| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 2 | g.136115514G>A | CA1890123 | CXCR4 | c.402C>T (p.Ile134=) c.369C>T (p.Ile123=) c.414C>T (p.Ile138=) c.426C>T (p.Ile142=) n.608C>T c.627C>T (p.Ile209=) c.513C>T (p.Ile171=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 2 | g.136115514G>C | CA348659160 | CXCR4 | c.402C>G (p.Ile134Met) c.369C>G (p.Ile123Met) c.414C>G (p.Ile138Met) c.426C>G (p.Ile142Met) n.608C>G c.627C>G (p.Ile209Met) c.513C>G (p.Ile171Met) | |
| 2 | g.136115514G= | CA1290966079 | CXCR4 | c.402C= (p.Ile134=) c.369C= (p.Ile123=) c.414C= (p.Ile138=) c.426C= (p.Ile142=) n.608C= c.627C= (p.Ile209=) c.513C= (p.Ile171=) | |
| 2 | g.136115514G>T | CA429206592 | CXCR4 | c.402C>A (p.Ile134=) c.369C>A (p.Ile123=) c.414C>A (p.Ile138=) c.426C>A (p.Ile142=) n.608C>A c.627C>A (p.Ile209=) c.513C>A (p.Ile171=) | |
| 2 | g.136115515A>C | CA348659162 | CXCR4 | c.401T>G (p.Ile134Ser) c.368T>G (p.Ile123Ser) c.413T>G (p.Ile138Ser) c.425T>G (p.Ile142Ser) n.607T>G c.626T>G (p.Ile209Ser) c.512T>G (p.Ile171Ser) | |
| 2 | g.136115515A>G | CA348659164 | CXCR4 | c.401T>C (p.Ile134Thr) c.368T>C (p.Ile123Thr) c.413T>C (p.Ile138Thr) c.425T>C (p.Ile142Thr) n.607T>C c.626T>C (p.Ile209Thr) c.512T>C (p.Ile171Thr) | |
| 2 | g.136115515A>T | CA348659166 | CXCR4 | c.401T>A (p.Ile134Asn) c.368T>A (p.Ile123Asn) c.413T>A (p.Ile138Asn) c.425T>A (p.Ile142Asn) n.607T>A c.626T>A (p.Ile209Asn) c.512T>A (p.Ile171Asn) | |
| 2 | g.136115516T>A | CA348659173 | CXCR4 | c.400A>T (p.Ile134Phe) c.367A>T (p.Ile123Phe) c.412A>T (p.Ile138Phe) c.424A>T (p.Ile142Phe) n.606A>T c.625A>T (p.Ile209Phe) c.511A>T (p.Ile171Phe) | |
| 2 | g.136115516T>C | CA348659168 | CXCR4 | c.400A>G (p.Ile134Val) c.367A>G (p.Ile123Val) c.412A>G (p.Ile138Val) c.424A>G (p.Ile142Val) n.606A>G c.625A>G (p.Ile209Val) c.511A>G (p.Ile171Val) | |
| 2 | g.136115516T>G | CA348659170 | CXCR4 | c.400A>C (p.Ile134Leu) c.367A>C (p.Ile123Leu) c.412A>C (p.Ile138Leu) c.424A>C (p.Ile142Leu) n.606A>C c.625A>C (p.Ile209Leu) c.511A>C (p.Ile171Leu) | |
| 2 | g.136115517G>A | CA429206599 | CXCR4 | c.399C>T (p.Ala133=) c.366C>T (p.Ala122=) c.411C>T (p.Ala137=) c.423C>T (p.Ala141=) n.605C>T c.624C>T (p.Ala208=) c.510C>T (p.Ala170=) | |
| 2 | g.136115517G>C | CA429206601 | CXCR4 | c.399C>G (p.Ala133=) c.366C>G (p.Ala122=) c.411C>G (p.Ala137=) c.423C>G (p.Ala141=) n.605C>G c.624C>G (p.Ala208=) c.510C>G (p.Ala170=) | |
| 2 | g.136115517G>T | CA429206602 | CXCR4 | c.399C>A (p.Ala133=) c.366C>A (p.Ala122=) c.411C>A (p.Ala137=) c.423C>A (p.Ala141=) n.605C>A c.624C>A (p.Ala208=) c.510C>A (p.Ala170=) | COSMIC COSMIC |
| 2 | g.136115518G>A | CA348659175 | CXCR4 | c.398C>T (p.Ala133Val) c.365C>T (p.Ala122Val) c.410C>T (p.Ala137Val) c.422C>T (p.Ala141Val) n.604C>T c.623C>T (p.Ala208Val) c.509C>T (p.Ala170Val) | |
| 2 | g.136115518G>C | CA348659177 | CXCR4 | c.398C>G (p.Ala133Gly) c.365C>G (p.Ala122Gly) c.410C>G (p.Ala137Gly) c.422C>G (p.Ala141Gly) n.604C>G c.623C>G (p.Ala208Gly) c.509C>G (p.Ala170Gly) | |
| 2 | g.136115518G>T | CA348659178 | CXCR4 | c.398C>A (p.Ala133Asp) c.365C>A (p.Ala122Asp) c.410C>A (p.Ala137Asp) c.422C>A (p.Ala141Asp) n.604C>A c.623C>A (p.Ala208Asp) c.509C>A (p.Ala170Asp) | |
| 2 | g.136115519C>A | CA348659179 | CXCR4 | c.397G>T (p.Ala133Ser) c.364G>T (p.Ala122Ser) c.409G>T (p.Ala137Ser) c.421G>T (p.Ala141Ser) n.603G>T c.622G>T (p.Ala208Ser) c.508G>T (p.Ala170Ser) | |
| 2 | g.136115519C>G | CA348659181 | CXCR4 | c.397G>C (p.Ala133Pro) c.364G>C (p.Ala122Pro) c.409G>C (p.Ala137Pro) c.421G>C (p.Ala141Pro) n.603G>C c.622G>C (p.Ala208Pro) c.508G>C (p.Ala170Pro) | |
| 2 | g.136115519C>T | CA348659184 | CXCR4 | c.397G>A (p.Ala133Thr) c.364G>A (p.Ala122Thr) c.409G>A (p.Ala137Thr) c.421G>A (p.Ala141Thr) n.603G>A c.622G>A (p.Ala208Thr) c.508G>A (p.Ala170Thr) | |
| 2 | g.136115520C>A | CA429206609 | CXCR4 | c.396G>T (p.Leu132=) c.363G>T (p.Leu121=) c.408G>T (p.Leu136=) c.420G>T (p.Leu140=) n.602G>T c.621G>T (p.Leu207=) c.507G>T (p.Leu169=) | |
| 2 | g.136115520C>G | CA429206611 | CXCR4 | c.396G>C (p.Leu132=) c.363G>C (p.Leu121=) c.408G>C (p.Leu136=) c.420G>C (p.Leu140=) n.602G>C c.621G>C (p.Leu207=) c.507G>C (p.Leu169=) | |
| 2 | g.136115520C>T | CA429206613 | CXCR4 | c.396G>A (p.Leu132=) c.363G>A (p.Leu121=) c.408G>A (p.Leu136=) c.420G>A (p.Leu140=) n.602G>A c.621G>A (p.Leu207=) c.507G>A (p.Leu169=) | |
| 2 | g.136115521A>C | CA348659188 | CXCR4 | c.395T>G (p.Leu132Arg) c.362T>G (p.Leu121Arg) c.407T>G (p.Leu136Arg) c.419T>G (p.Leu140Arg) n.601T>G c.620T>G (p.Leu207Arg) c.506T>G (p.Leu169Arg) | |
| 2 | g.136115521A>G | CA348659190 | CXCR4 | c.395T>C (p.Leu132Pro) c.362T>C (p.Leu121Pro) c.407T>C (p.Leu136Pro) c.419T>C (p.Leu140Pro) n.601T>C c.620T>C (p.Leu207Pro) c.506T>C (p.Leu169Pro) | |
| 2 | g.136115521A>T | CA348659192 | CXCR4 | c.395T>A (p.Leu132Gln) c.362T>A (p.Leu121Gln) c.407T>A (p.Leu136Gln) c.419T>A (p.Leu140Gln) n.601T>A c.620T>A (p.Leu207Gln) c.506T>A (p.Leu169Gln) | |
| 2 | g.136115522G>A | CA429206620 | CXCR4 | c.394C>T (p.Leu132=) c.361C>T (p.Leu121=) c.406C>T (p.Leu136=) c.418C>T (p.Leu140=) n.600C>T c.619C>T (p.Leu207=) c.505C>T (p.Leu169=) | gnomAD v4 |
| 2 | g.136115522G>C | CA348659195 | CXCR4 | c.394C>G (p.Leu132Val) c.361C>G (p.Leu121Val) c.406C>G (p.Leu136Val) c.418C>G (p.Leu140Val) n.600C>G c.619C>G (p.Leu207Val) c.505C>G (p.Leu169Val) | |
| 2 | g.136115522G>T | CA348659196 | CXCR4 | c.394C>A (p.Leu132Met) c.361C>A (p.Leu121Met) c.406C>A (p.Leu136Met) c.418C>A (p.Leu140Met) n.600C>A c.619C>A (p.Leu207Met) c.505C>A (p.Leu169Met) | |
| 2 | g.136115525_136115530del | CA2661289451 | CXCR4 | c.389_394del (p.Arg130_Tyr131del) c.356_361del (p.Arg119_Tyr120del) c.401_406del (p.Arg134_Tyr135del) c.413_418del (p.Arg138_Tyr139del) n.595_600del c.614_619del (p.Arg205_Tyr206del) c.500_505del (p.Arg167_Tyr168del) | gnomAD v4 |
| 2 | g.136115523G>A | CA429206626 | CXCR4 | c.393C>T (p.Tyr131=) c.360C>T (p.Tyr120=) c.405C>T (p.Tyr135=) c.417C>T (p.Tyr139=) n.599C>T c.618C>T (p.Tyr206=) c.504C>T (p.Tyr168=) | |
| 2 | g.136115523G>C | CA348659200 | CXCR4 | c.393C>G (p.Tyr131Ter) c.360C>G (p.Tyr120Ter) c.405C>G (p.Tyr135Ter) c.417C>G (p.Tyr139Ter) n.599C>G c.618C>G (p.Tyr206Ter) c.504C>G (p.Tyr168Ter) | |
| 2 | g.136115523G>T | CA348659197 | CXCR4 | c.393C>A (p.Tyr131Ter) c.360C>A (p.Tyr120Ter) c.405C>A (p.Tyr135Ter) c.417C>A (p.Tyr139Ter) n.599C>A c.618C>A (p.Tyr206Ter) c.504C>A (p.Tyr168Ter) | |
| 2 | g.136115524T>A | CA348659202 | CXCR4 | c.392A>T (p.Tyr131Phe) c.359A>T (p.Tyr120Phe) c.404A>T (p.Tyr135Phe) c.416A>T (p.Tyr139Phe) n.598A>T c.617A>T (p.Tyr206Phe) c.503A>T (p.Tyr168Phe) | |
| 2 | g.136115524T>C | CA348659203 | CXCR4 | c.392A>G (p.Tyr131Cys) c.359A>G (p.Tyr120Cys) c.404A>G (p.Tyr135Cys) c.416A>G (p.Tyr139Cys) n.598A>G c.617A>G (p.Tyr206Cys) c.503A>G (p.Tyr168Cys) | dbSNP gnomAD v2 gnomAD v4 |
| 2 | g.136115524T>G | CA348659205 | CXCR4 | c.392A>C (p.Tyr131Ser) c.359A>C (p.Tyr120Ser) c.404A>C (p.Tyr135Ser) c.416A>C (p.Tyr139Ser) n.598A>C c.617A>C (p.Tyr206Ser) c.503A>C (p.Tyr168Ser) | |
| 2 | g.136115524T= | CA1290966080 | CXCR4 | c.392A= (p.Tyr131=) c.359A= (p.Tyr120=) c.404A= (p.Tyr135=) c.416A= (p.Tyr139=) n.598A= c.617A= (p.Tyr206=) c.503A= (p.Tyr168=) | |
| 2 | g.136115525A>C | CA348659207 | CXCR4 | c.391T>G (p.Tyr131Asp) c.358T>G (p.Tyr120Asp) c.403T>G (p.Tyr135Asp) c.415T>G (p.Tyr139Asp) n.597T>G c.616T>G (p.Tyr206Asp) c.502T>G (p.Tyr168Asp) | |
| 2 | g.136115525A>G | CA348659210 | CXCR4 | c.391T>C (p.Tyr131His) c.358T>C (p.Tyr120His) c.403T>C (p.Tyr135His) c.415T>C (p.Tyr139His) n.597T>C c.616T>C (p.Tyr206His) c.502T>C (p.Tyr168His) | |
| 2 | g.136115525A>T | CA348659212 | CXCR4 | c.391T>A (p.Tyr131Asn) c.358T>A (p.Tyr120Asn) c.403T>A (p.Tyr135Asn) c.415T>A (p.Tyr139Asn) n.597T>A c.616T>A (p.Tyr206Asn) c.502T>A (p.Tyr168Asn) | |
| 2 | g.136115526G>A | CA429206633 | CXCR4 | c.390C>T (p.Arg130=) c.357C>T (p.Arg119=) c.402C>T (p.Arg134=) c.414C>T (p.Arg138=) n.596C>T c.615C>T (p.Arg205=) c.501C>T (p.Arg167=) | |
| 2 | g.136115526G>C | CA429206636 | CXCR4 | c.390C>G (p.Arg130=) c.357C>G (p.Arg119=) c.402C>G (p.Arg134=) c.414C>G (p.Arg138=) n.596C>G c.615C>G (p.Arg205=) c.501C>G (p.Arg167=) | |
| 2 | g.136115526G>T | CA429206637 | CXCR4 | c.390C>A (p.Arg130=) c.357C>A (p.Arg119=) c.402C>A (p.Arg134=) c.414C>A (p.Arg138=) n.596C>A c.615C>A (p.Arg205=) c.501C>A (p.Arg167=) | ClinVar dbSNP |
| 2 | g.136115527C>A | CA348659220 | CXCR4 | c.389G>T (p.Arg130Leu) c.356G>T (p.Arg119Leu) c.401G>T (p.Arg134Leu) c.413G>T (p.Arg138Leu) n.595G>T c.614G>T (p.Arg205Leu) c.500G>T (p.Arg167Leu) | COSMIC COSMIC |
| 2 | g.136115527C>G | CA348659216 | CXCR4 | c.389G>C (p.Arg130Pro) c.356G>C (p.Arg119Pro) c.401G>C (p.Arg134Pro) c.413G>C (p.Arg138Pro) n.595G>C c.614G>C (p.Arg205Pro) c.500G>C (p.Arg167Pro) | |
| 2 | g.136115527C>T | CA348659218 | CXCR4 | c.389G>A (p.Arg130His) c.356G>A (p.Arg119His) c.401G>A (p.Arg134His) c.413G>A (p.Arg138His) n.595G>A c.614G>A (p.Arg205His) c.500G>A (p.Arg167His) | gnomAD v4 COSMIC |
| 2 | g.136115528G>A | CA348659223 | CXCR4 | c.388C>T (p.Arg130Cys) c.355C>T (p.Arg119Cys) c.400C>T (p.Arg134Cys) c.412C>T (p.Arg138Cys) n.594C>T c.613C>T (p.Arg205Cys) c.499C>T (p.Arg167Cys) | gnomAD v4 |
| 2 | g.136115528G>C | CA348659225 | CXCR4 | c.388C>G (p.Arg130Gly) c.355C>G (p.Arg119Gly) c.400C>G (p.Arg134Gly) c.412C>G (p.Arg138Gly) n.594C>G c.613C>G (p.Arg205Gly) c.499C>G (p.Arg167Gly) | |
| 2 | g.136115528G>T | CA348659227 | CXCR4 | c.388C>A (p.Arg130Ser) c.355C>A (p.Arg119Ser) c.400C>A (p.Arg134Ser) c.412C>A (p.Arg138Ser) n.594C>A c.613C>A (p.Arg205Ser) c.499C>A (p.Arg167Ser) | |
| 2 | g.136115529G>A | CA429206643 | CXCR4 | c.387C>T (p.Asp129=) c.354C>T (p.Asp118=) c.399C>T (p.Asp133=) c.411C>T (p.Asp137=) n.593C>T c.612C>T (p.Asp204=) c.498C>T (p.Asp166=) | dbSNP gnomAD v3 gnomAD v4 |
| 2 | g.136115529G>C | CA348659229 | CXCR4 | c.387C>G (p.Asp129Glu) c.354C>G (p.Asp118Glu) c.399C>G (p.Asp133Glu) c.411C>G (p.Asp137Glu) n.593C>G c.612C>G (p.Asp204Glu) c.498C>G (p.Asp166Glu) |