Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
16 | g.67940299G>A | CA396376046 | LCAT | c.928C>T (p.His310Tyr) c.156-225C>T c.712C>T (p.His238Tyr) c.666C>T (n.666C>T) | gnomAD v4 |
16 | g.67940299G>C | CA396376047 | LCAT | c.928C>G (p.His310Asp) c.156-225C>G c.712C>G (p.His238Asp) c.666C>G (n.666C>G) | |
16 | g.67940299G>T | CA396376048 | LCAT | c.928C>A (p.His310Asn) c.156-225C>A c.712C>A (p.His238Asn) c.666C>A (n.666C>A) | |
16 | g.67940300C>A | CA496384124 | LCAT | c.927G>T (p.Leu309=) c.156-226G>T c.711G>T (p.Leu237=) c.665G>T (n.665G>T) | |
16 | g.67940300C= | CA2229563301 | LCAT | c.927G= (p.Leu309=) c.156-226G= c.711G= (p.Leu237=) c.665G= (n.665G=) | |
16 | g.67940300C>G | CA283160899 | LCAT | c.927G>C (p.Leu309=) c.156-226G>C c.711G>C (p.Leu237=) c.665G>C (n.665G>C) | dbSNP |
16 | g.67940300C>T | CA496384125 | LCAT | c.927G>A (p.Leu309=) c.156-226G>A c.711G>A (p.Leu237=) c.665G>A (n.665G>A) | gnomAD v4 |
16 | g.67940301A>C | CA396376049 | LCAT | c.926T>G (p.Leu309Arg) c.156-227T>G c.710T>G (p.Leu237Arg) c.664T>G (n.664T>G) | |
16 | g.67940301A>G | CA396376050 | LCAT | c.926T>C (p.Leu309Pro) c.156-227T>C c.710T>C (p.Leu237Pro) c.664T>C (n.664T>C) | gnomAD v4 |
16 | g.67940301A>T | CA396376051 | LCAT | c.926T>A (p.Leu309Gln) c.156-227T>A c.710T>A (p.Leu237Gln) c.664T>A (n.664T>A) | |
16 | g.67940302G>A | CA8120933 | LCAT | c.925C>T (p.Leu309=) c.156-228C>T c.709C>T (p.Leu237=) c.663C>T (n.663C>T) | dbSNP ExAC gnomAD v2 gnomAD v4 |
16 | g.67940302G>C | CA8120932 | LCAT | c.925C>G (p.Leu309Val) c.156-228C>G c.709C>G (p.Leu237Val) c.663C>G (n.663C>G) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.67940302G= | CA2229563302 | LCAT | c.925C= (p.Leu309=) c.156-228C= c.709C= (p.Leu237=) c.663C= (n.663C=) | |
16 | g.67940302G>T | CA396376052 | LCAT | c.925C>A (p.Leu309Met) c.156-228C>A c.709C>A (p.Leu237Met) c.663C>A (n.663C>A) | |
16 | g.67940303G>A | CA496384126 | LCAT | c.924C>T (p.Asp308=) c.156-229C>T c.708C>T (p.Asp236=) c.662C>T (n.662C>T) | |
16 | g.67940303G>C | CA396376053 | LCAT | c.924C>G (p.Asp308Glu) c.156-229C>G c.708C>G (p.Asp236Glu) c.662C>G (n.662C>G) | |
16 | g.67940303G>T | CA396376054 | LCAT | c.924C>A (p.Asp308Glu) c.156-229C>A c.708C>A (p.Asp236Glu) c.662C>A (n.662C>A) | gnomAD v4 |
16 | g.67940304T>A | CA396376055 | LCAT | c.923A>T (p.Asp308Val) c.156-230A>T c.707A>T (p.Asp236Val) c.661A>T (n.661A>T) | |
16 | g.67940304T>C | CA396376056 | LCAT | c.923A>G (p.Asp308Gly) c.156-230A>G c.707A>G (p.Asp236Gly) c.661A>G (n.661A>G) | |
16 | g.67940304T>G | CA396376057 | LCAT | c.923A>C (p.Asp308Ala) c.156-230A>C c.707A>C (p.Asp236Ala) c.661A>C (n.661A>C) | |
16 | g.67940305C>A | CA396376058 | LCAT | c.922G>T (p.Asp308Tyr) c.156-231G>T c.706G>T (p.Asp236Tyr) c.660G>T (n.660G>T) | |
16 | g.67940305C>G | CA396376059 | LCAT | c.922G>C (p.Asp308His) c.156-231G>C c.706G>C (p.Asp236His) c.660G>C (n.660G>C) | |
16 | g.67940305C>T | CA396376060 | LCAT | c.922G>A (p.Asp308Asn) c.156-231G>A c.706G>A (p.Asp236Asn) c.660G>A (n.660G>A) | |
16 | g.67940306T>A | CA496384127 | LCAT | c.921A>T (p.Ala307=) c.156-232A>T c.705A>T (p.Ala235=) c.659A>T (n.659A>T) | |
16 | g.67940306T>C | CA496384128 | LCAT | c.921A>G (p.Ala307=) c.156-232A>G c.705A>G (p.Ala235=) c.659A>G (n.659A>G) | |
16 | g.67940306T>G | CA496384129 | LCAT | c.921A>C (p.Ala307=) c.156-232A>C c.705A>C (p.Ala235=) c.659A>C (n.659A>C) | |
16 | g.67940307G>A | CA396376061 | LCAT | c.920C>T (p.Ala307Val) c.156-233C>T c.704C>T (p.Ala235Val) c.658C>T (n.658C>T) | |
16 | g.67940307G>C | CA396376062 | LCAT | c.920C>G (p.Ala307Gly) c.156-233C>G c.704C>G (p.Ala235Gly) c.658C>G (n.658C>G) | |
16 | g.67940307G>T | CA396376063 | LCAT | c.920C>A (p.Ala307Glu) c.156-233C>A c.704C>A (p.Ala235Glu) c.658C>A (n.658C>A) | |
16 | g.67940308C>A | CA396376064 | LCAT | c.919G>T (p.Ala307Ser) c.156-234G>T c.703G>T (p.Ala235Ser) c.657G>T (n.657G>T) | |
16 | g.67940308C>G | CA396376065 | LCAT | c.919G>C (p.Ala307Pro) c.156-234G>C c.703G>C (p.Ala235Pro) c.657G>C (n.657G>C) | |
16 | g.67940308C>T | CA396376066 | LCAT | c.919G>A (p.Ala307Thr) c.156-234G>A c.703G>A (p.Ala235Thr) c.657G>A (n.657G>A) | |
16 | g.67940309A= | CA2229563303 | LCAT | c.918T= (p.Phe306=) c.156-235T= c.702T= (p.Phe234=) c.656T= (n.656T=) | |
16 | g.67940309A>C | CA396376067 | LCAT | c.918T>G (p.Phe306Leu) c.156-235T>G c.702T>G (p.Phe234Leu) c.656T>G (n.656T>G) | |
16 | g.67940309A>G | CA496384130 | LCAT | c.918T>C (p.Phe306=) c.156-235T>C c.702T>C (p.Phe234=) c.656T>C (n.656T>C) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
16 | g.67940309A>T | CA396376068 | LCAT | c.918T>A (p.Phe306Leu) c.156-235T>A c.702T>A (p.Phe234Leu) c.656T>A (n.656T>A) | |
16 | g.67940310A>C | CA396376069 | LCAT | c.917T>G (p.Phe306Cys) c.156-236T>G c.701T>G (p.Phe234Cys) c.655T>G (n.655T>G) | |
16 | g.67940310A>G | CA396376070 | LCAT | c.917T>C (p.Phe306Ser) c.156-236T>C c.701T>C (p.Phe234Ser) c.655T>C (n.655T>C) | |
16 | g.67940310A>T | CA396376071 | LCAT | c.917T>A (p.Phe306Tyr) c.156-236T>A c.701T>A (p.Phe234Tyr) c.655T>A (n.655T>A) | |
16 | g.67940311A>C | CA396376072 | LCAT | c.916T>G (p.Phe306Val) c.156-237T>G c.700T>G (p.Phe234Val) c.654T>G (n.654T>G) | |
16 | g.67940311A>G | CA396376073 | LCAT | c.916T>C (p.Phe306Leu) c.156-237T>C c.700T>C (p.Phe234Leu) c.654T>C (n.654T>C) | gnomAD v4 |
16 | g.67940311A>T | CA396376074 | LCAT | c.916T>A (p.Phe306Ile) c.156-237T>A c.700T>A (p.Phe234Ile) c.654T>A (n.654T>A) | |
16 | g.67940312G>A | CA496384131 | LCAT | c.915C>T (p.Phe305=) c.156-238C>T c.699C>T (p.Phe233=) c.653C>T (n.653C>T) | |
16 | g.67940312G>C | CA396376075 | LCAT | c.915C>G (p.Phe305Leu) c.156-238C>G c.699C>G (p.Phe233Leu) c.653C>G (n.653C>G) | |
16 | g.67940312G>T | CA396376076 | LCAT | c.915C>A (p.Phe305Leu) c.156-238C>A c.699C>A (p.Phe233Leu) c.653C>A (n.653C>A) | |
16 | g.67940313A>C | CA396376077 | LCAT | c.914T>G (p.Phe305Cys) c.156-239T>G c.698T>G (p.Phe233Cys) c.652T>G (n.652T>G) | |
16 | g.67940313A>G | CA396376078 | LCAT | c.914T>C (p.Phe305Ser) c.156-239T>C c.698T>C (p.Phe233Ser) c.652T>C (n.652T>C) | |
16 | g.67940313A>T | CA396376079 | LCAT | c.914T>A (p.Phe305Tyr) c.156-239T>A c.698T>A (p.Phe233Tyr) c.652T>A (n.652T>A) | gnomAD v4 |
16 | g.67940314A>C | CA396376080 | LCAT | c.913T>G (p.Phe305Val) c.156-240T>G c.697T>G (p.Phe233Val) c.651T>G (n.651T>G) | |
16 | g.67940314A>G | CA396376082 | LCAT | c.913T>C (p.Phe305Leu) c.156-240T>C c.697T>C (p.Phe233Leu) c.651T>C (n.651T>C) | |
16 | g.67940314A>T | CA396376081 | LCAT | c.913T>A (p.Phe305Ile) c.156-240T>A c.697T>A (p.Phe233Ile) c.651T>A (n.651T>A) | |
16 | g.67940315G>A | CA496384132 | LCAT | c.912C>T (p.Arg304=) c.156-241C>T c.696C>T (p.Arg232=) c.650C>T (n.650C>T) | gnomAD v4 |
16 | g.67940315G>C | CA496384134 | LCAT | c.912C>G (p.Arg304=) c.156-241C>G c.696C>G (p.Arg232=) c.650C>G (n.650C>G) | |
16 | g.67940315G>T | CA496384133 | LCAT | c.912C>A (p.Arg304=) c.156-241C>A c.696C>A (p.Arg232=) c.650C>A (n.650C>A) | |
16 | g.67940316C>A | CA396376083 | LCAT | c.911G>T (p.Arg304Leu) c.156-242G>T c.695G>T (p.Arg232Leu) c.649G>T (n.649G>T) | |
16 | g.67940316C= | CA2229563304 | LCAT | c.911G= (p.Arg304=) c.156-242G= c.695G= (p.Arg232=) c.649G= (n.649G=) | |
16 | g.67940316C>G | CA396376085 | LCAT | c.911G>C (p.Arg304Pro) c.156-242G>C c.695G>C (p.Arg232Pro) c.649G>C (n.649G>C) | |
16 | g.67940316C>T | CA396376084 | LCAT | c.911G>A (p.Arg304His) c.156-242G>A c.695G>A (p.Arg232His) c.649G>A (n.649G>A) | dbSNP gnomAD v3 gnomAD v4 |
16 | g.67940317G>A | CA396376086 | LCAT | c.910C>T (p.Arg304Cys) c.156-243C>T c.694C>T (p.Arg232Cys) c.648C>T (n.648C>T) | dbSNP gnomAD v3 gnomAD v4 COSMIC |
16 | g.67940317G>C | CA396376087 | LCAT | c.910C>G (p.Arg304Gly) c.156-243C>G c.694C>G (p.Arg232Gly) c.648C>G (n.648C>G) | |
16 | g.67940317G= | CA2229563305 | LCAT | c.910C= (p.Arg304=) c.156-243C= c.694C= (p.Arg232=) c.648C= (n.648C=) | |
16 | g.67940317G>T | CA396376088 | LCAT | c.910C>A (p.Arg304Ser) c.156-243C>A c.694C>A (p.Arg232Ser) c.648C>A (n.648C>A) | |
16 | g.67940318T>A | CA396376089 | LCAT | c.909A>T (p.Gln303His) c.156-244A>T c.693A>T (p.Gln231His) c.647A>T (n.647A>T) | |
16 | g.67940318T>C | CA496384135 | LCAT | c.909A>G (p.Gln303=) c.156-244A>G c.693A>G (p.Gln231=) c.647A>G (n.647A>G) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.67940318T>G | CA396376090 | LCAT | c.909A>C (p.Gln303His) c.156-244A>C c.693A>C (p.Gln231His) c.647A>C (n.647A>C) | |
16 | g.67940318T= | CA2229563306 | LCAT | c.909A= (p.Gln303=) c.156-244A= c.693A= (p.Gln231=) c.647A= (n.647A=) | |
16 | g.67940319T>A | CA396376091 | LCAT | c.908A>T (p.Gln303Leu) c.156-245A>T c.692A>T (p.Gln231Leu) c.646A>T (n.646A>T) | |
16 | g.67940319T>C | CA396376092 | LCAT | c.908A>G (p.Gln303Arg) c.156-245A>G c.692A>G (p.Gln231Arg) c.646A>G (n.646A>G) | |
16 | g.67940319T>G | CA396376093 | LCAT | c.908A>C (p.Gln303Pro) c.156-245A>C c.692A>C (p.Gln231Pro) c.646A>C (n.646A>C) | |
16 | g.67940320G>A | CA396376094 | LCAT | c.907C>T (p.Gln303Ter) c.156-246C>T c.691C>T (p.Gln231Ter) c.645C>T (n.645C>T) | |
16 | g.67940320G>C | CA396376095 | LCAT | c.907C>G (p.Gln303Glu) c.156-246C>G c.691C>G (p.Gln231Glu) c.645C>G (n.645C>G) | |
16 | g.67940320G>T | CA396376096 | LCAT | c.907C>A (p.Gln303Lys) c.156-246C>A c.691C>A (p.Gln231Lys) c.645C>A (n.645C>A) | |
16 | g.67940321G>A | CA496384136 | LCAT | c.906C>T (p.Phe302=) c.156-247C>T c.690C>T (p.Phe230=) c.644C>T (n.644C>T) | |
16 | g.67940321G>C | CA396376097 | LCAT | c.906C>G (p.Phe302Leu) c.156-247C>G c.690C>G (p.Phe230Leu) c.644C>G (n.644C>G) | |
16 | g.67940321G>T | CA396376098 | LCAT | c.906C>A (p.Phe302Leu) c.156-247C>A c.690C>A (p.Phe230Leu) c.644C>A (n.644C>A) | |
16 | g.67940322A>C | CA396376101 | LCAT | c.905T>G (p.Phe302Cys) c.156-248T>G c.689T>G (p.Phe230Cys) c.643T>G (n.643T>G) | |
16 | g.67940322A>G | CA396376100 | LCAT | c.905T>C (p.Phe302Ser) c.156-248T>C c.689T>C (p.Phe230Ser) c.643T>C (n.643T>C) | |
16 | g.67940322A>T | CA396376099 | LCAT | c.905T>A (p.Phe302Tyr) c.156-248T>A c.689T>A (p.Phe230Tyr) c.643T>A (n.643T>A) | |
16 | g.67940323A>C | CA396376102 | LCAT | c.904T>G (p.Phe302Val) c.156-249T>G c.688T>G (p.Phe230Val) c.642T>G (n.642T>G) | gnomAD v4 |
16 | g.67940323A>G | CA396376103 | LCAT | c.904T>C (p.Phe302Leu) c.156-249T>C c.688T>C (p.Phe230Leu) c.642T>C (n.642T>C) | |
16 | g.67940323A>T | CA396376104 | LCAT | c.904T>A (p.Phe302Ile) c.156-249T>A c.688T>A (p.Phe230Ile) c.642T>A (n.642T>A) | |
16 | g.67940324G>A | CA8120934 | LCAT | c.903C>T (p.Asp301=) c.156-250C>T c.687C>T (p.Asp229=) c.641C>T (n.641C>T) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.67940324G>C | CA396376105 | LCAT | c.903C>G (p.Asp301Glu) c.156-250C>G c.687C>G (p.Asp229Glu) c.641C>G (n.641C>G) | |
16 | g.67940324G= | CA2229563307 | LCAT | c.903C= (p.Asp301=) c.156-250C= c.687C= (p.Asp229=) c.641C= (n.641C=) | |
16 | g.67940324G>T | CA8120935 | LCAT | c.903C>A (p.Asp301Glu) c.156-250C>A c.687C>A (p.Asp229Glu) c.641C>A (n.641C>A) | dbSNP ExAC gnomAD v2 gnomAD v4 |
16 | g.67940325T>A | CA396376106 | LCAT | c.902A>T (p.Asp301Val) c.156-251A>T c.686A>T (p.Asp229Val) c.640A>T (n.640A>T) | |
16 | g.67940325T>C | CA396376107 | LCAT | c.902A>G (p.Asp301Gly) c.156-251A>G c.686A>G (p.Asp229Gly) c.640A>G (n.640A>G) | gnomAD v4 |
16 | g.67940325T>G | CA396376108 | LCAT | c.902A>C (p.Asp301Ala) c.156-251A>C c.686A>C (p.Asp229Ala) c.640A>C (n.640A>C) | |
16 | g.67940326C>A | CA396376109 | LCAT | c.901G>T (p.Asp301Tyr) c.156-252G>T c.685G>T (p.Asp229Tyr) c.639G>T (n.639G>T) | |
16 | g.67940326C= | CA2229563308 | LCAT | c.901G= (p.Asp301=) c.156-252G= c.685G= (p.Asp229=) c.639G= (n.639G=) | |
16 | g.67940326C>G | CA396376110 | LCAT | c.901G>C (p.Asp301His) c.156-252G>C c.685G>C (p.Asp229His) c.639G>C (n.639G>C) | |
16 | g.67940326C>T | CA283160905 | LCAT | c.901G>A (p.Asp301Asn) c.156-252G>A c.685G>A (p.Asp229Asn) c.639G>A (n.639G>A) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
16 | g.67940327A= | CA2229563309 | LCAT | c.900T= (p.Arg300=) c.156-253T= c.684T= (p.Arg228=) c.638T= (n.638T=) | |
16 | g.67940327A>C | CA496384137 | LCAT | c.900T>G (p.Arg300=) c.156-253T>G c.684T>G (p.Arg228=) c.638T>G (n.638T>G) | gnomAD v4 |
16 | g.67940327A>G | CA283160910 | LCAT | c.900T>C (p.Arg300=) c.156-253T>C c.684T>C (p.Arg228=) c.638T>C (n.638T>C) | dbSNP gnomAD v3 gnomAD v4 |
16 | g.67940327A>T | CA496384138 | LCAT | c.900T>A (p.Arg300=) c.156-253T>A c.684T>A (p.Arg228=) c.638T>A (n.638T>A) | |
16 | g.67940328C>A | CA396376111 | LCAT | c.899G>T (p.Arg300Leu) c.156-254G>T c.683G>T (p.Arg228Leu) c.637G>T (n.637G>T) | |
16 | g.67940328C= | CA2229563310 | LCAT | c.899G= (p.Arg300=) c.156-254G= c.683G= (p.Arg228=) c.637G= (n.637G=) | |
16 | g.67940328C>G | CA396376112 | LCAT | c.899G>C (p.Arg300Pro) c.156-254G>C c.683G>C (p.Arg228Pro) c.637G>C (n.637G>C) | |
16 | g.67940328C>T | CA8120936 | LCAT | c.899G>A (p.Arg300His) c.156-254G>A c.683G>A (p.Arg228His) c.637G>A (n.637G>A) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.67940329G>A | CA8120937 | LCAT | c.898C>T (p.Arg300Cys) c.156-255C>T c.682C>T (p.Arg228Cys) c.636C>T (n.636C>T) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
16 | g.67940329G>C | CA396376113 | LCAT | c.898C>G (p.Arg300Gly) c.156-255C>G c.682C>G (p.Arg228Gly) c.636C>G (n.636C>G) | |
16 | g.67940329G= | CA2229563311 | LCAT | c.898C= (p.Arg300=) c.156-255C= c.682C= (p.Arg228=) c.636C= (n.636C=) | |
16 | g.67940329G>T | CA396376114 | LCAT | c.898C>A (p.Arg300Ser) c.156-255C>A c.682C>A (p.Arg228Ser) c.636C>A (n.636C>A) | |
16 | g.67940330G>A | CA496384141 | LCAT | c.897C>T (p.Gly299=) c.156-256C>T c.681C>T (p.Gly227=) c.635C>T (n.635C>T) | |
16 | g.67940330G>C | CA496384139 | LCAT | c.897C>G (p.Gly299=) c.156-256C>G c.681C>G (p.Gly227=) c.635C>G (n.635C>G) | |
16 | g.67940330G>T | CA496384140 | LCAT | c.897C>A (p.Gly299=) c.156-256C>A c.681C>A (p.Gly227=) c.635C>A (n.635C>A) | |
16 | g.67940331C>A | CA396376115 | LCAT | c.896G>T (p.Gly299Val) c.156-257G>T c.680G>T (p.Gly227Val) c.634G>T (n.634G>T) | |
16 | g.67940331C= | CA2229563312 | LCAT | c.896G= (p.Gly299=) c.156-257G= c.680G= (p.Gly227=) c.634G= (n.634G=) | |
16 | g.67940331C>G | CA396376116 | LCAT | c.896G>C (p.Gly299Ala) c.156-257G>C c.680G>C (p.Gly227Ala) c.634G>C (n.634G>C) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.67940331C>T | CA396376117 | LCAT | c.896G>A (p.Gly299Asp) c.156-257G>A c.680G>A (p.Gly227Asp) c.634G>A (n.634G>A) | |
16 | g.67940332C>A | CA396376118 | LCAT | c.895G>T (p.Gly299Cys) c.156-258G>T c.679G>T (p.Gly227Cys) c.633G>T (n.633G>T) | |
16 | g.67940332C>G | CA396376119 | LCAT | c.895G>C (p.Gly299Arg) c.156-258G>C c.679G>C (p.Gly227Arg) c.633G>C (n.633G>C) | |
16 | g.67940332C>T | CA396376120 | LCAT | c.895G>A (p.Gly299Ser) c.156-258G>A c.679G>A (p.Gly227Ser) c.633G>A (n.633G>A) | gnomAD v4 |
16 | g.67940333T>A | CA496384142 | LCAT | c.894A>T (p.Thr298=) c.156-259A>T c.678A>T (p.Thr226=) c.632A>T (n.632A>T) | |
16 | g.67940333T>C | CA496384143 | LCAT | c.894A>G (p.Thr298=) c.156-259A>G c.678A>G (p.Thr226=) c.632A>G (n.632A>G) | |
16 | g.67940333T>G | CA496384144 | LCAT | c.894A>C (p.Thr298=) c.156-259A>C c.678A>C (p.Thr226=) c.632A>C (n.632A>C) | |
16 | g.67940334G>A | CA396376121 | LCAT | c.893C>T (p.Thr298Ile) c.156-260C>T c.677C>T (p.Thr226Ile) c.631C>T (n.631C>T) | gnomAD v4 |
16 | g.67940334G>C | CA8120938 | LCAT | c.893C>G (p.Thr298Arg) c.156-260C>G c.677C>G (p.Thr226Arg) c.631C>G (n.631C>G) | dbSNP ExAC gnomAD v2 gnomAD v4 |
16 | g.67940334G= | CA2229563313 | LCAT | c.893C= (p.Thr298=) c.156-260C= c.677C= (p.Thr226=) c.631C= (n.631C=) | |
16 | g.67940334G>T | CA396376122 | LCAT | c.893C>A (p.Thr298Lys) c.156-260C>A c.677C>A (p.Thr226Lys) c.631C>A (n.631C>A) | COSMIC |
16 | g.67940335T>A | CA396376125 | LCAT | c.892A>T (p.Thr298Ser) c.156-261A>T c.676A>T (p.Thr226Ser) c.630A>T (n.630A>T) | |
16 | g.67940335T>C | CA396376123 | LCAT | c.892A>G (p.Thr298Ala) c.156-261A>G c.676A>G (p.Thr226Ala) c.630A>G (n.630A>G) | COSMIC |
16 | g.67940335T>G | CA396376124 | LCAT | c.892A>C (p.Thr298Pro) c.156-261A>C c.676A>C (p.Thr226Pro) c.630A>C (n.630A>C) | |
16 | g.67940336G>A | CA283160935 | LCAT | c.891C>T (p.Tyr297=) c.156-262C>T c.675C>T (p.Tyr225=) c.629C>T (n.629C>T) | dbSNP gnomAD v3 gnomAD v4 |
16 | g.67940336G>C | CA396376126 | LCAT | c.891C>G (p.Tyr297Ter) c.156-262C>G c.675C>G (p.Tyr225Ter) c.629C>G (n.629C>G) | |
16 | g.67940336G= | CA2229563314 | LCAT | c.891C= (p.Tyr297=) c.156-262C= c.675C= (p.Tyr225=) c.629C= (n.629C=) | |
16 | g.67940336G>T | CA396376127 | LCAT | c.891C>A (p.Tyr297Ter) c.156-262C>A c.675C>A (p.Tyr225Ter) c.629C>A (n.629C>A) | |
16 | g.67940337T>A | CA396376128 | LCAT | c.890A>T (p.Tyr297Phe) c.156-263A>T c.674A>T (p.Tyr225Phe) c.628A>T (n.628A>T) | |
16 | g.67940337T>C | CA396376129 | LCAT | c.890A>G (p.Tyr297Cys) c.156-263A>G c.674A>G (p.Tyr225Cys) c.628A>G (n.628A>G) | |
16 | g.67940337T>G | CA396376130 | LCAT | c.890A>C (p.Tyr297Ser) c.156-263A>C c.674A>C (p.Tyr225Ser) c.628A>C (n.628A>C) | |
16 | g.67940338A>C | CA396376131 | LCAT | c.889T>G (p.Tyr297Asp) c.156-264T>G c.673T>G (p.Tyr225Asp) c.627T>G (n.627T>G) | |
16 | g.67940338A>G | CA396376132 | LCAT | c.889T>C (p.Tyr297His) c.156-264T>C c.673T>C (p.Tyr225His) c.627T>C (n.627T>C) | |
16 | g.67940338A>T | CA396376133 | LCAT | c.889T>A (p.Tyr297Asn) c.156-264T>A c.673T>A (p.Tyr225Asn) c.627T>A (n.627T>A) | |
16 | g.67940339G>A | CA496384145 | LCAT | c.888C>T (p.Asn296=) c.156-265C>T c.672C>T (p.Asn224=) c.626C>T (n.626C>T) | gnomAD v4 |
16 | g.67940339G>C | CA396376134 | LCAT | c.888C>G (p.Asn296Lys) c.156-265C>G c.672C>G (p.Asn224Lys) c.626C>G (n.626C>G) | |
16 | g.67940339G>T | CA396376135 | LCAT | c.888C>A (p.Asn296Lys) c.156-265C>A c.672C>A (p.Asn224Lys) c.626C>A (n.626C>A) | |
16 | g.67940340T>A | CA396376138 | LCAT | c.887A>T (p.Asn296Ile) c.156-266A>T c.671A>T (p.Asn224Ile) c.625A>T (n.625A>T) | |
16 | g.67940340T>C | CA396376137 | LCAT | c.887A>G (p.Asn296Ser) c.156-266A>G c.671A>G (p.Asn224Ser) c.625A>G (n.625A>G) | |
16 | g.67940340T>G | CA396376136 | LCAT | c.887A>C (p.Asn296Thr) c.156-266A>C c.671A>C (p.Asn224Thr) c.625A>C (n.625A>C) | |
16 | g.67940341T>A | CA396376139 | LCAT | c.886A>T (p.Asn296Tyr) c.156-267A>T c.670A>T (p.Asn224Tyr) c.624A>T (n.624A>T) | |
16 | g.67940341T>C | CA396376141 | LCAT | c.886A>G (p.Asn296Asp) c.156-267A>G c.670A>G (p.Asn224Asp) c.624A>G (n.624A>G) | gnomAD v4 |
16 | g.67940341T>G | CA396376140 | LCAT | c.886A>C (p.Asn296His) c.156-267A>C c.670A>C (p.Asn224His) c.624A>C (n.624A>C) | |
16 | g.67940342G>A | CA496384146 | LCAT | c.885C>T (p.Phe295=) c.156-268C>T c.669C>T (p.Phe223=) c.623C>T (n.623C>T) | COSMIC |
16 | g.67940342G>C | CA396376142 | LCAT | c.885C>G (p.Phe295Leu) c.156-268C>G c.669C>G (p.Phe223Leu) c.623C>G (n.623C>G) | COSMIC |
16 | g.67940342G= | CA2229563315 | LCAT | c.885C= (p.Phe295=) c.156-268C= c.669C= (p.Phe223=) c.623C= (n.623C=) | |
16 | g.67940342G>T | CA396376143 | LCAT | c.885C>A (p.Phe295Leu) c.156-268C>A c.669C>A (p.Phe223Leu) c.623C>A (n.623C>A) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.67940343A>C | CA396376144 | LCAT | c.884T>G (p.Phe295Cys) c.156-269T>G c.668T>G (p.Phe223Cys) c.622T>G (n.622T>G) | |
16 | g.67940343A>G | CA396376145 | LCAT | c.884T>C (p.Phe295Ser) c.156-269T>C c.668T>C (p.Phe223Ser) c.622T>C (n.622T>C) | |
16 | g.67940343A>T | CA396376146 | LCAT | c.884T>A (p.Phe295Tyr) c.156-269T>A c.668T>A (p.Phe223Tyr) c.622T>A (n.622T>A) | |
16 | g.67940344A>C | CA396376147 | LCAT | c.883T>G (p.Phe295Val) c.156-270T>G c.667T>G (p.Phe223Val) c.621T>G (n.621T>G) | |
16 | g.67940344A>G | CA396376148 | LCAT | c.883T>C (p.Phe295Leu) c.156-270T>C c.667T>C (p.Phe223Leu) c.621T>C (n.621T>C) | gnomAD v4 |
16 | g.67940344A>T | CA396376149 | LCAT | c.883T>A (p.Phe295Ile) c.156-270T>A c.667T>A (p.Phe223Ile) c.621T>A (n.621T>A) | |
16 | g.67940345G>A | CA496384147 | LCAT | c.882C>T (p.Ser294=) c.156-271C>T c.666C>T (p.Ser222=) c.620C>T (n.620C>T) | |
16 | g.67940345G>C | CA396376150 | LCAT | c.882C>G (p.Ser294Arg) c.156-271C>G c.666C>G (p.Ser222Arg) c.620C>G (n.620C>G) | |
16 | g.67940345G>T | CA396376151 | LCAT | c.882C>A (p.Ser294Arg) c.156-271C>A c.666C>A (p.Ser222Arg) c.620C>A (n.620C>A) | |
16 | g.67940346C>A | CA396376152 | LCAT | c.881G>T (p.Ser294Ile) c.156-272G>T c.665G>T (p.Ser222Ile) c.619G>T (n.619G>T) | |
16 | g.67940346C>G | CA396376153 | LCAT | c.881G>C (p.Ser294Thr) c.156-272G>C c.665G>C (p.Ser222Thr) c.619G>C (n.619G>C) | |
16 | g.67940346C>T | CA396376154 | LCAT | c.881G>A (p.Ser294Asn) c.156-272G>A c.665G>A (p.Ser222Asn) c.619G>A (n.619G>A) | gnomAD v4 |
16 | g.67940347T>A | CA396376155 | LCAT | c.880A>T (p.Ser294Cys) c.156-273A>T c.664A>T (p.Ser222Cys) c.618A>T (n.618A>T) | gnomAD v4 |
16 | g.67940347T>C | CA396376157 | LCAT | c.880A>G (p.Ser294Gly) c.156-273A>G c.664A>G (p.Ser222Gly) c.618A>G (n.618A>G) | |
16 | g.67940347T>G | CA396376156 | LCAT | c.880A>C (p.Ser294Arg) c.156-273A>C c.664A>C (p.Ser222Arg) c.618A>C (n.618A>C) | |
16 | g.67940348G>A | CA8120939 | LCAT | c.879C>T (p.Pro293=) c.156-274C>T c.663C>T (p.Pro221=) c.617C>T (n.617C>T) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.67940348G>C | CA496383964 | LCAT | c.879C>G (p.Pro293=) c.156-274C>G c.663C>G (p.Pro221=) c.617C>G (n.617C>G) | |
16 | g.67940348G= | CA2229563316 | LCAT | c.879C= (p.Pro293=) c.156-274C= c.663C= (p.Pro221=) c.617C= (n.617C=) | |
16 | g.67940348G>T | CA496383967 | LCAT | c.879C>A (p.Pro293=) c.156-274C>A c.663C>A (p.Pro221=) c.617C>A (n.617C>A) | |
16 | g.67940349G>A | CA396376158 | LCAT | c.878C>T (p.Pro293Leu) c.156-275C>T c.662C>T (p.Pro221Leu) c.616C>T (n.616C>T) | |
16 | g.67940349G>C | CA396376159 | LCAT | c.878C>G (p.Pro293Arg) c.156-275C>G c.662C>G (p.Pro221Arg) c.616C>G (n.616C>G) | |
16 | g.67940349G>T | CA396376160 | LCAT | c.878C>A (p.Pro293His) c.156-275C>A c.662C>A (p.Pro221His) c.616C>A (n.616C>A) | |
16 | g.67940350G>A | CA396376161 | LCAT | c.877C>T (p.Pro293Ser) c.156-276C>T c.661C>T (p.Pro221Ser) c.615C>T (n.615C>T) | dbSNP gnomAD v2 gnomAD v4 |
16 | g.67940350G>C | CA396376162 | LCAT | c.877C>G (p.Pro293Ala) c.156-276C>G c.661C>G (p.Pro221Ala) c.615C>G (n.615C>G) | gnomAD v4 |
16 | g.67940350G= | CA2229563317 | LCAT | c.877C= (p.Pro293=) c.156-276C= c.661C= (p.Pro221=) c.615C= (n.615C=) | |
16 | g.67940350G>T | CA396376163 | LCAT | c.877C>A (p.Pro293Thr) c.156-276C>A c.661C>A (p.Pro221Thr) c.615C>A (n.615C>A) | |
16 | g.67940351T>A | CA496383971 | LCAT | c.876A>T (p.Thr292=) c.156-277A>T c.660A>T (p.Thr220=) c.614A>T (n.614A>T) | |
16 | g.67940351T>C | CA496383970 | LCAT | c.876A>G (p.Thr292=) c.156-277A>G c.660A>G (p.Thr220=) c.614A>G (n.614A>G) | gnomAD v4 |
16 | g.67940351T>G | CA496383969 | LCAT | c.876A>C (p.Thr292=) c.156-277A>C c.660A>C (p.Thr220=) c.614A>C (n.614A>C) | dbSNP |
16 | g.67940351T= | CA2229563318 | LCAT | c.876A= (p.Thr292=) c.156-277A= c.660A= (p.Thr220=) c.614A= (n.614A=) | |
16 | g.67940351_67940365delinsTGTGGAAATGAACAC | CA2229563319 | LCAT | c.862_876delinsGTGTTCATTTCCACA (p.Val288=) c.156-291_156-277delinsGTGTTCATTTCCACA c.646_660delinsGTGTTCATTTCCACA (p.Val216=) c.600_614delinsGTGTTCATTTCCACA (n.600_614delinsGTGTTCATTTCCACA) | |
16 | g.67940352G>A | CA396376164 | LCAT | c.875C>T (p.Thr292Ile) c.156-278C>T c.659C>T (p.Thr220Ile) c.613C>T (n.613C>T) | gnomAD v4 |
16 | g.67940352G>C | CA396376165 | LCAT | c.875C>G (p.Thr292Arg) c.156-278C>G c.659C>G (p.Thr220Arg) c.613C>G (n.613C>G) | |
16 | g.67940352G>T | CA396376166 | LCAT | c.875C>A (p.Thr292Lys) c.156-278C>A c.659C>A (p.Thr220Lys) c.613C>A (n.613C>A) | |
16 | g.67940356_67940369del | CA978460279 | LCAT | c.862_875del (p.Val288ThrfsTer9) c.156-291_156-278del c.646_659del (p.Val216ThrfsTer9) c.600_613del (n.600_613del) | dbSNP gnomAD v3 gnomAD v4 |
16 | g.67940353T>A | CA396376169 | LCAT | c.874A>T (p.Thr292Ser) c.156-279A>T c.658A>T (p.Thr220Ser) c.612A>T (n.612A>T) | |
16 | g.67940353T>C | CA396376168 | LCAT | c.874A>G (p.Thr292Ala) c.156-279A>G c.658A>G (p.Thr220Ala) c.612A>G (n.612A>G) | |
16 | g.67940353T>G | CA396376167 | LCAT | c.874A>C (p.Thr292Pro) c.156-279A>C c.658A>C (p.Thr220Pro) c.612A>C (n.612A>C) | |
16 | g.67940354G>A | CA496383976 | LCAT | c.873C>T (p.Ser291=) c.156-280C>T c.657C>T (p.Ser219=) c.611C>T (n.611C>T) | |
16 | g.67940354G>C | CA283160943 | LCAT | c.873C>G (p.Ser291=) c.156-280C>G c.657C>G (p.Ser219=) c.611C>G (n.611C>G) | dbSNP gnomAD v4 |
16 | g.67940354G= | CA2229563320 | LCAT | c.873C= (p.Ser291=) c.156-280C= c.657C= (p.Ser219=) c.611C= (n.611C=) | |
16 | g.67940354G>T | CA496383977 | LCAT | c.873C>A (p.Ser291=) c.156-280C>A c.657C>A (p.Ser219=) c.611C>A (n.611C>A) | |
16 | g.67940355G>A | CA396376170 | LCAT | c.872C>T (p.Ser291Phe) c.156-281C>T c.656C>T (p.Ser219Phe) c.610C>T (n.610C>T) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.67940355G>C | CA396376171 | LCAT | c.872C>G (p.Ser291Cys) c.156-281C>G c.656C>G (p.Ser219Cys) c.610C>G (n.610C>G) | |
16 | g.67940355G= | CA2229563321 | LCAT | c.872C= (p.Ser291=) c.156-281C= c.656C= (p.Ser219=) c.610C= (n.610C=) | |
16 | g.67940355G>T | CA396376172 | LCAT | c.872C>A (p.Ser291Tyr) c.156-281C>A c.656C>A (p.Ser219Tyr) c.610C>A (n.610C>A) | |
16 | g.67940356A>C | CA396376173 | LCAT | c.871T>G (p.Ser291Ala) c.156-282T>G c.655T>G (p.Ser219Ala) c.609T>G (n.609T>G) | |
16 | g.67940356A>G | CA396376174 | LCAT | c.871T>C (p.Ser291Pro) c.156-282T>C c.655T>C (p.Ser219Pro) c.609T>C (n.609T>C) | |
16 | g.67940356A>T | CA396376175 | LCAT | c.871T>A (p.Ser291Thr) c.156-282T>A c.655T>A (p.Ser219Thr) c.609T>A (n.609T>A) | |
16 | g.67940357A= | CA2229563322 | LCAT | c.870T= (p.Ile290=) c.156-283T= c.654T= (p.Ile218=) c.608T= (n.608T=) | |
16 | g.67940357A>C | CA396376176 | LCAT | c.870T>G (p.Ile290Met) c.156-283T>G c.654T>G (p.Ile218Met) c.608T>G (n.608T>G) | |
16 | g.67940357A>G | CA496383980 | LCAT | c.870T>C (p.Ile290=) c.156-283T>C c.654T>C (p.Ile218=) c.608T>C (n.608T>C) | dbSNP gnomAD v2 gnomAD v4 |
16 | g.67940357A>T | CA283160951 | LCAT | c.870T>A (p.Ile290=) c.156-283T>A c.654T>A (p.Ile218=) c.608T>A (n.608T>A) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.67940357_67940359dup | CA2573054258 | LCAT | c.868_870dup (p.Ile290_Ser291insIle) c.156-285_156-283dup c.652_654dup (p.Ile218_Ser219insIle) c.606_608dup (n.606_608dup) | ClinVar dbSNP |
16 | g.67940358A= | CA2229563323 | LCAT | c.869T= (p.Ile290=) c.156-284T= c.653T= (p.Ile218=) c.607T= (n.607T=) | |
16 | g.67940358A>C | CA396376177 | LCAT | c.869T>G (p.Ile290Ser) c.156-284T>G c.653T>G (p.Ile218Ser) c.607T>G (n.607T>G) | |
16 | g.67940358A>G | CA396376178 | LCAT | c.869T>C (p.Ile290Thr) c.156-284T>C c.653T>C (p.Ile218Thr) c.607T>C (n.607T>C) | dbSNP gnomAD v2 gnomAD v4 |
16 | g.67940358A>T | CA396376179 | LCAT | c.869T>A (p.Ile290Asn) c.156-284T>A c.653T>A (p.Ile218Asn) c.607T>A (n.607T>A) | |
16 | g.67940359T>A | CA396376180 | LCAT | c.868A>T (p.Ile290Phe) c.156-285A>T c.652A>T (p.Ile218Phe) c.606A>T (n.606A>T) | |
16 | g.67940359T>C | CA8120940 | LCAT | c.868A>G (p.Ile290Val) c.156-285A>G c.652A>G (p.Ile218Val) c.606A>G (n.606A>G) | dbSNP ExAC gnomAD v2 gnomAD v4 |
16 | g.67940359T>G | CA396376181 | LCAT | c.868A>C (p.Ile290Leu) c.156-285A>C c.652A>C (p.Ile218Leu) c.606A>C (n.606A>C) | |
16 | g.67940359T= | CA2229563324 | LCAT | c.868A= (p.Ile290=) c.156-285A= c.652A= (p.Ile218=) c.606A= (n.606A=) | |
16 | g.67940360G>A | CA496383986 | LCAT | c.867C>T (p.Phe289=) c.156-286C>T c.651C>T (p.Phe217=) c.605C>T (n.605C>T) | gnomAD v4 COSMIC |
16 | g.67940360G>C | CA396376182 | LCAT | c.867C>G (p.Phe289Leu) c.156-286C>G c.651C>G (p.Phe217Leu) c.605C>G (n.605C>G) | |
16 | g.67940360G= | CA2229563325 | LCAT | c.867C= (p.Phe289=) c.156-286C= c.651C= (p.Phe217=) c.605C= (n.605C=) | |
16 | g.67940360G>T | CA8120941 | LCAT | c.867C>A (p.Phe289Leu) c.156-286C>A c.651C>A (p.Phe217Leu) c.605C>A (n.605C>A) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.67940361A>C | CA396376183 | LCAT | c.866T>G (p.Phe289Cys) c.156-287T>G c.650T>G (p.Phe217Cys) c.604T>G (n.604T>G) | |
16 | g.67940361A>G | CA396376184 | LCAT | c.866T>C (p.Phe289Ser) c.156-287T>C c.650T>C (p.Phe217Ser) c.604T>C (n.604T>C) | |
16 | g.67940361A>T | CA396376185 | LCAT | c.866T>A (p.Phe289Tyr) c.156-287T>A c.650T>A (p.Phe217Tyr) c.604T>A (n.604T>A) | |
16 | g.67940362A>C | CA396376186 | LCAT | c.865T>G (p.Phe289Val) c.156-288T>G c.649T>G (p.Phe217Val) c.603T>G (n.603T>G) | |
16 | g.67940362A>G | CA396376187 | LCAT | c.865T>C (p.Phe289Leu) c.156-288T>C c.649T>C (p.Phe217Leu) c.603T>C (n.603T>C) | |
16 | g.67940362A>T | CA396376188 | LCAT | c.865T>A (p.Phe289Ile) c.156-288T>A c.649T>A (p.Phe217Ile) c.603T>A (n.603T>A) | |
16 | g.67940363C>A | CA496383992 | LCAT | c.864G>T (p.Val288=) c.156-289G>T c.648G>T (p.Val216=) c.602G>T (n.602G>T) | dbSNP gnomAD v4 |
16 | g.67940363C= | CA2229563326 | LCAT | c.864G= (p.Val288=) c.156-289G= c.648G= (p.Val216=) c.602G= (n.602G=) | |
16 | g.67940363C>G | CA496383994 | LCAT | c.864G>C (p.Val288=) c.156-289G>C c.648G>C (p.Val216=) c.602G>C (n.602G>C) | |
16 | g.67940363C>T | CA496383993 | LCAT | c.864G>A (p.Val288=) c.156-289G>A c.648G>A (p.Val216=) c.602G>A (n.602G>A) | gnomAD v4 |
16 | g.67940364A>C | CA396376189 | LCAT | c.863T>G (p.Val288Gly) c.156-290T>G c.647T>G (p.Val216Gly) c.601T>G (n.601T>G) | |
16 | g.67940364A>G | CA396376190 | LCAT | c.863T>C (p.Val288Ala) c.156-290T>C c.647T>C (p.Val216Ala) c.601T>C (n.601T>C) | ClinVar gnomAD v4 |
16 | g.67940364A>T | CA396376191 | LCAT | c.863T>A (p.Val288Glu) c.156-290T>A c.647T>A (p.Val216Glu) c.601T>A (n.601T>A) | |
16 | g.67940365del | CA2695223582 | LCAT | c.862del (p.Val288CysfsTer?) c.156-291del c.646del (p.Val216CysfsTer?) c.600del (n.600del) | |
16 | g.67940365C>A | CA396376192 | LCAT | c.862G>T (p.Val288Leu) c.156-291G>T c.646G>T (p.Val216Leu) c.600G>T (n.600G>T) | |
16 | g.67940365C= | CA2229563327 | LCAT | c.862G= (p.Val288=) c.156-291G= c.646G= (p.Val216=) c.600G= (n.600G=) | |
16 | g.67940365C>G | CA396376193 | LCAT | c.862G>C (p.Val288Leu) c.156-291G>C c.646G>C (p.Val216Leu) c.600G>C (n.600G>C) | |
16 | g.67940365C>T | CA396376194 | LCAT | c.862G>A (p.Val288Met) c.156-291G>A c.646G>A (p.Val216Met) c.600G>A (n.600G>A) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
16 | g.67940366G>A | CA8120942 | LCAT | c.861C>T (p.His287=) c.156-292C>T c.645C>T (p.His215=) c.599C>T (n.599C>T) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.67940366G>C | CA396376196 | LCAT | c.861C>G (p.His287Gln) c.156-292C>G c.645C>G (p.His215Gln) c.599C>G (n.599C>G) | gnomAD v4 |
16 | g.67940366G= | CA2229563328 | LCAT | c.861C= (p.His287=) c.156-292C= c.645C= (p.His215=) c.599C= (n.599C=) | |
16 | g.67940366G>T | CA396376195 | LCAT | c.861C>A (p.His287Gln) c.156-292C>A c.645C>A (p.His215Gln) c.599C>A (n.599C>A) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.67940367T>A | CA396376197 | LCAT | c.860A>T (p.His287Leu) c.156-293A>T c.644A>T (p.His215Leu) c.598A>T (n.598A>T) | |
16 | g.67940367T>C | CA8120943 | LCAT | c.860A>G (p.His287Arg) c.156-293A>G c.644A>G (p.His215Arg) c.598A>G (n.598A>G) | dbSNP ExAC gnomAD v2 gnomAD v4 |
16 | g.67940367T>G | CA396376198 | LCAT | c.860A>C (p.His287Pro) c.156-293A>C c.644A>C (p.His215Pro) c.598A>C (n.598A>C) | |
16 | g.67940367T= | CA2229563329 | LCAT | c.860A= (p.His287=) c.156-293A= c.644A= (p.His215=) c.598A= (n.598A=) | |
16 | g.67940368G>A | CA396376199 | LCAT | c.859C>T (p.His287Tyr) c.156-294C>T c.643C>T (p.His215Tyr) c.597C>T (n.597C>T) | gnomAD v4 |
16 | g.67940368G>C | CA396376201 | LCAT | c.859C>G (p.His287Asp) c.156-294C>G c.643C>G (p.His215Asp) c.597C>G (n.597C>G) | |
16 | g.67940368G>T | CA396376200 | LCAT | c.859C>A (p.His287Asn) c.156-294C>A c.643C>A (p.His215Asn) c.597C>A (n.597C>A) | |
16 | g.67940369G>A | CA496384001 | LCAT | c.858C>T (p.Asp286=) c.156-295C>T c.642C>T (p.Asp214=) c.596C>T (n.596C>T) | |
16 | g.67940369G>C | CA396376202 | LCAT | c.858C>G (p.Asp286Glu) c.156-295C>G c.642C>G (p.Asp214Glu) c.596C>G (n.596C>G) | |
16 | g.67940369G>T | CA396376203 | LCAT | c.858C>A (p.Asp286Glu) c.156-295C>A c.642C>A (p.Asp214Glu) c.596C>A (n.596C>A) | |
16 | g.67940370T>A | CA396376204 | LCAT | c.857A>T (p.Asp286Val) c.156-296A>T c.641A>T (p.Asp214Val) c.595A>T (n.595A>T) | |
16 | g.67940370T>C | CA396376205 | LCAT | c.857A>G (p.Asp286Gly) c.156-296A>G c.641A>G (p.Asp214Gly) c.595A>G (n.595A>G) | |
16 | g.67940370T>G | CA396376206 | LCAT | c.857A>C (p.Asp286Ala) c.156-296A>C c.641A>C (p.Asp214Ala) c.595A>C (n.595A>C) | |
16 | g.67940370_67940371delinsTC | CA2229563330 | LCAT | c.856_857delinsGA (p.Asp286=) c.156-297_156-296delinsGA c.640_641delinsGA (p.Asp214=) c.594_595delinsGA (n.594_595delinsGA) | |
16 | g.67940371C>A | CA396376209 | LCAT | c.856G>T (p.Asp286Tyr) c.156-297G>T c.640G>T (p.Asp214Tyr) c.594G>T (n.594G>T) | |
16 | g.67940371C>G | CA396376208 | LCAT | c.856G>C (p.Asp286His) c.156-297G>C c.640G>C (p.Asp214His) c.594G>C (n.594G>C) | |
16 | g.67940371C>T | CA396376207 | LCAT | c.856G>A (p.Asp286Asn) c.156-297G>A c.640G>A (p.Asp214Asn) c.594G>A (n.594G>A) | gnomAD v4 |
16 | g.67940372del | CA8120944 | LCAT | c.856del (p.Asp286ThrfsTer?) c.156-297del c.640del (p.Asp214ThrfsTer?) c.594del (n.594del) | dbSNP ExAC gnomAD v2 gnomAD v4 |
16 | g.67940372C>A | CA396376210 | LCAT | c.855G>T (p.Glu285Asp) c.156-298G>T c.639G>T (p.Glu213Asp) c.593G>T (n.593G>T) | |
16 | g.67940372C>G | CA396376211 | LCAT | c.855G>C (p.Glu285Asp) c.156-298G>C c.639G>C (p.Glu213Asp) c.593G>C (n.593G>C) | |
16 | g.67940372C>T | CA496384005 | LCAT | c.855G>A (p.Glu285=) c.156-298G>A c.639G>A (p.Glu213=) c.593G>A (n.593G>A) | |
16 | g.67940373T>A | CA396376212 | LCAT | c.854A>T (p.Glu285Val) c.156-299A>T c.638A>T (p.Glu213Val) c.592A>T (n.592A>T) | |
16 | g.67940373T>C | CA396376213 | LCAT | c.854A>G (p.Glu285Gly) c.156-299A>G c.638A>G (p.Glu213Gly) c.592A>G (n.592A>G) | |
16 | g.67940373T>G | CA396376214 | LCAT | c.854A>C (p.Glu285Ala) c.156-299A>C c.638A>C (p.Glu213Ala) c.592A>C (n.592A>C) | |
16 | g.67940374C>A | CA396376217 | LCAT | c.853G>T (p.Glu285Ter) c.156-300G>T c.637G>T (p.Glu213Ter) c.591G>T (n.591G>T) | |
16 | g.67940374C= | CA2229563331 | LCAT | c.853G= (p.Glu285=) c.156-300G= c.637G= (p.Glu213=) c.591G= (n.591G=) | |
16 | g.67940374C>G | CA396376215 | LCAT | c.853G>C (p.Glu285Gln) c.156-300G>C c.637G>C (p.Glu213Gln) c.591G>C (n.591G>C) | |
16 | g.67940374C>T | CA396376216 | LCAT | c.853G>A (p.Glu285Lys) c.156-300G>A c.637G>A (p.Glu213Lys) c.591G>A (n.591G>A) | dbSNP |
16 | g.67940375A= | CA2229563332 | LCAT | c.852T= (p.Pro284=) c.156-301T= c.636T= (p.Pro212=) c.590T= (n.590T=) | |
16 | g.67940375A>C | CA496384008 | LCAT | c.852T>G (p.Pro284=) c.156-301T>G c.636T>G (p.Pro212=) c.590T>G (n.590T>G) | |
16 | g.67940375A>G | CA8120945 | LCAT | c.852T>C (p.Pro284=) c.156-301T>C c.636T>C (p.Pro212=) c.590T>C (n.590T>C) | dbSNP ExAC gnomAD v2 gnomAD v4 |
16 | g.67940375A>T | CA496384009 | LCAT | c.852T>A (p.Pro284=) c.156-301T>A c.636T>A (p.Pro212=) c.590T>A (n.590T>A) | |
16 | g.67940376G>A | CA396376218 | LCAT | c.851C>T (p.Pro284Leu) c.156-302C>T c.635C>T (p.Pro212Leu) c.589C>T (n.589C>T) | |
16 | g.67940376G>C | CA396376219 | LCAT | c.851C>G (p.Pro284Arg) c.156-302C>G c.635C>G (p.Pro212Arg) c.589C>G (n.589C>G) | |
16 | g.67940376G>T | CA396376220 | LCAT | c.851C>A (p.Pro284His) c.156-302C>A c.635C>A (p.Pro212His) c.589C>A (n.589C>A) | |
16 | g.67940377G>A | CA396376221 | LCAT | c.850C>T (p.Pro284Ser) c.156-303C>T c.634C>T (p.Pro212Ser) c.588C>T (n.588C>T) | |
16 | g.67940377G>C | CA396376222 | LCAT | c.850C>G (p.Pro284Ala) c.156-303C>G c.634C>G (p.Pro212Ala) c.588C>G (n.588C>G) | |
16 | g.67940377G>T | CA396376223 | LCAT | c.850C>A (p.Pro284Thr) c.156-303C>A c.634C>A (p.Pro212Thr) c.588C>A (n.588C>A) | |
16 | g.67940378C>A | CA396376224 | LCAT | c.849G>T (p.Trp283Cys) c.156-304G>T c.633G>T (p.Trp211Cys) c.587G>T (n.587G>T) | |
16 | g.67940378C>G | CA396376225 | LCAT | c.849G>C (p.Trp283Cys) c.156-304G>C c.633G>C (p.Trp211Cys) c.587G>C (n.587G>C) | |
16 | g.67940378C>T | CA396376226 | LCAT | c.849G>A (p.Trp283Ter) c.156-304G>A c.633G>A (p.Trp211Ter) c.587G>A (n.587G>A) | ClinVar |
16 | g.67940379C>A | CA396376227 | LCAT | c.848G>T (p.Trp283Leu) c.156-305G>T c.632G>T (p.Trp211Leu) c.586G>T (n.586G>T) | gnomAD v4 |
16 | g.67940379C>G | CA396376228 | LCAT | c.848G>C (p.Trp283Ser) c.156-305G>C c.632G>C (p.Trp211Ser) c.586G>C (n.586G>C) | |
16 | g.67940379C>T | CA396376229 | LCAT | c.848G>A (p.Trp283Ter) c.156-305G>A c.632G>A (p.Trp211Ter) c.586G>A (n.586G>A) | |
16 | g.67940380del | CA2576033452 | LCAT | c.847del (p.Trp283GlyfsTer?) c.156-306del c.631del (p.Trp211GlyfsTer?) c.585del (n.585del) | |
16 | g.67940380A>C | CA396376232 | LCAT | c.847T>G (p.Trp283Gly) c.156-306T>G c.631T>G (p.Trp211Gly) c.585T>G (n.585T>G) | |
16 | g.67940380A>G | CA396376230 | LCAT | c.847T>C (p.Trp283Arg) c.156-306T>C c.631T>C (p.Trp211Arg) c.585T>C (n.585T>C) | |
16 | g.67940380A>T | CA396376231 | LCAT | c.847T>A (p.Trp283Arg) c.156-306T>A c.631T>A (p.Trp211Arg) c.585T>A (n.585T>A) | |
16 | g.67940381C>A | CA496384012 | LCAT | c.846G>T (p.Ala282=) c.156-307G>T c.630G>T (p.Ala210=) c.584G>T (n.584G>T) | |
16 | g.67940381C= | CA2229563333 | LCAT | c.846G= (p.Ala282=) c.156-307G= c.630G= (p.Ala210=) c.584G= (n.584G=) | |
16 | g.67940381C>G | CA496384013 | LCAT | c.846G>C (p.Ala282=) c.156-307G>C c.630G>C (p.Ala210=) c.584G>C (n.584G>C) | |
16 | g.67940381C>T | CA8120946 | LCAT | c.846G>A (p.Ala282=) c.156-307G>A c.630G>A (p.Ala210=) c.584G>A (n.584G>A) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.67940382G>A | CA396376233 | LCAT | c.845C>T (p.Ala282Val) c.156-308C>T c.629C>T (p.Ala210Val) c.583C>T (n.583C>T) | ClinVar dbSNP gnomAD v4 COSMIC |
16 | g.67940382G>C | CA396376234 | LCAT | c.845C>G (p.Ala282Gly) c.156-308C>G c.629C>G (p.Ala210Gly) c.583C>G (n.583C>G) | |
16 | g.67940382G= | CA2229563334 | LCAT | c.845C= (p.Ala282=) c.156-308C= c.629C= (p.Ala210=) c.583C= (n.583C=) | |
16 | g.67940382G>T | CA396376235 | LCAT | c.845C>A (p.Ala282Glu) c.156-308C>A c.629C>A (p.Ala210Glu) c.583C>A (n.583C>A) | |
16 | g.67940383C>A | CA396376236 | LCAT | c.844G>T (p.Ala282Ser) c.156-309G>T c.628G>T (p.Ala210Ser) c.582G>T (n.582G>T) | |
16 | g.67940383C>G | CA396376237 | LCAT | c.844G>C (p.Ala282Pro) c.156-309G>C c.628G>C (p.Ala210Pro) c.582G>C (n.582G>C) | |
16 | g.67940383C>T | CA396376238 | LCAT | c.844G>A (p.Ala282Thr) c.156-309G>A c.628G>A (p.Ala210Thr) c.582G>A (n.582G>A) | |
16 | g.67940384C>A | CA396376239 | LCAT | c.843G>T (p.Met281Ile) c.156-310G>T c.627G>T (p.Met209Ile) c.581G>T (n.581G>T) | |
16 | g.67940384C>G | CA396376240 | LCAT | c.843G>C (p.Met281Ile) c.156-310G>C c.627G>C (p.Met209Ile) c.581G>C (n.581G>C) | |
16 | g.67940384C>T | CA396376241 | LCAT | c.843G>A (p.Met281Ile) c.156-310G>A c.627G>A (p.Met209Ile) c.581G>A (n.581G>A) | gnomAD v4 |
16 | g.67940385A>C | CA396376242 | LCAT | c.842T>G (p.Met281Arg) c.156-311T>G c.626T>G (p.Met209Arg) c.580T>G (n.580T>G) | |
16 | g.67940385A>G | CA396376243 | LCAT | c.842T>C (p.Met281Thr) c.156-311T>C c.626T>C (p.Met209Thr) c.580T>C (n.580T>C) | gnomAD v4 |
16 | g.67940385A>T | CA396376244 | LCAT | c.842T>A (p.Met281Lys) c.156-311T>A c.626T>A (p.Met209Lys) c.580T>A (n.580T>A) | |
16 | g.67940386T>A | CA396376246 | LCAT | c.841A>T (p.Met281Leu) c.156-312A>T c.625A>T (p.Met209Leu) c.579A>T (n.579A>T) | |
16 | g.67940386T>C | CA8120947 | LCAT | c.841A>G (p.Met281Val) c.156-312A>G c.625A>G (p.Met209Val) c.579A>G (n.579A>G) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.67940386T>G | CA396376245 | LCAT | c.841A>C (p.Met281Leu) c.156-312A>C c.625A>C (p.Met209Leu) c.579A>C (n.579A>C) | |
16 | g.67940386T= | CA2229563335 | LCAT | c.841A= (p.Met281=) c.156-312A= c.625A= (p.Met209=) c.579A= (n.579A=) | |
16 | g.67940387G>A | CA283160990 | LCAT | c.840C>T (p.Arg280=) c.156-313C>T c.624C>T (p.Arg208=) c.578C>T (n.578C>T) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
16 | g.67940387G>C | CA496384017 | LCAT | c.840C>G (p.Arg280=) c.156-313C>G c.624C>G (p.Arg208=) c.578C>G (n.578C>G) | |
16 | g.67940387G= | CA2229563336 | LCAT | c.840C= (p.Arg280=) c.156-313C= c.624C= (p.Arg208=) c.578C= (n.578C=) | |
16 | g.67940387G>T | CA496384018 | LCAT | c.840C>A (p.Arg280=) c.156-313C>A c.624C>A (p.Arg208=) c.578C>A (n.578C>A) | |
16 | g.67940388C>A | CA396376247 | LCAT | c.839G>T (p.Arg280Leu) c.156-314G>T c.623G>T (p.Arg208Leu) c.577G>T (n.577G>T) | |
16 | g.67940388C= | CA2229563337 | LCAT | c.839G= (p.Arg280=) c.156-314G= c.623G= (p.Arg208=) c.577G= (n.577G=) | |
16 | g.67940388C>G | CA396376248 | LCAT | c.839G>C (p.Arg280Pro) c.156-314G>C c.623G>C (p.Arg208Pro) c.577G>C (n.577G>C) | gnomAD v4 |
16 | g.67940388C>T | CA8120948 | LCAT | c.839G>A (p.Arg280His) c.156-314G>A c.623G>A (p.Arg208His) c.577G>A (n.577G>A) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
16 | g.67940389G>A | CA8120949 | LCAT | c.838C>T (p.Arg280Cys) c.156-315C>T c.622C>T (p.Arg208Cys) c.576C>T (n.576C>T) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.67940389G>C | CA396376249 | LCAT | c.838C>G (p.Arg280Gly) c.156-315C>G c.622C>G (p.Arg208Gly) c.576C>G (n.576C>G) | |
16 | g.67940389G= | CA2229563338 | LCAT | c.838C= (p.Arg280=) c.156-315C= c.622C= (p.Arg208=) c.576C= (n.576C=) | |
16 | g.67940389G>T | CA396376250 | LCAT | c.838C>A (p.Arg280Ser) c.156-315C>A c.622C>A (p.Arg208Ser) c.576C>A (n.576C>A) | |
16 | g.67940392_67940393del | CA2580612821 | LCAT | c.837_838del (p.Arg280HisfsTer5) c.156-316_156-315del c.621_622del (p.Arg208HisfsTer5) c.575_576del (n.575_576del) | ClinVar dbSNP |
16 | g.67940390A>C | CA496384019 | LCAT | c.837T>G (p.Ser279=) c.156-316T>G c.621T>G (p.Ser207=) c.575T>G (n.575T>G) | |
16 | g.67940390A>G | CA496384020 | LCAT | c.837T>C (p.Ser279=) c.156-316T>C c.621T>C (p.Ser207=) c.575T>C (n.575T>C) | |
16 | g.67940390A>T | CA496384022 | LCAT | c.837T>A (p.Ser279=) c.156-316T>A c.621T>A (p.Ser207=) c.575T>A (n.575T>A) | |
16 | g.67940391G>A | CA396376251 | LCAT | c.836C>T (p.Ser279Phe) c.156-317C>T c.620C>T (p.Ser207Phe) c.574C>T (n.574C>T) | |
16 | g.67940391G>C | CA396376252 | LCAT | c.836C>G (p.Ser279Cys) c.156-317C>G c.620C>G (p.Ser207Cys) c.574C>G (n.574C>G) | |
16 | g.67940391G>T | CA396376253 | LCAT | c.836C>A (p.Ser279Tyr) c.156-317C>A c.620C>A (p.Ser207Tyr) c.574C>A (n.574C>A) | |
16 | g.67940392A>C | CA396376254 | LCAT | c.835T>G (p.Ser279Ala) c.156-318T>G c.619T>G (p.Ser207Ala) c.573T>G (n.573T>G) | |
16 | g.67940392A>G | CA396376255 | LCAT | c.835T>C (p.Ser279Pro) c.156-318T>C c.619T>C (p.Ser207Pro) c.573T>C (n.573T>C) | |
16 | g.67940392A>T | CA396376256 | LCAT | c.835T>A (p.Ser279Thr) c.156-318T>A c.619T>A (p.Ser207Thr) c.573T>A (n.573T>A) | |
16 | g.67940393G>A | CA496384025 | LCAT | c.834C>T (p.Pro278=) c.156-319C>T c.618C>T (p.Pro206=) c.572C>T (n.572C>T) | dbSNP gnomAD v3 gnomAD v4 |
16 | g.67940393G>C | CA496384023 | LCAT | c.834C>G (p.Pro278=) c.156-319C>G c.618C>G (p.Pro206=) c.572C>G (n.572C>G) | gnomAD v4 |
16 | g.67940393G= | CA2229563339 | LCAT | c.834C= (p.Pro278=) c.156-319C= c.618C= (p.Pro206=) c.572C= (n.572C=) | |
16 | g.67940393G>T | CA496384024 | LCAT | c.834C>A (p.Pro278=) c.156-319C>A c.618C>A (p.Pro206=) c.572C>A (n.572C>A) | |
16 | g.67940394G>A | CA396376259 | LCAT | c.833C>T (p.Pro278Leu) c.156-320C>T c.617C>T (p.Pro206Leu) c.571C>T (n.571C>T) | |
16 | g.67940394G>C | CA396376258 | LCAT | c.833C>G (p.Pro278Arg) c.156-320C>G c.617C>G (p.Pro206Arg) c.571C>G (n.571C>G) | |
16 | g.67940394G>T | CA396376257 | LCAT | c.833C>A (p.Pro278His) c.156-320C>A c.617C>A (p.Pro206His) c.571C>A (n.571C>A) | |
16 | g.67940395G>A | CA396376260 | LCAT | c.832C>T (p.Pro278Ser) c.156-321C>T c.616C>T (p.Pro206Ser) c.570C>T (n.570C>T) | ClinVar dbSNP gnomAD v4 COSMIC |
16 | g.67940395G>C | CA396376261 | LCAT | c.832C>G (p.Pro278Ala) c.156-321C>G c.616C>G (p.Pro206Ala) c.570C>G (n.570C>G) | |
16 | g.67940395G= | CA2229563340 | LCAT | c.832C= (p.Pro278=) c.156-321C= c.616C= (p.Pro206=) c.570C= (n.570C=) | |
16 | g.67940395G>T | CA396376262 | LCAT | c.832C>A (p.Pro278Thr) c.156-321C>A c.616C>A (p.Pro206Thr) c.570C>A (n.570C>A) | |
16 | g.67940396A>C | CA396376263 | LCAT | c.831T>G (p.Phe277Leu) c.156-322T>G c.615T>G (p.Phe205Leu) c.569T>G (n.569T>G) | |
16 | g.67940396A>G | CA496384027 | LCAT | c.831T>C (p.Phe277=) c.156-322T>C c.615T>C (p.Phe205=) c.569T>C (n.569T>C) | gnomAD v4 |
16 | g.67940396A>T | CA396376264 | LCAT | c.831T>A (p.Phe277Leu) c.156-322T>A c.615T>A (p.Phe205Leu) c.569T>A (n.569T>A) | |
16 | g.67940397A>C | CA396376267 | LCAT | c.830T>G (p.Phe277Cys) c.156-323T>G c.614T>G (p.Phe205Cys) c.568T>G (n.568T>G) | |
16 | g.67940397A>G | CA396376266 | LCAT | c.830T>C (p.Phe277Ser) c.156-323T>C c.614T>C (p.Phe205Ser) c.568T>C (n.568T>C) | |
16 | g.67940397A>T | CA396376265 | LCAT | c.830T>A (p.Phe277Tyr) c.156-323T>A c.614T>A (p.Phe205Tyr) c.568T>A (n.568T>A) | |
16 | g.67940398A>C | CA396376268 | LCAT | c.829T>G (p.Phe277Val) c.156-324T>G c.613T>G (p.Phe205Val) c.567T>G (n.567T>G) | |
16 | g.67940398A>G | CA396376269 | LCAT | c.829T>C (p.Phe277Leu) c.156-324T>C c.613T>C (p.Phe205Leu) c.567T>C (n.567T>C) | |
16 | g.67940398A>T | CA396376270 | LCAT | c.829T>A (p.Phe277Ile) c.156-324T>A c.613T>A (p.Phe205Ile) c.567T>A (n.567T>A) | |
16 | g.67940399_67940400dup | CA2554837458 | LCAT | c.828_829dup (p.Phe277CysfsTer?) c.156-325_156-324dup c.612_613dup (p.Phe205CysfsTer?) c.566_567dup (n.566_567dup) | |
16 | g.67940399C>A | CA396376271 | LCAT | c.828G>T (p.Met276Ile) c.156-325G>T c.612G>T (p.Met204Ile) c.566G>T (n.566G>T) | |
16 | g.67940399C= | CA2229563341 | LCAT | c.828G= (p.Met276=) c.156-325G= c.612G= (p.Met204=) c.566G= (n.566G=) | |
16 | g.67940399C>G | CA396376272 | LCAT | c.828G>C (p.Met276Ile) c.156-325G>C c.612G>C (p.Met204Ile) c.566G>C (n.566G>C) | |
16 | g.67940399C>T | CA8120950 | LCAT | c.828G>A (p.Met276Ile) c.156-325G>A c.612G>A (p.Met204Ile) c.566G>A (n.566G>A) | dbSNP ExAC gnomAD v2 gnomAD v4 |