Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.93898462G>ACA123035PROS1c.835C>T (p.Gln279Ter)
c.790C>T (p.Gln264Ter)
n.1003C>T
c.793C>T (p.Gln265Ter)
c.934C>T (n.934C>T)
c.931C>T (p.Gln311Ter)
c.442C>T (p.Gln148Ter)
ClinVar dbSNP gnomAD v4
3g.93898462G>CCA353672801PROS1c.835C>G (p.Gln279Glu)
c.790C>G (p.Gln264Glu)
n.1003C>G
c.793C>G (p.Gln265Glu)
c.934C>G (n.934C>G)
c.931C>G (p.Gln311Glu)
c.442C>G (p.Gln148Glu)
3g.93898462G=CA1385039107PROS1c.835C= (p.Gln279=)
c.790C= (p.Gln264=)
n.1003C=
c.793C= (p.Gln265=)
c.934C= (n.934C=)
c.931C= (p.Gln311=)
c.442C= (p.Gln148=)
3g.93898462G>TCA353672802PROS1c.835C>A (p.Gln279Lys)
c.790C>A (p.Gln264Lys)
n.1003C>A
c.793C>A (p.Gln265Lys)
c.934C>A (n.934C>A)
c.931C>A (p.Gln311Lys)
c.442C>A (p.Gln148Lys)
3g.93898463A=CA1385039108PROS1c.834T= (p.Asp278=)
c.789T= (p.Asp263=)
n.1002T=
c.792T= (p.Asp264=)
c.933T= (n.933T=)
c.930T= (p.Asp310=)
c.441T= (p.Asp147=)
3g.93898463A>CCA353672803PROS1c.834T>G (p.Asp278Glu)
c.789T>G (p.Asp263Glu)
n.1002T>G
c.792T>G (p.Asp264Glu)
c.933T>G (n.933T>G)
c.930T>G (p.Asp310Glu)
c.441T>G (p.Asp147Glu)
3g.93898463A>GCA434461256PROS1c.834T>C (p.Asp278=)
c.789T>C (p.Asp263=)
n.1002T>C
c.792T>C (p.Asp264=)
c.933T>C (n.933T>C)
c.930T>C (p.Asp310=)
c.441T>C (p.Asp147=)
dbSNP gnomAD v3 gnomAD v4
3g.93898463A>TCA353672804PROS1c.834T>A (p.Asp278Glu)
c.789T>A (p.Asp263Glu)
n.1002T>A
c.792T>A (p.Asp264Glu)
c.933T>A (n.933T>A)
c.930T>A (p.Asp310Glu)
c.441T>A (p.Asp147Glu)
3g.93898464T>ACA353672805PROS1c.833A>T (p.Asp278Val)
c.788A>T (p.Asp263Val)
n.1001A>T
c.791A>T (p.Asp264Val)
c.932A>T (n.932A>T)
c.929A>T (p.Asp310Val)
c.440A>T (p.Asp147Val)
3g.93898464T>CCA353672807PROS1c.833A>G (p.Asp278Gly)
c.788A>G (p.Asp263Gly)
n.1001A>G
c.791A>G (p.Asp264Gly)
c.932A>G (n.932A>G)
c.929A>G (p.Asp310Gly)
c.440A>G (p.Asp147Gly)
3g.93898464T>GCA353672806PROS1c.833A>C (p.Asp278Ala)
c.788A>C (p.Asp263Ala)
n.1001A>C
c.791A>C (p.Asp264Ala)
c.932A>C (n.932A>C)
c.929A>C (p.Asp310Ala)
c.440A>C (p.Asp147Ala)
3g.93898465C>ACA353672808PROS1c.832G>T (p.Asp278Tyr)
c.787G>T (p.Asp263Tyr)
n.1000G>T
c.790G>T (p.Asp264Tyr)
c.931G>T (n.931G>T)
c.928G>T (p.Asp310Tyr)
c.439G>T (p.Asp147Tyr)
3g.93898465C=CA1385039109PROS1c.832G= (p.Asp278=)
c.787G= (p.Asp263=)
n.1000G=
c.790G= (p.Asp264=)
c.931G= (n.931G=)
c.928G= (p.Asp310=)
c.439G= (p.Asp147=)
3g.93898465C>GCA353672809PROS1c.832G>C (p.Asp278His)
c.787G>C (p.Asp263His)
n.1000G>C
c.790G>C (p.Asp264His)
c.931G>C (n.931G>C)
c.928G>C (p.Asp310His)
c.439G>C (p.Asp147His)
3g.93898465C>TCA2503360PROS1c.832G>A (p.Asp278Asn)
c.787G>A (p.Asp263Asn)
n.1000G>A
c.790G>A (p.Asp264Asn)
c.931G>A (n.931G>A)
c.928G>A (p.Asp310Asn)
c.439G>A (p.Asp147Asn)
dbSNP ExAC gnomAD v2 gnomAD v4
3g.93898466T>ACA353672810PROS1c.831A>T (p.Gln277His)
c.786A>T (p.Gln262His)
n.999A>T
c.789A>T (p.Gln263His)
c.930A>T (n.930A>T)
c.927A>T (p.Gln309His)
c.438A>T (p.Gln146His)
3g.93898466T>CCA434461257PROS1c.831A>G (p.Gln277=)
c.786A>G (p.Gln262=)
n.999A>G
c.789A>G (p.Gln263=)
c.930A>G (n.930A>G)
c.927A>G (p.Gln309=)
c.438A>G (p.Gln146=)
3g.93898466T>GCA353672811PROS1c.831A>C (p.Gln277His)
c.786A>C (p.Gln262His)
n.999A>C
c.789A>C (p.Gln263His)
c.930A>C (n.930A>C)
c.927A>C (p.Gln309His)
c.438A>C (p.Gln146His)
3g.93898467T>ACA353672812PROS1c.830A>T (p.Gln277Leu)
c.785A>T (p.Gln262Leu)
n.998A>T
c.788A>T (p.Gln263Leu)
c.929A>T (n.929A>T)
c.926A>T (p.Gln309Leu)
c.437A>T (p.Gln146Leu)
3g.93898467T>CCA353672813PROS1c.830A>G (p.Gln277Arg)
c.785A>G (p.Gln262Arg)
n.998A>G
c.788A>G (p.Gln263Arg)
c.929A>G (n.929A>G)
c.926A>G (p.Gln309Arg)
c.437A>G (p.Gln146Arg)
3g.93898467T>GCA353672814PROS1c.830A>C (p.Gln277Pro)
c.785A>C (p.Gln262Pro)
n.998A>C
c.788A>C (p.Gln263Pro)
c.929A>C (n.929A>C)
c.926A>C (p.Gln309Pro)
c.437A>C (p.Gln146Pro)
3g.93898468G>ACA353672815PROS1c.829C>T (p.Gln277Ter)
c.784C>T (p.Gln262Ter)
n.997C>T
c.787C>T (p.Gln263Ter)
c.928C>T (n.928C>T)
c.925C>T (p.Gln309Ter)
c.436C>T (p.Gln146Ter)
gnomAD v4
3g.93898468G>CCA353672816PROS1c.829C>G (p.Gln277Glu)
c.784C>G (p.Gln262Glu)
n.997C>G
c.787C>G (p.Gln263Glu)
c.928C>G (n.928C>G)
c.925C>G (p.Gln309Glu)
c.436C>G (p.Gln146Glu)
3g.93898468G>TCA353672817PROS1c.829C>A (p.Gln277Lys)
c.784C>A (p.Gln262Lys)
n.997C>A
c.787C>A (p.Gln263Lys)
c.928C>A (n.928C>A)
c.925C>A (p.Gln309Lys)
c.436C>A (p.Gln146Lys)
gnomAD v4
3g.93898469G>ACA434461258PROS1c.828C>T (p.Ala276=)
c.783C>T (p.Ala261=)
n.996C>T
c.786C>T (p.Ala262=)
c.927C>T (n.927C>T)
c.924C>T (p.Ala308=)
c.435C>T (p.Ala145=)
gnomAD v4
3g.93898469G>CCA434461259PROS1c.828C>G (p.Ala276=)
c.783C>G (p.Ala261=)
n.996C>G
c.786C>G (p.Ala262=)
c.927C>G (n.927C>G)
c.924C>G (p.Ala308=)
c.435C>G (p.Ala145=)
3g.93898469G>TCA434461260PROS1c.828C>A (p.Ala276=)
c.783C>A (p.Ala261=)
n.996C>A
c.786C>A (p.Ala262=)
c.927C>A (n.927C>A)
c.924C>A (p.Ala308=)
c.435C>A (p.Ala145=)
3g.93898470G>ACA2503361PROS1c.827C>T (p.Ala276Val)
c.782C>T (p.Ala261Val)
n.995C>T
c.785C>T (p.Ala262Val)
c.926C>T (n.926C>T)
c.923C>T (p.Ala308Val)
c.434C>T (p.Ala145Val)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.93898470G>CCA353672819PROS1c.827C>G (p.Ala276Gly)
c.782C>G (p.Ala261Gly)
n.995C>G
c.785C>G (p.Ala262Gly)
c.926C>G (n.926C>G)
c.923C>G (p.Ala308Gly)
c.434C>G (p.Ala145Gly)
3g.93898470G=CA1385039110PROS1c.827C= (p.Ala276=)
c.782C= (p.Ala261=)
n.995C=
c.785C= (p.Ala262=)
c.926C= (n.926C=)
c.923C= (p.Ala308=)
c.434C= (p.Ala145=)
3g.93898470G>TCA353672818PROS1c.827C>A (p.Ala276Asp)
c.782C>A (p.Ala261Asp)
n.995C>A
c.785C>A (p.Ala262Asp)
c.926C>A (n.926C>A)
c.923C>A (p.Ala308Asp)
c.434C>A (p.Ala145Asp)
3g.93898471C>ACA353672820PROS1c.826G>T (p.Ala276Ser)
c.781G>T (p.Ala261Ser)
n.994G>T
c.784G>T (p.Ala262Ser)
c.925G>T (n.925G>T)
c.922G>T (p.Ala308Ser)
c.433G>T (p.Ala145Ser)
dbSNP
3g.93898471C=CA1385039111PROS1c.826G= (p.Ala276=)
c.781G= (p.Ala261=)
n.994G=
c.784G= (p.Ala262=)
c.925G= (n.925G=)
c.922G= (p.Ala308=)
c.433G= (p.Ala145=)
3g.93898471C>GCA353672821PROS1c.826G>C (p.Ala276Pro)
c.781G>C (p.Ala261Pro)
n.994G>C
c.784G>C (p.Ala262Pro)
c.925G>C (n.925G>C)
c.922G>C (p.Ala308Pro)
c.433G>C (p.Ala145Pro)
3g.93898471C>TCA353672822PROS1c.826G>A (p.Ala276Thr)
c.781G>A (p.Ala261Thr)
n.994G>A
c.784G>A (p.Ala262Thr)
c.925G>A (n.925G>A)
c.922G>A (p.Ala308Thr)
c.433G>A (p.Ala145Thr)
3g.93898472A=CA1385039112PROS1c.825T= (p.Leu275=)
c.780T= (p.Leu260=)
n.993T=
c.783T= (p.Leu261=)
c.924T= (n.924T=)
c.921T= (p.Leu307=)
c.432T= (p.Leu144=)
3g.93898472A>CCA434461263PROS1c.825T>G (p.Leu275=)
c.780T>G (p.Leu260=)
n.993T>G
c.783T>G (p.Leu261=)
c.924T>G (n.924T>G)
c.921T>G (p.Leu307=)
c.432T>G (p.Leu144=)
3g.93898472A>GCA434461262PROS1c.825T>C (p.Leu275=)
c.780T>C (p.Leu260=)
n.993T>C
c.783T>C (p.Leu261=)
c.924T>C (n.924T>C)
c.921T>C (p.Leu307=)
c.432T>C (p.Leu144=)
dbSNP
3g.93898472A>TCA434461261PROS1c.825T>A (p.Leu275=)
c.780T>A (p.Leu260=)
n.993T>A
c.783T>A (p.Leu261=)
c.924T>A (n.924T>A)
c.921T>A (p.Leu307=)
c.432T>A (p.Leu144=)
3g.93898473A=CA1385039113PROS1c.824T= (p.Leu275=)
c.779T= (p.Leu260=)
n.992T=
c.782T= (p.Leu261=)
c.923T= (n.923T=)
c.920T= (p.Leu307=)
c.431T= (p.Leu144=)
3g.93898473A>CCA353672823PROS1c.824T>G (p.Leu275Arg)
c.779T>G (p.Leu260Arg)
n.992T>G
c.782T>G (p.Leu261Arg)
c.923T>G (n.923T>G)
c.920T>G (p.Leu307Arg)
c.431T>G (p.Leu144Arg)
3g.93898473A>GCA78485268PROS1c.824T>C (p.Leu275Pro)
c.779T>C (p.Leu260Pro)
n.992T>C
c.782T>C (p.Leu261Pro)
c.923T>C (n.923T>C)
c.920T>C (p.Leu307Pro)
c.431T>C (p.Leu144Pro)
dbSNP gnomAD v3 gnomAD v4
3g.93898473A>TCA353672824PROS1c.824T>A (p.Leu275His)
c.779T>A (p.Leu260His)
n.992T>A
c.782T>A (p.Leu261His)
c.923T>A (n.923T>A)
c.920T>A (p.Leu307His)
c.431T>A (p.Leu144His)
3g.93898474G>ACA353672827PROS1c.823C>T (p.Leu275Phe)
c.778C>T (p.Leu260Phe)
n.991C>T
c.781C>T (p.Leu261Phe)
c.922C>T (n.922C>T)
c.919C>T (p.Leu307Phe)
c.430C>T (p.Leu144Phe)
gnomAD v4
3g.93898474G>CCA353672825PROS1c.823C>G (p.Leu275Val)
c.778C>G (p.Leu260Val)
n.991C>G
c.781C>G (p.Leu261Val)
c.922C>G (n.922C>G)
c.919C>G (p.Leu307Val)
c.430C>G (p.Leu144Val)
3g.93898474G>TCA353672826PROS1c.823C>A (p.Leu275Ile)
c.778C>A (p.Leu260Ile)
n.991C>A
c.781C>A (p.Leu261Ile)
c.922C>A (n.922C>A)
c.919C>A (p.Leu307Ile)
c.430C>A (p.Leu144Ile)
3g.93898475T>ACA353672828PROS1c.822A>T (p.Lys274Asn)
c.777A>T (p.Lys259Asn)
n.990A>T
c.780A>T (p.Lys260Asn)
c.921A>T (n.921A>T)
c.918A>T (p.Lys306Asn)
c.429A>T (p.Lys143Asn)
COSMIC
3g.93898475T>CCA434461264PROS1c.822A>G (p.Lys274=)
c.777A>G (p.Lys259=)
n.990A>G
c.780A>G (p.Lys260=)
c.921A>G (n.921A>G)
c.918A>G (p.Lys306=)
c.429A>G (p.Lys143=)
3g.93898475T>GCA353672829PROS1c.822A>C (p.Lys274Asn)
c.777A>C (p.Lys259Asn)
n.990A>C
c.780A>C (p.Lys260Asn)
c.921A>C (n.921A>C)
c.918A>C (p.Lys306Asn)
c.429A>C (p.Lys143Asn)
3g.93898476T>ACA353672830PROS1c.821A>T (p.Lys274Ile)
c.776A>T (p.Lys259Ile)
n.989A>T
c.779A>T (p.Lys260Ile)
c.920A>T (n.920A>T)
c.917A>T (p.Lys306Ile)
c.428A>T (p.Lys143Ile)

Number of alleles fetched