| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 4 | g.186208979_186208987del | CA2672897508 | CYP4V2 | c.1205_1213del (p.Val402_Glu404del) n.440_448del n.5903_5911del n.295_303del c.809_817del (p.Val270_Glu272del) | gnomAD v4 |
| 4 | g.186208987G>A | CA358950304 | CYP4V2,KLKB1 | c.1213G>A (p.Asp405Asn) n.448G>A n.5911G>A c.9G>A n.303G>A c.817G>A (p.Asp273Asn) | gnomAD v4 |
| 4 | g.186208987G>C | CA358950303 | CYP4V2,KLKB1 | c.1213G>C (p.Asp405His) n.448G>C n.5911G>C c.9G>C n.303G>C c.817G>C (p.Asp273His) | |
| 4 | g.186208987G= | CA1519891343 | CYP4V2,KLKB1 | c.1213G= (p.Asp405=) n.448G= n.5911G= c.9G= n.303G= c.817G= (p.Asp273=) | |
| 4 | g.186208987G>T | CA358950302 | CYP4V2,KLKB1 | c.1213G>T (p.Asp405Tyr) n.448G>T n.5911G>T c.9G>T n.303G>T c.817G>T (p.Asp273Tyr) | dbSNP |
| 4 | g.186208988A>C | CA358950305 | CYP4V2,KLKB1 | c.1214A>C (p.Asp405Ala) n.449A>C n.5912A>C c.10A>C n.304A>C c.818A>C (p.Asp273Ala) | |
| 4 | g.186208988A>G | CA358950306 | CYP4V2,KLKB1 | c.1214A>G (p.Asp405Gly) n.449A>G n.5912A>G c.10A>G n.304A>G c.818A>G (p.Asp273Gly) | |
| 4 | g.186208988A>T | CA358950307 | CYP4V2,KLKB1 | c.1214A>T (p.Asp405Val) n.449A>T n.5912A>T c.10A>T n.304A>T c.818A>T (p.Asp273Val) | |
| 4 | g.186208989T>A | CA358950308 | CYP4V2,KLKB1 | c.1215T>A (p.Asp405Glu) n.450T>A n.5913T>A c.11T>A n.305T>A c.819T>A (p.Asp273Glu) | |
| 4 | g.186208989T>C | CA442882237 | CYP4V2,KLKB1 | c.1215T>C (p.Asp405=) n.450T>C n.5913T>C c.11T>C n.305T>C c.819T>C (p.Asp273=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 4 | g.186208989T>G | CA358950309 | CYP4V2,KLKB1 | c.1215T>G (p.Asp405Glu) n.450T>G n.5913T>G c.11T>G n.305T>G c.819T>G (p.Asp273Glu) | |
| 4 | g.186208989T= | CA1519891344 | CYP4V2,KLKB1 | c.1215T= (p.Asp405=) n.450T= n.5913T= c.11T= n.305T= c.819T= (p.Asp273=) | |
| 4 | g.186208989_186208990insA | CA2672897509 | CYP4V2,KLKB1 | c.1215_1216insA (p.Cys406MetfsTer2) n.450_451insA n.5913_5914insA c.11_12insA n.305_306insA c.819_820insA (p.Cys274MetfsTer2) | gnomAD v4 |
| 4 | g.186208990T>A | CA358950310 | CYP4V2,KLKB1 | c.1216T>A (p.Cys406Ser) n.451T>A n.5914T>A c.12T>A n.306T>A c.820T>A (p.Cys274Ser) | |
| 4 | g.186208990T>C | CA3162788 | CYP4V2,KLKB1 | c.1216T>C (p.Cys406Arg) n.451T>C n.5914T>C c.12T>C n.306T>C c.820T>C (p.Cys274Arg) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 4 | g.186208990T>G | CA358950311 | CYP4V2,KLKB1 | c.1216T>G (p.Cys406Gly) n.451T>G n.5914T>G c.12T>G n.306T>G c.820T>G (p.Cys274Gly) | |
| 4 | g.186208990T= | CA1519891345 | CYP4V2,KLKB1 | c.1216T= (p.Cys406=) n.451T= n.5914T= c.12T= n.306T= c.820T= (p.Cys274=) | |
| 4 | g.186208991G>A | CA112134823 | CYP4V2,KLKB1 | c.1217G>A (p.Cys406Tyr) n.452G>A n.5915G>A c.13G>A n.307G>A c.821G>A (p.Cys274Tyr) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 4 | g.186208991G>C | CA358950312 | CYP4V2,KLKB1 | c.1217G>C (p.Cys406Ser) n.452G>C n.5915G>C c.13G>C n.307G>C c.821G>C (p.Cys274Ser) | |
| 4 | g.186208991G= | CA1519891346 | CYP4V2,KLKB1 | c.1217G= (p.Cys406=) n.452G= n.5915G= c.13G= n.307G= c.821G= (p.Cys274=) | |
| 4 | g.186208991G>T | CA358950313 | CYP4V2,KLKB1 | c.1217G>T (p.Cys406Phe) n.452G>T n.5915G>T c.13G>T n.307G>T c.821G>T (p.Cys274Phe) | dbSNP gnomAD v4 |
| 4 | g.186208992T>A | CA358950314 | CYP4V2,KLKB1 | c.1218T>A (p.Cys406Ter) n.453T>A n.5916T>A c.14T>A n.308T>A c.822T>A (p.Cys274Ter) | |
| 4 | g.186208992T>C | CA442882249 | CYP4V2,KLKB1 | c.1218T>C (p.Cys406=) n.453T>C n.5916T>C c.14T>C n.308T>C c.822T>C (p.Cys274=) | |
| 4 | g.186208992T>G | CA358950315 | CYP4V2,KLKB1 | c.1218T>G (p.Cys406Trp) n.453T>G n.5916T>G c.14T>G n.308T>G c.822T>G (p.Cys274Trp) | |
| 4 | g.186208993G>A | CA358950316 | CYP4V2,KLKB1 | c.1219G>A (p.Glu407Lys) n.454G>A n.5917G>A c.15G>A n.309G>A c.823G>A (p.Glu275Lys) | |
| 4 | g.186208993G>C | CA358950318 | CYP4V2,KLKB1 | c.1219G>C (p.Glu407Gln) n.454G>C n.5917G>C c.15G>C n.309G>C c.823G>C (p.Glu275Gln) | |
| 4 | g.186208993G>T | CA358950317 | CYP4V2,KLKB1 | c.1219G>T (p.Glu407Ter) n.454G>T n.5917G>T c.15G>T n.309G>T c.823G>T (p.Glu275Ter) | ClinVar dbSNP gnomAD v4 |
| 4 | g.186208994A>C | CA358950319 | CYP4V2,KLKB1 | c.1220A>C (p.Glu407Ala) n.455A>C n.5918A>C c.16A>C n.310A>C c.824A>C (p.Glu275Ala) | |
| 4 | g.186208994A>G | CA358950320 | CYP4V2,KLKB1 | c.1220A>G (p.Glu407Gly) n.455A>G n.5918A>G c.16A>G n.310A>G c.824A>G (p.Glu275Gly) | |
| 4 | g.186208994A>T | CA358950321 | CYP4V2,KLKB1 | c.1220A>T (p.Glu407Val) n.455A>T n.5918A>T c.16A>T n.310A>T c.824A>T (p.Glu275Val) | |
| 4 | g.186208995A>C | CA358950322 | CYP4V2,KLKB1 | c.1221A>C (p.Glu407Asp) n.456A>C n.5919A>C c.17A>C n.311A>C c.825A>C (p.Glu275Asp) | |
| 4 | g.186208995A>G | CA442882260 | CYP4V2,KLKB1 | c.1221A>G (p.Glu407=) n.456A>G n.5919A>G c.17A>G n.311A>G c.825A>G (p.Glu275=) | |
| 4 | g.186208995A>T | CA358950323 | CYP4V2,KLKB1 | c.1221A>T (p.Glu407Asp) n.456A>T n.5919A>T c.17A>T n.311A>T c.825A>T (p.Glu275Asp) | |
| 4 | g.186208996G>A | CA358950324 | CYP4V2,KLKB1 | c.1222G>A (p.Val408Met) n.457G>A n.5920G>A c.18G>A n.312G>A c.826G>A (p.Val276Met) | |
| 4 | g.186208996G>C | CA358950325 | CYP4V2,KLKB1 | c.1222G>C (p.Val408Leu) n.457G>C n.5920G>C c.18G>C n.312G>C c.826G>C (p.Val276Leu) | |
| 4 | g.186208996G= | CA1519891347 | CYP4V2,KLKB1 | c.1222G= (p.Val408=) n.457G= n.5920G= c.18G= n.312G= c.826G= (p.Val276=) | |
| 4 | g.186208996G>T | CA3162789 | CYP4V2,KLKB1 | c.1222G>T (p.Val408Leu) n.457G>T n.5920G>T c.18G>T n.312G>T c.826G>T (p.Val276Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 4 | g.186208997T>A | CA358950326 | CYP4V2,KLKB1 | c.1223T>A (p.Val408Glu) n.458T>A n.5921T>A c.19T>A n.313T>A c.827T>A (p.Val276Glu) | |
| 4 | g.186208997T>C | CA358950327 | CYP4V2,KLKB1 | c.1223T>C (p.Val408Ala) n.458T>C n.5921T>C c.19T>C n.313T>C c.827T>C (p.Val276Ala) | |
| 4 | g.186208997T>G | CA358950328 | CYP4V2,KLKB1 | c.1223T>G (p.Val408Gly) n.458T>G n.5921T>G c.19T>G n.313T>G c.827T>G (p.Val276Gly) | |
| 4 | g.186208998G>A | CA442882272 | CYP4V2,KLKB1 | c.1224G>A (p.Val408=) n.459G>A n.5922G>A c.20G>A n.314G>A c.828G>A (p.Val276=) | dbSNP gnomAD v3 gnomAD v4 |
| 4 | g.186208998G>C | CA442882273 | CYP4V2,KLKB1 | c.1224G>C (p.Val408=) n.459G>C n.5922G>C c.20G>C n.314G>C c.828G>C (p.Val276=) | |
| 4 | g.186208998G= | CA1519891348 | CYP4V2,KLKB1 | c.1224G= (p.Val408=) n.459G= n.5922G= c.20G= n.314G= c.828G= (p.Val276=) | |
| 4 | g.186208998G>T | CA442882274 | CYP4V2,KLKB1 | c.1224G>T (p.Val408=) n.459G>T n.5922G>T c.20G>T n.314G>T c.828G>T (p.Val276=) | |
| 4 | g.186208999G>A | CA358950331 | CYP4V2,KLKB1 | c.1225G>A (p.Ala409Thr) n.460G>A n.5923G>A c.21G>A n.315G>A c.1225G>A (p.Gly409Ser) c.829G>A (p.Ala277Thr) | dbSNP gnomAD v2 gnomAD v4 |
| 4 | g.186208999G>C | CA358950330 | CYP4V2,KLKB1 | c.1225G>C (p.Ala409Pro) n.460G>C n.5923G>C c.21G>C n.315G>C c.1225G>C (p.Gly409Arg) c.829G>C (p.Ala277Pro) | dbSNP |
| 4 | g.186208999G= | CA1519891349 | CYP4V2,KLKB1 | c.1225G= (p.Ala409=) n.460G= n.5923G= c.21G= n.315G= c.1225G= (p.Gly409=) c.829G= (p.Ala277=) | |
| 4 | g.186208999G>T | CA358950329 | CYP4V2,KLKB1 | c.1225G>T (p.Ala409Ser) n.460G>T n.5923G>T c.21G>T n.315G>T c.1225G>T (p.Gly409Cys) c.829G>T (p.Ala277Ser) | |
| 4 | g.186209000G>A | CA3162790 | CYP4V2,KLKB1 | c.1225+1G>A (n.1225+1G>A) n.460+1G>A n.5923+1G>A c.21+1G>A n.315+1G>A c.829+1G>A (n.829+1G>A) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 4 | g.186209000G>C | CA358950332 | CYP4V2,KLKB1 | c.1225+1G>C (n.1225+1G>C) n.460+1G>C n.5923+1G>C c.21+1G>C n.315+1G>C c.829+1G>C (n.829+1G>C) |