Chr Mutation (hg38) CAid Gene Transcript Linkouts
15g.38351101T>ACA391933203SPRED1c.772T>A (p.Tyr258Asn)
c.808T>A (p.Tyr270Asn)
c.550T>A (p.Tyr184Asn)
c.709T>A (p.Tyr237Asn)
15g.38351101T>CCA391933204SPRED1c.772T>C (p.Tyr258His)
c.808T>C (p.Tyr270His)
c.550T>C (p.Tyr184His)
c.709T>C (p.Tyr237His)
15g.38351101T>GCA391933205SPRED1c.772T>G (p.Tyr258Asp)
c.808T>G (p.Tyr270Asp)
c.550T>G (p.Tyr184Asp)
c.709T>G (p.Tyr237Asp)
15g.38351102A>CCA391933207SPRED1c.773A>C (p.Tyr258Ser)
c.809A>C (p.Tyr270Ser)
c.551A>C (p.Tyr184Ser)
c.710A>C (p.Tyr237Ser)
15g.38351102A>GCA391933208SPRED1c.773A>G (p.Tyr258Cys)
c.809A>G (p.Tyr270Cys)
c.551A>G (p.Tyr184Cys)
c.710A>G (p.Tyr237Cys)
 ClinVar dbSNP
15g.38351102A>TCA391933206SPRED1c.773A>T (p.Tyr258Phe)
c.809A>T (p.Tyr270Phe)
c.551A>T (p.Tyr184Phe)
c.710A>T (p.Tyr237Phe)
15g.38351103T>ACA391933210SPRED1c.774T>A (p.Tyr258Ter)
c.810T>A (p.Tyr270Ter)
c.552T>A (p.Tyr184Ter)
c.711T>A (p.Tyr237Ter)
15g.38351103T>CCA489922943SPRED1c.774T>C (p.Tyr258=)
c.810T>C (p.Tyr270=)
c.552T>C (p.Tyr184=)
c.711T>C (p.Tyr237=)
15g.38351103T>GCA391933209SPRED1c.774T>G (p.Tyr258Ter)
c.810T>G (p.Tyr270Ter)
c.552T>G (p.Tyr184Ter)
c.711T>G (p.Tyr237Ter)
 ClinVar dbSNP
15g.38351103T=CA2170812574SPRED1c.774T= (p.Tyr258=)
c.810T= (p.Tyr270=)
c.552T= (p.Tyr184=)
c.711T= (p.Tyr237=)
15g.38351104G>ACA391933211SPRED1c.775G>A (p.Ala259Thr)
c.811G>A (p.Ala271Thr)
c.553G>A (p.Ala185Thr)
c.712G>A (p.Ala238Thr)
15g.38351104G>CCA391933212SPRED1c.775G>C (p.Ala259Pro)
c.811G>C (p.Ala271Pro)
c.553G>C (p.Ala185Pro)
c.712G>C (p.Ala238Pro)
15g.38351104G>TCA391933213SPRED1c.775G>T (p.Ala259Ser)
c.811G>T (p.Ala271Ser)
c.553G>T (p.Ala185Ser)
c.712G>T (p.Ala238Ser)
15g.38351104_38351111delCA2695219957SPRED1c.775_782del (p.Ala259GlnfsTer4)
c.811_818del (p.Ala271GlnfsTer4)
c.553_560del (p.Ala185GlnfsTer4)
c.712_719del (p.Ala238GlnfsTer4)
15g.38351105C>ACA391933214SPRED1c.776C>A (p.Ala259Glu)
c.812C>A (p.Ala271Glu)
c.554C>A (p.Ala185Glu)
c.713C>A (p.Ala238Glu)
15g.38351105C=CA2170812575SPRED1c.776C= (p.Ala259=)
c.812C= (p.Ala271=)
c.554C= (p.Ala185=)
c.713C= (p.Ala238=)
15g.38351105C>GCA391933215SPRED1c.776C>G (p.Ala259Gly)
c.812C>G (p.Ala271Gly)
c.554C>G (p.Ala185Gly)
c.713C>G (p.Ala238Gly)
15g.38351105C>TCA391933216SPRED1c.776C>T (p.Ala259Val)
c.812C>T (p.Ala271Val)
c.554C>T (p.Ala185Val)
c.713C>T (p.Ala238Val)
 dbSNP gnomAD v2 gnomAD v4
15g.38351106A=CA2170812576SPRED1c.777A= (p.Ala259=)
c.813A= (p.Ala271=)
c.555A= (p.Ala185=)
c.714A= (p.Ala238=)
15g.38351106A>CCA489922944SPRED1c.777A>C (p.Ala259=)
c.813A>C (p.Ala271=)
c.555A>C (p.Ala185=)
c.714A>C (p.Ala238=)
15g.38351106A>GCA489922945SPRED1c.777A>G (p.Ala259=)
c.813A>G (p.Ala271=)
c.555A>G (p.Ala185=)
c.714A>G (p.Ala238=)
 dbSNP gnomAD v4
15g.38351106A>TCA489922946SPRED1c.777A>T (p.Ala259=)
c.813A>T (p.Ala271=)
c.555A>T (p.Ala185=)
c.714A>T (p.Ala238=)
 ClinVar
15g.38351107G>ACA391933217SPRED1c.778G>A (p.Asp260Asn)
c.814G>A (p.Asp272Asn)
c.556G>A (p.Asp186Asn)
c.715G>A (p.Asp239Asn)
15g.38351107G>CCA391933218SPRED1c.778G>C (p.Asp260His)
c.814G>C (p.Asp272His)
c.556G>C (p.Asp186His)
c.715G>C (p.Asp239His)
15g.38351107G>TCA391933219SPRED1c.778G>T (p.Asp260Tyr)
c.814G>T (p.Asp272Tyr)
c.556G>T (p.Asp186Tyr)
c.715G>T (p.Asp239Tyr)
15g.38351108A>CCA391933220SPRED1c.779A>C (p.Asp260Ala)
c.815A>C (p.Asp272Ala)
c.557A>C (p.Asp186Ala)
c.716A>C (p.Asp239Ala)
15g.38351108A>GCA391933221SPRED1c.779A>G (p.Asp260Gly)
c.815A>G (p.Asp272Gly)
c.557A>G (p.Asp186Gly)
c.716A>G (p.Asp239Gly)
15g.38351108A>TCA391933222SPRED1c.779A>T (p.Asp260Val)
c.815A>T (p.Asp272Val)
c.557A>T (p.Asp186Val)
c.716A>T (p.Asp239Val)
15g.38351109C>ACA391933224SPRED1c.780C>A (p.Asp260Glu)
c.816C>A (p.Asp272Glu)
c.558C>A (p.Asp186Glu)
c.717C>A (p.Asp239Glu)
15g.38351109C=CA2170812577SPRED1c.780C= (p.Asp260=)
c.816C= (p.Asp272=)
c.558C= (p.Asp186=)
c.717C= (p.Asp239=)
15g.38351109C>GCA391933223SPRED1c.780C>G (p.Asp260Glu)
c.816C>G (p.Asp272Glu)
c.558C>G (p.Asp186Glu)
c.717C>G (p.Asp239Glu)
 dbSNP gnomAD v2 gnomAD v4
15g.38351109C>TCA489922947SPRED1c.780C>T (p.Asp260=)
c.816C>T (p.Asp272=)
c.558C>T (p.Asp186=)
c.717C>T (p.Asp239=)
 gnomAD v4
15g.38351110delCA658761234SPRED1c.781del (p.Tyr261ThrfsTer?)
c.817del (p.Tyr273ThrfsTer?)
c.559del (p.Tyr187ThrfsTer?)
c.718del (p.Tyr240ThrfsTer?)
15g.38351110T>ACA391933225SPRED1c.781T>A (p.Tyr261Asn)
c.817T>A (p.Tyr273Asn)
c.559T>A (p.Tyr187Asn)
c.718T>A (p.Tyr240Asn)
15g.38351110T>CCA391933226SPRED1c.781T>C (p.Tyr261His)
c.817T>C (p.Tyr273His)
c.559T>C (p.Tyr187His)
c.718T>C (p.Tyr240His)
 COSMIC
15g.38351110T>GCA391933227SPRED1c.781T>G (p.Tyr261Asp)
c.817T>G (p.Tyr273Asp)
c.559T>G (p.Tyr187Asp)
c.718T>G (p.Tyr240Asp)
15g.38351111A>CCA391933228SPRED1c.782A>C (p.Tyr261Ser)
c.818A>C (p.Tyr273Ser)
c.560A>C (p.Tyr187Ser)
c.719A>C (p.Tyr240Ser)
15g.38351111A>GCA391933229SPRED1c.782A>G (p.Tyr261Cys)
c.818A>G (p.Tyr273Cys)
c.560A>G (p.Tyr187Cys)
c.719A>G (p.Tyr240Cys)
 ClinVar
15g.38351111A>TCA391933230SPRED1c.782A>T (p.Tyr261Phe)
c.818A>T (p.Tyr273Phe)
c.560A>T (p.Tyr187Phe)
c.719A>T (p.Tyr240Phe)
15g.38351112C>ACA391933231SPRED1c.783C>A (p.Tyr261Ter)
c.819C>A (p.Tyr273Ter)
c.561C>A (p.Tyr187Ter)
c.720C>A (p.Tyr240Ter)
 ClinVar dbSNP
15g.38351112C=CA2170812578SPRED1c.783C= (p.Tyr261=)
c.819C= (p.Tyr273=)
c.561C= (p.Tyr187=)
c.720C= (p.Tyr240=)
15g.38351112C>GCA391933232SPRED1c.783C>G (p.Tyr261Ter)
c.819C>G (p.Tyr273Ter)
c.561C>G (p.Tyr187Ter)
c.720C>G (p.Tyr240Ter)
15g.38351112C>TCA489922948SPRED1c.783C>T (p.Tyr261=)
c.819C>T (p.Tyr273=)
c.561C>T (p.Tyr187=)
c.720C>T (p.Tyr240=)
 dbSNP
15g.38351113A=CA2170812579SPRED1c.784A= (p.Arg262=)
c.820A= (p.Arg274=)
c.562A= (p.Arg188=)
c.721A= (p.Arg241=)
15g.38351113A>CCA490011761SPRED1c.784A>C (p.Arg262=)
c.820A>C (p.Arg274=)
c.562A>C (p.Arg188=)
c.721A>C (p.Arg241=)
15g.38351113A>GCA391933233SPRED1c.784A>G (p.Arg262Gly)
c.820A>G (p.Arg274Gly)
c.562A>G (p.Arg188Gly)
c.721A>G (p.Arg241Gly)
15g.38351113A>TCA251959SPRED1c.784A>T (p.Arg262Ter)
c.820A>T (p.Arg274Ter)
c.562A>T (p.Arg188Ter)
c.721A>T (p.Arg241Ter)
 ClinVar dbSNP
15g.38351114G>ACA391933234SPRED1c.785G>A (p.Arg262Lys)
c.821G>A (p.Arg274Lys)
c.563G>A (p.Arg188Lys)
c.722G>A (p.Arg241Lys)
15g.38351114G>CCA391933235SPRED1c.785G>C (p.Arg262Thr)
c.821G>C (p.Arg274Thr)
c.563G>C (p.Arg188Thr)
c.722G>C (p.Arg241Thr)
15g.38351114G>TCA391933236SPRED1c.785G>T (p.Arg262Ile)
c.821G>T (p.Arg274Ile)
c.563G>T (p.Arg188Ile)
c.722G>T (p.Arg241Ile)
15g.38351115A>CCA391933238SPRED1c.786A>C (p.Arg262Ser)
c.822A>C (p.Arg274Ser)
c.564A>C (p.Arg188Ser)
c.723A>C (p.Arg241Ser)
15g.38351115A>GCA490011762SPRED1c.786A>G (p.Arg262=)
c.822A>G (p.Arg274=)
c.564A>G (p.Arg188=)
c.723A>G (p.Arg241=)
 gnomAD v4
15g.38351115A>TCA391933237SPRED1c.786A>T (p.Arg262Ser)
c.822A>T (p.Arg274Ser)
c.564A>T (p.Arg188Ser)
c.723A>T (p.Arg241Ser)
15g.38351116C>ACA391933239SPRED1c.787C>A (p.His263Asn)
c.823C>A (p.His275Asn)
c.565C>A (p.His189Asn)
c.724C>A (p.His242Asn)
15g.38351116C>GCA391933241SPRED1c.787C>G (p.His263Asp)
c.823C>G (p.His275Asp)
c.565C>G (p.His189Asp)
c.724C>G (p.His242Asp)
15g.38351116C>TCA391933240SPRED1c.787C>T (p.His263Tyr)
c.823C>T (p.His275Tyr)
c.565C>T (p.His189Tyr)
c.724C>T (p.His242Tyr)
15g.38351117A>CCA391933242SPRED1c.788A>C (p.His263Pro)
c.824A>C (p.His275Pro)
c.566A>C (p.His189Pro)
c.725A>C (p.His242Pro)
15g.38351117A>GCA391933243SPRED1c.788A>G (p.His263Arg)
c.824A>G (p.His275Arg)
c.566A>G (p.His189Arg)
c.725A>G (p.His242Arg)
 ClinVar
15g.38351117A>TCA391933244SPRED1c.788A>T (p.His263Leu)
c.824A>T (p.His275Leu)
c.566A>T (p.His189Leu)
c.725A>T (p.His242Leu)
15g.38351118T>ACA391933245SPRED1c.789T>A (p.His263Gln)
c.825T>A (p.His275Gln)
c.567T>A (p.His189Gln)
c.726T>A (p.His242Gln)
15g.38351118T>CCA490011763SPRED1c.789T>C (p.His263=)
c.825T>C (p.His275=)
c.567T>C (p.His189=)
c.726T>C (p.His242=)
 gnomAD v4
15g.38351118T>GCA391933246SPRED1c.789T>G (p.His263Gln)
c.825T>G (p.His275Gln)
c.567T>G (p.His189Gln)
c.726T>G (p.His242Gln)
15g.38351119C>ACA391933247SPRED1c.790C>A (p.Pro264Thr)
c.826C>A (p.Pro276Thr)
c.568C>A (p.Pro190Thr)
c.727C>A (p.Pro243Thr)
15g.38351119C>GCA391933248SPRED1c.790C>G (p.Pro264Ala)
c.826C>G (p.Pro276Ala)
c.568C>G (p.Pro190Ala)
c.727C>G (p.Pro243Ala)
15g.38351119C>TCA391933249SPRED1c.790C>T (p.Pro264Ser)
c.826C>T (p.Pro276Ser)
c.568C>T (p.Pro190Ser)
c.727C>T (p.Pro243Ser)
15g.38351119delinsAACA2580089316SPRED1c.790delinsAA (p.Pro264AsnfsTer2)
c.826delinsAA (p.Pro276AsnfsTer2)
c.568delinsAA (p.Pro190AsnfsTer2)
c.727delinsAA (p.Pro243AsnfsTer2)
 ClinVar
15g.38351120C>ACA391933250SPRED1c.791C>A (p.Pro264His)
c.827C>A (p.Pro276His)
c.569C>A (p.Pro190His)
c.728C>A (p.Pro243His)
15g.38351120C>GCA391933251SPRED1c.791C>G (p.Pro264Arg)
c.827C>G (p.Pro276Arg)
c.569C>G (p.Pro190Arg)
c.728C>G (p.Pro243Arg)
15g.38351120C>TCA391933252SPRED1c.791C>T (p.Pro264Leu)
c.827C>T (p.Pro276Leu)
c.569C>T (p.Pro190Leu)
c.728C>T (p.Pro243Leu)
15g.38351121T>ACA490011764SPRED1c.792T>A (p.Pro264=)
c.828T>A (p.Pro276=)
c.570T>A (p.Pro190=)
c.729T>A (p.Pro243=)
15g.38351121T>CCA490011766SPRED1c.792T>C (p.Pro264=)
c.828T>C (p.Pro276=)
c.570T>C (p.Pro190=)
c.729T>C (p.Pro243=)
15g.38351121T>GCA490011765SPRED1c.792T>G (p.Pro264=)
c.828T>G (p.Pro276=)
c.570T>G (p.Pro190=)
c.729T>G (p.Pro243=)
15g.38351122G>ACA391933255SPRED1c.793G>A (p.Asp265Asn)
c.829G>A (p.Asp277Asn)
c.571G>A (p.Asp191Asn)
c.730G>A (p.Asp244Asn)
15g.38351122G>CCA391933254SPRED1c.793G>C (p.Asp265His)
c.829G>C (p.Asp277His)
c.571G>C (p.Asp191His)
c.730G>C (p.Asp244His)
15g.38351122G>TCA391933253SPRED1c.793G>T (p.Asp265Tyr)
c.829G>T (p.Asp277Tyr)
c.571G>T (p.Asp191Tyr)
c.730G>T (p.Asp244Tyr)
15g.38351123A>CCA391933256SPRED1c.794A>C (p.Asp265Ala)
c.830A>C (p.Asp277Ala)
c.572A>C (p.Asp191Ala)
c.731A>C (p.Asp244Ala)
15g.38351123A>GCA391933257SPRED1c.794A>G (p.Asp265Gly)
c.830A>G (p.Asp277Gly)
c.572A>G (p.Asp191Gly)
c.731A>G (p.Asp244Gly)
15g.38351123A>TCA391933258SPRED1c.794A>T (p.Asp265Val)
c.830A>T (p.Asp277Val)
c.572A>T (p.Asp191Val)
c.731A>T (p.Asp244Val)
15g.38351123dupCA2499222897SPRED1c.794dup (p.Asp265GlufsTer6)
c.830dup (p.Asp277GlufsTer6)
c.572dup (p.Asp191GlufsTer6)
c.731dup (p.Asp244GlufsTer6)
 ClinVar dbSNP
15g.38351124C>ACA391933259SPRED1c.795C>A (p.Asp265Glu)
c.831C>A (p.Asp277Glu)
c.573C>A (p.Asp191Glu)
c.732C>A (p.Asp244Glu)
15g.38351124C=CA2170812580SPRED1c.795C= (p.Asp265=)
c.831C= (p.Asp277=)
c.573C= (p.Asp191=)
c.732C= (p.Asp244=)
15g.38351124C>GCA391933260SPRED1c.795C>G (p.Asp265Glu)
c.831C>G (p.Asp277Glu)
c.573C>G (p.Asp191Glu)
c.732C>G (p.Asp244Glu)
15g.38351124C>TCA7470188SPRED1c.795C>T (p.Asp265=)
c.831C>T (p.Asp277=)
c.573C>T (p.Asp191=)
c.732C>T (p.Asp244=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.38351124_38351126delinsCATCA2170812581SPRED1c.795_797delinsCAT (p.Asp265=)
c.831_833delinsCAT (p.Asp277=)
c.573_575delinsCAT (p.Asp191=)
c.732_734delinsCAT (p.Asp244=)
15g.38351125A=CA2170812582SPRED1c.796A= (p.Met266=)
c.832A= (p.Met278=)
c.574A= (p.Met192=)
c.733A= (p.Met245=)
15g.38351125A>CCA391933261SPRED1c.796A>C (p.Met266Leu)
c.832A>C (p.Met278Leu)
c.574A>C (p.Met192Leu)
c.733A>C (p.Met245Leu)
 dbSNP gnomAD v2 gnomAD v4
15g.38351125A>GCA391933262SPRED1c.796A>G (p.Met266Val)
c.832A>G (p.Met278Val)
c.574A>G (p.Met192Val)
c.733A>G (p.Met245Val)
 dbSNP gnomAD v2 gnomAD v4
15g.38351125A>TCA391933263SPRED1c.796A>T (p.Met266Leu)
c.832A>T (p.Met278Leu)
c.574A>T (p.Met192Leu)
c.733A>T (p.Met245Leu)
 ClinVar dbSNP gnomAD v2 gnomAD v4
15g.38351125_38351126delCA348567SPRED1c.796_797del (p.Met266ValfsTer4)
c.832_833del (p.Met278ValfsTer4)
c.574_575del (p.Met192ValfsTer4)
c.733_734del (p.Met245ValfsTer4)
 ClinVar dbSNP gnomAD v4
15g.38351126T>ACA391933264SPRED1c.797T>A (p.Met266Lys)
c.833T>A (p.Met278Lys)
c.575T>A (p.Met192Lys)
c.734T>A (p.Met245Lys)
15g.38351126T>CCA391933265SPRED1c.797T>C (p.Met266Thr)
c.833T>C (p.Met278Thr)
c.575T>C (p.Met192Thr)
c.734T>C (p.Met245Thr)
 COSMIC
15g.38351126T>GCA391933266SPRED1c.797T>G (p.Met266Arg)
c.833T>G (p.Met278Arg)
c.575T>G (p.Met192Arg)
c.734T>G (p.Met245Arg)
15g.38351127G>ACA391933269SPRED1c.798G>A (p.Met266Ile)
c.834G>A (p.Met278Ile)
c.576G>A (p.Met192Ile)
c.735G>A (p.Met245Ile)
 ClinVar gnomAD v4
15g.38351127G>CCA391933268SPRED1c.798G>C (p.Met266Ile)
c.834G>C (p.Met278Ile)
c.576G>C (p.Met192Ile)
c.735G>C (p.Met245Ile)
 gnomAD v4
15g.38351127G>TCA391933267SPRED1c.798G>T (p.Met266Ile)
c.834G>T (p.Met278Ile)
c.576G>T (p.Met192Ile)
c.735G>T (p.Met245Ile)
15g.38351128T>ACA391933270SPRED1c.799T>A (p.Trp267Arg)
c.835T>A (p.Trp279Arg)
c.577T>A (p.Trp193Arg)
c.736T>A (p.Trp246Arg)
15g.38351128T>CCA391933272SPRED1c.799T>C (p.Trp267Arg)
c.835T>C (p.Trp279Arg)
c.577T>C (p.Trp193Arg)
c.736T>C (p.Trp246Arg)
15g.38351128T>GCA391933271SPRED1c.799T>G (p.Trp267Gly)
c.835T>G (p.Trp279Gly)
c.577T>G (p.Trp193Gly)
c.736T>G (p.Trp246Gly)
15g.38351129G>ACA391933273SPRED1c.800G>A (p.Trp267Ter)
c.836G>A (p.Trp279Ter)
c.578G>A (p.Trp193Ter)
c.737G>A (p.Trp246Ter)
 ClinVar dbSNP
15g.38351129G>CCA391933275SPRED1c.800G>C (p.Trp267Ser)
c.836G>C (p.Trp279Ser)
c.578G>C (p.Trp193Ser)
c.737G>C (p.Trp246Ser)
15g.38351129G=CA2170812583SPRED1c.800G= (p.Trp267=)
c.836G= (p.Trp279=)
c.578G= (p.Trp193=)
c.737G= (p.Trp246=)
15g.38351129G>TCA391933274SPRED1c.800G>T (p.Trp267Leu)
c.836G>T (p.Trp279Leu)
c.578G>T (p.Trp193Leu)
c.737G>T (p.Trp246Leu)
15g.38351130G>ACA391933276SPRED1c.801G>A (p.Trp267Ter)
c.837G>A (p.Trp279Ter)
c.579G>A (p.Trp193Ter)
c.738G>A (p.Trp246Ter)
15g.38351130G>CCA391933278SPRED1c.801G>C (p.Trp267Cys)
c.837G>C (p.Trp279Cys)
c.579G>C (p.Trp193Cys)
c.738G>C (p.Trp246Cys)
15g.38351130G>TCA391933277SPRED1c.801G>T (p.Trp267Cys)
c.837G>T (p.Trp279Cys)
c.579G>T (p.Trp193Cys)
c.738G>T (p.Trp246Cys)
15g.38351131A>CCA391933279SPRED1c.802A>C (p.Lys268Gln)
c.838A>C (p.Lys280Gln)
c.580A>C (p.Lys194Gln)
c.739A>C (p.Lys247Gln)
15g.38351131A>GCA391933281SPRED1c.802A>G (p.Lys268Glu)
c.838A>G (p.Lys280Glu)
c.580A>G (p.Lys194Glu)
c.739A>G (p.Lys247Glu)
15g.38351131A>TCA391933280SPRED1c.802A>T (p.Lys268Ter)
c.838A>T (p.Lys280Ter)
c.580A>T (p.Lys194Ter)
c.739A>T (p.Lys247Ter)
15g.38351132A>CCA391933282SPRED1c.803A>C (p.Lys268Thr)
c.839A>C (p.Lys280Thr)
c.581A>C (p.Lys194Thr)
c.740A>C (p.Lys247Thr)
15g.38351132A>GCA391933283SPRED1c.803A>G (p.Lys268Arg)
c.839A>G (p.Lys280Arg)
c.581A>G (p.Lys194Arg)
c.740A>G (p.Lys247Arg)
15g.38351132A>TCA391933284SPRED1c.803A>T (p.Lys268Ile)
c.839A>T (p.Lys280Ile)
c.581A>T (p.Lys194Ile)
c.740A>T (p.Lys247Ile)
15g.38351133A=CA2170812584SPRED1c.804A= (p.Lys268=)
c.840A= (p.Lys280=)
c.582A= (p.Lys194=)
c.741A= (p.Lys247=)
15g.38351133A>CCA391933285SPRED1c.804A>C (p.Lys268Asn)
c.840A>C (p.Lys280Asn)
c.582A>C (p.Lys194Asn)
c.741A>C (p.Lys247Asn)
15g.38351133A>GCA490011769SPRED1c.804A>G (p.Lys268=)
c.840A>G (p.Lys280=)
c.582A>G (p.Lys194=)
c.741A>G (p.Lys247=)
 dbSNP gnomAD v3 gnomAD v4
15g.38351133A>TCA391933286SPRED1c.804A>T (p.Lys268Asn)
c.840A>T (p.Lys280Asn)
c.582A>T (p.Lys194Asn)
c.741A>T (p.Lys247Asn)
15g.38351134A>CCA391933287SPRED1c.805A>C (p.Asn269His)
c.841A>C (p.Asn281His)
c.583A>C (p.Asn195His)
c.742A>C (p.Asn248His)
15g.38351134A>GCA391933288SPRED1c.805A>G (p.Asn269Asp)
c.841A>G (p.Asn281Asp)
c.583A>G (p.Asn195Asp)
c.742A>G (p.Asn248Asp)
15g.38351134A>TCA391933289SPRED1c.805A>T (p.Asn269Tyr)
c.841A>T (p.Asn281Tyr)
c.583A>T (p.Asn195Tyr)
c.742A>T (p.Asn248Tyr)
15g.38351135A>CCA391933290SPRED1c.806A>C (p.Asn269Thr)
c.842A>C (p.Asn281Thr)
c.584A>C (p.Asn195Thr)
c.743A>C (p.Asn248Thr)
15g.38351135A>GCA391933291SPRED1c.806A>G (p.Asn269Ser)
c.842A>G (p.Asn281Ser)
c.584A>G (p.Asn195Ser)
c.743A>G (p.Asn248Ser)
15g.38351135A>TCA391933292SPRED1c.806A>T (p.Asn269Ile)
c.842A>T (p.Asn281Ile)
c.584A>T (p.Asn195Ile)
c.743A>T (p.Asn248Ile)
15g.38351136T>ACA391933293SPRED1c.807T>A (p.Asn269Lys)
c.843T>A (p.Asn281Lys)
c.585T>A (p.Asn195Lys)
c.744T>A (p.Asn248Lys)
15g.38351136T>CCA490011773SPRED1c.807T>C (p.Asn269=)
c.843T>C (p.Asn281=)
c.585T>C (p.Asn195=)
c.744T>C (p.Asn248=)
15g.38351136T>GCA10603437SPRED1c.807T>G (p.Asn269Lys)
c.843T>G (p.Asn281Lys)
c.585T>G (p.Asn195Lys)
c.744T>G (p.Asn248Lys)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
15g.38351136T=CA2170812585SPRED1c.807T= (p.Asn269=)
c.843T= (p.Asn281=)
c.585T= (p.Asn195=)
c.744T= (p.Asn248=)
15g.38351137G>ACA391933294SPRED1c.808G>A (p.Asp270Asn)
c.844G>A (p.Asp282Asn)
c.586G>A (p.Asp196Asn)
c.745G>A (p.Asp249Asn)
15g.38351137G>CCA391933296SPRED1c.808G>C (p.Asp270His)
c.844G>C (p.Asp282His)
c.586G>C (p.Asp196His)
c.745G>C (p.Asp249His)
15g.38351137G=CA2170812586SPRED1c.808G= (p.Asp270=)
c.844G= (p.Asp282=)
c.586G= (p.Asp196=)
c.745G= (p.Asp249=)
15g.38351137G>TCA391933295SPRED1c.808G>T (p.Asp270Tyr)
c.844G>T (p.Asp282Tyr)
c.586G>T (p.Asp196Tyr)
c.745G>T (p.Asp249Tyr)
 ClinVar dbSNP gnomAD v2 gnomAD v4
15g.38351138A=CA2170812587SPRED1c.809A= (p.Asp270=)
c.845A= (p.Asp282=)
c.587A= (p.Asp196=)
c.746A= (p.Asp249=)
15g.38351138A>CCA391933297SPRED1c.809A>C (p.Asp270Ala)
c.845A>C (p.Asp282Ala)
c.587A>C (p.Asp196Ala)
c.746A>C (p.Asp249Ala)
 COSMIC
15g.38351138A>GCA391933298SPRED1c.809A>G (p.Asp270Gly)
c.845A>G (p.Asp282Gly)
c.587A>G (p.Asp196Gly)
c.746A>G (p.Asp249Gly)
 dbSNP gnomAD v2 gnomAD v4
15g.38351138A>TCA391933299SPRED1c.809A>T (p.Asp270Val)
c.845A>T (p.Asp282Val)
c.587A>T (p.Asp196Val)
c.746A>T (p.Asp249Val)
15g.38351139C>ACA391933300SPRED1c.810C>A (p.Asp270Glu)
c.846C>A (p.Asp282Glu)
c.588C>A (p.Asp196Glu)
c.747C>A (p.Asp249Glu)
15g.38351139C>GCA391933301SPRED1c.810C>G (p.Asp270Glu)
c.846C>G (p.Asp282Glu)
c.588C>G (p.Asp196Glu)
c.747C>G (p.Asp249Glu)
15g.38351139C>TCA490011776SPRED1c.810C>T (p.Asp270=)
c.846C>T (p.Asp282=)
c.588C>T (p.Asp196=)
c.747C>T (p.Asp249=)
15g.38351140T>ACA391933302SPRED1c.811T>A (p.Leu271Met)
c.847T>A (p.Leu283Met)
c.589T>A (p.Leu197Met)
c.748T>A (p.Leu250Met)
15g.38351140T>CCA490011778SPRED1c.811T>C (p.Leu271=)
c.847T>C (p.Leu283=)
c.589T>C (p.Leu197=)
c.748T>C (p.Leu250=)
15g.38351140T>GCA391933303SPRED1c.811T>G (p.Leu271Val)
c.847T>G (p.Leu283Val)
c.589T>G (p.Leu197Val)
c.748T>G (p.Leu250Val)
15g.38351141T>ACA391933304SPRED1c.812T>A (p.Leu271Ter)
c.848T>A (p.Leu283Ter)
c.590T>A (p.Leu197Ter)
c.749T>A (p.Leu250Ter)
15g.38351141T>CCA391933305SPRED1c.812T>C (p.Leu271Ser)
c.848T>C (p.Leu283Ser)
c.590T>C (p.Leu197Ser)
c.749T>C (p.Leu250Ser)
 dbSNP gnomAD v4
15g.38351141T>GCA391933306SPRED1c.812T>G (p.Leu271Trp)
c.848T>G (p.Leu283Trp)
c.590T>G (p.Leu197Trp)
c.749T>G (p.Leu250Trp)
15g.38351141T=CA2170812588SPRED1c.812T= (p.Leu271=)
c.848T= (p.Leu283=)
c.590T= (p.Leu197=)
c.749T= (p.Leu250=)
15g.38351142G>ACA490011784SPRED1c.813G>A (p.Leu271=)
c.849G>A (p.Leu283=)
c.591G>A (p.Leu197=)
c.750G>A (p.Leu250=)
15g.38351142G>CCA391933307SPRED1c.813G>C (p.Leu271Phe)
c.849G>C (p.Leu283Phe)
c.591G>C (p.Leu197Phe)
c.750G>C (p.Leu250Phe)
15g.38351142G>TCA391933308SPRED1c.813G>T (p.Leu271Phe)
c.849G>T (p.Leu283Phe)
c.591G>T (p.Leu197Phe)
c.750G>T (p.Leu250Phe)
15g.38351143G>ACA391933309SPRED1c.814G>A (p.Glu272Lys)
c.850G>A (p.Glu284Lys)
c.592G>A (p.Glu198Lys)
c.751G>A (p.Glu251Lys)
 COSMIC
15g.38351143G>CCA391933310SPRED1c.814G>C (p.Glu272Gln)
c.850G>C (p.Glu284Gln)
c.592G>C (p.Glu198Gln)
c.751G>C (p.Glu251Gln)
15g.38351143G>TCA391933311SPRED1c.814G>T (p.Glu272Ter)
c.850G>T (p.Glu284Ter)
c.592G>T (p.Glu198Ter)
c.751G>T (p.Glu251Ter)
15g.38351145_38351148delCA2627716205SPRED1c.816_819del (p.Arg273MetfsTer29)
c.852_855del (p.Arg285MetfsTer29)
c.594_597del (p.Arg199MetfsTer29)
c.753_756del (p.Arg252MetfsTer29)
 gnomAD v4
15g.38351144A>CCA391933312SPRED1c.815A>C (p.Glu272Ala)
c.851A>C (p.Glu284Ala)
c.593A>C (p.Glu198Ala)
c.752A>C (p.Glu251Ala)
15g.38351144A>GCA391933313SPRED1c.815A>G (p.Glu272Gly)
c.851A>G (p.Glu284Gly)
c.593A>G (p.Glu198Gly)
c.752A>G (p.Glu251Gly)
15g.38351144A>TCA391933314SPRED1c.815A>T (p.Glu272Val)
c.851A>T (p.Glu284Val)
c.593A>T (p.Glu198Val)
c.752A>T (p.Glu251Val)
15g.38351145A>CCA391933315SPRED1c.816A>C (p.Glu272Asp)
c.852A>C (p.Glu284Asp)
c.594A>C (p.Glu198Asp)
c.753A>C (p.Glu251Asp)
15g.38351145A>GCA490011789SPRED1c.816A>G (p.Glu272=)
c.852A>G (p.Glu284=)
c.594A>G (p.Glu198=)
c.753A>G (p.Glu251=)
15g.38351145A>TCA391933316SPRED1c.816A>T (p.Glu272Asp)
c.852A>T (p.Glu284Asp)
c.594A>T (p.Glu198Asp)
c.753A>T (p.Glu251Asp)
15g.38351146A=CA2170812589SPRED1c.817A= (p.Arg273=)
c.853A= (p.Arg285=)
c.595A= (p.Arg199=)
c.754A= (p.Arg252=)
15g.38351146A>CCA490011791SPRED1c.817A>C (p.Arg273=)
c.853A>C (p.Arg285=)
c.595A>C (p.Arg199=)
c.754A>C (p.Arg252=)
15g.38351146A>GCA269293443SPRED1c.817A>G (p.Arg273Gly)
c.853A>G (p.Arg285Gly)
c.595A>G (p.Arg199Gly)
c.754A>G (p.Arg252Gly)
 dbSNP gnomAD v4
15g.38351146A>TCA391933317SPRED1c.817A>T (p.Arg273Ter)
c.853A>T (p.Arg285Ter)
c.595A>T (p.Arg199Ter)
c.754A>T (p.Arg252Ter)
15g.38351147G>ACA391933318SPRED1c.818G>A (p.Arg273Lys)
c.854G>A (p.Arg285Lys)
c.596G>A (p.Arg199Lys)
c.755G>A (p.Arg252Lys)
15g.38351147G>CCA269293444SPRED1c.818G>C (p.Arg273Thr)
c.854G>C (p.Arg285Thr)
c.596G>C (p.Arg199Thr)
c.755G>C (p.Arg252Thr)
 dbSNP
15g.38351147G=CA2170812590SPRED1c.818G= (p.Arg273=)
c.854G= (p.Arg285=)
c.596G= (p.Arg199=)
c.755G= (p.Arg252=)
15g.38351147G>TCA391933319SPRED1c.818G>T (p.Arg273Ile)
c.854G>T (p.Arg285Ile)
c.596G>T (p.Arg199Ile)
c.755G>T (p.Arg252Ile)
 COSMIC
15g.38351148A>CCA391933320SPRED1c.819A>C (p.Arg273Ser)
c.855A>C (p.Arg285Ser)
c.597A>C (p.Arg199Ser)
c.756A>C (p.Arg252Ser)
15g.38351148A>GCA490011795SPRED1c.819A>G (p.Arg273=)
c.855A>G (p.Arg285=)
c.597A>G (p.Arg199=)
c.756A>G (p.Arg252=)
15g.38351148A>TCA391933321SPRED1c.819A>T (p.Arg273Ser)
c.855A>T (p.Arg285Ser)
c.597A>T (p.Arg199Ser)
c.756A>T (p.Arg252Ser)
15g.38351149G>ACA391933322SPRED1c.820G>A (p.Asp274Asn)
c.856G>A (p.Asp286Asn)
c.598G>A (p.Asp200Asn)
c.757G>A (p.Asp253Asn)
15g.38351149G>CCA391933323SPRED1c.820G>C (p.Asp274His)
c.856G>C (p.Asp286His)
c.598G>C (p.Asp200His)
c.757G>C (p.Asp253His)
 gnomAD v4
15g.38351149G>TCA391933324SPRED1c.820G>T (p.Asp274Tyr)
c.856G>T (p.Asp286Tyr)
c.598G>T (p.Asp200Tyr)
c.757G>T (p.Asp253Tyr)
 gnomAD v4
15g.38351150A=CA2170812591SPRED1c.821A= (p.Asp274=)
c.857A= (p.Asp286=)
c.599A= (p.Asp200=)
c.758A= (p.Asp253=)
15g.38351150A>CCA391933325SPRED1c.821A>C (p.Asp274Ala)
c.857A>C (p.Asp286Ala)
c.599A>C (p.Asp200Ala)
c.758A>C (p.Asp253Ala)
 COSMIC
15g.38351150A>GCA269293445SPRED1c.821A>G (p.Asp274Gly)
c.857A>G (p.Asp286Gly)
c.599A>G (p.Asp200Gly)
c.758A>G (p.Asp253Gly)
 dbSNP gnomAD v4
15g.38351150A>TCA391933326SPRED1c.821A>T (p.Asp274Val)
c.857A>T (p.Asp286Val)
c.599A>T (p.Asp200Val)
c.758A>T (p.Asp253Val)
15g.38351151T>ACA391933327SPRED1c.822T>A (p.Asp274Glu)
c.858T>A (p.Asp286Glu)
c.600T>A (p.Asp200Glu)
c.759T>A (p.Asp253Glu)
15g.38351151T>CCA490011800SPRED1c.822T>C (p.Asp274=)
c.858T>C (p.Asp286=)
c.600T>C (p.Asp200=)
c.759T>C (p.Asp253=)
15g.38351151T>GCA391933328SPRED1c.822T>G (p.Asp274Glu)
c.858T>G (p.Asp286Glu)
c.600T>G (p.Asp200Glu)
c.759T>G (p.Asp253Glu)
15g.38351152G>ACA391933329SPRED1c.823G>A (p.Asp275Asn)
c.859G>A (p.Asp287Asn)
c.601G>A (p.Asp201Asn)
c.760G>A (p.Asp254Asn)
15g.38351152G>CCA391933330SPRED1c.823G>C (p.Asp275His)
c.859G>C (p.Asp287His)
c.601G>C (p.Asp201His)
c.760G>C (p.Asp254His)
15g.38351152G=CA2170812592SPRED1c.823G= (p.Asp275=)
c.859G= (p.Asp287=)
c.601G= (p.Asp201=)
c.760G= (p.Asp254=)
15g.38351152G>TCA7470189SPRED1c.823G>T (p.Asp275Tyr)
c.859G>T (p.Asp287Tyr)
c.601G>T (p.Asp201Tyr)
c.760G>T (p.Asp254Tyr)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
15g.38351153A>CCA391933333SPRED1c.824A>C (p.Asp275Ala)
c.860A>C (p.Asp287Ala)
c.602A>C (p.Asp201Ala)
c.761A>C (p.Asp254Ala)
15g.38351153A>GCA391933332SPRED1c.824A>G (p.Asp275Gly)
c.860A>G (p.Asp287Gly)
c.602A>G (p.Asp201Gly)
c.761A>G (p.Asp254Gly)
15g.38351153A>TCA391933331SPRED1c.824A>T (p.Asp275Val)
c.860A>T (p.Asp287Val)
c.602A>T (p.Asp201Val)
c.761A>T (p.Asp254Val)
15g.38351154T>ACA391933334SPRED1c.825T>A (p.Asp275Glu)
c.861T>A (p.Asp287Glu)
c.603T>A (p.Asp201Glu)
c.762T>A (p.Asp254Glu)
15g.38351154T>CCA490011803SPRED1c.825T>C (p.Asp275=)
c.861T>C (p.Asp287=)
c.603T>C (p.Asp201=)
c.762T>C (p.Asp254=)
15g.38351154T>GCA391933335SPRED1c.825T>G (p.Asp275Glu)
c.861T>G (p.Asp287Glu)
c.603T>G (p.Asp201Glu)
c.762T>G (p.Asp254Glu)
15g.38351155G>ACA391933336SPRED1c.826G>A (p.Ala276Thr)
c.862G>A (p.Ala288Thr)
c.604G>A (p.Ala202Thr)
c.763G>A (p.Ala255Thr)
 ClinVar dbSNP gnomAD v2 gnomAD v4
15g.38351155G>CCA391933337SPRED1c.826G>C (p.Ala276Pro)
c.862G>C (p.Ala288Pro)
c.604G>C (p.Ala202Pro)
c.763G>C (p.Ala255Pro)
15g.38351155G=CA2170812593SPRED1c.826G= (p.Ala276=)
c.862G= (p.Ala288=)
c.604G= (p.Ala202=)
c.763G= (p.Ala255=)
15g.38351155G>TCA391933338SPRED1c.826G>T (p.Ala276Ser)
c.862G>T (p.Ala288Ser)
c.604G>T (p.Ala202Ser)
c.763G>T (p.Ala255Ser)
15g.38351156C>ACA391933339SPRED1c.827C>A (p.Ala276Asp)
c.863C>A (p.Ala288Asp)
c.605C>A (p.Ala202Asp)
c.764C>A (p.Ala255Asp)
15g.38351156C>GCA391933340SPRED1c.827C>G (p.Ala276Gly)
c.863C>G (p.Ala288Gly)
c.605C>G (p.Ala202Gly)
c.764C>G (p.Ala255Gly)
15g.38351156C>TCA391933341SPRED1c.827C>T (p.Ala276Val)
c.863C>T (p.Ala288Val)
c.605C>T (p.Ala202Val)
c.764C>T (p.Ala255Val)
15g.38351157T>ACA490011808SPRED1c.828T>A (p.Ala276=)
c.864T>A (p.Ala288=)
c.606T>A (p.Ala202=)
c.765T>A (p.Ala255=)
15g.38351157T>CCA490011809SPRED1c.828T>C (p.Ala276=)
c.864T>C (p.Ala288=)
c.606T>C (p.Ala202=)
c.765T>C (p.Ala255=)
15g.38351157T>GCA490011810SPRED1c.828T>G (p.Ala276=)
c.864T>G (p.Ala288=)
c.606T>G (p.Ala202=)
c.765T>G (p.Ala255=)
15g.38351158G>ACA269293446SPRED1c.829G>A (p.Asp277Asn)
c.865G>A (p.Asp289Asn)
c.607G>A (p.Asp203Asn)
c.766G>A (p.Asp256Asn)
 ClinVar dbSNP gnomAD v3 gnomAD v4
15g.38351158G>CCA391933342SPRED1c.829G>C (p.Asp277His)
c.865G>C (p.Asp289His)
c.607G>C (p.Asp203His)
c.766G>C (p.Asp256His)
15g.38351158G=CA2170812594SPRED1c.829G= (p.Asp277=)
c.865G= (p.Asp289=)
c.607G= (p.Asp203=)
c.766G= (p.Asp256=)
15g.38351158G>TCA391933343SPRED1c.829G>T (p.Asp277Tyr)
c.865G>T (p.Asp289Tyr)
c.607G>T (p.Asp203Tyr)
c.766G>T (p.Asp256Tyr)
15g.38351159A>CCA391933344SPRED1c.830A>C (p.Asp277Ala)
c.866A>C (p.Asp289Ala)
c.608A>C (p.Asp203Ala)
c.767A>C (p.Asp256Ala)
15g.38351159A>GCA391933345SPRED1c.830A>G (p.Asp277Gly)
c.866A>G (p.Asp289Gly)
c.608A>G (p.Asp203Gly)
c.767A>G (p.Asp256Gly)
15g.38351159A>TCA391933346SPRED1c.830A>T (p.Asp277Val)
c.866A>T (p.Asp289Val)
c.608A>T (p.Asp203Val)
c.767A>T (p.Asp256Val)
15g.38351160T>ACA391933348SPRED1c.831T>A (p.Asp277Glu)
c.867T>A (p.Asp289Glu)
c.609T>A (p.Asp203Glu)
c.768T>A (p.Asp256Glu)
15g.38351160T>CCA490011815SPRED1c.831T>C (p.Asp277=)
c.867T>C (p.Asp289=)
c.609T>C (p.Asp203=)
c.768T>C (p.Asp256=)
15g.38351160T>GCA391933347SPRED1c.831T>G (p.Asp277Glu)
c.867T>G (p.Asp289Glu)
c.609T>G (p.Asp203Glu)
c.768T>G (p.Asp256Glu)
15g.38351161dupCA658761235SPRED1c.832dup (p.Ser278PhefsTer7)
c.868dup (p.Ser290PhefsTer7)
c.610dup (p.Ser204PhefsTer7)
c.769dup (p.Ser257PhefsTer7)
 gnomAD v4
15g.38351161T>ACA391933349SPRED1c.832T>A (p.Ser278Thr)
c.868T>A (p.Ser290Thr)
c.610T>A (p.Ser204Thr)
c.769T>A (p.Ser257Thr)
15g.38351161T>CCA391933350SPRED1c.832T>C (p.Ser278Pro)
c.868T>C (p.Ser290Pro)
c.610T>C (p.Ser204Pro)
c.769T>C (p.Ser257Pro)
15g.38351161T>GCA391933351SPRED1c.832T>G (p.Ser278Ala)
c.868T>G (p.Ser290Ala)
c.610T>G (p.Ser204Ala)
c.769T>G (p.Ser257Ala)
15g.38351162C>ACA391933352SPRED1c.833C>A (p.Ser278Tyr)
c.869C>A (p.Ser290Tyr)
c.611C>A (p.Ser204Tyr)
c.770C>A (p.Ser257Tyr)
15g.38351162C>GCA391933353SPRED1c.833C>G (p.Ser278Cys)
c.869C>G (p.Ser290Cys)
c.611C>G (p.Ser204Cys)
c.770C>G (p.Ser257Cys)
15g.38351162C>TCA391933354SPRED1c.833C>T (p.Ser278Phe)
c.869C>T (p.Ser290Phe)
c.611C>T (p.Ser204Phe)
c.770C>T (p.Ser257Phe)
15g.38351163C>ACA490011818SPRED1c.834C>A (p.Ser278=)
c.870C>A (p.Ser290=)
c.612C>A (p.Ser204=)
c.771C>A (p.Ser257=)
15g.38351163C>GCA490011820SPRED1c.834C>G (p.Ser278=)
c.870C>G (p.Ser290=)
c.612C>G (p.Ser204=)
c.771C>G (p.Ser257=)
15g.38351163C>TCA490011821SPRED1c.834C>T (p.Ser278=)
c.870C>T (p.Ser290=)
c.612C>T (p.Ser204=)
c.771C>T (p.Ser257=)
15g.38351164A=CA2170812595SPRED1c.835A= (p.Ser279=)
c.871A= (p.Ser291=)
c.613A= (p.Ser205=)
c.772A= (p.Ser258=)
15g.38351164A>CCA391933355SPRED1c.835A>C (p.Ser279Arg)
c.871A>C (p.Ser291Arg)
c.613A>C (p.Ser205Arg)
c.772A>C (p.Ser258Arg)
15g.38351164A>GCA7470190SPRED1c.835A>G (p.Ser279Gly)
c.871A>G (p.Ser291Gly)
c.613A>G (p.Ser205Gly)
c.772A>G (p.Ser258Gly)
 dbSNP ExAC gnomAD v2 gnomAD v4
15g.38351164A>TCA391933356SPRED1c.835A>T (p.Ser279Cys)
c.871A>T (p.Ser291Cys)
c.613A>T (p.Ser205Cys)
c.772A>T (p.Ser258Cys)
15g.38351165G>ACA269293447SPRED1c.836G>A (p.Ser279Asn)
c.872G>A (p.Ser291Asn)
c.614G>A (p.Ser205Asn)
c.773G>A (p.Ser258Asn)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
15g.38351165G>CCA391933357SPRED1c.836G>C (p.Ser279Thr)
c.872G>C (p.Ser291Thr)
c.614G>C (p.Ser205Thr)
c.773G>C (p.Ser258Thr)
 gnomAD v4
15g.38351165G=CA2170812596SPRED1c.836G= (p.Ser279=)
c.872G= (p.Ser291=)
c.614G= (p.Ser205=)
c.773G= (p.Ser258=)
15g.38351165G>TCA391933358SPRED1c.836G>T (p.Ser279Ile)
c.872G>T (p.Ser291Ile)
c.614G>T (p.Ser205Ile)
c.773G>T (p.Ser258Ile)
 dbSNP
15g.38351166T>ACA391933360SPRED1c.837T>A (p.Ser279Arg)
c.873T>A (p.Ser291Arg)
c.615T>A (p.Ser205Arg)
c.774T>A (p.Ser258Arg)
 dbSNP
15g.38351166T>CCA490011827SPRED1c.837T>C (p.Ser279=)
c.873T>C (p.Ser291=)
c.615T>C (p.Ser205=)
c.774T>C (p.Ser258=)
 dbSNP gnomAD v3 gnomAD v4
15g.38351166T>GCA391933359SPRED1c.837T>G (p.Ser279Arg)
c.873T>G (p.Ser291Arg)
c.615T>G (p.Ser205Arg)
c.774T>G (p.Ser258Arg)
15g.38351166T=CA2170812597SPRED1c.837T= (p.Ser279=)
c.873T= (p.Ser291=)
c.615T= (p.Ser205=)
c.774T= (p.Ser258=)
15g.38351167A=CA2170812598SPRED1c.838A= (p.Ile280=)
c.874A= (p.Ile292=)
c.616A= (p.Ile206=)
c.775A= (p.Ile259=)
15g.38351167A>CCA391933361SPRED1c.838A>C (p.Ile280Leu)
c.874A>C (p.Ile292Leu)
c.616A>C (p.Ile206Leu)
c.775A>C (p.Ile259Leu)
15g.38351167A>GCA391933362SPRED1c.838A>G (p.Ile280Val)
c.874A>G (p.Ile292Val)
c.616A>G (p.Ile206Val)
c.775A>G (p.Ile259Val)
 dbSNP gnomAD v4
15g.38351167A>TCA391933363SPRED1c.838A>T (p.Ile280Phe)
c.874A>T (p.Ile292Phe)
c.616A>T (p.Ile206Phe)
c.775A>T (p.Ile259Phe)
15g.38351168T>ACA391933364SPRED1c.839T>A (p.Ile280Asn)
c.875T>A (p.Ile292Asn)
c.617T>A (p.Ile206Asn)
c.776T>A (p.Ile259Asn)
15g.38351168T>CCA391933365SPRED1c.839T>C (p.Ile280Thr)
c.875T>C (p.Ile292Thr)
c.617T>C (p.Ile206Thr)
c.776T>C (p.Ile259Thr)
15g.38351168T>GCA391933366SPRED1c.839T>G (p.Ile280Ser)
c.875T>G (p.Ile292Ser)
c.617T>G (p.Ile206Ser)
c.776T>G (p.Ile259Ser)
15g.38351169T>ACA490011835SPRED1c.840T>A (p.Ile280=)
c.876T>A (p.Ile292=)
c.618T>A (p.Ile206=)
c.777T>A (p.Ile259=)
15g.38351169T>CCA490011834SPRED1c.840T>C (p.Ile280=)
c.876T>C (p.Ile292=)
c.618T>C (p.Ile206=)
c.777T>C (p.Ile259=)
15g.38351169T>GCA391933367SPRED1c.840T>G (p.Ile280Met)
c.876T>G (p.Ile292Met)
c.618T>G (p.Ile206Met)
c.777T>G (p.Ile259Met)
15g.38351170C>ACA391933368SPRED1c.841C>A (p.Gln281Lys)
c.877C>A (p.Gln293Lys)
c.619C>A (p.Gln207Lys)
c.778C>A (p.Gln260Lys)
15g.38351170C=CA2170812599SPRED1c.841C= (p.Gln281=)
c.877C= (p.Gln293=)
c.619C= (p.Gln207=)
c.778C= (p.Gln260=)
15g.38351170C>GCA391933369SPRED1c.841C>G (p.Gln281Glu)
c.877C>G (p.Gln293Glu)
c.619C>G (p.Gln207Glu)
c.778C>G (p.Gln260Glu)
15g.38351170C>TCA7470191SPRED1c.841C>T (p.Gln281Ter)
c.877C>T (p.Gln293Ter)
c.619C>T (p.Gln207Ter)
c.778C>T (p.Gln260Ter)
 ClinVar dbSNP ExAC
15g.38351171A=CA2170812600SPRED1c.842A= (p.Gln281=)
c.878A= (p.Gln293=)
c.620A= (p.Gln207=)
c.779A= (p.Gln260=)
15g.38351171A>CCA391933370SPRED1c.842A>C (p.Gln281Pro)
c.878A>C (p.Gln293Pro)
c.620A>C (p.Gln207Pro)
c.779A>C (p.Gln260Pro)
15g.38351171A>GCA391933371SPRED1c.842A>G (p.Gln281Arg)
c.878A>G (p.Gln293Arg)
c.620A>G (p.Gln207Arg)
c.779A>G (p.Gln260Arg)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
15g.38351171A>TCA391933372SPRED1c.842A>T (p.Gln281Leu)
c.878A>T (p.Gln293Leu)
c.620A>T (p.Gln207Leu)
c.779A>T (p.Gln260Leu)
15g.38351172G>ACA490011838SPRED1c.843G>A (p.Gln281=)
c.879G>A (p.Gln293=)
c.621G>A (p.Gln207=)
c.780G>A (p.Gln260=)
 ClinVar dbSNP
15g.38351172G>CCA391933374SPRED1c.843G>C (p.Gln281His)
c.879G>C (p.Gln293His)
c.621G>C (p.Gln207His)
c.780G>C (p.Gln260His)
 gnomAD v4
15g.38351172G=CA2170812601SPRED1c.843G= (p.Gln281=)
c.879G= (p.Gln293=)
c.621G= (p.Gln207=)
c.780G= (p.Gln260=)
15g.38351172G>TCA391933373SPRED1c.843G>T (p.Gln281His)
c.879G>T (p.Gln293His)
c.621G>T (p.Gln207His)
c.780G>T (p.Gln260His)
 dbSNP gnomAD v2 gnomAD v4
15g.38351173T>ACA391933375SPRED1c.844T>A (p.Phe282Ile)
c.880T>A (p.Phe294Ile)
c.622T>A (p.Phe208Ile)
c.781T>A (p.Phe261Ile)
15g.38351173T>CCA391933376SPRED1c.844T>C (p.Phe282Leu)
c.880T>C (p.Phe294Leu)
c.622T>C (p.Phe208Leu)
c.781T>C (p.Phe261Leu)
15g.38351173T>GCA391933377SPRED1c.844T>G (p.Phe282Val)
c.880T>G (p.Phe294Val)
c.622T>G (p.Phe208Val)
c.781T>G (p.Phe261Val)
15g.38351174T>ACA391933378SPRED1c.845T>A (p.Phe282Tyr)
c.881T>A (p.Phe294Tyr)
c.623T>A (p.Phe208Tyr)
c.782T>A (p.Phe261Tyr)
15g.38351174T>CCA391933379SPRED1c.845T>C (p.Phe282Ser)
c.881T>C (p.Phe294Ser)
c.623T>C (p.Phe208Ser)
c.782T>C (p.Phe261Ser)
15g.38351174T>GCA391933380SPRED1c.845T>G (p.Phe282Cys)
c.881T>G (p.Phe294Cys)
c.623T>G (p.Phe208Cys)
c.782T>G (p.Phe261Cys)
15g.38351175T>ACA391933381SPRED1c.846T>A (p.Phe282Leu)
c.882T>A (p.Phe294Leu)
c.624T>A (p.Phe208Leu)
c.783T>A (p.Phe261Leu)
15g.38351175T>CCA490011844SPRED1c.846T>C (p.Phe282=)
c.882T>C (p.Phe294=)
c.624T>C (p.Phe208=)
c.783T>C (p.Phe261=)
15g.38351175T>GCA391933382SPRED1c.846T>G (p.Phe282Leu)
c.882T>G (p.Phe294Leu)
c.624T>G (p.Phe208Leu)
c.783T>G (p.Phe261Leu)
15g.38351176T>ACA391933383SPRED1c.847T>A (p.Ser283Thr)
c.883T>A (p.Ser295Thr)
c.625T>A (p.Ser209Thr)
c.784T>A (p.Ser262Thr)
15g.38351176T>CCA391933384SPRED1c.847T>C (p.Ser283Pro)
c.883T>C (p.Ser295Pro)
c.625T>C (p.Ser209Pro)
c.784T>C (p.Ser262Pro)
15g.38351176T>GCA391933385SPRED1c.847T>G (p.Ser283Ala)
c.883T>G (p.Ser295Ala)
c.625T>G (p.Ser209Ala)
c.784T>G (p.Ser262Ala)
 gnomAD v4
15g.38351177C>ACA391933386SPRED1c.848C>A (p.Ser283Tyr)
c.884C>A (p.Ser295Tyr)
c.626C>A (p.Ser209Tyr)
c.785C>A (p.Ser262Tyr)
15g.38351177C>GCA391933387SPRED1c.848C>G (p.Ser283Cys)
c.884C>G (p.Ser295Cys)
c.626C>G (p.Ser209Cys)
c.785C>G (p.Ser262Cys)
15g.38351177C>TCA391933388SPRED1c.848C>T (p.Ser283Phe)
c.884C>T (p.Ser295Phe)
c.626C>T (p.Ser209Phe)
c.785C>T (p.Ser262Phe)
15g.38351178T>ACA490011849SPRED1c.849T>A (p.Ser283=)
c.885T>A (p.Ser295=)
c.627T>A (p.Ser209=)
c.786T>A (p.Ser262=)
15g.38351178T>CCA490011850SPRED1c.849T>C (p.Ser283=)
c.885T>C (p.Ser295=)
c.627T>C (p.Ser209=)
c.786T>C (p.Ser262=)
 dbSNP gnomAD v2 gnomAD v4
15g.38351178T>GCA490011851SPRED1c.849T>G (p.Ser283=)
c.885T>G (p.Ser295=)
c.627T>G (p.Ser209=)
c.786T>G (p.Ser262=)
 dbSNP gnomAD v4
15g.38351178T=CA2170812602SPRED1c.849T= (p.Ser283=)
c.885T= (p.Ser295=)
c.627T= (p.Ser209=)
c.786T= (p.Ser262=)
15g.38351179A>CCA391933391SPRED1c.850A>C (p.Lys284Gln)
c.886A>C (p.Lys296Gln)
c.628A>C (p.Lys210Gln)
c.787A>C (p.Lys263Gln)
15g.38351179A>GCA391933390SPRED1c.850A>G (p.Lys284Glu)
c.886A>G (p.Lys296Glu)
c.628A>G (p.Lys210Glu)
c.787A>G (p.Lys263Glu)
15g.38351179A>TCA391933389SPRED1c.850A>T (p.Lys284Ter)
c.886A>T (p.Lys296Ter)
c.628A>T (p.Lys210Ter)
c.787A>T (p.Lys263Ter)
15g.38351180A>CCA391933393SPRED1c.851A>C (p.Lys284Thr)
c.887A>C (p.Lys296Thr)
c.629A>C (p.Lys210Thr)
c.788A>C (p.Lys263Thr)
15g.38351180A>GCA391933392SPRED1c.851A>G (p.Lys284Arg)
c.887A>G (p.Lys296Arg)
c.629A>G (p.Lys210Arg)
c.788A>G (p.Lys263Arg)
15g.38351180A>TCA391933394SPRED1c.851A>T (p.Lys284Ile)
c.887A>T (p.Lys296Ile)
c.629A>T (p.Lys210Ile)
c.788A>T (p.Lys263Ile)
15g.38351181A=CA2170812603SPRED1c.852A= (p.Lys284=)
c.888A= (p.Lys296=)
c.630A= (p.Lys210=)
c.789A= (p.Lys263=)
15g.38351181A>CCA391933395SPRED1c.852A>C (p.Lys284Asn)
c.888A>C (p.Lys296Asn)
c.630A>C (p.Lys210Asn)
c.789A>C (p.Lys263Asn)
 dbSNP gnomAD v2
15g.38351181A>GCA490011854SPRED1c.852A>G (p.Lys284=)
c.888A>G (p.Lys296=)
c.630A>G (p.Lys210=)
c.789A>G (p.Lys263=)
 ClinVar dbSNP gnomAD v3 gnomAD v4
15g.38351181A>TCA391933396SPRED1c.852A>T (p.Lys284Asn)
c.888A>T (p.Lys296Asn)
c.630A>T (p.Lys210Asn)
c.789A>T (p.Lys263Asn)
15g.38351182C>ACA391933397SPRED1c.853C>A (p.Pro285Thr)
c.889C>A (p.Pro297Thr)
c.631C>A (p.Pro211Thr)
c.790C>A (p.Pro264Thr)
 gnomAD v4
15g.38351182C>GCA391933398SPRED1c.853C>G (p.Pro285Ala)
c.889C>G (p.Pro297Ala)
c.631C>G (p.Pro211Ala)
c.790C>G (p.Pro264Ala)
15g.38351182C>TCA391933399SPRED1c.853C>T (p.Pro285Ser)
c.889C>T (p.Pro297Ser)
c.631C>T (p.Pro211Ser)
c.790C>T (p.Pro264Ser)
15g.38351183C>ACA391933400SPRED1c.854C>A (p.Pro285Gln)
c.890C>A (p.Pro297Gln)
c.632C>A (p.Pro211Gln)
c.791C>A (p.Pro264Gln)
15g.38351183C=CA2170812604SPRED1c.854C= (p.Pro285=)
c.890C= (p.Pro297=)
c.632C= (p.Pro211=)
c.791C= (p.Pro264=)
15g.38351183C>GCA391933401SPRED1c.854C>G (p.Pro285Arg)
c.890C>G (p.Pro297Arg)
c.632C>G (p.Pro211Arg)
c.791C>G (p.Pro264Arg)
15g.38351183C>TCA269293448SPRED1c.854C>T (p.Pro285Leu)
c.890C>T (p.Pro297Leu)
c.632C>T (p.Pro211Leu)
c.791C>T (p.Pro264Leu)
 ClinVar dbSNP
15g.38351184A>CCA490011858SPRED1c.855A>C (p.Pro285=)
c.891A>C (p.Pro297=)
c.633A>C (p.Pro211=)
c.792A>C (p.Pro264=)
15g.38351184A>GCA490011859SPRED1c.855A>G (p.Pro285=)
c.891A>G (p.Pro297=)
c.633A>G (p.Pro211=)
c.792A>G (p.Pro264=)
15g.38351184A>TCA490011860SPRED1c.855A>T (p.Pro285=)
c.891A>T (p.Pro297=)
c.633A>T (p.Pro211=)
c.792A>T (p.Pro264=)
15g.38351185G>ACA391933402SPRED1c.856G>A (p.Asp286Asn)
c.892G>A (p.Asp298Asn)
c.634G>A (p.Asp212Asn)
c.793G>A (p.Asp265Asn)
 ClinVar dbSNP
15g.38351185G>CCA391933403SPRED1c.856G>C (p.Asp286His)
c.892G>C (p.Asp298His)
c.634G>C (p.Asp212His)
c.793G>C (p.Asp265His)
 gnomAD v4
15g.38351185G>TCA391933404SPRED1c.856G>T (p.Asp286Tyr)
c.892G>T (p.Asp298Tyr)
c.634G>T (p.Asp212Tyr)
c.793G>T (p.Asp265Tyr)
15g.38351186A>CCA391933405SPRED1c.857A>C (p.Asp286Ala)
c.893A>C (p.Asp298Ala)
c.635A>C (p.Asp212Ala)
c.794A>C (p.Asp265Ala)
15g.38351186A>GCA391933406SPRED1c.857A>G (p.Asp286Gly)
c.893A>G (p.Asp298Gly)
c.635A>G (p.Asp212Gly)
c.794A>G (p.Asp265Gly)
15g.38351186A>TCA391933407SPRED1c.857A>T (p.Asp286Val)
c.893A>T (p.Asp298Val)
c.635A>T (p.Asp212Val)
c.794A>T (p.Asp265Val)
15g.38351187C>ACA391933408SPRED1c.858C>A (p.Asp286Glu)
c.894C>A (p.Asp298Glu)
c.636C>A (p.Asp212Glu)
c.795C>A (p.Asp265Glu)
15g.38351187C=CA2170812605SPRED1c.858C= (p.Asp286=)
c.894C= (p.Asp298=)
c.636C= (p.Asp212=)
c.795C= (p.Asp265=)
15g.38351187C>GCA391933409SPRED1c.858C>G (p.Asp286Glu)
c.894C>G (p.Asp298Glu)
c.636C>G (p.Asp212Glu)
c.795C>G (p.Asp265Glu)
 dbSNP gnomAD v2 gnomAD v4
15g.38351187C>TCA490011865SPRED1c.858C>T (p.Asp286=)
c.894C>T (p.Asp298=)
c.636C>T (p.Asp212=)
c.795C>T (p.Asp265=)
15g.38351188A>CCA391933410SPRED1c.859A>C (p.Ser287Arg)
c.895A>C (p.Ser299Arg)
c.637A>C (p.Ser213Arg)
c.796A>C (p.Ser266Arg)
15g.38351188A>GCA391933411SPRED1c.859A>G (p.Ser287Gly)
c.895A>G (p.Ser299Gly)
c.637A>G (p.Ser213Gly)
c.796A>G (p.Ser266Gly)
 gnomAD v4
15g.38351188A>TCA391933412SPRED1c.859A>T (p.Ser287Cys)
c.895A>T (p.Ser299Cys)
c.637A>T (p.Ser213Cys)
c.796A>T (p.Ser266Cys)
15g.38351189G>ACA391933413SPRED1c.860G>A (p.Ser287Asn)
c.896G>A (p.Ser299Asn)
c.638G>A (p.Ser213Asn)
c.797G>A (p.Ser266Asn)
 ClinVar gnomAD v4
15g.38351189G>CCA391933414SPRED1c.860G>C (p.Ser287Thr)
c.896G>C (p.Ser299Thr)
c.638G>C (p.Ser213Thr)
c.797G>C (p.Ser266Thr)
15g.38351189G>TCA391933415SPRED1c.860G>T (p.Ser287Ile)
c.896G>T (p.Ser299Ile)
c.638G>T (p.Ser213Ile)
c.797G>T (p.Ser266Ile)
15g.38351190T>ACA391933416SPRED1c.861T>A (p.Ser287Arg)
c.897T>A (p.Ser299Arg)
c.639T>A (p.Ser213Arg)
c.798T>A (p.Ser266Arg)
15g.38351190T>CCA490011870SPRED1c.861T>C (p.Ser287=)
c.897T>C (p.Ser299=)
c.639T>C (p.Ser213=)
c.798T>C (p.Ser266=)
 ClinVar gnomAD v4
15g.38351190T>GCA391933417SPRED1c.861T>G (p.Ser287Arg)
c.897T>G (p.Ser299Arg)
c.639T>G (p.Ser213Arg)
c.798T>G (p.Ser266Arg)
15g.38351190T=CA2170812606SPRED1c.861T= (p.Ser287=)
c.897T= (p.Ser299=)
c.639T= (p.Ser213=)
c.798T= (p.Ser266=)
15g.38351191A=CA2170812607SPRED1c.862A= (p.Lys288=)
c.898A= (p.Lys300=)
c.640A= (p.Lys214=)
c.799A= (p.Lys267=)
15g.38351191A>CCA391933418SPRED1c.862A>C (p.Lys288Gln)
c.898A>C (p.Lys300Gln)
c.640A>C (p.Lys214Gln)
c.799A>C (p.Lys267Gln)
15g.38351191A>GCA391933419SPRED1c.862A>G (p.Lys288Glu)
c.898A>G (p.Lys300Glu)
c.640A>G (p.Lys214Glu)
c.799A>G (p.Lys267Glu)
 dbSNP gnomAD v4
15g.38351191A>TCA391933420SPRED1c.862A>T (p.Lys288Ter)
c.898A>T (p.Lys300Ter)
c.640A>T (p.Lys214Ter)
c.799A>T (p.Lys267Ter)
15g.38351196dupCA617561332SPRED1c.867dup (p.Ser290IlefsTer10)
c.903dup (p.Ser302IlefsTer10)
c.645dup (p.Ser216IlefsTer10)
c.804dup (p.Ser269IlefsTer10)
 ClinVar dbSNP gnomAD v2 gnomAD v4
15g.38351192A>CCA391933422SPRED1c.863A>C (p.Lys288Thr)
c.899A>C (p.Lys300Thr)
c.641A>C (p.Lys214Thr)
c.800A>C (p.Lys267Thr)
 gnomAD v4 COSMIC
15g.38351192A>GCA391933423SPRED1c.863A>G (p.Lys288Arg)
c.899A>G (p.Lys300Arg)
c.641A>G (p.Lys214Arg)
c.800A>G (p.Lys267Arg)
15g.38351192A>TCA391933421SPRED1c.863A>T (p.Lys288Ile)
c.899A>T (p.Lys300Ile)
c.641A>T (p.Lys214Ile)
c.800A>T (p.Lys267Ile)
15g.38351193A=CA2170812608SPRED1c.864A= (p.Lys288=)
c.900A= (p.Lys300=)
c.642A= (p.Lys214=)
c.801A= (p.Lys267=)
15g.38351193A>CCA7470192SPRED1c.864A>C (p.Lys288Asn)
c.900A>C (p.Lys300Asn)
c.642A>C (p.Lys214Asn)
c.801A>C (p.Lys267Asn)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
15g.38351193A>GCA490011875SPRED1c.864A>G (p.Lys288=)
c.900A>G (p.Lys300=)
c.642A>G (p.Lys214=)
c.801A>G (p.Lys267=)
15g.38351193A>TCA391933424SPRED1c.864A>T (p.Lys288Asn)
c.900A>T (p.Lys300Asn)
c.642A>T (p.Lys214Asn)
c.801A>T (p.Lys267Asn)
15g.38351194A>CCA391933425SPRED1c.865A>C (p.Lys289Gln)
c.901A>C (p.Lys301Gln)
c.643A>C (p.Lys215Gln)
c.802A>C (p.Lys268Gln)
15g.38351194A>GCA391933426SPRED1c.865A>G (p.Lys289Glu)
c.901A>G (p.Lys301Glu)
c.643A>G (p.Lys215Glu)
c.802A>G (p.Lys268Glu)
15g.38351194A>TCA391933427SPRED1c.865A>T (p.Lys289Ter)
c.901A>T (p.Lys301Ter)
c.643A>T (p.Lys215Ter)
c.802A>T (p.Lys268Ter)
15g.38351194_38351203delinsAAATCAGACTCA2170812609SPRED1c.865_874delinsAAATCAGACT (p.Lys289=)
c.901_910delinsAAATCAGACT (p.Lys301=)
c.643_652delinsAAATCAGACT (p.Lys215=)
c.802_811delinsAAATCAGACT (p.Lys268=)
15g.38351195A=CA2170812610SPRED1c.866A= (p.Lys289=)
c.902A= (p.Lys301=)
c.644A= (p.Lys215=)
c.803A= (p.Lys268=)
15g.38351195A>CCA7470194SPRED1c.866A>C (p.Lys289Thr)
c.902A>C (p.Lys301Thr)
c.644A>C (p.Lys215Thr)
c.803A>C (p.Lys268Thr)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.38351195A>GCA391933428SPRED1c.866A>G (p.Lys289Arg)
c.902A>G (p.Lys301Arg)
c.644A>G (p.Lys215Arg)
c.803A>G (p.Lys268Arg)
15g.38351195A>TCA391933429SPRED1c.866A>T (p.Lys289Ile)
c.902A>T (p.Lys301Ile)
c.644A>T (p.Lys215Ile)
c.803A>T (p.Lys268Ile)
 dbSNP gnomAD v2 gnomAD v4
15g.38351196_38351204delCA7470193SPRED1c.867_875del (p.Lys289_Tyr292delinsAsn)
c.903_911del (p.Lys301_Tyr304delinsAsn)
c.645_653del (p.Lys215_Tyr218delinsAsn)
c.804_812del (p.Lys268_Tyr271delinsAsn)
 dbSNP ExAC gnomAD v2 gnomAD v4
15g.38351196A=CA2170812611SPRED1c.867A= (p.Lys289=)
c.903A= (p.Lys301=)
c.645A= (p.Lys215=)
c.804A= (p.Lys268=)
15g.38351196A>CCA391933430SPRED1c.867A>C (p.Lys289Asn)
c.903A>C (p.Lys301Asn)
c.645A>C (p.Lys215Asn)
c.804A>C (p.Lys268Asn)
15g.38351196A>GCA490011880SPRED1c.867A>G (p.Lys289=)
c.903A>G (p.Lys301=)
c.645A>G (p.Lys215=)
c.804A>G (p.Lys268=)
15g.38351196A>TCA391933431SPRED1c.867A>T (p.Lys289Asn)
c.903A>T (p.Lys301Asn)
c.645A>T (p.Lys215Asn)
c.804A>T (p.Lys268Asn)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
15g.38351197T>ACA391933433SPRED1c.868T>A (p.Ser290Thr)
c.904T>A (p.Ser302Thr)
c.646T>A (p.Ser216Thr)
c.805T>A (p.Ser269Thr)
15g.38351197T>CCA391933434SPRED1c.868T>C (p.Ser290Pro)
c.904T>C (p.Ser302Pro)
c.646T>C (p.Ser216Pro)
c.805T>C (p.Ser269Pro)
15g.38351197T>GCA391933432SPRED1c.868T>G (p.Ser290Ala)
c.904T>G (p.Ser302Ala)
c.646T>G (p.Ser216Ala)
c.805T>G (p.Ser269Ala)
15g.38351198C>ACA391933435SPRED1c.869C>A (p.Ser290Ter)
c.905C>A (p.Ser302Ter)
c.647C>A (p.Ser216Ter)
c.806C>A (p.Ser269Ter)
15g.38351198C>GCA391933436SPRED1c.869C>G (p.Ser290Ter)
c.905C>G (p.Ser302Ter)
c.647C>G (p.Ser216Ter)
c.806C>G (p.Ser269Ter)
15g.38351198C>TCA391933437SPRED1c.869C>T (p.Ser290Leu)
c.905C>T (p.Ser302Leu)
c.647C>T (p.Ser216Leu)
c.806C>T (p.Ser269Leu)
15g.38351199A>CCA490011888SPRED1c.870A>C (p.Ser290=)
c.906A>C (p.Ser302=)
c.648A>C (p.Ser216=)
c.807A>C (p.Ser269=)
15g.38351199A>GCA490011890SPRED1c.870A>G (p.Ser290=)
c.906A>G (p.Ser302=)
c.648A>G (p.Ser216=)
c.807A>G (p.Ser269=)
15g.38351199A>TCA490011893SPRED1c.870A>T (p.Ser290=)
c.906A>T (p.Ser302=)
c.648A>T (p.Ser216=)
c.807A>T (p.Ser269=)
15g.38351200G>ACA391933438SPRED1c.871G>A (p.Asp291Asn)
c.907G>A (p.Asp303Asn)
c.649G>A (p.Asp217Asn)
c.808G>A (p.Asp270Asn)
15g.38351200G>CCA391933439SPRED1c.871G>C (p.Asp291His)
c.907G>C (p.Asp303His)
c.649G>C (p.Asp217His)
c.808G>C (p.Asp270His)
15g.38351200G>TCA391933440SPRED1c.871G>T (p.Asp291Tyr)
c.907G>T (p.Asp303Tyr)
c.649G>T (p.Asp217Tyr)
c.808G>T (p.Asp270Tyr)
15g.38351201A>CCA391933441SPRED1c.872A>C (p.Asp291Ala)
c.908A>C (p.Asp303Ala)
c.650A>C (p.Asp217Ala)
c.809A>C (p.Asp270Ala)
15g.38351201A>GCA391933443SPRED1c.872A>G (p.Asp291Gly)
c.908A>G (p.Asp303Gly)
c.650A>G (p.Asp217Gly)
c.809A>G (p.Asp270Gly)
15g.38351201A>TCA391933442SPRED1c.872A>T (p.Asp291Val)
c.908A>T (p.Asp303Val)
c.650A>T (p.Asp217Val)
c.809A>T (p.Asp270Val)
 ClinVar

Number of alleles fetched