| 13 | g.52397701C>A | CA388037932 | THSD1 | c.552G>T (p.Gln184His)
| |
| 13 | g.52397701C>G | CA388037934 | THSD1 | c.552G>C (p.Gln184His)
| |
| 13 | g.52397701C>T | CA484028459 | THSD1 | c.552G>A (p.Gln184=)
| gnomAD v4 |
| 13 | g.52397701_52397702insA | CA2557528149 | THSD1 | c.551_552insT (p.Gln184HisfsTer20)
| |
| 13 | g.52397702T>A | CA388037938 | THSD1 | c.551A>T (p.Gln184Leu)
| |
| 13 | g.52397702T>C | CA6992177 | THSD1 | c.551A>G (p.Gln184Arg)
| dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.52397702T>G | CA388037942 | THSD1 | c.551A>C (p.Gln184Pro)
| |
| 13 | g.52397702T= | CA2091759610 | THSD1 | c.551A= (p.Gln184=)
| |
| 13 | g.52397703G>A | CA6992178 | THSD1 | c.550C>T (p.Gln184Ter)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
| 13 | g.52397703G>C | CA250097302 | THSD1 | c.550C>G (p.Gln184Glu)
| dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.52397703G= | CA2091759614 | THSD1 | c.550C= (p.Gln184=)
| |
| 13 | g.52397703G>T | CA388037946 | THSD1 | c.550C>A (p.Gln184Lys)
| |
| 13 | g.52397704T>A | CA388037951 | THSD1 | c.549A>T (p.Arg183Ser)
| |
| 13 | g.52397704T>C | CA484028467 | THSD1 | c.549A>G (p.Arg183=)
| dbSNP gnomAD v3 gnomAD v4 |
| 13 | g.52397704T>G | CA250097310 | THSD1 | c.549A>C (p.Arg183Ser)
| dbSNP gnomAD v4 |
| 13 | g.52397704T= | CA2091759617 | THSD1 | c.549A= (p.Arg183=)
| |
| 13 | g.52397705C>A | CA388037961 | THSD1 | c.548G>T (p.Arg183Ile)
| |
| 13 | g.52397705C>G | CA388037962 | THSD1 | c.548G>C (p.Arg183Thr)
| |
| 13 | g.52397705C>T | CA388037966 | THSD1 | c.548G>A (p.Arg183Lys)
| |
| 13 | g.52397706T>A | CA388037971 | THSD1 | c.547A>T (p.Arg183Ter)
| |
| 13 | g.52397706T>C | CA388037973 | THSD1 | c.547A>G (p.Arg183Gly)
| dbSNP gnomAD v4 |
| 13 | g.52397706T>G | CA484028469 | THSD1 | c.547A>C (p.Arg183=)
| |
| 13 | g.52397706T= | CA2091759620 | THSD1 | c.547A= (p.Arg183=)
| |
| 13 | g.52397707T>A | CA484028470 | THSD1 | c.546A>T (p.Ser182=)
| |
| 13 | g.52397707T>C | CA484028471 | THSD1 | c.546A>G (p.Ser182=)
| dbSNP gnomAD v3 gnomAD v4 |
| 13 | g.52397707T>G | CA484028472 | THSD1 | c.546A>C (p.Ser182=)
| |
| 13 | g.52397707T= | CA2091759623 | THSD1 | c.546A= (p.Ser182=)
| |
| 13 | g.52397708G>A | CA388037982 | THSD1 | c.545C>T (p.Ser182Leu)
| |
| 13 | g.52397708G>C | CA388037979 | THSD1 | c.545C>G (p.Ser182Ter)
| |
| 13 | g.52397708G>T | CA388037977 | THSD1 | c.545C>A (p.Ser182Ter)
| |
| 13 | g.52397709A>C | CA388037983 | THSD1 | c.544T>G (p.Ser182Ala)
| |
| 13 | g.52397709A>G | CA388037986 | THSD1 | c.544T>C (p.Ser182Pro)
| |
| 13 | g.52397709A>T | CA388037989 | THSD1 | c.544T>A (p.Ser182Thr)
| |
| 13 | g.52397710A>C | CA388037992 | THSD1 | c.543T>G (p.Asn181Lys)
| |
| 13 | g.52397710A>G | CA484028476 | THSD1 | c.543T>C (p.Asn181=)
| |
| 13 | g.52397710A>T | CA388037994 | THSD1 | c.543T>A (p.Asn181Lys)
| |
| 13 | g.52397710_52397716del | CA2569554637 | THSD1 | c.537_543del (p.Arg179SerfsTer8)
| |
| 13 | g.52397711T>A | CA388037999 | THSD1 | c.542A>T (p.Asn181Ile)
| |
| 13 | g.52397711T>C | CA388038000 | THSD1 | c.542A>G (p.Asn181Ser)
| |
| 13 | g.52397711T>G | CA388038002 | THSD1 | c.542A>C (p.Asn181Thr)
| |
| 13 | g.52397712T>A | CA388038006 | THSD1 | c.541A>T (p.Asn181Tyr)
| |
| 13 | g.52397712T>C | CA388038009 | THSD1 | c.541A>G (p.Asn181Asp)
| |
| 13 | g.52397712T>G | CA388038012 | THSD1 | c.541A>C (p.Asn181His)
| |
| 13 | g.52397713T>A | CA388038016 | THSD1 | c.540A>T (p.Arg180Ser)
| |
| 13 | g.52397713T>C | CA484028478 | THSD1 | c.540A>G (p.Arg180=)
| |
| 13 | g.52397713T>G | CA388038017 | THSD1 | c.540A>C (p.Arg180Ser)
| |
| 13 | g.52397714C>A | CA388038023 | THSD1 | c.539G>T (p.Arg180Ile)
| |
| 13 | g.52397714C>G | CA388038026 | THSD1 | c.539G>C (p.Arg180Thr)
| |
| 13 | g.52397714C>T | CA388038020 | THSD1 | c.539G>A (p.Arg180Lys)
| |
| 13 | g.52397715T>A | CA388038029 | THSD1 | c.538A>T (p.Arg180Ter)
| |
| 13 | g.52397715T>C | CA388038032 | THSD1 | c.538A>G (p.Arg180Gly)
| |
| 13 | g.52397715T>G | CA484028481 | THSD1 | c.538A>C (p.Arg180=)
| |
| 13 | g.52397716T>A | CA388038035 | THSD1 | c.537A>T (p.Arg179Ser)
| |
| 13 | g.52397716T>C | CA484028482 | THSD1 | c.537A>G (p.Arg179=)
| |
| 13 | g.52397716T>G | CA388038038 | THSD1 | c.537A>C (p.Arg179Ser)
| |
| 13 | g.52397717C>A | CA388038042 | THSD1 | c.536G>T (p.Arg179Ile)
| |
| 13 | g.52397717C>G | CA388038044 | THSD1 | c.536G>C (p.Arg179Thr)
| |
| 13 | g.52397717C>T | CA388038047 | THSD1 | c.536G>A (p.Arg179Lys)
| gnomAD v4 |
| 13 | g.52397717_52397718insCCGCCC | CA2565195912 | THSD1 | c.536_537insGGCGGG (p.Arg179_Arg180insAlaGly)
| |
| 13 | g.52397718T>A | CA388038049 | THSD1 | c.535A>T (p.Arg179Ter)
| |
| 13 | g.52397718T>C | CA388038052 | THSD1 | c.535A>G (p.Arg179Gly)
| |
| 13 | g.52397718T>G | CA484028484 | THSD1 | c.535A>C (p.Arg179=)
| |
| 13 | g.52397719T>A | CA484028487 | THSD1 | c.534A>T (p.Ala178=)
| |
| 13 | g.52397719T>C | CA484028488 | THSD1 | c.534A>G (p.Ala178=)
| |
| 13 | g.52397719T>G | CA484028490 | THSD1 | c.534A>C (p.Ala178=)
| |
| 13 | g.52397720G>A | CA388038056 | THSD1 | c.533C>T (p.Ala178Val)
| |
| 13 | g.52397720G>C | CA388038059 | THSD1 | c.533C>G (p.Ala178Gly)
| |
| 13 | g.52397720G>T | CA388038064 | THSD1 | c.533C>A (p.Ala178Glu)
| |
| 13 | g.52397721C>A | CA388038077 | THSD1 | c.532G>T (p.Ala178Ser)
| |
| 13 | g.52397721C>G | CA388038067 | THSD1 | c.532G>C (p.Ala178Pro)
| |
| 13 | g.52397721C>T | CA388038075 | THSD1 | c.532G>A (p.Ala178Thr)
| |
| 13 | g.52397722C>A | CA388038080 | THSD1 | c.531G>T (p.Glu177Asp)
| |
| 13 | g.52397722C>G | CA388038082 | THSD1 | c.531G>C (p.Glu177Asp)
| |
| 13 | g.52397722C>T | CA484028491 | THSD1 | c.531G>A (p.Glu177=)
| gnomAD v4 |
| 13 | g.52397723T>A | CA388038083 | THSD1 | c.530A>T (p.Glu177Val)
| |
| 13 | g.52397723T>C | CA388038084 | THSD1 | c.530A>G (p.Glu177Gly)
| COSMIC |
| 13 | g.52397723T>G | CA388038086 | THSD1 | c.530A>C (p.Glu177Ala)
| |
| 13 | g.52397724C>A | CA388038088 | THSD1 | c.529G>T (p.Glu177Ter)
| |
| 13 | g.52397724C= | CA2091759625 | THSD1 | c.529G= (p.Glu177=)
| |
| 13 | g.52397724C>G | CA388038091 | THSD1 | c.529G>C (p.Glu177Gln)
| |
| 13 | g.52397724C>T | CA6992179 | THSD1 | c.529G>A (p.Glu177Lys)
| dbSNP ExAC gnomAD v2 COSMIC |
| 13 | g.52397725A= | CA2091759629 | THSD1 | c.528T= (p.Pro176=)
| |
| 13 | g.52397725A>C | CA484028494 | THSD1 | c.528T>G (p.Pro176=)
| dbSNP gnomAD v4 |
| 13 | g.52397725A>G | CA484028495 | THSD1 | c.528T>C (p.Pro176=)
| |
| 13 | g.52397725A>T | CA484028496 | THSD1 | c.528T>A (p.Pro176=)
| |
| 13 | g.52397726G>A | CA6992180 | THSD1 | c.527C>T (p.Pro176Leu)
| dbSNP ExAC |
| 13 | g.52397726G>C | CA388038095 | THSD1 | c.527C>G (p.Pro176Arg)
| dbSNP |
| 13 | g.52397726G= | CA2091759633 | THSD1 | c.527C= (p.Pro176=)
| |
| 13 | g.52397726G>T | CA388038100 | THSD1 | c.527C>A (p.Pro176His)
| |
| 13 | g.52397727G>A | CA388038109 | THSD1 | c.526C>T (p.Pro176Ser)
| |
| 13 | g.52397727G>C | CA388038108 | THSD1 | c.526C>G (p.Pro176Ala)
| |
| 13 | g.52397727G= | CA2091759638 | THSD1 | c.526C= (p.Pro176=)
| |
| 13 | g.52397727G>T | CA6992181 | THSD1 | c.526C>A (p.Pro176Thr)
| dbSNP ExAC |
| 13 | g.52397728A= | CA2091759641 | THSD1 | c.525T= (p.Leu175=)
| |
| 13 | g.52397728A>C | CA484028501 | THSD1 | c.525T>G (p.Leu175=)
| |
| 13 | g.52397728A>G | CA484028502 | THSD1 | c.525T>C (p.Leu175=)
| dbSNP |
| 13 | g.52397728A>T | CA484028503 | THSD1 | c.525T>A (p.Leu175=)
| |
| 13 | g.52397729A= | CA2091759645 | THSD1 | c.524T= (p.Leu175=)
| |
| 13 | g.52397729A>C | CA388038111 | THSD1 | c.524T>G (p.Leu175Arg)
| ClinVar dbSNP gnomAD v4 |
| 13 | g.52397729A>G | CA388038117 | THSD1 | c.524T>C (p.Leu175Pro)
| |
| 13 | g.52397729A>T | CA388038114 | THSD1 | c.524T>A (p.Leu175His)
| |
| 13 | g.52397730G>A | CA388038121 | THSD1 | c.523C>T (p.Leu175Phe)
| |
| 13 | g.52397730G>C | CA388038123 | THSD1 | c.523C>G (p.Leu175Val)
| |
| 13 | g.52397730G>T | CA388038125 | THSD1 | c.523C>A (p.Leu175Ile)
| |
| 13 | g.52397731A>C | CA388038128 | THSD1 | c.522T>G (p.Ser174Arg)
| |
| 13 | g.52397731A>G | CA484028509 | THSD1 | c.522T>C (p.Ser174=)
| gnomAD v4 |
| 13 | g.52397731A>T | CA388038131 | THSD1 | c.522T>A (p.Ser174Arg)
| |
| 13 | g.52397732C>A | CA388038135 | THSD1 | c.521G>T (p.Ser174Ile)
| |
| 13 | g.52397732C>G | CA388038140 | THSD1 | c.521G>C (p.Ser174Thr)
| |
| 13 | g.52397732C>T | CA388038142 | THSD1 | c.521G>A (p.Ser174Asn)
| gnomAD v4 |
| 13 | g.52397733T>A | CA388038143 | THSD1 | c.520A>T (p.Ser174Cys)
| |
| 13 | g.52397733T>C | CA388038148 | THSD1 | c.520A>G (p.Ser174Gly)
| |
| 13 | g.52397733T>G | CA388038150 | THSD1 | c.520A>C (p.Ser174Arg)
| |
| 13 | g.52397734G>A | CA6992182 | THSD1 | c.519C>T (p.Asn173=)
| dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.52397734G>C | CA388038158 | THSD1 | c.519C>G (p.Asn173Lys)
| |
| 13 | g.52397734G= | CA2091759647 | THSD1 | c.519C= (p.Asn173=)
| |
| 13 | g.52397734G>T | CA388038155 | THSD1 | c.519C>A (p.Asn173Lys)
| gnomAD v4 |
| 13 | g.52397735T>A | CA388038165 | THSD1 | c.518A>T (p.Asn173Ile)
| |
| 13 | g.52397735T>C | CA388038167 | THSD1 | c.518A>G (p.Asn173Ser)
| |
| 13 | g.52397735T>G | CA388038171 | THSD1 | c.518A>C (p.Asn173Thr)
| |
| 13 | g.52397735_52397738delinsTTGG | CA2091759651 | THSD1 | c.515_518delinsCCAA (p.Thr172=)
| |
| 13 | g.52397736T>A | CA388038175 | THSD1 | c.517A>T (p.Asn173Tyr)
| |
| 13 | g.52397736T>C | CA388038177 | THSD1 | c.517A>G (p.Asn173Asp)
| |
| 13 | g.52397736T>G | CA388038178 | THSD1 | c.517A>C (p.Asn173His)
| |
| 13 | g.52397738_52397740del | CA2091759654 | THSD1 | c.515_517del (p.Thr172del)
| dbSNP |
| 13 | g.52397737G>A | CA484028516 | THSD1 | c.516C>T (p.Thr172=)
| |
| 13 | g.52397737G>C | CA484028518 | THSD1 | c.516C>G (p.Thr172=)
| |
| 13 | g.52397737G>T | CA484028517 | THSD1 | c.516C>A (p.Thr172=)
| |
| 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)
| |
