Chr Mutation (hg38) CAid Gene Transcript Linkouts
5g.177992900_177992906delinsCTGGTGGCA1603814029PROP1c.484_490delinsCCACCAG (p.Pro162=)
5g.177992901T>ACA448354954PROP1c.489A>T (p.Pro163=)
5g.177992901T>CCA448354956PROP1c.489A>G (p.Pro163=)
5g.177992901T>GCA448354951PROP1c.489A>C (p.Pro163=)
5g.177992912_177992914dupCA3587515PROP1c.487_489dup (p.Pro163_Val164insPro)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
5g.177992912_177992914delCA3587514PROP1c.487_489del (p.Pro163del)
dbSNP ExAC gnomAD v2 gnomAD v4
5g.177992909_177992914delCA808117610PROP1c.484_489del (p.Pro162_Pro163del)
dbSNP
5g.177992902G>ACA362378624PROP1c.488C>T (p.Pro163Leu)
5g.177992902G>CCA362378625PROP1c.488C>G (p.Pro163Arg)
5g.177992902G=CA1603814030PROP1c.488C= (p.Pro163=)
5g.177992902G>TCA3587516PROP1c.488C>A (p.Pro163Gln)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
5g.177992903G>ACA362378626PROP1c.487C>T (p.Pro163Ser)
5g.177992903G>CCA362378627PROP1c.487C>G (p.Pro163Ala)
5g.177992903G>TCA362378628PROP1c.487C>A (p.Pro163Thr)
5g.177992904T>ACA448354965PROP1c.486A>T (p.Pro162=)
5g.177992904T>CCA448354968PROP1c.486A>G (p.Pro162=)
5g.177992904T>GCA448354970PROP1c.486A>C (p.Pro162=)
5g.177992905G>ACA3587517PROP1c.485C>T (p.Pro162Leu)
dbSNP ExAC gnomAD v2 gnomAD v4
5g.177992905G>CCA362378629PROP1c.485C>G (p.Pro162Arg)
5g.177992905G=CA1603814031PROP1c.485C= (p.Pro162=)
5g.177992905G>TCA362378630PROP1c.485C>A (p.Pro162Gln)
dbSNP gnomAD v2 gnomAD v4
5g.177992906G>ACA362378633PROP1c.484C>T (p.Pro162Ser)
dbSNP gnomAD v3 gnomAD v4
5g.177992906G>CCA362378631PROP1c.484C>G (p.Pro162Ala)
5g.177992906G=CA1603814032PROP1c.484C= (p.Pro162=)
5g.177992906G>TCA362378632PROP1c.484C>A (p.Pro162Thr)
5g.177992907T>ACA448354980PROP1c.483A>T (p.Pro161=)
5g.177992907T>CCA448354984PROP1c.483A>G (p.Pro161=)
5g.177992907T>GCA448354981PROP1c.483A>C (p.Pro161=)
5g.177992907T=CA1603814033PROP1c.483A= (p.Pro161=)
5g.177992908G>ACA132897251PROP1c.482C>T (p.Pro161Leu)
dbSNP
5g.177992908G>CCA362378634PROP1c.482C>G (p.Pro161Arg)
gnomAD v4
5g.177992908G=CA1603814035PROP1c.482C= (p.Pro161=)
5g.177992908G>TCA362378635PROP1c.482C>A (p.Pro161Gln)
gnomAD v4
5g.177992909dupCA1603814034PROP1c.482dup (p.Pro162ThrfsTer?)
dbSNP
5g.177992909G>ACA362378636PROP1c.481C>T (p.Pro161Ser)
5g.177992909G>CCA362378637PROP1c.481C>G (p.Pro161Ala)
5g.177992909G>TCA362378638PROP1c.481C>A (p.Pro161Thr)
5g.177992910T>ACA448354994PROP1c.480A>T (p.Pro160=)
COSMIC
5g.177992910T>CCA448354996PROP1c.480A>G (p.Pro160=)
5g.177992910T>GCA448354998PROP1c.480A>C (p.Pro160=)
5g.177992911G>ACA362378639PROP1c.479C>T (p.Pro160Leu)
dbSNP
5g.177992911G>CCA362378640PROP1c.479C>G (p.Pro160Arg)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
5g.177992911G=CA1603814036PROP1c.479C= (p.Pro160=)
5g.177992911G>TCA362378641PROP1c.479C>A (p.Pro160Gln)
5g.177992912G>ACA362378642PROP1c.478C>T (p.Pro160Ser)
5g.177992912G>CCA362378643PROP1c.478C>G (p.Pro160Ala)
dbSNP gnomAD v4
5g.177992912G=CA1603814037PROP1c.478C= (p.Pro160=)
5g.177992912G>TCA362378644PROP1c.478C>A (p.Pro160Thr)
5g.177992913T>ACA448355010PROP1c.477A>T (p.Ala159=)
5g.177992913T>CCA448355012PROP1c.477A>G (p.Ala159=)
ClinVar dbSNP gnomAD v3 gnomAD v4
5g.177992913T>GCA448355014PROP1c.477A>C (p.Ala159=)
5g.177992913T=CA1603814038PROP1c.477A= (p.Ala159=)
5g.177992916_177992918dupCA132897255PROP1c.475_477dup (p.Ala159_Pro160insAla)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
5g.177992914G>ACA132897258PROP1c.476C>T (p.Ala159Val)
dbSNP
5g.177992914G>CCA362378646PROP1c.476C>G (p.Ala159Gly)
5g.177992914G=CA1603814039PROP1c.476C= (p.Ala159=)
5g.177992914G>TCA362378645PROP1c.476C>A (p.Ala159Glu)
5g.177992915C>ACA362378647PROP1c.475G>T (p.Ala159Ser)
5g.177992915C>GCA362378649PROP1c.475G>C (p.Ala159Pro)
5g.177992915C>TCA362378648PROP1c.475G>A (p.Ala159Thr)
5g.177992916T>ACA448355026PROP1c.474A>T (p.Ala158=)
ClinVar
5g.177992916T>CCA448355025PROP1c.474A>G (p.Ala158=)
5g.177992916T>GCA448355023PROP1c.474A>C (p.Ala158=)
5g.177992917G>ACA362378650PROP1c.473C>T (p.Ala158Val)
5g.177992917G>CCA362378652PROP1c.473C>G (p.Ala158Gly)
5g.177992917G=CA1603814040PROP1c.473C= (p.Ala158=)
5g.177992917G>TCA362378651PROP1c.473C>A (p.Ala158Glu)
dbSNP gnomAD v3 gnomAD v4
5g.177992918C>ACA362378653PROP1c.472G>T (p.Ala158Ser)
5g.177992918C=CA1603814041PROP1c.472G= (p.Ala158=)
5g.177992918C>GCA362378654PROP1c.472G>C (p.Ala158Pro)
dbSNP gnomAD v2 gnomAD v4
5g.177992918C>TCA3587518PROP1c.472G>A (p.Ala158Thr)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
5g.177992919G>ACA3587519PROP1c.471C>T (p.Tyr157=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
5g.177992919G>CCA3587520PROP1c.471C>G (p.Tyr157Ter)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
5g.177992919G=CA1603814042PROP1c.471C= (p.Tyr157=)
5g.177992919G>TCA362378655PROP1c.471C>A (p.Tyr157Ter)
5g.177992920T>ACA362378656PROP1c.470A>T (p.Tyr157Phe)
5g.177992920T>CCA362378657PROP1c.470A>G (p.Tyr157Cys)
gnomAD v4
5g.177992920T>GCA362378658PROP1c.470A>C (p.Tyr157Ser)
5g.177992920_177992921delinsTACA1603814043PROP1c.469_470delinsTA (p.Tyr157=)
5g.177992921A>CCA362378661PROP1c.469T>G (p.Tyr157Asp)
5g.177992921A>GCA362378660PROP1c.469T>C (p.Tyr157His)
5g.177992921A>TCA362378659PROP1c.469T>A (p.Tyr157Asn)
5g.177992922delCA1084892861PROP1c.469del (p.Tyr157ThrfsTer8)
dbSNP gnomAD v3 gnomAD v4
5g.177992923_177992925delCA2676775100PROP1c.467_469del (p.Ser156del)
gnomAD v4
5g.177992922A>CCA448355047PROP1c.468T>G (p.Ser156=)
5g.177992922A>GCA448355049PROP1c.468T>C (p.Ser156=)
5g.177992922A>TCA448355050PROP1c.468T>A (p.Ser156=)
5g.177992923G>ACA362378662PROP1c.467C>T (p.Ser156Phe)
gnomAD v4
5g.177992923G>CCA362378663PROP1c.467C>G (p.Ser156Cys)
gnomAD v4
5g.177992923G>TCA362378664PROP1c.467C>A (p.Ser156Tyr)
5g.177992924A=CA1603814044PROP1c.466T= (p.Ser156=)
5g.177992924A>CCA362378665PROP1c.466T>G (p.Ser156Ala)
5g.177992924A>GCA3587521PROP1c.466T>C (p.Ser156Pro)
dbSNP ExAC gnomAD v2 gnomAD v4
5g.177992924A>TCA362378666PROP1c.466T>A (p.Ser156Thr)
5g.177992925dupCA2695205845PROP1c.466dup (p.Ser156PhefsTer?)
5g.177992925A>CCA362378667PROP1c.465T>G (p.Tyr155Ter)
5g.177992925A>GCA448355062PROP1c.465T>C (p.Tyr155=)
gnomAD v4
5g.177992925A>TCA362378668PROP1c.465T>A (p.Tyr155Ter)
5g.177992926delCA2578500627PROP1c.464del (p.Tyr155PhefsTer10)
5g.177992926T>ACA362378669PROP1c.464A>T (p.Tyr155Phe)
5g.177992926T>CCA3587522PROP1c.464A>G (p.Tyr155Cys)
dbSNP ExAC gnomAD v2 gnomAD v4
5g.177992926T>GCA362378670PROP1c.464A>C (p.Tyr155Ser)
5g.177992926T=CA1603814045PROP1c.464A= (p.Tyr155=)
5g.177992927delCA2580074075PROP1c.463del (p.Tyr155IlefsTer10)
ClinVar gnomAD v4
5g.177992927A=CA1603814046PROP1c.463T= (p.Tyr155=)
5g.177992927A>CCA362378672PROP1c.463T>G (p.Tyr155Asp)
5g.177992927A>GCA362378673PROP1c.463T>C (p.Tyr155His)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
5g.177992927A>TCA362378671PROP1c.463T>A (p.Tyr155Asn)
5g.177992928G>ACA448355073PROP1c.462C>T (p.Pro154=)
5g.177992928G>CCA448355078PROP1c.462C>G (p.Pro154=)
ClinVar
5g.177992928G>TCA448355075PROP1c.462C>A (p.Pro154=)
COSMIC
5g.177992929G>ACA362378674PROP1c.461C>T (p.Pro154Leu)
gnomAD v4
5g.177992929G>CCA362378675PROP1c.461C>G (p.Pro154Arg)
5g.177992929G>TCA362378676PROP1c.461C>A (p.Pro154His)
5g.177992930G>ACA362378677PROP1c.460C>T (p.Pro154Ser)
gnomAD v4
5g.177992930G>CCA362378678PROP1c.460C>G (p.Pro154Ala)
dbSNP gnomAD v3 gnomAD v4
5g.177992930G=CA1603814047PROP1c.460C= (p.Pro154=)
5g.177992930G>TCA362378679PROP1c.460C>A (p.Pro154Thr)
5g.177992931G>ACA448355088PROP1c.459C>T (p.Cys153=)
ClinVar gnomAD v4
5g.177992931G>CCA362378680PROP1c.459C>G (p.Cys153Trp)
5g.177992931G>TCA362378681PROP1c.459C>A (p.Cys153Ter)
5g.177992932C>ACA362378682PROP1c.458G>T (p.Cys153Phe)
gnomAD v4
5g.177992932C=CA1603814048PROP1c.458G= (p.Cys153=)
5g.177992932C>GCA362378683PROP1c.458G>C (p.Cys153Ser)
dbSNP
5g.177992932C>TCA362378684PROP1c.458G>A (p.Cys153Tyr)
gnomAD v4
5g.177992933A>CCA362378687PROP1c.457T>G (p.Cys153Gly)
5g.177992933A>GCA362378686PROP1c.457T>C (p.Cys153Arg)
5g.177992933A>TCA362378685PROP1c.457T>A (p.Cys153Ser)
5g.177992934A=CA1603814049PROP1c.456T= (p.Ala152=)
5g.177992934A>CCA448355101PROP1c.456T>G (p.Ala152=)
5g.177992934A>GCA243390PROP1c.456T>C (p.Ala152=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
5g.177992934A>TCA448355104PROP1c.456T>A (p.Ala152=)
5g.177992935G>ACA362378688PROP1c.455C>T (p.Ala152Val)
gnomAD v4
5g.177992935G>CCA362378689PROP1c.455C>G (p.Ala152Gly)
5g.177992935G>TCA362378690PROP1c.455C>A (p.Ala152Asp)
5g.177992936C>ACA362378691PROP1c.454G>T (p.Ala152Ser)
5g.177992936C>GCA362378692PROP1c.454G>C (p.Ala152Pro)
5g.177992936C>TCA362378693PROP1c.454G>A (p.Ala152Thr)
5g.177992937A=CA1603814050PROP1c.453T= (p.Thr151=)
5g.177992937A>CCA448355115PROP1c.453T>G (p.Thr151=)
dbSNP
5g.177992937A>GCA448355117PROP1c.453T>C (p.Thr151=)
5g.177992937A>TCA448355113PROP1c.453T>A (p.Thr151=)
5g.177992938G>ACA3587523PROP1c.452C>T (p.Thr151Ile)
dbSNP ExAC gnomAD v2
5g.177992938G>CCA362378694PROP1c.452C>G (p.Thr151Ser)
5g.177992938G=CA1603814051PROP1c.452C= (p.Thr151=)
5g.177992938G>TCA362378695PROP1c.452C>A (p.Thr151Asn)
5g.177992939T>ACA362378696PROP1c.451A>T (p.Thr151Ser)
5g.177992939T>CCA362378697PROP1c.451A>G (p.Thr151Ala)
gnomAD v4
5g.177992939T>GCA362378698PROP1c.451A>C (p.Thr151Pro)
5g.177992940G>ACA448355127PROP1c.450C>T (p.Ser150=)
5g.177992940G>CCA448355128PROP1c.450C>G (p.Ser150=)
5g.177992940G>TCA448355130PROP1c.450C>A (p.Ser150=)
5g.177992941G>ACA362378700PROP1c.449C>T (p.Ser150Phe)
gnomAD v4
5g.177992941G>CCA362378701PROP1c.449C>G (p.Ser150Cys)
5g.177992941G>TCA362378699PROP1c.449C>A (p.Ser150Tyr)
5g.177992942A=CA1603814052PROP1c.448T= (p.Ser150=)
5g.177992942A>CCA362378704PROP1c.448T>G (p.Ser150Ala)
5g.177992942A>GCA362378702PROP1c.448T>C (p.Ser150Pro)
5g.177992942A>TCA362378703PROP1c.448T>A (p.Ser150Thr)
dbSNP
5g.177992943C>ACA362378705PROP1c.447G>T (p.Glu149Asp)
5g.177992943C=CA1603814053PROP1c.447G= (p.Glu149=)
5g.177992943C>GCA362378706PROP1c.447G>C (p.Glu149Asp)
5g.177992943C>TCA3587524PROP1c.447G>A (p.Glu149=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
5g.177992944T>ACA362378707PROP1c.446A>T (p.Glu149Val)
5g.177992944T>CCA362378708PROP1c.446A>G (p.Glu149Gly)
gnomAD v4
5g.177992944T>GCA362378709PROP1c.446A>C (p.Glu149Ala)
5g.177992945C>ACA362378710PROP1c.445G>T (p.Glu149Ter)
5g.177992945C>GCA362378711PROP1c.445G>C (p.Glu149Gln)
5g.177992945C>TCA362378712PROP1c.445G>A (p.Glu149Lys)
5g.177992946T>ACA448355146PROP1c.444A>T (p.Pro148=)
5g.177992946T>CCA3587525PROP1c.444A>G (p.Pro148=)
dbSNP ExAC gnomAD v2 gnomAD v4
5g.177992946T>GCA448355149PROP1c.444A>C (p.Pro148=)
5g.177992946T=CA1603814054PROP1c.444A= (p.Pro148=)
5g.177992947G>ACA362378715PROP1c.443C>T (p.Pro148Leu)
dbSNP gnomAD v3 gnomAD v4
5g.177992947G>CCA362378714PROP1c.443C>G (p.Pro148Arg)
5g.177992947G=CA1603814055PROP1c.443C= (p.Pro148=)
5g.177992947G>TCA362378713PROP1c.443C>A (p.Pro148Gln)
COSMIC
5g.177992948G>ACA362378716PROP1c.442C>T (p.Pro148Ser)
5g.177992948G>CCA362378717PROP1c.442C>G (p.Pro148Ala)
5g.177992948G>TCA362378718PROP1c.442C>A (p.Pro148Thr)
5g.177992949C>ACA362378719PROP1c.441G>T (p.Leu147Phe)
5g.177992949C>GCA362378720PROP1c.441G>C (p.Leu147Phe)
5g.177992949C>TCA448355162PROP1c.441G>A (p.Leu147=)
5g.177992950A>CCA362378721PROP1c.440T>G (p.Leu147Trp)
5g.177992950A>GCA362378722PROP1c.440T>C (p.Leu147Ser)
5g.177992950A>TCA362378723PROP1c.440T>A (p.Leu147Ter)
5g.177992953_177992955delCA2769598627PROP1c.438_440del (p.Phe146del)
5g.177992951A=CA1603814056PROP1c.439T= (p.Leu147=)
5g.177992951A>CCA362378724PROP1c.439T>G (p.Leu147Val)
5g.177992951A>GCA448355168PROP1c.439T>C (p.Leu147=)
dbSNP gnomAD v2 gnomAD v4
5g.177992951A>TCA362378725PROP1c.439T>A (p.Leu147Met)
5g.177992952G>ACA448355172PROP1c.438C>T (p.Phe146=)
5g.177992952G>CCA362378726PROP1c.438C>G (p.Phe146Leu)
5g.177992952G>TCA362378727PROP1c.438C>A (p.Phe146Leu)
5g.177992953A>CCA362378730PROP1c.437T>G (p.Phe146Cys)
5g.177992953A>GCA362378729PROP1c.437T>C (p.Phe146Ser)
5g.177992953A>TCA362378728PROP1c.437T>A (p.Phe146Tyr)
5g.177992954A=CA1603814057PROP1c.436T= (p.Phe146=)
5g.177992954A>CCA362378731PROP1c.436T>G (p.Phe146Val)
dbSNP gnomAD v3 gnomAD v4
5g.177992954A>GCA362378732PROP1c.436T>C (p.Phe146Leu)
dbSNP gnomAD v3 gnomAD v4
5g.177992954A>TCA362378733PROP1c.436T>A (p.Phe146Ile)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
5g.177992955G>ACA448355184PROP1c.435C>T (p.Ser145=)
5g.177992955G>CCA362378734PROP1c.435C>G (p.Ser145Arg)
5g.177992955G>TCA362378735PROP1c.435C>A (p.Ser145Arg)
5g.177992956C>ACA362378738PROP1c.434G>T (p.Ser145Ile)
dbSNP
5g.177992956C=CA1603814058PROP1c.434G= (p.Ser145=)
5g.177992956C>GCA362378737PROP1c.434G>C (p.Ser145Thr)
5g.177992956C>TCA362378736PROP1c.434G>A (p.Ser145Asn)
5g.177992957T>ACA362378739PROP1c.433A>T (p.Ser145Cys)
5g.177992957T>CCA362378740PROP1c.433A>G (p.Ser145Gly)
ClinVar gnomAD v4
5g.177992957T>GCA362378741PROP1c.433A>C (p.Ser145Arg)
5g.177992958G>ACA448355197PROP1c.432C>T (p.Ser144=)
5g.177992958G>CCA448355201PROP1c.432C>G (p.Ser144=)
5g.177992958G>TCA448355199PROP1c.432C>A (p.Ser144=)
5g.177992959G>ACA362378742PROP1c.431C>T (p.Ser144Phe)
gnomAD v4
5g.177992959G>CCA362378743PROP1c.431C>G (p.Ser144Cys)
5g.177992959G>TCA362378744PROP1c.431C>A (p.Ser144Tyr)
5g.177992960A>CCA362378745PROP1c.430T>G (p.Ser144Ala)
5g.177992960A>GCA362378747PROP1c.430T>C (p.Ser144Pro)
5g.177992960A>TCA362378746PROP1c.430T>A (p.Ser144Thr)
gnomAD v4
5g.177992963delCA2676775129PROP1c.430del (p.Ser144ProfsTer21)
gnomAD v4
5g.177992961A>CCA362378748PROP1c.429T>G (p.Phe143Leu)
5g.177992961A>GCA448355212PROP1c.429T>C (p.Phe143=)
5g.177992961A>TCA362378749PROP1c.429T>A (p.Phe143Leu)
5g.177992962A>CCA362378750PROP1c.428T>G (p.Phe143Cys)
5g.177992962A>GCA362378751PROP1c.428T>C (p.Phe143Ser)
5g.177992962A>TCA362378752PROP1c.428T>A (p.Phe143Tyr)
5g.177992963A>CCA362378753PROP1c.427T>G (p.Phe143Val)
5g.177992963A>GCA362378754PROP1c.427T>C (p.Phe143Leu)
5g.177992963A>TCA362378755PROP1c.427T>A (p.Phe143Ile)
5g.177992964G>ACA132897332PROP1c.426C>T (p.Ala142=)
ClinVar dbSNP
5g.177992964G>CCA448355214PROP1c.426C>G (p.Ala142=)
5g.177992964G=CA1603814059PROP1c.426C= (p.Ala142=)
5g.177992964G>TCA448355216PROP1c.426C>A (p.Ala142=)
ClinVar
5g.177992965G>ACA243388PROP1c.425C>T (p.Ala142Val)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
5g.177992965G>CCA362378756PROP1c.425C>G (p.Ala142Gly)
5g.177992965G=CA1603814060PROP1c.425C= (p.Ala142=)
5g.177992965G>TCA362378757PROP1c.425C>A (p.Ala142Asp)
5g.177992966C>ACA362378759PROP1c.424G>T (p.Ala142Ser)
5g.177992966C=CA1603814061PROP1c.424G= (p.Ala142=)
5g.177992966C>GCA362378758PROP1c.424G>C (p.Ala142Pro)
5g.177992966C>TCA202375PROP1c.424G>A (p.Ala142Thr)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
5g.177992967G>ACA3587526PROP1c.423C>T (p.Ala141=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
5g.177992967G>CCA448355228PROP1c.423C>G (p.Ala141=)
5g.177992967G=CA1603814062PROP1c.423C= (p.Ala141=)
5g.177992967G>TCA448355230PROP1c.423C>A (p.Ala141=)
5g.177992968G>ACA362378762PROP1c.422C>T (p.Ala141Val)
gnomAD v4
5g.177992968G>CCA362378760PROP1c.422C>G (p.Ala141Gly)
5g.177992968G>TCA362378761PROP1c.422C>A (p.Ala141Asp)
5g.177992969C>ACA362378763PROP1c.421G>T (p.Ala141Ser)
5g.177992969C=CA1603814063PROP1c.421G= (p.Ala141=)
5g.177992969C>GCA362378764PROP1c.421G>C (p.Ala141Pro)
dbSNP
5g.177992969C>TCA362378765PROP1c.421G>A (p.Ala141Thr)
5g.177992970A=CA1603814064PROP1c.420T= (p.Pro140=)
5g.177992970A>CCA448355239PROP1c.420T>G (p.Pro140=)
5g.177992970A>GCA448355243PROP1c.420T>C (p.Pro140=)
dbSNP gnomAD v3 gnomAD v4
5g.177992970A>TCA448355241PROP1c.420T>A (p.Pro140=)
5g.177992971G>ACA362378768PROP1c.419C>T (p.Pro140Leu)
5g.177992971G>CCA362378767PROP1c.419C>G (p.Pro140Arg)
5g.177992971G>TCA362378766PROP1c.419C>A (p.Pro140His)
5g.177992972G>ACA362378769PROP1c.418C>T (p.Pro140Ser)
gnomAD v4
5g.177992972G>CCA362378770PROP1c.418C>G (p.Pro140Ala)
5g.177992972G>TCA362378771PROP1c.418C>A (p.Pro140Thr)
5g.177992973A>CCA448355253PROP1c.417T>G (p.Ser139=)
5g.177992973A>GCA448355254PROP1c.417T>C (p.Ser139=)
5g.177992973A>TCA448355257PROP1c.417T>A (p.Ser139=)
5g.177992974G>ACA3587527PROP1c.416C>T (p.Ser139Phe)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
5g.177992974G>CCA362378772PROP1c.416C>G (p.Ser139Cys)
5g.177992974G=CA1603814065PROP1c.416C= (p.Ser139=)
5g.177992974G>TCA362378773PROP1c.416C>A (p.Ser139Tyr)
5g.177992975A>CCA362378776PROP1c.415T>G (p.Ser139Ala)
5g.177992975A>GCA362378774PROP1c.415T>C (p.Ser139Pro)
5g.177992975A>TCA362378775PROP1c.415T>A (p.Ser139Thr)
5g.177992976C>ACA448355265PROP1c.414G>T (p.Leu138=)
5g.177992976C=CA1603814066PROP1c.414G= (p.Leu138=)
5g.177992976C>GCA448355267PROP1c.414G>C (p.Leu138=)
5g.177992976C>TCA448355269PROP1c.414G>A (p.Leu138=)
ClinVar dbSNP gnomAD v2 gnomAD v4
5g.177992977A>CCA362378777PROP1c.413T>G (p.Leu138Arg)
5g.177992977A>GCA362378778PROP1c.413T>C (p.Leu138Pro)
5g.177992977A>TCA362378779PROP1c.413T>A (p.Leu138Gln)
5g.177992978G>ACA448355276PROP1c.412C>T (p.Leu138=)
dbSNP
5g.177992978G>CCA362378780PROP1c.412C>G (p.Leu138Val)
5g.177992978G=CA1603814067PROP1c.412C= (p.Leu138=)
5g.177992978G>TCA362378781PROP1c.412C>A (p.Leu138Met)
5g.177992979A=CA1603814069PROP1c.411T= (p.His137=)
5g.177992979A>CCA362378782PROP1c.411T>G (p.His137Gln)
dbSNP gnomAD v3 gnomAD v4
5g.177992979A>GCA448355281PROP1c.411T>C (p.His137=)
ClinVar dbSNP
5g.177992979A>TCA362378783PROP1c.411T>A (p.His137Gln)
5g.177992979_177992984dupCA1603814068PROP1c.406_411dup (p.His137_Leu138insAlaHis)
dbSNP
5g.177992980T>ACA362378784PROP1c.410A>T (p.His137Leu)
5g.177992980T>CCA362378785PROP1c.410A>G (p.His137Arg)
gnomAD v4
5g.177992980T>GCA362378786PROP1c.410A>C (p.His137Pro)
5g.177992981G>ACA362378787PROP1c.409C>T (p.His137Tyr)
gnomAD v4
5g.177992981G>CCA362378788PROP1c.409C>G (p.His137Asp)
5g.177992981G>TCA362378789PROP1c.409C>A (p.His137Asn)
5g.177992982G>ACA448355293PROP1c.408C>T (p.Ala136=)
gnomAD v4
5g.177992982G>CCA448355295PROP1c.408C>G (p.Ala136=)
5g.177992982G>TCA448355297PROP1c.408C>A (p.Ala136=)
ClinVar gnomAD v4
5g.177992983G>ACA362378792PROP1c.407C>T (p.Ala136Val)
5g.177992983G>CCA362378790PROP1c.407C>G (p.Ala136Gly)
5g.177992983G>TCA362378791PROP1c.407C>A (p.Ala136Asp)
5g.177992984C>ACA362378793PROP1c.406G>T (p.Ala136Ser)
dbSNP
5g.177992984C=CA1603814070PROP1c.406G= (p.Ala136=)
5g.177992984C>GCA362378794PROP1c.406G>C (p.Ala136Pro)
5g.177992984C>TCA362378795PROP1c.406G>A (p.Ala136Thr)
5g.177992985C>ACA448355307PROP1c.405G>T (p.Leu135=)
5g.177992985C>GCA448355308PROP1c.405G>C (p.Leu135=)
5g.177992985C>TCA448355311PROP1c.405G>A (p.Leu135=)
5g.177992986A>CCA362378796PROP1c.404T>G (p.Leu135Arg)
5g.177992986A>GCA362378797PROP1c.404T>C (p.Leu135Pro)
5g.177992986A>TCA362378798PROP1c.404T>A (p.Leu135Gln)
5g.177992987G>ACA448355318PROP1c.403C>T (p.Leu135=)
5g.177992987G>CCA3587528PROP1c.403C>G (p.Leu135Val)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
5g.177992987G=CA1603814071PROP1c.403C= (p.Leu135=)
5g.177992987G>TCA362378799PROP1c.403C>A (p.Leu135Met)
5g.177992988A>CCA448355322PROP1c.402T>G (p.Pro134=)
5g.177992988A>GCA448355323PROP1c.402T>C (p.Pro134=)
5g.177992988A>TCA448355325PROP1c.402T>A (p.Pro134=)
5g.177992989G>ACA362378800PROP1c.401C>T (p.Pro134Leu)
5g.177992989G>CCA362378801PROP1c.401C>G (p.Pro134Arg)
5g.177992989G>TCA362378802PROP1c.401C>A (p.Pro134His)
5g.177992990G>ACA362378803PROP1c.400C>T (p.Pro134Ser)
gnomAD v4
5g.177992990G>CCA362378804PROP1c.400C>G (p.Pro134Ala)
5g.177992990G>TCA362378805PROP1c.400C>A (p.Pro134Thr)
5g.177992991C>ACA362378806PROP1c.399G>T (p.Gln133His)
5g.177992991C>GCA362378807PROP1c.399G>C (p.Gln133His)
5g.177992991C>TCA448355337PROP1c.399G>A (p.Gln133=)
gnomAD v4
5g.177992992T>ACA362378808PROP1c.398A>T (p.Gln133Leu)
5g.177992992T>CCA362378809PROP1c.398A>G (p.Gln133Arg)
5g.177992992T>GCA362378810PROP1c.398A>C (p.Gln133Pro)
5g.177992993G>ACA362378811PROP1c.397C>T (p.Gln133Ter)
gnomAD v4
5g.177992993G>CCA362378812PROP1c.397C>G (p.Gln133Glu)
5g.177992993G>TCA362378813PROP1c.397C>A (p.Gln133Lys)
5g.177992994A>CCA448355350PROP1c.396T>G (p.Leu132=)
5g.177992994A>GCA448355352PROP1c.396T>C (p.Leu132=)
ClinVar
5g.177992994A>TCA448355353PROP1c.396T>A (p.Leu132=)
5g.177992995A=CA1603814072PROP1c.395T= (p.Leu132=)
5g.177992995A>CCA362378814PROP1c.395T>G (p.Leu132Arg)
dbSNP gnomAD v4
5g.177992995A>GCA362378815PROP1c.395T>C (p.Leu132Pro)
5g.177992995A>TCA362378816PROP1c.395T>A (p.Leu132His)
5g.177992996G>ACA362378817PROP1c.394C>T (p.Leu132Phe)
5g.177992996G>CCA362378818PROP1c.394C>G (p.Leu132Val)
5g.177992996G>TCA362378819PROP1c.394C>A (p.Leu132Ile)
5g.177992997C>ACA448355368PROP1c.393G>T (p.Leu131=)
5g.177992997C=CA1603814073PROP1c.393G= (p.Leu131=)
5g.177992997C>GCA448355364PROP1c.393G>C (p.Leu131=)
5g.177992997C>TCA448355366PROP1c.393G>A (p.Leu131=)
ClinVar dbSNP gnomAD v4
5g.177992998A>CCA362378820PROP1c.392T>G (p.Leu131Arg)
5g.177992998A>GCA362378822PROP1c.392T>C (p.Leu131Pro)
gnomAD v4
5g.177992998A>TCA362378821PROP1c.392T>A (p.Leu131Gln)
5g.177992998_177993000delinsAGTCA1603814074PROP1c.390_392delinsACT (p.Ser130=)
5g.177992999G>ACA448355375PROP1c.391C>T (p.Leu131=)
ClinVar dbSNP
5g.177992999G>CCA362378823PROP1c.391C>G (p.Leu131Val)
5g.177992999G=CA1603814075PROP1c.391C= (p.Leu131=)
5g.177992999G>TCA362378824PROP1c.391C>A (p.Leu131Met)
5g.177993000_177993001delCA16041002PROP1c.390_391del (p.Leu131AlafsTer?)
ClinVar dbSNP
5g.177993000T>ACA448355378PROP1c.390A>T (p.Ser130=)
5g.177993000T>CCA448355379PROP1c.390A>G (p.Ser130=)
ClinVar dbSNP
5g.177993000T>GCA448355382PROP1c.390A>C (p.Ser130=)
ClinVar
5g.177993001G>ACA362378825PROP1c.389C>T (p.Ser130Leu)
5g.177993001G>CCA362378826PROP1c.389C>G (p.Ser130Ter)
5g.177993001G>TCA362378827PROP1c.389C>A (p.Ser130Ter)

Number of alleles fetched