192T>C) | |
| 5 | g.174729347T>G | CA362230158 | MSX2 | c.568T>G (p.Phe190Val) c.*192T>G (n.*192T>G) | |
| 5 | g.174729348T>A | CA362230159 | MSX2 | c.569T>A (p.Phe190Tyr) c.*193T>A (n.*193T>A) | gnomAD v4 |
| 5 | g.174729348T>C | CA362230160 | MSX2 | c.569T>C (p.Phe190Ser) c.*193T>C (n.*193T>C) | |
| 5 | g.174729348T>G | CA362230161 | MSX2 | c.569T>G (p.Phe190Cys) c.*193T>G (n.*193T>G) | |
| 5 | g.174729349C>A | CA362230162 | MSX2 | c.570C>A (p.Phe190Leu) c.*194C>A (n.*194C>A) | |
| 5 | g.174729349C= | CA1602356194 | MSX2 | c.570C= (p.Phe190=) c.*194C= (n.*194C=) | |
| 5 | g.174729349C>G | CA362230163 | MSX2 | c.570C>G (p.Phe190Leu) c.*194C>G (n.*194C>G) | dbSNP gnomAD v2 gnomAD v4 |
| 5 | g.174729349C>T | CA3565229 | MSX2 | c.570C>T (p.Phe190=) c.*194C>T (n.*194C>T) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 5 | g.174729350C>A | CA362230164 | MSX2 | c.571C>A (p.Gln191Lys) c.*195C>A (n.*195C>A) | |
| 5 | g.174729350C>G | CA362230165 | MSX2 | c.571C>G (p.Gln191Glu) c.*195C>G (n.*195C>G) | |
| 5 | g.174729350C>T | CA362230166 | MSX2 | c.571C>T (p.Gln191Ter) c.*195C>T (n.*195C>T) | |
| 5 | g.174729351A= | CA1602356204 | MSX2 | c.572A= (p.Gln191=) c.*196A= (n.*196A=) | |
| 5 | g.174729351A>C | CA362230167 | MSX2 | c.572A>C (p.Gln191Pro) c.*196A>C (n.*196A>C) | |
| 5 | g.174729351A>G | CA362230169 | MSX2 | c.572A>G (p.Gln191Arg) c.*196A>G (n.*196A>G) | ClinVar dbSNP |
| 5 | g.174729351A>T | CA362230168 | MSX2 | c.572A>T (p.Gln191Leu) c.*196A>T (n.*196A>T) | |
| 5 | g.174729352G>A | CA447978918 | MSX2 | c.573G>A (p.Gln191=) c.*197G>A (n.*197G>A) | dbSNP gnomAD v2 gnomAD v4 |
| 5 | g.174729352G>C | CA362230170 | MSX2 | c.573G>C (p.Gln191His) c.*197G>C (n.*197G>C) | |
| 5 | g.174729352G= | CA1602356214 | MSX2 | c.573G= (p.Gln191=) c.*197G= (n.*197G=) | |
| 5 | g.174729352G>T | CA362230171 | MSX2 | c.573G>T (p.Gln191His) c.*197G>T (n.*197G>T) | |
| 5 | g.174729353A>C | CA362230172 | MSX2 | c.574A>C (p.Asn192His) c.*198A>C (n.*198A>C) | |
| 5 | g.174729353A>G | CA362230173 | MSX2 | c.574A>G (p.Asn192Asp) c.*198A>G (n.*198A>G) | |
| 5 | g.174729353A>T | CA362230174 | MSX2 | c.574A>T (p.Asn192Tyr) c.*198A>T (n.*198A>T) | |
| 5 | g.174729354A>C | CA362230175 | MSX2 | c.575A>C (p.Asn192Thr) c.*199A>C (n.*199A>C) | |
| 5 | g.174729354A>G | CA362230176 | MSX2 | c.575A>G (p.Asn192Ser) c.*199A>G (n.*199A>G) | |
| 5 | g.174729354A>T | CA362230177 | MSX2 | c.575A>T (p.Asn192Ile) c.*199A>T (n.*199A>T) | |
| 5 | g.174729355C>A | CA362230178 | MSX2 | c.576C>A (p.Asn192Lys) c.*200C>A (n.*200C>A) | |
| 5 | g.174729355C>G | CA362230179 | MSX2 | c.576C>G (p.Asn192Lys) c.*200C>G (n.*200C>G) | |
| 5 | g.174729355C>T | CA447978923 | MSX2 | c.576C>T (p.Asn192=) c.*200C>T (n.*200C>T) | |
| 5 | g.174729356C>A | CA447978926 | MSX2 | c.577C>A (p.Arg193=) c.*201C>A (n.*201C>A) | |
| 5 | g.174729356C= | CA1602356216 | MSX2 | c.577C= (p.Arg193=) c.*201C= (n.*201C=) | |
| 5 | g.174729356C>G | CA362230181 | MSX2 | c.577C>G (p.Arg193Gly) c.*201C>G (n.*201C>G) | |
| 5 | g.174729356C>T | CA362230180 | MSX2 | c.577C>T (p.Arg193Ter) c.*201C>T (n.*201C>T) | ClinVar dbSNP gnomAD v4 |
| 5 | g.174729357G>A | CA362230182 | MSX2 | c.578G>A (p.Arg193Gln) c.*202G>A (n.*202G>A) | gnomAD v4 COSMIC |
| 5 | g.174729357G>C | CA362230183 | MSX2 | c.578G>C (p.Arg193Pro) c.*202G>C (n.*202G>C) | |
| 5 | g.174729357G>T | CA362230184 | MSX2 | c.578G>T (p.Arg193Leu) c.*202G>T (n.*202G>T) | |
| 5 | g.174729358A>C | CA447978928 | MSX2 | c.579A>C (p.Arg193=) c.*203A>C (n.*203A>C) | |
| 5 | g.174729358A>G | CA447978929 | MSX2 | c.579A>G (p.Arg193=) c.*203A>G (n.*203A>G) | |
| 5 | g.174729358A>T | CA447978930 | MSX2 | c.579A>T (p.Arg193=) c.*203A>T (n.*203A>T) | |
| 5 | g.174729359A>C | CA447978931 | MSX2 | c.580A>C (p.Arg194=) c.*204A>C (n.*204A>C) | |
| 5 | g.174729359A>G | CA362230185 | MSX2 | c.580A>G (p.Arg194Gly) c.*204A>G (n.*204A>G) | |
| 5 | g.174729359A>T | CA362230186 | MSX2 | c.580A>T (p.Arg194Trp) c.*204A>T (n.*204A>T) | |
| 5 | g.174729360G>A | CA362230187 | MSX2 | c.581G>A (p.Arg194Lys) c.*205G>A (n.*205G>A) | |
| 5 | g.174729360G>C | CA362230188 | MSX2 | c.581G>C (p.Arg194Thr) c.*205G>C (n.*205G>C) | |
| 5 | g.174729360G>T | CA362230189 | MSX2 | c.581G>T (p.Arg194Met) c.*205G>T (n.*205G>T) | |
| 5 | g.174729361G>A | CA447978935 | MSX2 | c.582G>A (p.Arg194=) c.*206G>A (n.*206G>A) | gnomAD v4 |
| 5 | g.174729361G>C | CA362230190 | MSX2 | c.582G>C (p.Arg194Ser) c.*206G>C (n.*206G>C) | |
| 5 | g.174729361G>T | CA362230191 | MSX2 | c.582G>T (p.Arg194Ser) c.*206G>T (n.*206G>T) | |
| 5 | g.174729362G>A | CA362230192 | MSX2 | c.583G>A (p.Ala195Thr) c.*207G>A (n.*207G>A) | gnomAD v4 |
| 5 | g.174729362G>C | CA362230193 | MSX2 | c.583G>C (p.Ala195Pro) c.*207G>C (n.*207G>C) | |
| 5 | g.174729362G>T | CA362230194 | MSX2 | c.583G>T (p.Ala195Ser) c.*207G>T (n.*207G>T) | |
| 5 | g.174729363C>A | CA362230197 | MSX2 | c.584C>A (p.Ala195Asp) c.*208C>A (n.*208C>A) | |
| 5 | g.174729363C= | CA1602356221 | MSX2 | c.584C= (p.Ala195=) c.*208C= (n.*208C=) | |
| 5 | g.174729363C>G | CA362230195 | MSX2 | c.584C>G (p.Ala195Gly) c.*208C>G (n.*208C>G) | dbSNP gnomAD v2 gnomAD v4 |
| 5 | g.174729363C>T | CA362230196 | MSX2 | c.584C>T (p.Ala195Val) c.*208C>T (n.*208C>T) | dbSNP gnomAD v3 gnomAD v4 |
| 5 | g.174729364C>A | CA447978936 | MSX2 | c.585C>A (p.Ala195=) c.*209C>A (n.*209C>A) | |
| 5 | g.174729364C= | CA1602356225 | MSX2 | c.585C= (p.Ala195=) c.*209C= (n.*209C=) | |
| 5 | g.174729364C>G | CA3565230 | MSX2 | c.585C>G (p.Ala195=) c.*209C>G (n.*209C>G) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 5 | g.174729364C>T | CA447978937 | MSX2 | c.585C>T (p.Ala195=) c.*209C>T (n.*209C>T) | |
| 5 | g.174729365A>C | CA362230198 | MSX2 | c.586A>C (p.Lys196Gln) c.*210A>C (n.*210A>C) | |
| 5 | g.174729365A>G | CA362230199 | MSX2 | c.586A>G (p.Lys196Glu) c.*210A>G (n.*210A>G) | |
| 5 | g.174729365A>T | CA362230200 | MSX2 | c.586A>T (p.Lys196Ter) c.*210A>T (n.*210A>T) | |
| 5 | g.174729366A= | CA1602356229 | MSX2 | c.587A= (p.Lys196=) c.*211A= (n.*211A=) | |
| 5 | g.174729366A>C | CA362230201 | MSX2 | c.587A>C (p.Lys196Thr) c.*211A>C (n.*211A>C) | |
| 5 | g.174729366A>G | CA362230202 | MSX2 | c.587A>G (p.Lys196Arg) c.*211A>G (n.*211A>G) | dbSNP gnomAD v2 gnomAD v4 |
| 5 | g.174729366A>T | CA362230203 | MSX2 | c.587A>T (p.Lys196Met) c.*211A>T (n.*211A>T) | |
| 5 | g.174729367G>A | CA447978940 | MSX2 | c.588G>A (p.Lys196=) c.*212G>A (n.*212G>A) | |
| 5 | g.174729367G>C | CA362230204 | MSX2 | c.588G>C (p.Lys196Asn) c.*212G>C (n.*212G>C) | |
| 5 | g.174729367G>T | CA362230205 | MSX2 | c.588G>T (p.Lys196Asn) c.*212G>T (n.*212G>T) | |
| 5 | g.174729368G>A | CA362230206 | MSX2 | c.589G>A (p.Ala197Thr) c.*213G>A (n.*213G>A) | |
| 5 | g.174729368G>C | CA362230207 | MSX2 | c.589G>C (p.Ala197Pro) c.*213G>C (n.*213G>C) | |
| 5 | g.174729368G>T | CA362230208 | MSX2 | c.589G>T (p.Ala197Ser) c.*213G>T (n.*213G>T) | |
| 5 | g.174729369C>A | CA3565231 | MSX2 | c.590C>A (p.Ala197Glu) c.*214C>A (n.*214C>A) | dbSNP ExAC gnomAD v2 |
| 5 | g.174729369C= | CA1602356234 | MSX2 | c.590C= (p.Ala197=) c.*214C= (n.*214C=) | |
| 5 | g.174729369C>G | CA362230209 | MSX2 | c.590C>G (p.Ala197Gly) c.*214C>G (n.*214C>G) | |
| 5 | g.174729369C>T | CA3565232 | MSX2 | c.590C>T (p.Ala197Val) c.*214C>T (n.*214C>T) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 5 | g.174729370G>A | CA3565233 | MSX2 | c.591G>A (p.Ala197=) c.*215G>A (n.*215G>A) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 5 | g.174729370G>C | CA447978947 | MSX2 | c.591G>C (p.Ala197=) c.*215G>C (n.*215G>C) | |
| 5 | g.174729370G= | CA1602356242 | MSX2 | c.591G= (p.Ala197=) c.*215G= (n.*215G=) | |
| 5 | g.174729370G>T | CA447978948 | MSX2 | c.591G>T (p.Ala197=) c.*215G>T (n.*215G>T) | COSMIC |
| 5 | g.174729371A= | CA1602356245 | MSX2 | c.592A= (p.Lys198=) c.*216A= (n.*216A=) | |
| 5 | g.174729371A>C | CA362230211 | MSX2 | c.592A>C (p.Lys198Gln) c.*216A>C (n.*216A>C) | |
| 5 | g.174729371A>G | CA362230210 | MSX2 | c.592A>G (p.Lys198Glu) c.*216A>G (n.*216A>G) | ClinVar dbSNP |
| 5 | g.174729371A>T | CA362230212 | MSX2 | c.592A>T (p.Lys198Ter) c.*216A>T (n.*216A>T) | |
| 5 | g.174729372A>C | CA362230213 | MSX2 | c.593A>C (p.Lys198Thr) c.*217A>C (n.*217A>C) | |
| 5 | g.174729372A>G | CA362230214 | MSX2 | c.593A>G (p.Lys198Arg) c.*217A>G (n.*217A>G) | |
| 5 | g.174729372A>T | CA362230215 | MSX2 | c.593A>T (p.Lys198Ile) c.*217A>T (n.*217A>T) | |
| 5 | g.174729373A>C | CA362230216 | MSX2 | c.594A>C (p.Lys198Asn) c.*218A>C (n.*218A>C) | |
| 5 | g.174729373A>G | CA447978950 | MSX2 | c.594A>G (p.Lys198=) c.*218A>G (n.*218A>G) | |
| 5 | g.174729373A>T | CA362230217 | MSX2 | c.594A>T (p.Lys198Asn) c.*218A>T (n.*218A>T) | |
| 5 | g.174729374A>C | CA447978951 | MSX2 | c.595A>C (p.Arg199=) c.*219A>C (n.*219A>C) | gnomAD v4 |
| 5 | g.174729374A>G | CA362230218 | MSX2 | c.595A>G (p.Arg199Gly) c.*219A>G (n.*219A>G) | |
| 5 | g.174729374A>T | CA362230219 | MSX2 | c.595A>T (p.Arg199Ter) c.*219A>T (n.*219A>T) | COSMIC |
| 5 | g.174729375G>A | CA362230220 | MSX2 | c.596G>A (p.Arg199Lys) c.*220G>A (n.*220G>A) | gnomAD v4 |
| 5 | g.174729375G>C | CA362230221 | MSX2 | c.596G>C (p.Arg199Thr) c.*220G>C (n.*220G>C) | |
| 5 | g.174729375G= | CA1602356248 | MSX2 | c.596G= (p.Arg199=) c.*220G= (n.*220G=) | |
| 5 | g.174729375G>T | CA132701454 | MSX2 | c.596G>T (p.Arg199Ile) c.*220G>T (n.*220G>T) | dbSNP gnomAD v3 gnomAD v4 |
| 5 | g.174729376A>C | CA362230222 | MSX2 | c.597A>C (p.Arg199Ser) c.*221A>C (n.*221A>C) | |
| 5 | g.174729376A>G | CA447978952 | MSX2 | c.597A>G (p.Arg199=) c.*221A>G (n.*221A>G) | ClinVar gnomAD v4 |
| 5 | g.174729376A>T | CA362230223 | MSX2 | c.597A>T (p.Arg199Ser) c.*221A>T (n.*221A>T) | |
| 5 | g.174729377C>A | CA362230225 | MSX2 | c.598C>A (p.Leu200Met) c.*222C>A (n.*222C>A) | |
| 5 | g.174729377C= | CA1602356254 | MSX2 | c.598C= (p.Leu200=) c.*222C= (n.*222C=) | |
| 5 | g.174729377C>G | CA362230224 | MSX2 | c.598C>G (p.Leu200Val) c.*222C>G (n.*222C>G) | dbSNP |
| 5 | g.174729377C>T | CA447978953 | MSX2 | c.598C>T (p.Leu200=) c.*222C>T (n.*222C>T) | |
| 5 | g.174729378T>A | CA362230226 | MSX2 | c.599T>A (p.Leu200Gln) c.*223T>A (n.*223T>A) | |
| 5 | g.174729378T>C | CA362230227 | MSX2 | c.599T>C (p.Leu200Pro) c.*223T>C (n.*223T>C) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 5 | g.174729378T>G | CA362230228 | MSX2 | c.599T>G (p.Leu200Arg) c.*223T>G (n.*223T>G) | |
| 5 | g.174729378T= | CA1602356257 | MSX2 | c.599T= (p.Leu200=) c.*223T= (n.*223T=) | |
| 5 | g.174729379G>A | CA447978954 | MSX2 | c.600G>A (p.Leu200=) c.*224G>A (n.*224G>A) | |
| 5 | g.174729379G>C | CA447978955 | MSX2 | c.600G>C (p.Leu200=) c.*224G>C (n.*224G>C) | |
| 5 | g.174729379G= | CA1602356263 | MSX2 | c.600G= (p.Leu200=) c.*224G= (n.*224G=) | |
| 5 | g.174729379G>T | CA447978956 | MSX2 | c.600G>T (p.Leu200=) c.*224G>T (n.*224G>T) | dbSNP gnomAD v2 gnomAD v4 |
| 5 | g.174729380C>A | CA362230229 | MSX2 | c.601C>A (p.Gln201Lys) c.*225C>A (n.*225C>A) | |
| 5 | g.174729380C>G | CA362230230 | MSX2 | c.601C>G (p.Gln201Glu) c.*225C>G (n.*225C>G) | |
| 5 | g.174729380C>T | CA362230231 | MSX2 | c.601C>T (p.Gln201Ter) c.*225C>T (n.*225C>T) | |
| 5 | g.174729381A= | CA1602356267 | MSX2 | c.602A= (p.Gln201=) c.*226A= (n.*226A=) | |
| 5 | g.174729381A>C | CA362230232 | MSX2 | c.602A>C (p.Gln201Pro) c.*226A>C (n.*226A>C) | |
| 5 | g.174729381A>G | CA362230233 | MSX2 | c.602A>G (p.Gln201Arg) c.*226A>G (n.*226A>G) | dbSNP gnomAD v2 gnomAD v4 |
| 5 | g.174729381A>T | CA362230234 | MSX2 | c.602A>T (p.Gln201Leu) c.*226A>T (n.*226A>T) | |
| 5 | g.174729382G>A | CA447978957 | MSX2 | c.603G>A (p.Gln201=) c.*227G>A (n.*227G>A) | |
| 5 | g.174729382G>C | CA362230235 | MSX2 | c.603G>C (p.Gln201His) c.*227G>C (n.*227G>C) | |
| 5 | g.174729382G>T | CA362230236 | MSX2 | c.603G>T (p.Gln201His) c.*227G>T (n.*227G>T) | |
| 5 | g.174729383dup | CA132701455 | MSX2 | c.604dup (p.Glu202GlyfsTer?) c.*228dup (n.*228dup) | dbSNP |
| 5 | g.174729383G>A | CA362230238 | MSX2 | c.604G>A (p.Glu202Lys) c.*228G>A (n.*228G>A) | |
| 5 | g.174729383G>C | CA3565234 | MSX2 | c.604G>C (p.Glu202Gln) c.*228G>C (n.*228G>C) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 5 | g.174729383G= | CA1602356274 | MSX2 | c.604G= (p.Glu202=) c.*228G= (n.*228G=) | |
| 5 | g.174729383G>T | CA362230237 | MSX2 | c.604G>T (p.Glu202Ter) c.*228G>T (n.*228G>T) | |
| 5 | g.174729384A>C | CA362230241 | MSX2 | c.605A>C (p.Glu202Ala) c.*229A>C (n.*229A>C) | |
| 5 | g.174729384A>G | CA362230239 | MSX2 | c.605A>G (p.Glu202Gly) c.*229A>G (n.*229A>G) | |
| 5 | g.174729384A>T | CA362230240 | MSX2 | c.605A>T (p.Glu202Val) c.*229A>T (n.*229A>T) | |
| 5 | g.174729385G>A | CA447978958 | MSX2 | c.606G>A (p.Glu202=) c.*230G>A (n.*230G>A) | |
| 5 | g.174729385G>C | CA362230242 | MSX2 | c.606G>C (p.Glu202Asp) c.*230G>C (n.*230G>C) | |
| 5 | g.174729385G>T | CA362230243 | MSX2 | c.606G>T (p.Glu202Asp) c.*230G>T (n.*230G>T) | |
| 5 | g.174729386G>A | CA362230244 | MSX2 | c.607G>A (p.Ala203Thr) c.*231G>A (n.*231G>A) | |
| 5 | g.174729386G>C | CA362230245 | MSX2 | c.607G>C (p.Ala203Pro) c.*231G>C (n.*231G>C) | |
| 5 | g.174729386G>T | CA362230246 | MSX2 | c.607G>T (p.Ala203Ser) c.*231G>T (n.*231G>T) | |
| 5 | g.174729387C>A | CA362230247 | MSX2 | c.608C>A (p.Ala203Glu) c.*232C>A (n.*232C>A) | |
| 5 | g.174729387C>G | CA362230248 | MSX2 | c.608C>G (p.Ala203Gly) c.*232C>G (n.*232C>G) | |
| 5 | g.174729387C>T | CA362230249 | MSX2 | c.608C>T (p.Ala203Val) c.*232C>T (n.*232C>T) | |
| 5 | g.174729388A>C | CA447978959 | MSX2 | c.609A>C (p.Ala203=) c.*233A>C (n.*233A>C) | |
| 5 | g.174729388A>G | CA447978960 | MSX2 | c.609A>G (p.Ala203=) c.*233A>G (n.*233A>G) | |
| 5 | g.174729388A>T | CA447978961 | MSX2 | c.609A>T (p.Ala203=) c.*233A>T (n.*233A>T) | |
| 5 | g.174729389G>A | CA362230250 | MSX2 | c.610G>A (p.Glu204Lys) c.*234G>A (n.*234G>A) | |
| 5 | g.174729389G>C | CA362230251 | MSX2 | c.610G>C (p.Glu204Gln) c.*234G>C (n.*234G>C) | |
| 5 | g.174729389G>T | CA362230252 | MSX2 | c.610G>T (p.Glu204Ter) c.*234G>T (n.*234G>T) | |
| 5 | g.174729390A>C | CA362230255 | MSX2 | c.611A>C (p.Glu204Ala) c.*235A>C (n.*235A>C) | |
| 5 | g.174729390A>G | CA362230253 | MSX2 | c.611A>G (p.Glu204Gly) c.*235A>G (n.*235A>G) | |
| 5 | g.174729390A>T | CA362230254 | MSX2 | c.611A>T (p.Glu204Val) c.*235A>T (n.*235A>T) | |
| 5 | g.174729391A>C | CA362230256 | MSX2 | c.612A>C (p.Glu204Asp) c.*236A>C (n.*236A>C) | |
| 5 | g.174729391A>G | CA447978962 | MSX2 | c.612A>G (p.Glu204=) c.*236A>G (n.*236A>G) | |
| 5 | g.174729391A>T | CA362230257 | MSX2 | c.612A>T (p.Glu204Asp) c.*236A>T (n.*236A>T) | |
| 5 | g.174729392C>A | CA362230258 | MSX2 | c.613C>A (p.Leu205Met) c.*237C>A (n.*237C>A) | gnomAD v4 |
| 5 | g.174729392C= | CA1602356276 | MSX2 | c.613C= (p.Leu205=) c.*237C= (n.*237C=) | |
| 5 | g.174729392C>G | CA362230259 | MSX2 | c.613C>G (p.Leu205Val) c.*237C>G (n.*237C>G) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 5 | g.174729392C>T | CA132701456 | MSX2 | c.613C>T (p.Leu205=) c.*237C>T (n.*237C>T) | dbSNP gnomAD v4 |
| 5 | g.174729393T>A | CA362230260 | MSX2 | c.614T>A (p.Leu205Gln) c.*238T>A (n.*238T>A) | |
| 5 | g.174729393T>C | CA362230261 | MSX2 | c.614T>C (p.Leu205Pro) c.*238T>C (n.*238T>C) | |
| 5 | g.174729393T>G | CA362230262 | MSX2 | c.614T>G (p.Leu205Arg) c.*238T>G (n.*238T>G) | |
| 5 | g.174729394G>A | CA3565235 | MSX2 | c.615G>A (p.Leu205=) c.*239G>A (n.*239G>A) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 5 | g.174729394G>C | CA447978731 | MSX2 | c.615G>C (p.Leu205=) c.*239G>C (n.*239G>C) | dbSNP |
| 5 | g.174729394G= | CA1602356280 | MSX2 | c.615G= (p.Leu205=) c.*239G= (n.*239G=) | |
| 5 | g.174729394G>T | CA447978733 | MSX2 | c.615G>T (p.Leu205=) c.*239G>T (n.*239G>T) | |
| 5 | g.174729395G>A | CA362230263 | MSX2 | c.616G>A (p.Glu206Lys) c.*240G>A (n.*240G>A) | |
| 5 | g.174729395G>C | CA362230264 | MSX2 | c.616G>C (p.Glu206Gln) c.*240G>C (n.*240G>C) | |
| 5 | g.174729395G>T | CA362230265 | MSX2 | c.616G>T (p.Glu206Ter) c.*240G>T (n.*240G>T) | |
| 5 | g.174729396A>C | CA362230267 | MSX2 | c.617A>C (p.Glu206Ala) c.*241A>C (n.*241A>C) | |
| 5 | g.174729396A>G | CA362230268 | MSX2 | c.617A>G (p.Glu206Gly) c.*241A>G (n.*241A>G) | |
| 5 | g.174729396A>T | CA362230266 | MSX2 | c.617A>T (p.Glu206Val) c.*241A>T (n.*241A>T) | gnomAD v4 |
| 5 | g.174729397A= | CA1602356282 | MSX2 | c.618A= (p.Glu206=) c.*242A= (n.*242A=) | |
| 5 | g.174729397A>C | CA362230269 | MSX2 | c.618A>C (p.Glu206Asp) c.*242A>C (n.*242A>C) | |
| 5 | g.174729397A>G | CA447978737 | MSX2 | c.618A>G (p.Glu206=) c.*242A>G (n.*242A>G) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 5 | g.174729397A>T | CA362230270 | MSX2 | c.618A>T (p.Glu206Asp) c.*242A>T (n.*242A>T) | |
| 5 | g.174729398A= | CA1602356285 | MSX2 | c.619A= (p.Lys207=) c.*243A= (n.*243A=) | |
| 5 | g.174729398A>C | CA132701457 | MSX2 | c.619A>C (p.Lys207Gln) c.*243A>C (n.*243A>C) | dbSNP gnomAD v4 |
| 5 | g.174729398A>G | CA362230271 | MSX2 | c.619A>G (p.Lys207Glu) c.*243A>G (n.*243A>G) | |
| 5 | g.174729398A>T | CA362230272 | MSX2 | c.619A>T (p.Lys207Ter) c.*243A>T (n.*243A>T) | |
| 5 | g.174729399A>C | CA362230273 | MSX2 | c.620A>C (p.Lys207Thr) c.*244A>C (n.*244A>C) | |
| 5 | g.174729399A>G | CA362230274 | MSX2 | c.620A>G (p.Lys207Arg) c.*244A>G (n.*244A>G) | |
| 5 | g.174729399A>T | CA362230275 | MSX2 | c.620A>T (p.Lys207Met) c.*244A>T (n.*244A>T) | |
| 5 | g.174729400G>A | CA447978742 | MSX2 | c.621G>A (p.Lys207=) c.*245G>A (n.*245G>A) | |
| 5 | g.174729400G>C | CA362230276 | MSX2 | c.621G>C (p.Lys207Asn) c.*245G>C (n.*245G>C) | |
| 5 | g.174729400G>T | CA362230277 | MSX2 | c.621G>T (p.Lys207Asn) c.*245G>T (n.*245G>T) | |
| 5 | g.174729401C>A | CA362230278 | MSX2 | c.622C>A (p.Leu208Met) c.*246C>A (n.*246C>A) | |
| 5 | g.174729401C= | CA1602356289 | MSX2 | c.622C= (p.Leu208=) c.*246C= (n.*246C=) | |
| 5 | g.174729401C>G | CA362230279 | MSX2 | c.622C>G (p.Leu208Val) c.*246C>G (n.*246C>G) | dbSNP |
| 5 | g.174729401C>T | CA447978744 | MSX2 | c.622C>T (p.Leu208=) c.*246C>T (n.*246C>T) |