| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 3 | g.93900830T>A | CA353673122 | PROS1 | c.701A>T (p.Tyr234Phe) c.656A>T (p.Tyr219Phe) n.869A>T c.659A>T (p.Tyr220Phe) c.800A>T (n.800A>T) c.797A>T (p.Tyr266Phe) c.308A>T (p.Tyr103Phe) | |
| 3 | g.93900830T>C | CA128690 | PROS1 | c.701A>G (p.Tyr234Cys) c.656A>G (p.Tyr219Cys) n.869A>G c.659A>G (p.Tyr220Cys) c.800A>G (n.800A>G) c.797A>G (p.Tyr266Cys) c.308A>G (p.Tyr103Cys) | ClinVar dbSNP gnomAD v2 COSMIC |
| 3 | g.93900830T>G | CA353673123 | PROS1 | c.701A>C (p.Tyr234Ser) c.656A>C (p.Tyr219Ser) n.869A>C c.659A>C (p.Tyr220Ser) c.800A>C (n.800A>C) c.797A>C (p.Tyr266Ser) c.308A>C (p.Tyr103Ser) | |
| 3 | g.93900830T= | CA1385040189 | PROS1 | c.701A= (p.Tyr234=) c.656A= (p.Tyr219=) n.869A= c.659A= (p.Tyr220=) c.800A= (n.800A=) c.797A= (p.Tyr266=) c.308A= (p.Tyr103=) | |
| 3 | g.93900831A>C | CA353673124 | PROS1 | c.700T>G (p.Tyr234Asp) c.655T>G (p.Tyr219Asp) n.868T>G c.658T>G (p.Tyr220Asp) c.799T>G (n.799T>G) c.796T>G (p.Tyr266Asp) c.307T>G (p.Tyr103Asp) | |
| 3 | g.93900831A>G | CA353673125 | PROS1 | c.700T>C (p.Tyr234His) c.655T>C (p.Tyr219His) n.868T>C c.658T>C (p.Tyr220His) c.799T>C (n.799T>C) c.796T>C (p.Tyr266His) c.307T>C (p.Tyr103His) | |
| 3 | g.93900831A>T | CA353673126 | PROS1 | c.700T>A (p.Tyr234Asn) c.655T>A (p.Tyr219Asn) n.868T>A c.658T>A (p.Tyr220Asn) c.799T>A (n.799T>A) c.796T>A (p.Tyr266Asn) c.307T>A (p.Tyr103Asn) | |
| 3 | g.93900832T>A | CA353673128 | PROS1 | c.699A>T (p.Arg233Ser) c.654A>T (p.Arg218Ser) n.867A>T c.657A>T (p.Arg219Ser) c.798A>T (n.798A>T) c.795A>T (p.Arg265Ser) c.306A>T (p.Arg102Ser) | |
| 3 | g.93900832T>C | CA434461652 | PROS1 | c.699A>G (p.Arg233=) c.654A>G (p.Arg218=) n.867A>G c.657A>G (p.Arg219=) c.798A>G (n.798A>G) c.795A>G (p.Arg265=) c.306A>G (p.Arg102=) | |
| 3 | g.93900832T>G | CA353673127 | PROS1 | c.699A>C (p.Arg233Ser) c.654A>C (p.Arg218Ser) n.867A>C c.657A>C (p.Arg219Ser) c.798A>C (n.798A>C) c.795A>C (p.Arg265Ser) c.306A>C (p.Arg102Ser) | |
| 3 | g.93900832T= | CA1385040190 | PROS1 | c.699A= (p.Arg233=) c.654A= (p.Arg218=) n.867A= c.657A= (p.Arg219=) c.798A= (n.798A=) c.795A= (p.Arg265=) c.306A= (p.Arg102=) | |
| 3 | g.93900832_93900833insA | CA78486999 | PROS1 | c.698_699insT (p.Arg233SerfsTer3) c.653_654insT (p.Arg218SerfsTer3) n.866_867insT c.656_657insT (p.Arg219SerfsTer3) c.797_798insT (n.797_798insT) c.794_795insT (p.Arg265SerfsTer3) c.305_306insT (p.Arg102SerfsTer3) | dbSNP |
| 3 | g.93900833C>A | CA353673129 | PROS1 | c.698G>T (p.Arg233Ile) c.653G>T (p.Arg218Ile) n.866G>T c.656G>T (p.Arg219Ile) c.797G>T (n.797G>T) c.794G>T (p.Arg265Ile) c.305G>T (p.Arg102Ile) | |
| 3 | g.93900833C= | CA1385040191 | PROS1 | c.698G= (p.Arg233=) c.653G= (p.Arg218=) n.866G= c.656G= (p.Arg219=) c.797G= (n.797G=) c.794G= (p.Arg265=) c.305G= (p.Arg102=) | |
| 3 | g.93900833C>G | CA353673130 | PROS1 | c.698G>C (p.Arg233Thr) c.653G>C (p.Arg218Thr) n.866G>C c.656G>C (p.Arg219Thr) c.797G>C (n.797G>C) c.794G>C (p.Arg265Thr) c.305G>C (p.Arg102Thr) | |
| 3 | g.93900833C>T | CA211741 | PROS1 | c.698G>A (p.Arg233Lys) c.653G>A (p.Arg218Lys) n.866G>A c.656G>A (p.Arg219Lys) c.797G>A (n.797G>A) c.794G>A (p.Arg265Lys) c.305G>A (p.Arg102Lys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 3 | g.93900834T>A | CA353673131 | PROS1 | c.697A>T (p.Arg233Ter) c.652A>T (p.Arg218Ter) n.865A>T c.655A>T (p.Arg219Ter) c.796A>T (n.796A>T) c.793A>T (p.Arg265Ter) c.304A>T (p.Arg102Ter) | |
| 3 | g.93900834T>C | CA353673132 | PROS1 | c.697A>G (p.Arg233Gly) c.652A>G (p.Arg218Gly) n.865A>G c.655A>G (p.Arg219Gly) c.796A>G (n.796A>G) c.793A>G (p.Arg265Gly) c.304A>G (p.Arg102Gly) | |
| 3 | g.93900834T>G | CA434461653 | PROS1 | c.697A>C (p.Arg233=) c.652A>C (p.Arg218=) n.865A>C c.655A>C (p.Arg219=) c.796A>C (n.796A>C) c.793A>C (p.Arg265=) c.304A>C (p.Arg102=) | |
| 3 | g.93900835G>A | CA434461654 | PROS1 | c.696C>T (p.Tyr232=) c.651C>T (p.Tyr217=) n.864C>T c.654C>T (p.Tyr218=) c.795C>T (n.795C>T) c.792C>T (p.Tyr264=) c.303C>T (p.Tyr101=) | gnomAD v4 |
| 3 | g.93900835G>C | CA353673133 | PROS1 | c.696C>G (p.Tyr232Ter) c.651C>G (p.Tyr217Ter) n.864C>G c.654C>G (p.Tyr218Ter) c.795C>G (n.795C>G) c.792C>G (p.Tyr264Ter) c.303C>G (p.Tyr101Ter) | |
| 3 | g.93900835G>T | CA353673134 | PROS1 | c.696C>A (p.Tyr232Ter) c.651C>A (p.Tyr217Ter) n.864C>A c.654C>A (p.Tyr218Ter) c.795C>A (n.795C>A) c.792C>A (p.Tyr264Ter) c.303C>A (p.Tyr101Ter) | |
| 3 | g.93900836T>A | CA353673135 | PROS1 | c.695A>T (p.Tyr232Phe) c.650A>T (p.Tyr217Phe) n.863A>T c.653A>T (p.Tyr218Phe) c.794A>T (n.794A>T) c.791A>T (p.Tyr264Phe) c.302A>T (p.Tyr101Phe) | |
| 3 | g.93900836T>C | CA2503408 | PROS1 | c.695A>G (p.Tyr232Cys) c.650A>G (p.Tyr217Cys) n.863A>G c.653A>G (p.Tyr218Cys) c.794A>G (n.794A>G) c.791A>G (p.Tyr264Cys) c.302A>G (p.Tyr101Cys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 3 | g.93900836T>G | CA353673136 | PROS1 | c.695A>C (p.Tyr232Ser) c.650A>C (p.Tyr217Ser) n.863A>C c.653A>C (p.Tyr218Ser) c.794A>C (n.794A>C) c.791A>C (p.Tyr264Ser) c.302A>C (p.Tyr101Ser) | |
| 3 | g.93900836T= | CA1385040192 | PROS1 | c.695A= (p.Tyr232=) c.650A= (p.Tyr217=) n.863A= c.653A= (p.Tyr218=) c.794A= (n.794A=) c.791A= (p.Tyr264=) c.302A= (p.Tyr101=) | |
| 3 | g.93900837A>C | CA353673138 | PROS1 | c.694T>G (p.Tyr232Asp) c.649T>G (p.Tyr217Asp) n.862T>G c.652T>G (p.Tyr218Asp) c.793T>G (n.793T>G) c.790T>G (p.Tyr264Asp) c.301T>G (p.Tyr101Asp) | |
| 3 | g.93900837A>G | CA353673139 | PROS1 | c.694T>C (p.Tyr232His) c.649T>C (p.Tyr217His) n.862T>C c.652T>C (p.Tyr218His) c.793T>C (n.793T>C) c.790T>C (p.Tyr264His) c.301T>C (p.Tyr101His) | gnomAD v4 |
| 3 | g.93900837A>T | CA353673137 | PROS1 | c.694T>A (p.Tyr232Asn) c.649T>A (p.Tyr217Asn) n.862T>A c.652T>A (p.Tyr218Asn) c.793T>A (n.793T>A) c.790T>A (p.Tyr264Asn) c.301T>A (p.Tyr101Asn) | |
| 3 | g.93900838G>A | CA434461655 | PROS1 | c.693C>T (p.Gly231=) c.648C>T (p.Gly216=) n.861C>T c.651C>T (p.Gly217=) c.792C>T (n.792C>T) c.789C>T (p.Gly263=) c.300C>T (p.Gly100=) | |
| 3 | g.93900838G>C | CA434461656 | PROS1 | c.693C>G (p.Gly231=) c.648C>G (p.Gly216=) n.861C>G c.651C>G (p.Gly217=) c.792C>G (n.792C>G) c.789C>G (p.Gly263=) c.300C>G (p.Gly100=) | |
| 3 | g.93900838G>T | CA434461657 | PROS1 | c.693C>A (p.Gly231=) c.648C>A (p.Gly216=) n.861C>A c.651C>A (p.Gly217=) c.792C>A (n.792C>A) c.789C>A (p.Gly263=) c.300C>A (p.Gly100=) | |
| 3 | g.93900839C>A | CA353673140 | PROS1 | c.692G>T (p.Gly231Val) c.647G>T (p.Gly216Val) n.860G>T c.650G>T (p.Gly217Val) c.791G>T (n.791G>T) c.788G>T (p.Gly263Val) c.299G>T (p.Gly100Val) | |
| 3 | g.93900839C= | CA1385040193 | PROS1 | c.692G= (p.Gly231=) c.647G= (p.Gly216=) n.860G= c.650G= (p.Gly217=) c.791G= (n.791G=) c.788G= (p.Gly263=) c.299G= (p.Gly100=) | |
| 3 | g.93900839C>G | CA353673141 | PROS1 | c.692G>C (p.Gly231Ala) c.647G>C (p.Gly216Ala) n.860G>C c.650G>C (p.Gly217Ala) c.791G>C (n.791G>C) c.788G>C (p.Gly263Ala) c.299G>C (p.Gly100Ala) | |
| 3 | g.93900839C>T | CA353673142 | PROS1 | c.692G>A (p.Gly231Asp) c.647G>A (p.Gly216Asp) n.860G>A c.650G>A (p.Gly217Asp) c.791G>A (n.791G>A) c.788G>A (p.Gly263Asp) c.299G>A (p.Gly100Asp) | dbSNP gnomAD v4 |
| 3 | g.93900840C>A | CA353673143 | PROS1 | c.691G>T (p.Gly231Cys) c.646G>T (p.Gly216Cys) n.859G>T c.649G>T (p.Gly217Cys) c.790G>T (n.790G>T) c.787G>T (p.Gly263Cys) c.298G>T (p.Gly100Cys) | |
| 3 | g.93900840C= | CA1385040194 | PROS1 | c.691G= (p.Gly231=) c.646G= (p.Gly216=) n.859G= c.649G= (p.Gly217=) c.790G= (n.790G=) c.787G= (p.Gly263=) c.298G= (p.Gly100=) | |
| 3 | g.93900840C>G | CA353673144 | PROS1 | c.691G>C (p.Gly231Arg) c.646G>C (p.Gly216Arg) n.859G>C c.649G>C (p.Gly217Arg) c.790G>C (n.790G>C) c.787G>C (p.Gly263Arg) c.298G>C (p.Gly100Arg) | |
| 3 | g.93900840C>T | CA2503409 | PROS1 | c.691G>A (p.Gly231Ser) c.646G>A (p.Gly216Ser) n.859G>A c.649G>A (p.Gly217Ser) c.790G>A (n.790G>A) c.787G>A (p.Gly263Ser) c.298G>A (p.Gly100Ser) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 3 | g.93900841T>A | CA353673145 | PROS1 | c.690A>T (p.Glu230Asp) c.645A>T (p.Glu215Asp) n.858A>T c.648A>T (p.Glu216Asp) c.789A>T (n.789A>T) c.786A>T (p.Glu262Asp) c.297A>T (p.Glu99Asp) | |
| 3 | g.93900841T>C | CA434461658 | PROS1 | c.690A>G (p.Glu230=) c.645A>G (p.Glu215=) n.858A>G c.648A>G (p.Glu216=) c.789A>G (n.789A>G) c.786A>G (p.Glu262=) c.297A>G (p.Glu99=) | |
| 3 | g.93900841T>G | CA353673146 | PROS1 | c.690A>C (p.Glu230Asp) c.645A>C (p.Glu215Asp) n.858A>C c.648A>C (p.Glu216Asp) c.789A>C (n.789A>C) c.786A>C (p.Glu262Asp) c.297A>C (p.Glu99Asp) | |
| 3 | g.93900842T>A | CA353673147 | PROS1 | c.689A>T (p.Glu230Val) c.644A>T (p.Glu215Val) n.857A>T c.647A>T (p.Glu216Val) c.788A>T (n.788A>T) c.785A>T (p.Glu262Val) c.296A>T (p.Glu99Val) | |
| 3 | g.93900842T>C | CA353673148 | PROS1 | c.689A>G (p.Glu230Gly) c.644A>G (p.Glu215Gly) n.857A>G c.647A>G (p.Glu216Gly) c.788A>G (n.788A>G) c.785A>G (p.Glu262Gly) c.296A>G (p.Glu99Gly) | |
| 3 | g.93900842T>G | CA353673149 | PROS1 | c.689A>C (p.Glu230Ala) c.644A>C (p.Glu215Ala) n.857A>C c.647A>C (p.Glu216Ala) c.788A>C (n.788A>C) c.785A>C (p.Glu262Ala) c.296A>C (p.Glu99Ala) | |
| 3 | g.93900843C>A | CA353673150 | PROS1 | c.688G>T (p.Glu230Ter) c.643G>T (p.Glu215Ter) n.856G>T c.646G>T (p.Glu216Ter) c.787G>T (n.787G>T) c.784G>T (p.Glu262Ter) c.295G>T (p.Glu99Ter) | |
| 3 | g.93900843C= | CA1385040195 | PROS1 | c.688G= (p.Glu230=) c.643G= (p.Glu215=) n.856G= c.646G= (p.Glu216=) c.787G= (n.787G=) c.784G= (p.Glu262=) c.295G= (p.Glu99=) | |
| 3 | g.93900843C>G | CA353673151 | PROS1 | c.688G>C (p.Glu230Gln) c.643G>C (p.Glu215Gln) n.856G>C c.646G>C (p.Glu216Gln) c.787G>C (n.787G>C) c.784G>C (p.Glu262Gln) c.295G>C (p.Glu99Gln) | |
| 3 | g.93900843C>T | CA2503410 | PROS1 | c.688G>A (p.Glu230Lys) c.643G>A (p.Glu215Lys) n.856G>A c.646G>A (p.Glu216Lys) c.787G>A (n.787G>A) c.784G>A (p.Glu262Lys) c.295G>A (p.Glu99Lys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |