| 13 | g.52397735_52397738delinsTTGG | CA2091759651 | THSD1 | c.515_518delinsCCAA (p.Thr172=)
| |
| 13 | g.52397738_52397740del | CA2091759654 | THSD1 | c.515_517del (p.Thr172del)
| dbSNP |
| 13 | g.52397738G>A | CA388038181 | THSD1 | c.515C>T (p.Thr172Ile)
| gnomAD v4 |
| 13 | g.52397738G>C | CA388038183 | THSD1 | c.515C>G (p.Thr172Ser)
| |
| 13 | g.52397738G>T | CA388038185 | THSD1 | c.515C>A (p.Thr172Asn)
| |
| 13 | g.52397739T>A | CA388038188 | THSD1 | c.514A>T (p.Thr172Ser)
| |
| 13 | g.52397739T>C | CA388038191 | THSD1 | c.514A>G (p.Thr172Ala)
| |
| 13 | g.52397739T>G | CA388038193 | THSD1 | c.514A>C (p.Thr172Pro)
| |
| 13 | g.52397740G>A | CA484028523 | THSD1 | c.513C>T (p.Phe171=)
| dbSNP gnomAD v4 |
| 13 | g.52397740G>C | CA388038201 | THSD1 | c.513C>G (p.Phe171Leu)
| |
| 13 | g.52397740G= | CA2091759656 | THSD1 | c.513C= (p.Phe171=)
| |
| 13 | g.52397740G>T | CA388038198 | THSD1 | c.513C>A (p.Phe171Leu)
| |
| 13 | g.52397741A>C | CA388038204 | THSD1 | c.512T>G (p.Phe171Cys)
| |
| 13 | g.52397741A>G | CA388038205 | THSD1 | c.512T>C (p.Phe171Ser)
| |
| 13 | g.52397741A>T | CA388038208 | THSD1 | c.512T>A (p.Phe171Tyr)
| |
| 13 | g.52397742A= | CA2091759661 | THSD1 | c.511T= (p.Phe171=)
| |
| 13 | g.52397742A>C | CA388038211 | THSD1 | c.511T>G (p.Phe171Val)
| |
| 13 | g.52397742A>G | CA6992183 | THSD1 | c.511T>C (p.Phe171Leu)
| dbSNP ExAC gnomAD v2 |
| 13 | g.52397742A>T | CA388038216 | THSD1 | c.511T>A (p.Phe171Ile)
| |
| 13 | g.52397743G>A | CA484028527 | THSD1 | c.510C>T (p.Ile170=)
| gnomAD v4 |
| 13 | g.52397743G>C | CA388038219 | THSD1 | c.510C>G (p.Ile170Met)
| |
| 13 | g.52397743G>T | CA484028528 | THSD1 | c.510C>A (p.Ile170=)
| |
| 13 | g.52397744A= | CA2091759663 | THSD1 | c.509T= (p.Ile170=)
| |
| 13 | g.52397744A>C | CA388038224 | THSD1 | c.509T>G (p.Ile170Ser)
| |
| 13 | g.52397744A>G | CA6992184 | THSD1 | c.509T>C (p.Ile170Thr)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
| 13 | g.52397744A>T | CA388038227 | THSD1 | c.509T>A (p.Ile170Asn)
| |
| 13 | g.52397745T>A | CA388038231 | THSD1 | c.508A>T (p.Ile170Phe)
| |
| 13 | g.52397745T>C | CA388038234 | THSD1 | c.508A>G (p.Ile170Val)
| dbSNP gnomAD v4 |
| 13 | g.52397745T>G | CA388038236 | THSD1 | c.508A>C (p.Ile170Leu)
| |
| 13 | g.52397745T= | CA2091759668 | THSD1 | c.508A= (p.Ile170=)
| |
| 13 | g.52397746G>A | CA6992186 | THSD1 | c.507C>T (p.Val169=)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
| 13 | g.52397746G>C | CA484028532 | THSD1 | c.507C>G (p.Val169=)
| |
| 13 | g.52397746G= | CA2091759672 | THSD1 | c.507C= (p.Val169=)
| |
| 13 | g.52397746G>T | CA6992185 | THSD1 | c.507C>A (p.Val169=)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
| 13 | g.52397747A>C | CA388038244 | THSD1 | c.506T>G (p.Val169Gly)
| |
| 13 | g.52397747A>G | CA388038247 | THSD1 | c.506T>C (p.Val169Ala)
| |
| 13 | g.52397747A>T | CA388038249 | THSD1 | c.506T>A (p.Val169Asp)
| |
| 13 | g.52397748C>A | CA388038252 | THSD1 | c.505G>T (p.Val169Phe)
| |
| 13 | g.52397748C>G | CA388038254 | THSD1 | c.505G>C (p.Val169Leu)
| gnomAD v4 |
| 13 | g.52397748C>T | CA388038256 | THSD1 | c.505G>A (p.Val169Ile)
| gnomAD v4 |
| 13 | g.52397749A= | CA2091759674 | THSD1 | c.504T= (p.Asp168=)
| |
| 13 | g.52397749A>C | CA388038261 | THSD1 | c.504T>G (p.Asp168Glu)
| gnomAD v4 |
| 13 | g.52397749A>G | CA484028537 | THSD1 | c.504T>C (p.Asp168=)
| |
| 13 | g.52397749A>T | CA6992187 | THSD1 | c.504T>A (p.Asp168Glu)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
| 13 | g.52397750T>A | CA388038266 | THSD1 | c.503A>T (p.Asp168Val)
| |
| 13 | g.52397750T>C | CA388038268 | THSD1 | c.503A>G (p.Asp168Gly)
| |
| 13 | g.52397750T>G | CA388038271 | THSD1 | c.503A>C (p.Asp168Ala)
| |
| 13 | g.52397751C>A | CA388038275 | THSD1 | c.502G>T (p.Asp168Tyr)
| |
| 13 | g.52397751C= | CA2091759677 | THSD1 | c.502G= (p.Asp168=)
| |
| 13 | g.52397751C>G | CA388038278 | THSD1 | c.502G>C (p.Asp168His)
| |
| 13 | g.52397751C>T | CA388038281 | THSD1 | c.502G>A (p.Asp168Asn)
| dbSNP |
| 13 | g.52397752C>A | CA484028543 | THSD1 | c.501G>T (p.Val167=)
| |
| 13 | g.52397752C>G | CA484028545 | THSD1 | c.501G>C (p.Val167=)
| |
| 13 | g.52397752C>T | CA484028546 | THSD1 | c.501G>A (p.Val167=)
| |
| 13 | g.52397753A>C | CA388038288 | THSD1 | c.500T>G (p.Val167Gly)
| |
| 13 | g.52397753A>G | CA388038286 | THSD1 | c.500T>C (p.Val167Ala)
| |
| 13 | g.52397753A>T | CA388038284 | THSD1 | c.500T>A (p.Val167Glu)
| |
| 13 | g.52397754C>A | CA388038292 | THSD1 | c.499G>T (p.Val167Leu)
| |
| 13 | g.52397754C= | CA2091759679 | THSD1 | c.499G= (p.Val167=)
| |
| 13 | g.52397754C>G | CA388038290 | THSD1 | c.499G>C (p.Val167Leu)
| dbSNP |
| 13 | g.52397754C>T | CA388038293 | THSD1 | c.499G>A (p.Val167Met)
| |
| 13 | g.52397754_52397755del | CA2551395105 | THSD1 | c.498_499del (p.Val167GlyfsTer10)
| |
| 13 | g.52397755T>A | CA484028549 | THSD1 | c.498A>T (p.Val166=)
| |
| 13 | g.52397755T>C | CA484028550 | THSD1 | c.498A>G (p.Val166=)
| gnomAD v4 |
| 13 | g.52397755T>G | CA484028552 | THSD1 | c.498A>C (p.Val166=)
| |
| 13 | g.52397756A= | CA2091759682 | THSD1 | c.497T= (p.Val166=)
| |
| 13 | g.52397756A>C | CA388038297 | THSD1 | c.497T>G (p.Val166Gly)
| |
| 13 | g.52397756A>G | CA388038301 | THSD1 | c.497T>C (p.Val166Ala)
| dbSNP |
| 13 | g.52397756A>T | CA388038300 | THSD1 | c.497T>A (p.Val166Glu)
| |
| 13 | g.52397757C>A | CA388038305 | THSD1 | c.496G>T (p.Val166Leu)
| gnomAD v4 |
| 13 | g.52397757C= | CA2091759686 | THSD1 | c.496G= (p.Val166=)
| |
| 13 | g.52397757C>G | CA388038307 | THSD1 | c.496G>C (p.Val166Leu)
| |
| 13 | g.52397757C>T | CA388038310 | THSD1 | c.496G>A (p.Val166Ile)
| ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 13 | g.52397757_52397758insAA | CA2572298733 | THSD1 | c.495_496insTT (p.Val166LeufsTer2)
| |
| 13 | g.52397758G>A | CA6992188 | THSD1 | c.495C>T (p.Ile165=)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.52397758G>C | CA388038315 | THSD1 | c.495C>G (p.Ile165Met)
| |
| 13 | g.52397758G= | CA2091759690 | THSD1 | c.495C= (p.Ile165=)
| |
| 13 | g.52397758G>T | CA484028557 | THSD1 | c.495C>A (p.Ile165=)
| |
| 13 | g.52397759A>C | CA388038324 | THSD1 | c.494T>G (p.Ile165Ser)
| |
| 13 | g.52397759A>G | CA388038322 | THSD1 | c.494T>C (p.Ile165Thr)
| |
| 13 | g.52397759A>T | CA388038319 | THSD1 | c.494T>A (p.Ile165Asn)
| gnomAD v4 |
| 13 | g.52397760T>A | CA388038327 | THSD1 | c.493A>T (p.Ile165Phe)
| |
| 13 | g.52397760T>C | CA6992189 | THSD1 | c.493A>G (p.Ile165Val)
| dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.52397760T>G | CA388038332 | THSD1 | c.493A>C (p.Ile165Leu)
| |
| 13 | g.52397760T= | CA2091759694 | THSD1 | c.493A= (p.Ile165=)
| |
| 13 | g.52397761G>A | CA6992190 | THSD1 | c.492C>T (p.Asn164=)
| dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.52397761G>C | CA388038337 | THSD1 | c.492C>G (p.Asn164Lys)
| |
| 13 | g.52397761G= | CA2091759696 | THSD1 | c.492C= (p.Asn164=)
| |
| 13 | g.52397761G>T | CA388038339 | THSD1 | c.492C>A (p.Asn164Lys)
| |
| 13 | g.52397762T>A | CA388038341 | THSD1 | c.491A>T (p.Asn164Ile)
| |
| 13 | g.52397762T>C | CA388038345 | THSD1 | c.491A>G (p.Asn164Ser)
| gnomAD v4 COSMIC |
| 13 | g.52397762T>G | CA388038343 | THSD1 | c.491A>C (p.Asn164Thr)
| |
| 13 | g.52397763T>A | CA388038349 | THSD1 | c.490A>T (p.Asn164Tyr)
| |
| 13 | g.52397763T>C | CA388038351 | THSD1 | c.490A>G (p.Asn164Asp)
| |
| 13 | g.52397763T>G | CA388038354 | THSD1 | c.490A>C (p.Asn164His)
| |
| 13 | g.52397764G>A | CA484028562 | THSD1 | c.489C>T (p.Pro163=)
| |
| 13 | g.52397764G>C | CA484028563 | THSD1 | c.489C>G (p.Pro163=)
| |
| 13 | g.52397764G>T | CA484028566 | THSD1 | c.489C>A (p.Pro163=)
| |
| 13 | g.52397765G>A | CA388038358 | THSD1 | c.488C>T (p.Pro163Leu)
| |
| 13 | g.52397765G>C | CA388038361 | THSD1 | c.488C>G (p.Pro163Arg)
| gnomAD v4 |
| 13 | g.52397765G>T | CA388038363 | THSD1 | c.488C>A (p.Pro163His)
| |
| 13 | g.52397766G>A | CA388038366 | THSD1 | c.487C>T (p.Pro163Ser)
| |
| 13 | g.52397766G>C | CA388038368 | THSD1 | c.487C>G (p.Pro163Ala)
| |
| 13 | g.52397766G>T | CA388038370 | THSD1 | c.487C>A (p.Pro163Thr)
| |
| 13 | g.52397767C>A | CA388038374 | THSD1 | c.486G>T (p.Lys162Asn)
| |
| 13 | g.52397767C>G | CA388038376 | THSD1 | c.486G>C (p.Lys162Asn)
| |
| 13 | g.52397767C>T | CA484028571 | THSD1 | c.486G>A (p.Lys162=)
| |
| 13 | g.52397768T>A | CA388038381 | THSD1 | c.485A>T (p.Lys162Met)
| gnomAD v4 |
| 13 | g.52397768T>C | CA388038386 | THSD1 | c.485A>G (p.Lys162Arg)
| |
| 13 | g.52397768T>G | CA388038384 | THSD1 | c.485A>C (p.Lys162Thr)
| |
| 13 | g.52397769T>A | CA388038387 | THSD1 | c.484A>T (p.Lys162Ter)
| |
| 13 | g.52397769T>C | CA388038388 | THSD1 | c.484A>G (p.Lys162Glu)
| gnomAD v4 |
| 13 | g.52397769T>G | CA388038389 | THSD1 | c.484A>C (p.Lys162Gln)
| |
| 13 | g.52397770G>A | CA484028578 | THSD1 | c.483C>T (p.Asp161=)
| |
| 13 | g.52397770G>C | CA250097332 | THSD1 | c.483C>G (p.Asp161Glu)
| dbSNP gnomAD v3 gnomAD v4 |
| 13 | g.52397770G= | CA2091759699 | THSD1 | c.483C= (p.Asp161=)
| |
| 13 | g.52397770G>T | CA388038391 | THSD1 | c.483C>A (p.Asp161Glu)
| |
| 13 | g.52397771T>A | CA388038397 | THSD1 | c.482A>T (p.Asp161Val)
| gnomAD v4 |
| 13 | g.52397771T>C | CA388038400 | THSD1 | c.482A>G (p.Asp161Gly)
| |
| 13 | g.52397771T>G | CA388038402 | THSD1 | c.482A>C (p.Asp161Ala)
| |
| 13 | g.52397772C>A | CA388038407 | THSD1 | c.481G>T (p.Asp161Tyr)
| |
| 13 | g.52397772C= | CA2091759702 | THSD1 | c.481G= (p.Asp161=)
| |
| 13 | g.52397772C>G | CA388038409 | THSD1 | c.481G>C (p.Asp161His)
| |
| 13 | g.52397772C>T | CA6992191 | THSD1 | c.481G>A (p.Asp161Asn)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
| 13 | g.52397773C>A | CA484028583 | THSD1 | c.480G>T (p.Val160=)
| |
| 13 | g.52397773C>G | CA484028584 | THSD1 | c.480G>C (p.Val160=)
| |
| 13 | g.52397773C>T | CA484028585 | THSD1 | c.480G>A (p.Val160=)
| |
| 13 | g.52397774A>C | CA388038419 | THSD1 | c.479T>G (p.Val160Gly)
| |
| 13 | g.52397774A>G | CA388038414 | THSD1 | c.479T>C (p.Val160Ala)
| |
| 13 | g.52397774A>T | CA388038416 | THSD1 | c.479T>A (p.Val160Glu)
| |
| 13 | g.52397775C>A | CA388038422 | THSD1 | c.478G>T (p.Val160Leu)
| gnomAD v4 |
| 13 | g.52397775C>G | CA388038425 | THSD1 | c.478G>C (p.Val160Leu)
| |
| 13 | g.52397775C>T | CA388038427 | THSD1 | c.478G>A (p.Val160Met)
| |
| 13 | g.52397776A>C | CA484028589 | THSD1 | c.477T>G (p.Pro159=)
| |
| 13 | g.52397776A>G | CA484028590 | THSD1 | c.477T>C (p.Pro159=)
| |
| 13 | g.52397776A>T | CA484028591 | THSD1 | c.477T>A (p.Pro159=)
| |
| 13 | g.52397777G>A | CA388038431 | THSD1 | c.476C>T (p.Pro159Leu)
| dbSNP gnomAD v4 |
| 13 | g.52397777G>C | CA388038433 | THSD1 | c.476C>G (p.Pro159Arg)
| |
| 13 | g.52397777G>T | CA388038436 | THSD1 | c.476C>A (p.Pro159His)
| |
| 13 | g.52397778G>A | CA388038439 | THSD1 | c.475C>T (p.Pro159Ser)
| dbSNP COSMIC |
| 13 | g.52397778G>C | CA388038440 | THSD1 | c.475C>G (p.Pro159Ala)
| dbSNP gnomAD v2 gnomAD v4 |
| 13 | g.52397778G= | CA2091759706 | THSD1 | c.475C= (p.Pro159=)
| |
| 13 | g.52397778G>T | CA388038442 | THSD1 | c.475C>A (p.Pro159Thr)
| |
| 13 | g.52397779A>C | CA388038446 | THSD1 | c.474T>G (p.Phe158Leu)
| gnomAD v4 |
| 13 | g.52397779A>G | CA484028597 | THSD1 | c.474T>C (p.Phe158=)
| |
| 13 | g.52397779A>T | CA388038447 | THSD1 | c.474T>A (p.Phe158Leu)
| |
| 13 | g.52397780A>C | CA388038451 | THSD1 | c.473T>G (p.Phe158Cys)
| gnomAD v4 |
| 13 | g.52397780A>G | CA388038460 | THSD1 | c.473T>C (p.Phe158Ser)
| |
| 13 | g.52397780A>T | CA388038450 | THSD1 | c.473T>A (p.Phe158Tyr)
| |
| 13 | g.52397781A>C | CA388038468 | THSD1 | c.472T>G (p.Phe158Val)
| |
| 13 | g.52397781A>G | CA388038463 | THSD1 | c.472T>C (p.Phe158Leu)
| |
| 13 | g.52397781A>T | CA388038465 | THSD1 | c.472T>A (p.Phe158Ile)
| |
| 13 | g.52397782C>A | CA484028601 | THSD1 | c.471G>T (p.Pro157=)
| dbSNP |
| 13 | g.52397782C= | CA2091759709 | THSD1 | c.471G= (p.Pro157=)
| |
| 13 | g.52397782C>G | CA484028602 | THSD1 | c.471G>C (p.Pro157=)
| |
| 13 | g.52397782C>T | CA6992192 | THSD1 | c.471G>A (p.Pro157=)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 13 | g.52397782_52397783delinsCG | CA2091759711 | THSD1 | c.470_471delinsCG (p.Pro157=)
| |
| 13 | g.52397783G>A | CA250097337 | THSD1 | c.470C>T (p.Pro157Leu)
| dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 13 | g.52397783G>C | CA388038478 | THSD1 | c.470C>G (p.Pro157Arg)
| |
| 13 | g.52397783G= | CA2091759715 | THSD1 | c.470C= (p.Pro157=)
| |
| 13 | g.52397783G>T | CA6992193 | THSD1 | c.470C>A (p.Pro157Gln)
| dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.52397785del | CA698993994 | THSD1 | c.470del (p.Pro157ArgfsTer10)
| dbSNP gnomAD v4 |
| 13 | g.52397784G>A | CA388038483 | THSD1 | c.469C>T (p.Pro157Ser)
| |
| 13 | g.52397784G>C | CA388038486 | THSD1 | c.469C>G (p.Pro157Ala)
| |
| 13 | g.52397784G>T | CA388038487 | THSD1 | c.469C>A (p.Pro157Thr)
| |
| 13 | g.52397785G>A | CA250097343 | THSD1 | c.468C>T (p.Cys156=)
| dbSNP gnomAD v4 |
| 13 | g.52397785G>C | CA388038494 | THSD1 | c.468C>G (p.Cys156Trp)
| |
| 13 | g.52397785G= | CA2091759717 | THSD1 | c.468C= (p.Cys156=)
| |
| 13 | g.52397785G>T | CA388038497 | THSD1 | c.468C>A (p.Cys156Ter)
| |
| 13 | g.52397786C>A | CA388038505 | THSD1 | c.467G>T (p.Cys156Phe)
| COSMIC |
| 13 | g.52397786C>G | CA388038502 | THSD1 | c.467G>C (p.Cys156Ser)
| |
| 13 | g.52397786C>T | CA388038503 | THSD1 | c.467G>A (p.Cys156Tyr)
| |
| 13 | g.52397787A>C | CA388038508 | THSD1 | c.466T>G (p.Cys156Gly)
| |
| 13 | g.52397787A>G | CA388038509 | THSD1 | c.466T>C (p.Cys156Arg)
| |
| 13 | g.52397787A>T | CA388038511 | THSD1 | c.466T>A (p.Cys156Ser)
| |
| 13 | g.52397788C>A | CA484028611 | THSD1 | c.465G>T (p.Leu155=)
| |
| 13 | g.52397788C= | CA2091759720 | THSD1 | c.465G= (p.Leu155=)
| |
| 13 | g.52397788C>G | CA484028612 | THSD1 | c.465G>C (p.Leu155=)
| |
| 13 | g.52397788C>T | CA484028613 | THSD1 | c.465G>A (p.Leu155=)
| dbSNP |
| 13 | g.52397789A= | CA2091759722 | THSD1 | c.464T= (p.Leu155=)
| |
| 13 | g.52397789A>C | CA6992195 | THSD1 | c.464T>G (p.Leu155Arg)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
| 13 | g.52397789A>G | CA6992194 | THSD1 | c.464T>C (p.Leu155Pro)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.52397789A>T | CA388038517 | THSD1 | c.464T>A (p.Leu155Gln)
| |
| 13 | g.52397790G>A | CA484028614 | THSD1 | c.463C>T (p.Leu155=)
| |
| 13 | g.52397790G>C | CA388038521 | THSD1 | c.463C>G (p.Leu155Val)
| |
| 13 | g.52397790G>T | CA388038524 | THSD1 | c.463C>A (p.Leu155Met)
| |
| 13 | g.52397791T>A | CA484028617 | THSD1 | c.462A>T (p.Pro154=)
| |
| 13 | g.52397791T>C | CA484028620 | THSD1 | c.462A>G (p.Pro154=)
| gnomAD v4 |
| 13 | g.52397791T>G | CA484028618 | THSD1 | c.462A>C (p.Pro154=)
| |
| 13 | g.52397792G>A | CA388038534 | THSD1 | c.461C>T (p.Pro154Leu)
| |
| 13 | g.52397792G>C | CA388038536 | THSD1 | c.461C>G (p.Pro154Arg)
| |
| 13 | g.52397792G>T | CA388038539 | THSD1 | c.461C>A (p.Pro154Gln)
| |
| 13 | g.52397793G>A | CA6992196 | THSD1 | c.460C>T (p.Pro154Ser)
| dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.52397793G>C | CA388038546 | THSD1 | c.460C>G (p.Pro154Ala)
| gnomAD v4 |
| 13 | g.52397793G= | CA2091759727 | THSD1 | c.460C= (p.Pro154=)
| |
| 13 | g.52397793G>T | CA388038542 | THSD1 | c.460C>A (p.Pro154Thr)
| |
| 13 | g.52397794T>A | CA388038549 | THSD1 | c.459A>T (p.Gln153His)
| |
| 13 | g.52397794T>C | CA484028624 | THSD1 | c.459A>G (p.Gln153=)
| gnomAD v4 |
| 13 | g.52397794T>G | CA388038551 | THSD1 | c.459A>C (p.Gln153His)
| dbSNP gnomAD v4 |
| 13 | g.52397795T>A | CA388038554 | THSD1 | c.458A>T (p.Gln153Leu)
| |
| 13 | g.52397795T>C | CA388038559 | THSD1 | c.458A>G (p.Gln153Arg)
| gnomAD v4 |
| 13 | g.52397795T>G | CA388038561 | THSD1 | c.458A>C (p.Gln153Pro)
| |
| 13 | g.52397796G>A | CA388038568 | THSD1 | c.457C>T (p.Gln153Ter)
| |
| 13 | g.52397796G>C | CA388038565 | THSD1 | c.457C>G (p.Gln153Glu)
| |
| 13 | g.52397796G>T | CA388038563 | THSD1 | c.457C>A (p.Gln153Lys)
| COSMIC |
| 13 | g.52397797A= | CA2091759731 | THSD1 | c.456T= (p.Ser152=)
| |
| 13 | g.52397797A>C | CA388038571 | THSD1 | c.456T>G (p.Ser152Arg)
| |
| 13 | g.52397797A>G | CA6992197 | THSD1 | c.456T>C (p.Ser152=)
| dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.52397797A>T | CA388038573 | THSD1 | c.456T>A (p.Ser152Arg)
| |
| 13 | g.52397798C>A | CA388038577 | THSD1 | c.455G>T (p.Ser152Ile)
| |
| 13 | g.52397798C>G | CA388038580 | THSD1 | c.455G>C (p.Ser152Thr)
| gnomAD v4 |
| 13 | g.52397798C>T | CA388038582 | THSD1 | c.455G>A (p.Ser152Asn)
| |
| 13 | g.52397799T>A | CA388038586 | THSD1 | c.454A>T (p.Ser152Cys)
| |
| 13 | g.52397799T>C | CA388038590 | THSD1 | c.454A>G (p.Ser152Gly)
| |
| 13 | g.52397799T>G | CA388038587 | THSD1 | c.454A>C (p.Ser152Arg)
| |
| 13 | g.52397800G>A | CA484028632 | THSD1 | c.453C>T (p.Thr151=)
| |
| 13 | g.52397800G>C | CA6992199 | THSD1 | c.453C>G (p.Thr151=)
| dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.52397800G= | CA2091759736 | THSD1 | c.453C= (p.Thr151=)
| |
| 13 | g.52397800G>T | CA6992198 | THSD1 | c.453C>A (p.Thr151=)
| dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.52397801G>A | CA6992200 | THSD1 | c.452C>T (p.Thr151Ile)
| dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.52397801G>C | CA388038597 | THSD1 | c.452C>G (p.Thr151Ser)
| |
| 13 | g.52397801G= | CA2091759739 | THSD1 | c.452C= (p.Thr151=)
| |
| 13 | g.52397801G>T | CA388038600 | THSD1 | c.452C>A (p.Thr151Asn)
| |
| 13 | g.52397802T>A | CA388038603 | THSD1 | c.451A>T (p.Thr151Ser)
| gnomAD v4 |
| 13 | g.52397802T>C | CA388038606 | THSD1 | c.451A>G (p.Thr151Ala)
| dbSNP gnomAD v4 |
| 13 | g.52397802T>G | CA388038609 | THSD1 | c.451A>C (p.Thr151Pro)
| |
| 13 | g.52397802T= | CA2091759743 | THSD1 | c.451A= (p.Thr151=)
| |
| 13 | g.52397803A>C | CA388038614 | THSD1 | c.450T>G (p.Phe150Leu)
| |
| 13 | g.52397803A>G | CA484028636 | THSD1 | c.450T>C (p.Phe150=)
| |
| 13 | g.52397803A>T | CA388038615 | THSD1 | c.450T>A (p.Phe150Leu)
| |
| 13 | g.52397804A>C | CA388038620 | THSD1 | c.449T>G (p.Phe150Cys)
| |
| 13 | g.52397804A>G | CA388038623 | THSD1 | c.449T>C (p.Phe150Ser)
| |
| 13 | g.52397804A>T | CA388038625 | THSD1 | c.449T>A (p.Phe150Tyr)
| |
| 13 | g.52397805A>C | CA388038633 | THSD1 | c.448T>G (p.Phe150Val)
| |
| 13 | g.52397805A>G | CA388038635 | THSD1 | c.448T>C (p.Phe150Leu)
| |
| 13 | g.52397805A>T | CA388038629 | THSD1 | c.448T>A (p.Phe150Ile)
| |
| 13 | g.52397806T>A | CA484028641 | THSD1 | c.447A>T (p.Leu149=)
| |
| 13 | g.52397806T>C | CA484028642 | THSD1 | c.447A>G (p.Leu149=)
| dbSNP gnomAD v4 |
| 13 | g.52397806T>G | CA484028643 | THSD1 | c.447A>C (p.Leu149=)
| |
| 13 | g.52397806T= | CA2091759745 | THSD1 | c.447A= (p.Leu149=)
| |
| 13 | g.52397807A>C | CA388038641 | THSD1 | c.446T>G (p.Leu149Arg)
| |
| 13 | g.52397807A>G | CA388038639 | THSD1 | c.446T>C (p.Leu149Pro)
| |
| 13 | g.52397807A>T | CA388038640 | THSD1 | c.446T>A (p.Leu149Gln)
| |
| 13 | g.52397808G>A | CA484028646 | THSD1 | c.445C>T (p.Leu149=)
| |
| 13 | g.52397808G>C | CA388038643 | THSD1 | c.445C>G (p.Leu149Val)
| |
| 13 | g.52397808G>T | CA388038645 | THSD1 | c.445C>A (p.Leu149Ile)
| |
| 13 | g.52397809G>A | CA484028649 | THSD1 | c.444C>T (p.Gly148=)
| |
| 13 | g.52397809G>C | CA484028650 | THSD1 | c.444C>G (p.Gly148=)
| |
| 13 | g.52397809G>T | CA484028651 | THSD1 | c.444C>A (p.Gly148=)
| |
| 13 | g.52397809_52397810delinsGC | CA2091759746 | THSD1 | c.443_444delinsGC (p.Gly148=)
| |
| 13 | g.52397810C>A | CA6992201 | THSD1 | c.443G>T (p.Gly148Val)
| dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.52397810C= | CA2091759750 | THSD1 | c.443G= (p.Gly148=)
| |
| 13 | g.52397810C>G | CA388038651 | THSD1 | c.443G>C (p.Gly148Ala)
| |
| 13 | g.52397810C>T | CA388038653 | THSD1 | c.443G>A (p.Gly148Asp)
| |
| 13 | g.52397812del | CA610426197 | THSD1 | c.443del (p.Gly148AlafsTer19)
| dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.52397811C>A | CA388038656 | THSD1 | c.442G>T (p.Gly148Cys)
| |
| 13 | g.52397811C>G | CA388038658 | THSD1 | c.442G>C (p.Gly148Arg)
| |
| 13 | g.52397811C>T | CA388038659 | THSD1 | c.442G>A (p.Gly148Ser)
| |
| 13 | g.52397812C>A | CA484028652 | THSD1 | c.441G>T (p.Val147=)
| |
| 13 | g.52397812C= | CA2091759752 | THSD1 | c.441G= (p.Val147=)
| |
| 13 | g.52397812C>G | CA484028654 | THSD1 | c.441G>C (p.Val147=)
| dbSNP |
| 13 | g.52397812C>T | CA484028653 | THSD1 | c.441G>A (p.Val147=)
| |
| 13 | g.52397813A>C | CA388038664 | THSD1 | c.440T>G (p.Val147Gly)
| |
| 13 | g.52397813A>G | CA388038666 | THSD1 | c.440T>C (p.Val147Ala)
| |
| 13 | g.52397813A>T | CA388038667 | THSD1 | c.440T>A (p.Val147Glu)
| |
| 13 | g.52397814C>A | CA388038673 | THSD1 | c.439G>T (p.Val147Leu)
| |
| 13 | g.52397814C= | CA2091759755 | THSD1 | c.439G= (p.Val147=)
| |
| 13 | g.52397814C>G | CA388038672 | THSD1 | c.439G>C (p.Val147Leu)
| gnomAD v4 |
| 13 | g.52397814C>T | CA250097405 | THSD1 | c.439G>A (p.Val147Met)
| dbSNP gnomAD v3 gnomAD v4 |
| 13 | g.52397815T>A | CA388038677 | THSD1 | c.438A>T (p.Gln146His)
| |
| 13 | g.52397815T>C | CA6992202 | THSD1 | c.438A>G (p.Gln146=)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
| 13 | g.52397815T>G | CA388038681 | THSD1 | c.438A>C (p.Gln146His)
| |
| 13 | g.52397815T= | CA2091759759 | THSD1 | c.438A= (p.Gln146=)
| |
| 13 | g.52397816T>A | CA388038690 | THSD1 | c.437A>T (p.Gln146Leu)
| |
| 13 | g.52397816T>C | CA388038691 | THSD1 | c.437A>G (p.Gln146Arg)
| |
| 13 | g.52397816T>G | CA388038693 | THSD1 | c.437A>C (p.Gln146Pro)
| |
| 13 | g.52397817G>A | CA388038697 | THSD1 | c.436C>T (p.Gln146Ter)
| dbSNP gnomAD v3 gnomAD v4 |
| 13 | g.52397817G>C | CA388038700 | THSD1 | c.436C>G (p.Gln146Glu)
| |
| 13 | g.52397817G= | CA2091759762 | THSD1 | c.436C= (p.Gln146=)
| |
| 13 | g.52397817G>T | CA388038702 | THSD1 | c.436C>A (p.Gln146Lys)
| |
| 13 | g.52397818G>A | CA484028660 | THSD1 | c.435C>T (p.Phe145=)
| |
| 13 | g.52397818G>C | CA388038707 | THSD1 | c.435C>G (p.Phe145Leu)
| dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.52397818G= | CA2091759766 | THSD1 | c.435C= (p.Phe145=)
| |
| 13 | g.52397818G>T | CA388038708 | THSD1 | c.435C>A (p.Phe145Leu)
| |
| 13 | g.52397819A>C | CA388038712 | THSD1 | c.434T>G (p.Phe145Cys)
| |
| 13 | g.52397819A>G | CA388038715 | THSD1 | c.434T>C (p.Phe145Ser)
| |
| 13 | g.52397819A>T | CA388038717 | THSD1 | c.434T>A (p.Phe145Tyr)
| |
| 13 | g.52397820A>C | CA388038724 | THSD1 | c.433T>G (p.Phe145Val)
| |
| 13 | g.52397820A>G | CA388038725 | THSD1 | c.433T>C (p.Phe145Leu)
| |
| 13 | g.52397820A>T | CA388038721 | THSD1 | c.433T>A (p.Phe145Ile)
| |
| 13 | g.52397821G>A | CA484028664 | THSD1 | c.432C>T (p.Thr144=)
| dbSNP |
| 13 | g.52397821G>C | CA484028665 | THSD1 | c.432C>G (p.Thr144=)
| |
| 13 | g.52397821G= | CA2091759768 | THSD1 | c.432C= (p.Thr144=)
| |
| 13 | g.52397821G>T | CA484028666 | THSD1 | c.432C>A (p.Thr144=)
| |
| 13 | g.52397822G>A | CA388038728 | THSD1 | c.431C>T (p.Thr144Ile)
| dbSNP gnomAD v3 gnomAD v4 |
| 13 | g.52397822G>C | CA388038731 | THSD1 | c.431C>G (p.Thr144Ser)
| |
| 13 | g.52397822G= | CA2091759770 | THSD1 | c.431C= (p.Thr144=)
| |
| 13 | g.52397822G>T | CA388038734 | THSD1 | c.431C>A (p.Thr144Asn)
| dbSNP |
| 13 | g.52397823T>A | CA388038737 | THSD1 | c.430A>T (p.Thr144Ser)
| |
| 13 | g.52397823T>C | CA388038739 | THSD1 | c.430A>G (p.Thr144Ala)
| |
| 13 | g.52397823T>G | CA388038741 | THSD1 | c.430A>C (p.Thr144Pro)
| |
| 13 | g.52397824G>A | CA484028668 | THSD1 | c.429C>T (p.Gly143=)
| |
| 13 | g.52397824G>C | CA484028669 | THSD1 | c.429C>G (p.Gly143=)
| |
| 13 | g.52397824G>T | CA484028670 | THSD1 | c.429C>A (p.Gly143=)
| |
| 13 | g.52397825C>A | CA388038746 | THSD1 | c.428G>T (p.Gly143Val)
| |
| 13 | g.52397825C= | CA2091759775 | THSD1 | c.428G= (p.Gly143=)
| |
| 13 | g.52397825C>G | CA388038748 | THSD1 | c.428G>C (p.Gly143Ala)
| gnomAD v4 |
| 13 | g.52397825C>T | CA388038750 | THSD1 | c.428G>A (p.Gly143Asp)
| dbSNP gnomAD v3 gnomAD v4 |
| 13 | g.52397826dup | CA2575422252 | THSD1 | c.428dup (p.Thr144HisfsTer?)
| |
| 13 | g.52397826C>A | CA250097409 | THSD1 | c.427G>T (p.Gly143Cys)
| dbSNP gnomAD v3 gnomAD v4 |
| 13 | g.52397826C= | CA2091759777 | THSD1 | c.427G= (p.Gly143=)
| |
| 13 | g.52397826C>G | CA388038755 | THSD1 | c.427G>C (p.Gly143Arg)
| |
| 13 | g.52397826C>T | CA6992203 | THSD1 | c.427G>A (p.Gly143Ser)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
| 13 | g.52397827T>A | CA388038764 | THSD1 | c.426A>T (p.Glu142Asp)
| |
| 13 | g.52397827T>C | CA6992204 | THSD1 | c.426A>G (p.Glu142=)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
| 13 | g.52397827T>G | CA388038760 | THSD1 | c.426A>C (p.Glu142Asp)
| |
| 13 | g.52397827T= | CA2091759782 | THSD1 | c.426A= (p.Glu142=)
| |
| 13 | g.52397828T>A | CA388038767 | THSD1 | c.425A>T (p.Glu142Val)
| |
| 13 | g.52397828T>C | CA388038769 | THSD1 | c.425A>G (p.Glu142Gly)
| |
| 13 | g.52397828T>G | CA388038772 | THSD1 | c.425A>C (p.Glu142Ala)
| |
| 13 | g.52397829C>A | CA388038776 | THSD1 | c.424G>T (p.Glu142Ter)
| |
| 13 | g.52397829C>G | CA388038778 | THSD1 | c.424G>C (p.Glu142Gln)
| |
| 13 | g.52397829C>T | CA388038781 | THSD1 | c.424G>A (p.Glu142Lys)
| |
| 13 | g.52397830T>A | CA484028672 | THSD1 | c.423A>T (p.Ala141=)
| |
| 13 | g.52397830T>C | CA484028673 | THSD1 | c.423A>G (p.Ala141=)
| |
| 13 | g.52397830T>G | CA484028674 | THSD1 | c.423A>C (p.Ala141=)
| |
| 13 | g.52397831G>A | CA388038785 | THSD1 | c.422C>T (p.Ala141Val)
| |
| 13 | g.52397831G>C | CA388038788 | THSD1 | c.422C>G (p.Ala141Gly)
| |
| 13 | g.52397831G>T | CA388038790 | THSD1 | c.422C>A (p.Ala141Glu)
| |
| 13 | g.52397832C>A | CA388038794 | THSD1 | c.421G>T (p.Ala141Ser)
| |
| 13 | g.52397832C= | CA2091759787 | THSD1 | c.421G= (p.Ala141=)
| |
| 13 | g.52397832C>G | CA388038797 | THSD1 | c.421G>C (p.Ala141Pro)
| |
| 13 | g.52397832C>T | CA388038800 | THSD1 | c.421G>A (p.Ala141Thr)
| dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.52397833T>A | CA484028676 | THSD1 | c.420A>T (p.Ala140=)
| |
| 13 | g.52397833T>C | CA484028678 | THSD1 | c.420A>G (p.Ala140=)
| |
| 13 | g.52397833T>G | CA484028677 | THSD1 | c.420A>C (p.Ala140=)
| |
| 13 | g.52397834G>A | CA388038808 | THSD1 | c.419C>T (p.Ala140Val)
| |
| 13 | g.52397834G>C | CA388038807 | THSD1 | c.419C>G (p.Ala140Gly)
| |
| 13 | g.52397834G>T | CA388038805 | THSD1 | c.419C>A (p.Ala140Glu)
| |
| 13 | g.52397835C>A | CA388038813 | THSD1 | c.418G>T (p.Ala140Ser)
| |
| 13 | g.52397835C>G | CA388038817 | THSD1 | c.418G>C (p.Ala140Pro)
| |
| 13 | g.52397835C>T | CA388038816 | THSD1 | c.418G>A (p.Ala140Thr)
| |
| 13 | g.52397836C>A | CA388038821 | THSD1 | c.417G>T (p.Lys139Asn)
| |
| 13 | g.52397836C= | CA2091759794 | THSD1 | c.417G= (p.Lys139=)
| |
| 13 | g.52397836C>G | CA388038824 | THSD1 | c.417G>C (p.Lys139Asn)
| |
| 13 | g.52397836C>T | CA250097426 | THSD1 | c.417G>A (p.Lys139=)
| dbSNP gnomAD v4 |
| 13 | g.52397837T>A | CA388038827 | THSD1 | c.416A>T (p.Lys139Met)
| |
| 13 | g.52397837T>C | CA388038831 | THSD1 | c.416A>G (p.Lys139Arg)
| |
| 13 | g.52397837T>G | CA13876337 | THSD1 | c.416A>C (p.Lys139Thr)
| dbSNP |
| 13 | g.52397837T= | CA2091759795 | THSD1 | c.416A= (p.Lys139=)
| |
| 13 | g.52397838T>A | CA388038836 | THSD1 | c.415A>T (p.Lys139Ter)
| |
| 13 | g.52397838T>C | CA388038838 | THSD1 | c.415A>G (p.Lys139Glu)
| |
| 13 | g.52397838T>G | CA388038841 | THSD1 | c.415A>C (p.Lys139Gln)
| |
