Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.93896676G>ACA78484097PROS1c.865C>T (p.Leu289Phe)
c.820C>T (p.Leu274Phe)
n.1033C>T
c.823C>T (p.Leu275Phe)
c.964C>T (n.964C>T)
c.961C>T (p.Leu321Phe)
c.472C>T (p.Leu158Phe)
dbSNP gnomAD v3 gnomAD v4
3g.93896676G>CCA353672723PROS1c.865C>G (p.Leu289Val)
c.820C>G (p.Leu274Val)
n.1033C>G
c.823C>G (p.Leu275Val)
c.964C>G (n.964C>G)
c.961C>G (p.Leu321Val)
c.472C>G (p.Leu158Val)
3g.93896676G=CA1385038334PROS1c.865C= (p.Leu289=)
c.820C= (p.Leu274=)
n.1033C=
c.823C= (p.Leu275=)
c.964C= (n.964C=)
c.961C= (p.Leu321=)
c.472C= (p.Leu158=)
3g.93896676G>TCA353672724PROS1c.865C>A (p.Leu289Ile)
c.820C>A (p.Leu274Ile)
n.1033C>A
c.823C>A (p.Leu275Ile)
c.964C>A (n.964C>A)
c.961C>A (p.Leu321Ile)
c.472C>A (p.Leu158Ile)
3g.93896677G>ACA2503336PROS1c.864C>T (p.Cys288=)
c.819C>T (p.Cys273=)
n.1032C>T
c.822C>T (p.Cys274=)
c.963C>T (n.963C>T)
c.960C>T (p.Cys320=)
c.471C>T (p.Cys157=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
3g.93896677G>CCA353672725PROS1c.864C>G (p.Cys288Trp)
c.819C>G (p.Cys273Trp)
n.1032C>G
c.822C>G (p.Cys274Trp)
c.963C>G (n.963C>G)
c.960C>G (p.Cys320Trp)
c.471C>G (p.Cys157Trp)
3g.93896677G=CA1385038335PROS1c.864C= (p.Cys288=)
c.819C= (p.Cys273=)
n.1032C=
c.822C= (p.Cys274=)
c.963C= (n.963C=)
c.960C= (p.Cys320=)
c.471C= (p.Cys157=)
3g.93896677G>TCA353672726PROS1c.864C>A (p.Cys288Ter)
c.819C>A (p.Cys273Ter)
n.1032C>A
c.822C>A (p.Cys274Ter)
c.963C>A (n.963C>A)
c.960C>A (p.Cys320Ter)
c.471C>A (p.Cys157Ter)
ClinVar dbSNP
3g.93896678C>ACA353672727PROS1c.863G>T (p.Cys288Phe)
c.818G>T (p.Cys273Phe)
n.1031G>T
c.821G>T (p.Cys274Phe)
c.962G>T (n.962G>T)
c.959G>T (p.Cys320Phe)
c.470G>T (p.Cys157Phe)
3g.93896678C>GCA353672728PROS1c.863G>C (p.Cys288Ser)
c.818G>C (p.Cys273Ser)
n.1031G>C
c.821G>C (p.Cys274Ser)
c.962G>C (n.962G>C)
c.959G>C (p.Cys320Ser)
c.470G>C (p.Cys157Ser)
3g.93896678C>TCA353672729PROS1c.863G>A (p.Cys288Tyr)
c.818G>A (p.Cys273Tyr)
n.1031G>A
c.821G>A (p.Cys274Tyr)
c.962G>A (n.962G>A)
c.959G>A (p.Cys320Tyr)
c.470G>A (p.Cys157Tyr)
gnomAD v4 COSMIC
3g.93896679A>CCA353672731PROS1c.862T>G (p.Cys288Gly)
c.817T>G (p.Cys273Gly)
n.1030T>G
c.820T>G (p.Cys274Gly)
c.961T>G (n.961T>G)
c.958T>G (p.Cys320Gly)
c.469T>G (p.Cys157Gly)
3g.93896679A>GCA353672732PROS1c.862T>C (p.Cys288Arg)
c.817T>C (p.Cys273Arg)
n.1030T>C
c.820T>C (p.Cys274Arg)
c.961T>C (n.961T>C)
c.958T>C (p.Cys320Arg)
c.469T>C (p.Cys157Arg)
3g.93896679A>TCA353672730PROS1c.862T>A (p.Cys288Ser)
c.817T>A (p.Cys273Ser)
n.1030T>A
c.820T>A (p.Cys274Ser)
c.961T>A (n.961T>A)
c.958T>A (p.Cys320Ser)
c.469T>A (p.Cys157Ser)
3g.93896680C>ACA434460889PROS1c.861G>T (p.Val287=)
c.816G>T (p.Val272=)
n.1029G>T
c.819G>T (p.Val273=)
c.960G>T (n.960G>T)
c.957G>T (p.Val319=)
c.468G>T (p.Val156=)
3g.93896680C>GCA434460891PROS1c.861G>C (p.Val287=)
c.816G>C (p.Val272=)
n.1029G>C
c.819G>C (p.Val273=)
c.960G>C (n.960G>C)
c.957G>C (p.Val319=)
c.468G>C (p.Val156=)
3g.93896680C>TCA434460892PROS1c.861G>A (p.Val287=)
c.816G>A (p.Val272=)
n.1029G>A
c.819G>A (p.Val273=)
c.960G>A (n.960G>A)
c.957G>A (p.Val319=)
c.468G>A (p.Val156=)
gnomAD v4
3g.93896681A=CA1385038336PROS1c.860T= (p.Val287=)
c.815T= (p.Val272=)
n.1028T=
c.818T= (p.Val273=)
c.959T= (n.959T=)
c.956T= (p.Val319=)
c.467T= (p.Val156=)
3g.93896681A>CCA353672733PROS1c.860T>G (p.Val287Gly)
c.815T>G (p.Val272Gly)
n.1028T>G
c.818T>G (p.Val273Gly)
c.959T>G (n.959T>G)
c.956T>G (p.Val319Gly)
c.467T>G (p.Val156Gly)
dbSNP gnomAD v4
3g.93896681A>GCA2503337PROS1c.860T>C (p.Val287Ala)
c.815T>C (p.Val272Ala)
n.1028T>C
c.818T>C (p.Val273Ala)
c.959T>C (n.959T>C)
c.956T>C (p.Val319Ala)
c.467T>C (p.Val156Ala)
dbSNP ExAC gnomAD v2 gnomAD v4
3g.93896681A>TCA353672734PROS1c.860T>A (p.Val287Glu)
c.815T>A (p.Val272Glu)
n.1028T>A
c.818T>A (p.Val273Glu)
c.959T>A (n.959T>A)
c.956T>A (p.Val319Glu)
c.467T>A (p.Val156Glu)
3g.93896681dupCA2586972702PROS1c.860dup (p.Cys288ValfsTer7)
c.815dup (p.Cys273ValfsTer7)
n.1028dup
c.818dup (p.Cys274ValfsTer7)
c.959dup (n.959dup)
c.956dup (p.Cys320ValfsTer7)
c.467dup (p.Cys157ValfsTer7)
3g.93896682C>ACA353672735PROS1c.859G>T (p.Val287Leu)
c.814G>T (p.Val272Leu)
n.1027G>T
c.817G>T (p.Val273Leu)
c.958G>T (n.958G>T)
c.955G>T (p.Val319Leu)
c.466G>T (p.Val156Leu)
3g.93896682C>GCA353672737PROS1c.859G>C (p.Val287Leu)
c.814G>C (p.Val272Leu)
n.1027G>C
c.817G>C (p.Val273Leu)
c.958G>C (n.958G>C)
c.955G>C (p.Val319Leu)
c.466G>C (p.Val156Leu)
gnomAD v4
3g.93896682C>TCA353672736PROS1c.859G>A (p.Val287Met)
c.814G>A (p.Val272Met)
n.1027G>A
c.817G>A (p.Val273Met)
c.958G>A (n.958G>A)
c.955G>A (p.Val319Met)
c.466G>A (p.Val156Met)
3g.93896683T>ACA78484119PROS1c.858A>T (p.Ser286=)
c.813A>T (p.Ser271=)
n.1026A>T
c.816A>T (p.Ser272=)
c.957A>T (n.957A>T)
c.954A>T (p.Ser318=)
c.465A>T (p.Ser155=)
dbSNP gnomAD v2 gnomAD v4
3g.93896683T>CCA434460902PROS1c.858A>G (p.Ser286=)
c.813A>G (p.Ser271=)
n.1026A>G
c.816A>G (p.Ser272=)
c.957A>G (n.957A>G)
c.954A>G (p.Ser318=)
c.465A>G (p.Ser155=)
3g.93896683T>GCA434460904PROS1c.858A>C (p.Ser286=)
c.813A>C (p.Ser271=)
n.1026A>C
c.816A>C (p.Ser272=)
c.957A>C (n.957A>C)
c.954A>C (p.Ser318=)
c.465A>C (p.Ser155=)
3g.93896683T=CA1385038337PROS1c.858A= (p.Ser286=)
c.813A= (p.Ser271=)
n.1026A=
c.816A= (p.Ser272=)
c.957A= (n.957A=)
c.954A= (p.Ser318=)
c.465A= (p.Ser155=)
3g.93896684G>ACA353672738PROS1c.857C>T (p.Ser286Leu)
c.812C>T (p.Ser271Leu)
n.1025C>T
c.815C>T (p.Ser272Leu)
c.956C>T (n.956C>T)
c.953C>T (p.Ser318Leu)
c.464C>T (p.Ser155Leu)
COSMIC
3g.93896684G>CCA353672740PROS1c.857C>G (p.Ser286Ter)
c.812C>G (p.Ser271Ter)
n.1025C>G
c.815C>G (p.Ser272Ter)
c.956C>G (n.956C>G)
c.953C>G (p.Ser318Ter)
c.464C>G (p.Ser155Ter)
3g.93896684G>TCA353672739PROS1c.857C>A (p.Ser286Ter)
c.812C>A (p.Ser271Ter)
n.1025C>A
c.815C>A (p.Ser272Ter)
c.956C>A (n.956C>A)
c.953C>A (p.Ser318Ter)
c.464C>A (p.Ser155Ter)
3g.93896685A>CCA353672741PROS1c.856T>G (p.Ser286Ala)
c.811T>G (p.Ser271Ala)
n.1024T>G
c.814T>G (p.Ser272Ala)
c.955T>G (n.955T>G)
c.952T>G (p.Ser318Ala)
c.463T>G (p.Ser155Ala)
3g.93896685A>GCA353672742PROS1c.856T>C (p.Ser286Pro)
c.811T>C (p.Ser271Pro)
n.1024T>C
c.814T>C (p.Ser272Pro)
c.955T>C (n.955T>C)
c.952T>C (p.Ser318Pro)
c.463T>C (p.Ser155Pro)
3g.93896685A>TCA353672743PROS1c.856T>A (p.Ser286Thr)
c.811T>A (p.Ser271Thr)
n.1024T>A
c.814T>A (p.Ser272Thr)
c.955T>A (n.955T>A)
c.952T>A (p.Ser318Thr)
c.463T>A (p.Ser155Thr)
3g.93896685_93896688delinsAAACCA1385038338PROS1c.853_856delinsGTTT (p.Val285=)
c.808_811delinsGTTT (p.Val270=)
n.1021_1024delinsGTTT
c.811_814delinsGTTT (p.Val271=)
c.952_955delinsGTTT (n.952_955delinsGTTT)
c.949_952delinsGTTT (p.Val317=)
c.460_463delinsGTTT (p.Val154=)
3g.93896686A=CA1385038339PROS1c.855T= (p.Val285=)
c.810T= (p.Val270=)
n.1023T=
c.813T= (p.Val271=)
c.954T= (n.954T=)
c.951T= (p.Val317=)
c.462T= (p.Val154=)
3g.93896686A>CCA2503338PROS1c.855T>G (p.Val285=)
c.810T>G (p.Val270=)
n.1023T>G
c.813T>G (p.Val271=)
c.954T>G (n.954T>G)
c.951T>G (p.Val317=)
c.462T>G (p.Val154=)
dbSNP ExAC gnomAD v2 gnomAD v4
3g.93896686A>GCA434460915PROS1c.855T>C (p.Val285=)
c.810T>C (p.Val270=)
n.1023T>C
c.813T>C (p.Val271=)
c.954T>C (n.954T>C)
c.951T>C (p.Val317=)
c.462T>C (p.Val154=)
3g.93896686A>TCA434460916PROS1c.855T>A (p.Val285=)
c.810T>A (p.Val270=)
n.1023T>A
c.813T>A (p.Val271=)
c.954T>A (n.954T>A)
c.951T>A (p.Val317=)
c.462T>A (p.Val154=)
3g.93896689_93896691delCA544750412PROS1c.853_855del (p.Val285del)
c.808_810del (p.Val270del)
n.1021_1023del
c.811_813del (p.Val271del)
c.952_954del (n.952_954del)
c.949_951del (p.Val317del)
c.460_462del (p.Val154del)
dbSNP gnomAD v2 gnomAD v4
3g.93896687A>CCA353672744PROS1c.854T>G (p.Val285Gly)
c.809T>G (p.Val270Gly)
n.1022T>G
c.812T>G (p.Val271Gly)
c.953T>G (n.953T>G)
c.950T>G (p.Val317Gly)
c.461T>G (p.Val154Gly)
3g.93896687A>GCA353672745PROS1c.854T>C (p.Val285Ala)
c.809T>C (p.Val270Ala)
n.1022T>C
c.812T>C (p.Val271Ala)
c.953T>C (n.953T>C)
c.950T>C (p.Val317Ala)
c.461T>C (p.Val154Ala)
3g.93896687A>TCA353672746PROS1c.854T>A (p.Val285Asp)
c.809T>A (p.Val270Asp)
n.1022T>A
c.812T>A (p.Val271Asp)
c.953T>A (n.953T>A)
c.950T>A (p.Val317Asp)
c.461T>A (p.Val154Asp)
COSMIC
3g.93896688C>ACA353672747PROS1c.853G>T (p.Val285Phe)
c.808G>T (p.Val270Phe)
n.1021G>T
c.811G>T (p.Val271Phe)
c.952G>T (n.952G>T)
c.949G>T (p.Val317Phe)
c.460G>T (p.Val154Phe)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.93896688C=CA1385038340PROS1c.853G= (p.Val285=)
c.808G= (p.Val270=)
n.1021G=
c.811G= (p.Val271=)
c.952G= (n.952G=)
c.949G= (p.Val317=)
c.460G= (p.Val154=)
3g.93896688C>GCA353672748PROS1c.853G>C (p.Val285Leu)
c.808G>C (p.Val270Leu)
n.1021G>C
c.811G>C (p.Val271Leu)
c.952G>C (n.952G>C)
c.949G>C (p.Val317Leu)
c.460G>C (p.Val154Leu)
3g.93896688C>TCA353672749PROS1c.853G>A (p.Val285Ile)
c.808G>A (p.Val270Ile)
n.1021G>A
c.811G>A (p.Val271Ile)
c.952G>A (n.952G>A)
c.949G>A (p.Val317Ile)
c.460G>A (p.Val154Ile)
3g.93896689A=CA1385038341PROS1c.852T= (p.Val284=)
c.807T= (p.Val269=)
n.1020T=
c.810T= (p.Val270=)
c.951T= (n.951T=)
c.948T= (p.Val316=)
c.459T= (p.Val153=)
3g.93896689A>CCA2503339PROS1c.852T>G (p.Val284=)
c.807T>G (p.Val269=)
n.1020T>G
c.810T>G (p.Val270=)
c.951T>G (n.951T>G)
c.948T>G (p.Val316=)
c.459T>G (p.Val153=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4

Number of alleles fetched