Chr Mutation (hg38) CAid Gene Transcript Linkouts
9g.136673795_136673855delCA2692653751AGPAT2c.734_794del (p.Val245GlyfsTer22)
c.638_698del (p.Val213GlyfsTer22)
n.662_722del
 gnomAD v4
9g.136673829_136673837delCA16042192AGPAT2c.755_763del (p.Met252_Thr254del)
c.659_667del (p.Met220_Thr222del)
n.683_691del
 ClinVar dbSNP gnomAD v4
9g.136673829T>ACA375577263AGPAT2c.760A>T (p.Thr254Ser)
c.664A>T (p.Thr222Ser)
n.688A>T
9g.136673829T>CCA375577264AGPAT2c.760A>G (p.Thr254Ala)
c.664A>G (p.Thr222Ala)
n.688A>G
9g.136673829T>GCA375577265AGPAT2c.760A>C (p.Thr254Pro)
c.664A>C (p.Thr222Pro)
n.688A>C
9g.136673830C>ACA375577267AGPAT2c.759G>T (p.Arg253Ser)
c.663G>T (p.Arg221Ser)
n.687G>T
 gnomAD v4
9g.136673830C>GCA375577269AGPAT2c.759G>C (p.Arg253Ser)
c.663G>C (p.Arg221Ser)
n.687G>C
9g.136673830C>TCA467737008AGPAT2c.759G>A (p.Arg253=)
c.663G>A (p.Arg221=)
n.687G>A
 dbSNP
9g.136673831C>ACA375577271AGPAT2c.758G>T (p.Arg253Met)
c.662G>T (p.Arg221Met)
n.686G>T
 COSMIC
9g.136673831C>GCA375577272AGPAT2c.758G>C (p.Arg253Thr)
c.662G>C (p.Arg221Thr)
n.686G>C
9g.136673831C>TCA5342827AGPAT2c.758G>A (p.Arg253Lys)
c.662G>A (p.Arg221Lys)
n.686G>A
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
9g.136673832T>ACA375577274AGPAT2c.757A>T (p.Arg253Trp)
c.661A>T (p.Arg221Trp)
n.685A>T
9g.136673832T>CCA375577273AGPAT2c.757A>G (p.Arg253Gly)
c.661A>G (p.Arg221Gly)
n.685A>G
 gnomAD v4
9g.136673832T>GCA467737009AGPAT2c.757A>C (p.Arg253=)
c.661A>C (p.Arg221=)
n.685A>C
9g.136673833C>ACA375577276AGPAT2c.756G>T (p.Met252Ile)
c.660G>T (p.Met220Ile)
n.684G>T
9g.136673833C>GCA375577278AGPAT2c.756G>C (p.Met252Ile)
c.660G>C (p.Met220Ile)
n.684G>C
9g.136673833C>TCA375577279AGPAT2c.756G>A (p.Met252Ile)
c.660G>A (p.Met220Ile)
n.684G>A
 dbSNP gnomAD v3 gnomAD v4
9g.136673834_136673840dupCA2692653754AGPAT2c.750_756dup (p.Arg253GlyfsTer?)
c.654_660dup (p.Arg221GlyfsTer?)
n.678_684dup
 gnomAD v4
9g.136673834A>CCA375577281AGPAT2c.755T>G (p.Met252Arg)
c.659T>G (p.Met220Arg)
n.683T>G
9g.136673834A>GCA375577283AGPAT2c.755T>C (p.Met252Thr)
c.659T>C (p.Met220Thr)
n.683T>C
 ClinVar dbSNP gnomAD v2 gnomAD v4
9g.136673834A>TCA375577284AGPAT2c.755T>A (p.Met252Lys)
c.659T>A (p.Met220Lys)
n.683T>A
9g.136673835T>ACA375577285AGPAT2c.754A>T (p.Met252Leu)
c.658A>T (p.Met220Leu)
n.682A>T
9g.136673835T>CCA5342828AGPAT2c.754A>G (p.Met252Val)
c.658A>G (p.Met220Val)
n.682A>G
 dbSNP ExAC gnomAD v2 gnomAD v4
9g.136673835T>GCA375577288AGPAT2c.754A>C (p.Met252Leu)
c.658A>C (p.Met220Leu)
n.682A>C
9g.136673836G>ACA467737010AGPAT2c.753C>T (p.Ala251=)
c.657C>T (p.Ala219=)
n.681C>T
 gnomAD v4
9g.136673836G>CCA467737011AGPAT2c.753C>G (p.Ala251=)
c.657C>G (p.Ala219=)
n.681C>G
9g.136673836G>TCA467737012AGPAT2c.753C>A (p.Ala251=)
c.657C>A (p.Ala219=)
n.681C>A
9g.136673837G>ACA375577290AGPAT2c.752C>T (p.Ala251Val)
c.656C>T (p.Ala219Val)
n.680C>T
 gnomAD v4
9g.136673837G>CCA375577291AGPAT2c.752C>G (p.Ala251Gly)
c.656C>G (p.Ala219Gly)
n.680C>G
9g.136673837G>TCA375577292AGPAT2c.752C>A (p.Ala251Asp)
c.656C>A (p.Ala219Asp)
n.680C>A
9g.136673838C>ACA375577293AGPAT2c.751G>T (p.Ala251Ser)
c.655G>T (p.Ala219Ser)
n.679G>T
9g.136673838C>GCA375577296AGPAT2c.751G>C (p.Ala251Pro)
c.655G>C (p.Ala219Pro)
n.679G>C
9g.136673838C>TCA375577294AGPAT2c.751G>A (p.Ala251Thr)
c.655G>A (p.Ala219Thr)
n.679G>A
 dbSNP gnomAD v2 gnomAD v4
9g.136673839C>ACA467737013AGPAT2c.750G>T (p.Arg250=)
c.654G>T (p.Arg218=)
n.678G>T
9g.136673839C>GCA467737014AGPAT2c.750G>C (p.Arg250=)
c.654G>C (p.Arg218=)
n.678G>C
9g.136673839C>TCA467737015AGPAT2c.750G>A (p.Arg250=)
c.654G>A (p.Arg218=)
n.678G>A
9g.136673840C>ACA375577298AGPAT2c.749G>T (p.Arg250Leu)
c.653G>T (p.Arg218Leu)
n.677G>T
 gnomAD v4
9g.136673840C>GCA375577301AGPAT2c.749G>C (p.Arg250Pro)
c.653G>C (p.Arg218Pro)
n.677G>C
 gnomAD v4
9g.136673840C>TCA5342829AGPAT2c.749G>A (p.Arg250Gln)
c.653G>A (p.Arg218Gln)
n.677G>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
9g.136673842_136673861dupCA2692653755AGPAT2c.730_749dup (p.Ala251SerfsTer9)
c.634_653dup (p.Ala219SerfsTer9)
n.658_677dup
 gnomAD v4
9g.136673841G>ACA5342830AGPAT2c.748C>T (p.Arg250Trp)
c.652C>T (p.Arg218Trp)
n.676C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
9g.136673841G>CCA375577306AGPAT2c.748C>G (p.Arg250Gly)
c.652C>G (p.Arg218Gly)
n.676C>G
 dbSNP
9g.136673841G>TCA467737016AGPAT2c.748C>A (p.Arg250=)
c.652C>A (p.Arg218=)
n.676C>A
 gnomAD v4 COSMIC
9g.136673845_136673851dupCA2579519878AGPAT2c.742_748dup (p.Arg250LeufsTer?)
c.646_652dup (p.Arg218LeufsTer?)
n.670_676dup
 gnomAD v4
9g.136673843_136673865dupCA2692653756AGPAT2c.726_748dup (p.Arg250LeufsTer11)
c.630_652dup (p.Arg218LeufsTer11)
n.654_676dup
 gnomAD v4
9g.136673842G>ACA5342831AGPAT2c.747C>T (p.His249=)
c.651C>T (p.His217=)
n.675C>T
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
9g.136673842G>CCA375577309AGPAT2c.747C>G (p.His249Gln)
c.651C>G (p.His217Gln)
n.675C>G
9g.136673842G>TCA375577310AGPAT2c.747C>A (p.His249Gln)
c.651C>A (p.His217Gln)
n.675C>A
9g.136673844_136673852dupCA591367748AGPAT2c.739_747dup (p.His249_Arg250insThrCysHis)
c.643_651dup (p.His217_Arg218insThrCysHis)
n.667_675dup
 dbSNP gnomAD v2 gnomAD v4
9g.136673843T>ACA375577312AGPAT2c.746A>T (p.His249Leu)
c.650A>T (p.His217Leu)
n.674A>T
9g.136673843T>CCA375577313AGPAT2c.746A>G (p.His249Arg)
c.650A>G (p.His217Arg)
n.674A>G
9g.136673843T>GCA375577314AGPAT2c.746A>C (p.His249Pro)
c.650A>C (p.His217Pro)
n.674A>C
 dbSNP
9g.136673844G>ACA201626841AGPAT2c.745C>T (p.His249Tyr)
c.649C>T (p.His217Tyr)
n.673C>T
 dbSNP gnomAD v3 gnomAD v4
9g.136673844G>CCA375577317AGPAT2c.745C>G (p.His249Asp)
c.649C>G (p.His217Asp)
n.673C>G
 gnomAD v4
9g.136673844G>TCA375577319AGPAT2c.745C>A (p.His249Asn)
c.649C>A (p.His217Asn)
n.673C>A
9g.136673844_136673853dupCA2579519879AGPAT2c.736_745dup (p.His249ArgfsTer?)
c.640_649dup (p.His217ArgfsTer?)
n.664_673dup
9g.136673845G>ACA201626851AGPAT2c.744C>T (p.Cys248=)
c.648C>T (p.Cys216=)
n.672C>T
 dbSNP gnomAD v4
9g.136673845G>CCA375577321AGPAT2c.744C>G (p.Cys248Trp)
c.648C>G (p.Cys216Trp)
n.672C>G
9g.136673845G>TCA375577323AGPAT2c.744C>A (p.Cys248Ter)
c.648C>A (p.Cys216Ter)
n.672C>A
9g.136673847_136673860dupCA2692653757AGPAT2c.731_744dup (p.His249SerfsTer9)
c.635_648dup (p.His217SerfsTer9)
n.659_672dup
 gnomAD v4
9g.136673846C>ACA375577326AGPAT2c.743G>T (p.Cys248Phe)
c.647G>T (p.Cys216Phe)
n.671G>T
 gnomAD v4
9g.136673846C>GCA375577329AGPAT2c.743G>C (p.Cys248Ser)
c.647G>C (p.Cys216Ser)
n.671G>C
9g.136673846C>TCA375577327AGPAT2c.743G>A (p.Cys248Tyr)
c.647G>A (p.Cys216Tyr)
n.671G>A
9g.136673847_136673853delCA2579519880AGPAT2c.737_743del (p.Asp246AlafsTer5)
c.641_647del (p.Asp214AlafsTer5)
n.665_671del
9g.136673847_136673868dupCA2786279702AGPAT2c.722_743dup (p.His249ProfsTer?)
c.626_647dup (p.His217ProfsTer?)
n.650_671dup
9g.136673847A>CCA375577332AGPAT2c.742T>G (p.Cys248Gly)
c.646T>G (p.Cys216Gly)
n.670T>G
 dbSNP
9g.136673847A>GCA375577333AGPAT2c.742T>C (p.Cys248Arg)
c.646T>C (p.Cys216Arg)
n.670T>C
 gnomAD v4
9g.136673847A>TCA375577335AGPAT2c.742T>A (p.Cys248Ser)
c.646T>A (p.Cys216Ser)
n.670T>A
9g.136673847_136673848delCA2579519881AGPAT2c.741_742del (p.Cys248ProfsTer?)
c.645_646del (p.Cys216ProfsTer?)
n.669_670del
9g.136673848G>ACA5342832AGPAT2c.741C>T (p.Thr247=)
c.645C>T (p.Thr215=)
n.669C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
9g.136673848G>CCA467737017AGPAT2c.741C>G (p.Thr247=)
c.645C>G (p.Thr215=)
n.669C>G
9g.136673848G=CA2580903230AGPAT2c.741C= (p.Thr247=)
c.645C= (p.Thr215=)
n.669C=
9g.136673848G>TCA467737018AGPAT2c.741C>A (p.Thr247=)
c.645C>A (p.Thr215=)
n.669C>A
 gnomAD v4
9g.136673849G>ACA201626858AGPAT2c.740C>T (p.Thr247Ile)
c.644C>T (p.Thr215Ile)
n.668C>T
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
9g.136673849G>CCA375577338AGPAT2c.740C>G (p.Thr247Ser)
c.644C>G (p.Thr215Ser)
n.668C>G
9g.136673849G>TCA375577340AGPAT2c.740C>A (p.Thr247Asn)
c.644C>A (p.Thr215Asn)
n.668C>A
 gnomAD v4
9g.136673850T>ACA375577342AGPAT2c.739A>T (p.Thr247Ser)
c.643A>T (p.Thr215Ser)
n.667A>T
9g.136673850T>CCA375577344AGPAT2c.739A>G (p.Thr247Ala)
c.643A>G (p.Thr215Ala)
n.667A>G
 gnomAD v4
9g.136673850T>GCA375577346AGPAT2c.739A>C (p.Thr247Pro)
c.643A>C (p.Thr215Pro)
n.667A>C
 dbSNP
9g.136673857_136673858insTTGTCCACGCA2692653758AGPAT2c.739_740insACGTGGACA (p.Asp246_Thr247insAsnValAsp)
c.643_644insACGTGGACA (p.Asp214_Thr215insAsnValAsp)
n.667_668insACGTGGACA
 gnomAD v4
9g.136673851G>ACA467737019AGPAT2c.738C>T (p.Asp246=)
c.642C>T (p.Asp214=)
n.666C>T
 dbSNP gnomAD v3 gnomAD v4
9g.136673851G>CCA375577349AGPAT2c.738C>G (p.Asp246Glu)
c.642C>G (p.Asp214Glu)
n.666C>G
9g.136673851G>TCA375577347AGPAT2c.738C>A (p.Asp246Glu)
c.642C>A (p.Asp214Glu)
n.666C>A
9g.136673851_136673859delCA2497275506AGPAT2c.730_738del (p.Leu244_Asp246del)
c.634_642del (p.Leu212_Asp214del)
n.658_666del
 dbSNP
9g.136673852T>ACA375577350AGPAT2c.737A>T (p.Asp246Val)
c.641A>T (p.Asp214Val)
n.665A>T
9g.136673852T>CCA375577351AGPAT2c.737A>G (p.Asp246Gly)
c.641A>G (p.Asp214Gly)
n.665A>G
 gnomAD v4
9g.136673852T>GCA375577352AGPAT2c.737A>C (p.Asp246Ala)
c.641A>C (p.Asp214Ala)
n.665A>C
9g.136673853C>ACA375577354AGPAT2c.736G>T (p.Asp246Tyr)
c.640G>T (p.Asp214Tyr)
n.664G>T
9g.136673853C>GCA375577356AGPAT2c.736G>C (p.Asp246His)
c.640G>C (p.Asp214His)
n.664G>C
9g.136673853C>TCA375577358AGPAT2c.736G>A (p.Asp246Asn)
c.640G>A (p.Asp214Asn)
n.664G>A
9g.136673853_136673865dupCA591367749AGPAT2c.724_736dup (p.Asp246AlafsTer?)
c.628_640dup (p.Asp214AlafsTer?)
n.652_664dup
 dbSNP gnomAD v2 gnomAD v4
9g.136673854C>ACA467737026AGPAT2c.735G>T (p.Val245=)
c.639G>T (p.Val213=)
n.663G>T
9g.136673854C>GCA467737028AGPAT2c.735G>C (p.Val245=)
c.639G>C (p.Val213=)
n.663G>C
9g.136673854C>TCA467737030AGPAT2c.735G>A (p.Val245=)
c.639G>A (p.Val213=)
n.663G>A
9g.136673855A>CCA375577360AGPAT2c.734T>G (p.Val245Gly)
c.638T>G (p.Val213Gly)
n.662T>G
 dbSNP
9g.136673855A>GCA375577362AGPAT2c.734T>C (p.Val245Ala)
c.638T>C (p.Val213Ala)
n.662T>C
9g.136673855A>TCA375577364AGPAT2c.734T>A (p.Val245Glu)
c.638T>A (p.Val213Glu)
n.662T>A
9g.136673856C>ACA375577367AGPAT2c.733G>T (p.Val245Leu)
c.637G>T (p.Val213Leu)
n.661G>T
9g.136673856C>GCA375577369AGPAT2c.733G>C (p.Val245Leu)
c.637G>C (p.Val213Leu)
n.661G>C
 dbSNP gnomAD v2 gnomAD v4
9g.136673856C>TCA5342833AGPAT2c.733G>A (p.Val245Met)
c.637G>A (p.Val213Met)
n.661G>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
9g.136673858_136673861dupCA2497275507AGPAT2c.730_733dup (p.Val245AlafsTer?)
c.634_637dup (p.Val213AlafsTer?)
n.658_661dup
 dbSNP
9g.136673858_136673873dupCA2692653759AGPAT2c.718_733dup (p.Val245GlyfsTer?)
c.622_637dup (p.Val213GlyfsTer?)
n.646_661dup
 gnomAD v4
9g.136673857_136673874dupCA591367750AGPAT2c.716_733dup (p.Leu244_Val245insAlaAspValProAlaLeu)
c.620_637dup (p.Leu212_Val213insAlaAspValProAlaLeu)
n.644_661dup
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
9g.136673858_136673876dupCA2692653760AGPAT2c.715_733dup (p.Val245GlyfsTer?)
c.619_637dup (p.Val213GlyfsTer?)
n.643_661dup
 gnomAD v4
9g.136673857G>ACA5342834AGPAT2c.732C>T (p.Leu244=)
c.636C>T (p.Leu212=)
n.660C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
9g.136673857G>CCA467737041AGPAT2c.732C>G (p.Leu244=)
c.636C>G (p.Leu212=)
n.660C>G
9g.136673857G>TCA467737042AGPAT2c.732C>A (p.Leu244=)
c.636C>A (p.Leu212=)
n.660C>A
 gnomAD v4
9g.136673858A>CCA375577375AGPAT2c.731T>G (p.Leu244Arg)
c.635T>G (p.Leu212Arg)
n.659T>G
9g.136673858A>GCA375577381AGPAT2c.731T>C (p.Leu244Pro)
c.635T>C (p.Leu212Pro)
n.659T>C
9g.136673858A>TCA375577378AGPAT2c.731T>A (p.Leu244His)
c.635T>A (p.Leu212His)
n.659T>A
9g.136673859G>ACA375577384AGPAT2c.730C>T (p.Leu244Phe)
c.634C>T (p.Leu212Phe)
n.658C>T
9g.136673859G>CCA375577387AGPAT2c.730C>G (p.Leu244Val)
c.634C>G (p.Leu212Val)
n.658C>G
9g.136673859G>TCA375577390AGPAT2c.730C>A (p.Leu244Ile)
c.634C>A (p.Leu212Ile)
n.658C>A
 gnomAD v4
9g.136673859_136673870dupCA2579519882AGPAT2c.719_730dup (p.Ala243_Leu244insHisValProAla)
c.623_634dup (p.Ala211_Leu212insHisValProAla)
n.647_658dup
9g.136673860delCA2692653761AGPAT2c.729del (p.Leu244SerfsTer9)
c.633del (p.Leu212SerfsTer9)
n.657del
 gnomAD v4
9g.136673860C>ACA5342836AGPAT2c.729G>T (p.Ala243=)
c.633G>T (p.Ala211=)
n.657G>T
 dbSNP ExAC gnomAD v2 gnomAD v4
9g.136673860C>GCA467737048AGPAT2c.729G>C (p.Ala243=)
c.633G>C (p.Ala211=)
n.657G>C
 gnomAD v4
9g.136673860C>TCA5342835AGPAT2c.729G>A (p.Ala243=)
c.633G>A (p.Ala211=)
n.657G>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
9g.136673861delCA2692653762AGPAT2c.728del (p.Ala243GlyfsTer10)
c.632del (p.Ala211GlyfsTer10)
n.656del
 gnomAD v4
9g.136673861G>ACA5342838AGPAT2c.728C>T (p.Ala243Val)
c.632C>T (p.Ala211Val)
n.656C>T
 dbSNP ExAC gnomAD v3 gnomAD v4 COSMIC
9g.136673861G>CCA375577399AGPAT2c.728C>G (p.Ala243Gly)
c.632C>G (p.Ala211Gly)
n.656C>G
9g.136673861G>TCA5342837AGPAT2c.728C>A (p.Ala243Glu)
c.632C>A (p.Ala211Glu)
n.656C>A
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
9g.136673862C>ACA375577403AGPAT2c.727G>T (p.Ala243Ser)
c.631G>T (p.Ala211Ser)
n.655G>T
 gnomAD v4
9g.136673862C>GCA375577405AGPAT2c.727G>C (p.Ala243Pro)
c.631G>C (p.Ala211Pro)
n.655G>C
9g.136673862C>TCA375577408AGPAT2c.727G>A (p.Ala243Thr)
c.631G>A (p.Ala211Thr)
n.655G>A
9g.136673863A>CCA467737059AGPAT2c.726T>G (p.Pro242=)
c.630T>G (p.Pro210=)
n.654T>G
9g.136673863A>GCA467737060AGPAT2c.726T>C (p.Pro242=)
c.630T>C (p.Pro210=)
n.654T>C
9g.136673863A>TCA467737062AGPAT2c.726T>A (p.Pro242=)
c.630T>A (p.Pro210=)
n.654T>A
 gnomAD v4
9g.136673863_136673869delCA2692653763AGPAT2c.720_726del (p.Asp240GlufsTer11)
c.624_630del (p.Asp208GlufsTer11)
n.648_654del
 gnomAD v4
9g.136673864G>ACA375577415AGPAT2c.725C>T (p.Pro242Leu)
c.629C>T (p.Pro210Leu)
n.653C>T
 gnomAD v4
9g.136673864G>CCA375577417AGPAT2c.725C>G (p.Pro242Arg)
c.629C>G (p.Pro210Arg)
n.653C>G
9g.136673864G>TCA375577412AGPAT2c.725C>A (p.Pro242His)
c.629C>A (p.Pro210His)
n.653C>A
9g.136673865G>ACA375577424AGPAT2c.724C>T (p.Pro242Ser)
c.628C>T (p.Pro210Ser)
n.652C>T
9g.136673865G>CCA5342839AGPAT2c.724C>G (p.Pro242Ala)
c.628C>G (p.Pro210Ala)
n.652C>G
 dbSNP ExAC gnomAD v2 gnomAD v4
9g.136673865G>TCA375577422AGPAT2c.724C>A (p.Pro242Thr)
c.628C>A (p.Pro210Thr)
n.652C>A
9g.136673866_136673869delCA2579519883AGPAT2c.721_724del (p.Val241LeufsTer11)
c.625_628del (p.Val209LeufsTer11)
n.649_652del
9g.136673875_136673876insTCACTGGACGTCCGCCCA2692653764AGPAT2c.724_725insAGTGAGGCGGACGTCC (p.Pro242GlnfsTer2)
c.628_629insAGTGAGGCGGACGTCC (p.Pro210GlnfsTer2)
n.652_653insAGTGAGGCGGACGTCC
 gnomAD v4
9g.136673866G>ACA467737070AGPAT2c.723C>T (p.Val241=)
c.627C>T (p.Val209=)
n.651C>T
 dbSNP gnomAD v3 gnomAD v4
9g.136673866G>CCA467737072AGPAT2c.723C>G (p.Val241=)
c.627C>G (p.Val209=)
n.651C>G
9g.136673866G>TCA467737074AGPAT2c.723C>A (p.Val241=)
c.627C>A (p.Val209=)
n.651C>A
9g.136673867_136673873dupCA2692653765AGPAT2c.717_723dup (p.Pro242GlyfsTer?)
c.621_627dup (p.Pro210GlyfsTer?)
n.645_651dup
 gnomAD v4
9g.136673867A>CCA375577427AGPAT2c.722T>G (p.Val241Gly)
c.626T>G (p.Val209Gly)
n.650T>G
9g.136673867A>GCA375577429AGPAT2c.722T>C (p.Val241Ala)
c.626T>C (p.Val209Ala)
n.650T>C
 gnomAD v4
9g.136673867A>TCA375577432AGPAT2c.722T>A (p.Val241Asp)
c.626T>A (p.Val209Asp)
n.650T>A
9g.136673868delCA861080682AGPAT2c.721del (p.Val241SerfsTer12)
c.625del (p.Val209SerfsTer12)
n.649del
 dbSNP gnomAD v3 gnomAD v4
9g.136673868C>ACA201626880AGPAT2c.721G>T (p.Val241Phe)
c.625G>T (p.Val209Phe)
n.649G>T
 dbSNP gnomAD v4
9g.136673868C>GCA5342840AGPAT2c.721G>C (p.Val241Leu)
c.625G>C (p.Val209Leu)
n.649G>C
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
9g.136673868C>TCA5342841AGPAT2c.721G>A (p.Val241Ile)
c.625G>A (p.Val209Ile)
n.649G>A
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
9g.136673869_136673874dupCA2692653766AGPAT2c.716_721dup (p.Asp240_Val241insAlaAsp)
c.620_625dup (p.Asp208_Val209insAlaAsp)
n.644_649dup
 gnomAD v4
9g.136673870_136673887dupCA2692653767AGPAT2c.704_721dup (p.Asp240_Val241insGlyLeuThrAlaAlaAsp)
c.608_625dup (p.Asp208_Val209insGlyLeuThrAlaAlaAsp)
n.632_649dup
 gnomAD v4
9g.136673869G>ACA5342842AGPAT2c.720C>T (p.Asp240=)
c.624C>T (p.Asp208=)
n.648C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
9g.136673869G>CCA375577454AGPAT2c.720C>G (p.Asp240Glu)
c.624C>G (p.Asp208Glu)
n.648C>G
9g.136673869G>TCA375577459AGPAT2c.720C>A (p.Asp240Glu)
c.624C>A (p.Asp208Glu)
n.648C>A
9g.136673870T>ACA375577463AGPAT2c.719A>T (p.Asp240Val)
c.623A>T (p.Asp208Val)
n.647A>T
9g.136673870T>CCA375577466AGPAT2c.719A>G (p.Asp240Gly)
c.623A>G (p.Asp208Gly)
n.647A>G
 COSMIC
9g.136673870T>GCA5342843AGPAT2c.719A>C (p.Asp240Ala)
c.623A>C (p.Asp208Ala)
n.647A>C
 dbSNP ExAC gnomAD v2 gnomAD v4
9g.136673871C>ACA375577472AGPAT2c.718G>T (p.Asp240Tyr)
c.622G>T (p.Asp208Tyr)
n.646G>T
 gnomAD v4
9g.136673871C>GCA375577476AGPAT2c.718G>C (p.Asp240His)
c.622G>C (p.Asp208His)
n.646G>C
9g.136673871C>TCA375577475AGPAT2c.718G>A (p.Asp240Asn)
c.622G>A (p.Asp208Asn)
n.646G>A
9g.136673872_136673875dupCA591367757AGPAT2c.715_718dup (p.Asp240GlyfsTer?)
c.619_622dup (p.Asp208GlyfsTer?)
n.643_646dup
 dbSNP gnomAD v2 gnomAD v4
9g.136673875_136673888delCA1130033196AGPAT2c.705_718del (p.Leu236ArgfsTer?)
c.609_622del (p.Leu204ArgfsTer?)
n.633_646del
 gnomAD v3 gnomAD v4
9g.136673872C>ACA467737091AGPAT2c.717G>T (p.Ala239=)
c.621G>T (p.Ala207=)
n.645G>T
 gnomAD v4
9g.136673872C>GCA467737095AGPAT2c.717G>C (p.Ala239=)
c.621G>C (p.Ala207=)
n.645G>C
9g.136673872C>TCA5342844AGPAT2c.717G>A (p.Ala239=)
c.621G>A (p.Ala207=)
n.645G>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
9g.136673873G>ACA5342845AGPAT2c.716C>T (p.Ala239Val)
c.620C>T (p.Ala207Val)
n.644C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
9g.136673873G>CCA375577479AGPAT2c.716C>G (p.Ala239Gly)
c.620C>G (p.Ala207Gly)
n.644C>G
 dbSNP gnomAD v2 gnomAD v4
9g.136673873G>TCA375577480AGPAT2c.716C>A (p.Ala239Glu)
c.620C>A (p.Ala207Glu)
n.644C>A
 gnomAD v4
9g.136673873dupCA2579519884AGPAT2c.716dup (p.Asp240GlyfsTer?)
c.620dup (p.Asp208GlyfsTer?)
n.644dup
9g.136673874C>ACA375577484AGPAT2c.715G>T (p.Ala239Ser)
c.619G>T (p.Ala207Ser)
n.643G>T
9g.136673874C>GCA375577487AGPAT2c.715G>C (p.Ala239Pro)
c.619G>C (p.Ala207Pro)
n.643G>C
9g.136673874C>TCA375577491AGPAT2c.715G>A (p.Ala239Thr)
c.619G>A (p.Ala207Thr)
n.643G>A
 gnomAD v4
9g.136673875dupCA591367763AGPAT2c.715dup (p.Ala239GlyfsTer?)
c.619dup (p.Ala207GlyfsTer?)
n.643dup
 dbSNP gnomAD v2 gnomAD v4
9g.136673875C>ACA467737117AGPAT2c.714G>T (p.Ala238=)
c.618G>T (p.Ala206=)
n.642G>T
 gnomAD v4
9g.136673875C>GCA467737119AGPAT2c.714G>C (p.Ala238=)
c.618G>C (p.Ala206=)
n.642G>C
 dbSNP gnomAD v4
9g.136673875C>TCA5342846AGPAT2c.714G>A (p.Ala238=)
c.618G>A (p.Ala206=)
n.642G>A
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
9g.136673876G>ACA5342847AGPAT2c.713C>T (p.Ala238Val)
c.617C>T (p.Ala206Val)
n.641C>T
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
9g.136673876G>CCA5342848AGPAT2c.713C>G (p.Ala238Gly)
c.617C>G (p.Ala206Gly)
n.641C>G
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
9g.136673876G>TCA375577502AGPAT2c.713C>A (p.Ala238Glu)
c.617C>A (p.Ala206Glu)
n.641C>A
 gnomAD v4
9g.136673877_136673879delCA591367767AGPAT2c.711_713del (p.Ala238del)
c.615_617del (p.Ala206del)
n.639_641del
 dbSNP gnomAD v2 gnomAD v4
9g.136673877_136673881delCA1130033214AGPAT2c.709_713del (p.Thr237GlyfsTer?)
c.613_617del (p.Thr205GlyfsTer?)
n.637_641del
 gnomAD v3 gnomAD v4
9g.136673877C>ACA375577512AGPAT2c.712G>T (p.Ala238Ser)
c.616G>T (p.Ala206Ser)
n.640G>T
9g.136673877C>GCA375577509AGPAT2c.712G>C (p.Ala238Pro)
c.616G>C (p.Ala206Pro)
n.640G>C
9g.136673877C>TCA375577507AGPAT2c.712G>A (p.Ala238Thr)
c.616G>A (p.Ala206Thr)
n.640G>A
 gnomAD v4 COSMIC
9g.136673878_136673886delCA2579519885AGPAT2c.704_712del (p.Gly235_Thr237del)
c.608_616del (p.Gly203_Thr205del)
n.632_640del
9g.136673878A>CCA467737132AGPAT2c.711T>G (p.Thr237=)
c.615T>G (p.Thr205=)
n.639T>G
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
9g.136673878A>GCA5342849AGPAT2c.711T>C (p.Thr237=)
c.615T>C (p.Thr205=)
n.639T>C
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
9g.136673878A>TCA467737135AGPAT2c.711T>A (p.Thr237=)
c.615T>A (p.Thr205=)
n.639T>A
 gnomAD v4
9g.136673879delCA861080724AGPAT2c.710del (p.Thr237MetfsTer16)
c.614del (p.Thr205MetfsTer16)
n.638del
 dbSNP gnomAD v4
9g.136673879G>ACA375577516AGPAT2c.710C>T (p.Thr237Ile)
c.614C>T (p.Thr205Ile)
n.638C>T
 gnomAD v4
9g.136673879G>CCA375577518AGPAT2c.710C>G (p.Thr237Ser)
c.614C>G (p.Thr205Ser)
n.638C>G
9g.136673879G>TCA375577520AGPAT2c.710C>A (p.Thr237Asn)
c.614C>A (p.Thr205Asn)
n.638C>A
9g.136673880T>ACA375577525AGPAT2c.709A>T (p.Thr237Ser)
c.613A>T (p.Thr205Ser)
n.637A>T
9g.136673880T>CCA375577528AGPAT2c.709A>G (p.Thr237Ala)
c.613A>G (p.Thr205Ala)
n.637A>G
9g.136673880T>GCA375577531AGPAT2c.709A>C (p.Thr237Pro)
c.613A>C (p.Thr205Pro)
n.637A>C
9g.136673881G>ACA467737143AGPAT2c.708C>T (p.Leu236=)
c.612C>T (p.Leu204=)
n.636C>T
9g.136673881G>CCA467737145AGPAT2c.708C>G (p.Leu236=)
c.612C>G (p.Leu204=)
n.636C>G
9g.136673881G>TCA467737146AGPAT2c.708C>A (p.Leu236=)
c.612C>A (p.Leu204=)
n.636C>A
 gnomAD v4
9g.136673882A>CCA375577534AGPAT2c.707T>G (p.Leu236Arg)
c.611T>G (p.Leu204Arg)
n.635T>G
9g.136673882A>GCA375577537AGPAT2c.707T>C (p.Leu236Pro)
c.611T>C (p.Leu204Pro)
n.635T>C
 gnomAD v4
9g.136673882A>TCA375577540AGPAT2c.707T>A (p.Leu236His)
c.611T>A (p.Leu204His)
n.635T>A
9g.136673883G>ACA5342850AGPAT2c.706C>T (p.Leu236Phe)
c.610C>T (p.Leu204Phe)
n.634C>T
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
9g.136673883G>CCA375577545AGPAT2c.706C>G (p.Leu236Val)
c.610C>G (p.Leu204Val)
n.634C>G
 gnomAD v4
9g.136673883G>TCA375577548AGPAT2c.706C>A (p.Leu236Ile)
c.610C>A (p.Leu204Ile)
n.634C>A
 gnomAD v4
9g.136673884G>ACA467737152AGPAT2c.705C>T (p.Gly235=)
c.609C>T (p.Gly203=)
n.633C>T
 dbSNP gnomAD v2 gnomAD v4
9g.136673884G>CCA467737154AGPAT2c.705C>G (p.Gly235=)
c.609C>G (p.Gly203=)
n.633C>G
9g.136673884G>TCA467737156AGPAT2c.705C>A (p.Gly235=)
c.609C>A (p.Gly203=)
n.633C>A
 gnomAD v4
9g.136673884_136673885delCA2692653768AGPAT2c.704_705del (p.Gly235AlafsTer?)
c.608_609del (p.Gly203AlafsTer?)
n.632_633del
 gnomAD v4
9g.136673885C>ACA375577556AGPAT2c.704G>T (p.Gly235Val)
c.608G>T (p.Gly203Val)
n.632G>T
 gnomAD v4
9g.136673885C>GCA375577552AGPAT2c.704G>C (p.Gly235Ala)
c.608G>C (p.Gly203Ala)
n.632G>C
 gnomAD v4
9g.136673885C>TCA375577555AGPAT2c.704G>A (p.Gly235Asp)
c.608G>A (p.Gly203Asp)
n.632G>A
 gnomAD v4
9g.136673886dupCA2692653769AGPAT2c.704dup (p.Leu236ProfsTer?)
c.608dup (p.Leu204ProfsTer?)
n.632dup
 gnomAD v4
9g.136673886C>ACA375577561AGPAT2c.703G>T (p.Gly235Cys)
c.607G>T (p.Gly203Cys)
n.631G>T
 gnomAD v4
9g.136673886C>GCA375577564AGPAT2c.703G>C (p.Gly235Arg)
c.607G>C (p.Gly203Arg)
n.631G>C
9g.136673886C>TCA5342851AGPAT2c.703G>A (p.Gly235Ser)
c.607G>A (p.Gly203Ser)
n.631G>A
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
9g.136673887G>ACA151608AGPAT2c.702C>T (p.Ser234=)
c.606C>T (p.Ser202=)
n.630C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
9g.136673887G>CCA375577571AGPAT2c.702C>G (p.Ser234Arg)
c.606C>G (p.Ser202Arg)
n.630C>G
9g.136673887G>TCA375577575AGPAT2c.702C>A (p.Ser234Arg)
c.606C>A (p.Ser202Arg)
n.630C>A
 gnomAD v4
9g.136673888C>ACA375577578AGPAT2c.701G>T (p.Ser234Ile)
c.605G>T (p.Ser202Ile)
n.629G>T
9g.136673888C>GCA375577581AGPAT2c.701G>C (p.Ser234Thr)
c.605G>C (p.Ser202Thr)
n.629G>C
9g.136673888C>TCA375577584AGPAT2c.701G>A (p.Ser234Asn)
c.605G>A (p.Ser202Asn)
n.629G>A
9g.136673889_136673905delCA2692653770AGPAT2c.685_701del (p.Glu229ArgfsTer?)
c.589_605del (p.Glu197ArgfsTer?)
n.613_629del
 gnomAD v4
9g.136673889T>ACA375577588AGPAT2c.700A>T (p.Ser234Cys)
c.604A>T (p.Ser202Cys)
n.628A>T
9g.136673889T>CCA375577590AGPAT2c.700A>G (p.Ser234Gly)
c.604A>G (p.Ser202Gly)
n.628A>G
 gnomAD v4
9g.136673889T>GCA375577594AGPAT2c.700A>C (p.Ser234Arg)
c.604A>C (p.Ser202Arg)
n.628A>C
9g.136673890G>ACA467737165AGPAT2c.699C>T (p.Thr233=)
c.603C>T (p.Thr201=)
n.627C>T
 gnomAD v4
9g.136673890G>CCA467737166AGPAT2c.699C>G (p.Thr233=)
c.603C>G (p.Thr201=)
n.627C>G
9g.136673890G>TCA467737167AGPAT2c.699C>A (p.Thr233=)
c.603C>A (p.Thr201=)
n.627C>A
 gnomAD v4
9g.136673891G>ACA5342852AGPAT2c.698C>T (p.Thr233Ile)
c.602C>T (p.Thr201Ile)
n.626C>T
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
9g.136673891G>CCA375577600AGPAT2c.698C>G (p.Thr233Ser)
c.602C>G (p.Thr201Ser)
n.626C>G
9g.136673891G>TCA375577599AGPAT2c.698C>A (p.Thr233Asn)
c.602C>A (p.Thr201Asn)
n.626C>A
 ClinVar dbSNP gnomAD v4
9g.136673892T>ACA375577605AGPAT2c.697A>T (p.Thr233Ser)
c.601A>T (p.Thr201Ser)
n.625A>T
9g.136673892T>CCA375577610AGPAT2c.697A>G (p.Thr233Ala)
c.601A>G (p.Thr201Ala)
n.625A>G
9g.136673892T>GCA375577607AGPAT2c.697A>C (p.Thr233Pro)
c.601A>C (p.Thr201Pro)
n.625A>C
9g.136673893G>ACA467737170AGPAT2c.696C>T (p.Pro232=)
c.600C>T (p.Pro200=)
n.624C>T
 gnomAD v4
9g.136673893G>CCA467737174AGPAT2c.696C>G (p.Pro232=)
c.600C>G (p.Pro200=)
n.624C>G
9g.136673893G>TCA467737172AGPAT2c.696C>A (p.Pro232=)
c.600C>A (p.Pro200=)
n.624C>A
9g.136673894G>ACA375577613AGPAT2c.695C>T (p.Pro232Leu)
c.599C>T (p.Pro200Leu)
n.623C>T
 gnomAD v4
9g.136673894G>CCA375577617AGPAT2c.695C>G (p.Pro232Arg)
c.599C>G (p.Pro200Arg)
n.623C>G
9g.136673894G>TCA375577615AGPAT2c.695C>A (p.Pro232His)
c.599C>A (p.Pro200His)
n.623C>A
 gnomAD v4
9g.136673895G>ACA375577620AGPAT2c.694C>T (p.Pro232Ser)
c.598C>T (p.Pro200Ser)
n.622C>T
 gnomAD v4
9g.136673895G>CCA375577622AGPAT2c.694C>G (p.Pro232Ala)
c.598C>G (p.Pro200Ala)
n.622C>G
9g.136673895G>TCA375577625AGPAT2c.694C>A (p.Pro232Thr)
c.598C>A (p.Pro200Thr)
n.622C>A
9g.136673896G>ACA467737175AGPAT2c.693C>T (p.Ile231=)
c.597C>T (p.Ile199=)
n.621C>T
 gnomAD v4
9g.136673896G>CCA375577632AGPAT2c.693C>G (p.Ile231Met)
c.597C>G (p.Ile199Met)
n.621C>G
9g.136673896G>TCA467737176AGPAT2c.693C>A (p.Ile231=)
c.597C>A (p.Ile199=)
n.621C>A
9g.136673897A>CCA375577635AGPAT2c.692T>G (p.Ile231Ser)
c.596T>G (p.Ile199Ser)
n.620T>G
9g.136673897A>GCA5342853AGPAT2c.692T>C (p.Ile231Thr)
c.596T>C (p.Ile199Thr)
n.620T>C
 dbSNP ExAC gnomAD v2 gnomAD v4
9g.136673897A>TCA375577636AGPAT2c.692T>A (p.Ile231Asn)
c.596T>A (p.Ile199Asn)
n.620T>A
 dbSNP gnomAD v4
9g.136673898T>ACA375577640AGPAT2c.691A>T (p.Ile231Phe)
c.595A>T (p.Ile199Phe)
n.619A>T
 gnomAD v4
9g.136673898T>CCA375577643AGPAT2c.691A>G (p.Ile231Val)
c.595A>G (p.Ile199Val)
n.619A>G
9g.136673898T>GCA375577646AGPAT2c.691A>C (p.Ile231Leu)
c.595A>C (p.Ile199Leu)
n.619A>C
9g.136673899G>ACA467737179AGPAT2c.690C>T (p.Ala230=)
c.594C>T (p.Ala198=)
n.618C>T
 gnomAD v4
9g.136673899G>CCA467737177AGPAT2c.690C>G (p.Ala230=)
c.594C>G (p.Ala198=)
n.618C>G
9g.136673899G>TCA467737178AGPAT2c.690C>A (p.Ala230=)
c.594C>A (p.Ala198=)
n.618C>A
9g.136673900G>ACA375577651AGPAT2c.689C>T (p.Ala230Val)
c.593C>T (p.Ala198Val)
n.617C>T
 gnomAD v4
9g.136673900G>CCA375577653AGPAT2c.689C>G (p.Ala230Gly)
c.593C>G (p.Ala198Gly)
n.617C>G
9g.136673900G>TCA375577654AGPAT2c.689C>A (p.Ala230Asp)
c.593C>A (p.Ala198Asp)
n.617C>A
 gnomAD v4
9g.136673901C>ACA375577662AGPAT2c.688G>T (p.Ala230Ser)
c.592G>T (p.Ala198Ser)
n.616G>T
 gnomAD v4
9g.136673901C>GCA375577658AGPAT2c.688G>C (p.Ala230Pro)
c.592G>C (p.Ala198Pro)
n.616G>C
9g.136673901C>TCA375577656AGPAT2c.688G>A (p.Ala230Thr)
c.592G>A (p.Ala198Thr)
n.616G>A
 gnomAD v4
9g.136673902T>ACA375577665AGPAT2c.687A>T (p.Glu229Asp)
c.591A>T (p.Glu197Asp)
n.615A>T
9g.136673902T>CCA467737180AGPAT2c.687A>G (p.Glu229=)
c.591A>G (p.Glu197=)
n.615A>G
 gnomAD v4
9g.136673902T>GCA375577667AGPAT2c.687A>C (p.Glu229Asp)
c.591A>C (p.Glu197Asp)
n.615A>C
9g.136673903delCA2692653771AGPAT2c.687del (p.Ala230ProfsTer23)
c.591del (p.Ala198ProfsTer23)
n.615del
 gnomAD v4
9g.136673903T>ACA375577671AGPAT2c.686A>T (p.Glu229Val)
c.590A>T (p.Glu197Val)
n.614A>T
9g.136673903T>CCA375577673AGPAT2c.686A>G (p.Glu229Gly)
c.590A>G (p.Glu197Gly)
n.614A>G
9g.136673903T>GCA375577676AGPAT2c.686A>C (p.Glu229Ala)
c.590A>C (p.Glu197Ala)
n.614A>C
9g.136673904C>ACA375577678AGPAT2c.685G>T (p.Glu229Ter)
c.589G>T (p.Glu197Ter)
n.613G>T
 ClinVar dbSNP gnomAD v4
9g.136673904C>GCA375577679AGPAT2c.685G>C (p.Glu229Gln)
c.589G>C (p.Glu197Gln)
n.613G>C
9g.136673904C>TCA375577680AGPAT2c.685G>A (p.Glu229Lys)
c.589G>A (p.Glu197Lys)
n.613G>A
 dbSNP gnomAD v2
9g.136673905C>ACA467737181AGPAT2c.684G>T (p.Leu228=)
c.588G>T (p.Leu196=)
n.612G>T
 gnomAD v4
9g.136673905C>GCA467737182AGPAT2c.684G>C (p.Leu228=)
c.588G>C (p.Leu196=)
n.612G>C
9g.136673905C>TCA467737183AGPAT2c.684G>A (p.Leu228=)
c.588G>A (p.Leu196=)
n.612G>A
 gnomAD v4
9g.136673906A>CCA375577681AGPAT2c.683T>G (p.Leu228Arg)
c.587T>G (p.Leu196Arg)
n.611T>G
9g.136673906A>GCA277946AGPAT2c.683T>C (p.Leu228Pro)
c.587T>C (p.Leu196Pro)
n.611T>C
 ClinVar dbSNP gnomAD v4
9g.136673906A>TCA375577682AGPAT2c.683T>A (p.Leu228Gln)
c.587T>A (p.Leu196Gln)
n.611T>A
9g.136673907G>ACA467737186AGPAT2c.682C>T (p.Leu228=)
c.586C>T (p.Leu196=)
n.610C>T
 gnomAD v4
9g.136673907G>CCA375577687AGPAT2c.682C>G (p.Leu228Val)
c.586C>G (p.Leu196Val)
n.610C>G
 gnomAD v4
9g.136673907G>TCA375577690AGPAT2c.682C>A (p.Leu228Met)
c.586C>A (p.Leu196Met)
n.610C>A
9g.136673908C>ACA467737190AGPAT2c.681G>T (p.Val227=)
c.585G>T (p.Val195=)
n.609G>T
 gnomAD v4
9g.136673908C>GCA467737192AGPAT2c.681G>C (p.Val227=)
c.585G>C (p.Val195=)
n.609G>C
9g.136673908C>TCA467737194AGPAT2c.681G>A (p.Val227=)
c.585G>A (p.Val195=)
n.609G>A
 dbSNP gnomAD v2 gnomAD v4
9g.136673908_136673922delCA2692653772AGPAT2c.667_681del (p.Val223_Val227del)
c.571_585del (p.Val191_Val195del)
n.595_609del
 gnomAD v4
9g.136673909A>CCA375577703AGPAT2c.680T>G (p.Val227Gly)
c.584T>G (p.Val195Gly)
n.608T>G
9g.136673909A>GCA375577709AGPAT2c.680T>C (p.Val227Ala)
c.584T>C (p.Val195Ala)
n.608T>C
 gnomAD v4
9g.136673909A>TCA375577694AGPAT2c.680T>A (p.Val227Glu)
c.584T>A (p.Val195Glu)
n.608T>A
9g.136673910C>ACA375577715AGPAT2c.679G>T (p.Val227Leu)
c.583G>T (p.Val195Leu)
n.607G>T
9g.136673910C>GCA375577717AGPAT2c.679G>C (p.Val227Leu)
c.583G>C (p.Val195Leu)
n.607G>C
9g.136673910C>TCA5342854AGPAT2c.679G>A (p.Val227Met)
c.583G>A (p.Val195Met)
n.607G>A
 dbSNP ExAC gnomAD v2 gnomAD v4
9g.136673911C>ACA375577721AGPAT2c.678G>T (p.Gln226His)
c.582G>T (p.Gln194His)
n.606G>T
 gnomAD v4
9g.136673911C>GCA375577722AGPAT2c.678G>C (p.Gln226His)
c.582G>C (p.Gln194His)
n.606G>C
9g.136673911C>TCA467737204AGPAT2c.678G>A (p.Gln226=)
c.582G>A (p.Gln194=)
n.606G>A
 ClinVar dbSNP gnomAD v2 gnomAD v4
9g.136673912T>ACA375577726AGPAT2c.677A>T (p.Gln226Leu)
c.581A>T (p.Gln194Leu)
n.605A>T
 gnomAD v4
9g.136673912T>CCA375577730AGPAT2c.677A>G (p.Gln226Arg)
c.581A>G (p.Gln194Arg)
n.605A>G
 dbSNP gnomAD v4
9g.136673912T>GCA375577734AGPAT2c.677A>C (p.Gln226Pro)
c.581A>C (p.Gln194Pro)
n.605A>C
9g.136673913G>ACA16042193AGPAT2c.676C>T (p.Gln226Ter)
c.580C>T (p.Gln194Ter)
n.604C>T
 ClinVar dbSNP gnomAD v4
9g.136673913G>CCA375577739AGPAT2c.676C>G (p.Gln226Glu)
c.580C>G (p.Gln194Glu)
n.604C>G
9g.136673913G>TCA375577742AGPAT2c.676C>A (p.Gln226Lys)
c.580C>A (p.Gln194Lys)
n.604C>A
 gnomAD v4
9g.136673914C>ACA467737213AGPAT2c.675G>T (p.Val225=)
c.579G>T (p.Val193=)
n.603G>T
 gnomAD v4
9g.136673914C>GCA5342855AGPAT2c.675G>C (p.Val225=)
c.579G>C (p.Val193=)
n.603G>C
 dbSNP ExAC gnomAD v2 gnomAD v4
9g.136673914C>TCA5342856AGPAT2c.675G>A (p.Val225=)
c.579G>A (p.Val193=)
n.603G>A
 dbSNP ExAC gnomAD v2 gnomAD v4
9g.136673915A>CCA375577747AGPAT2c.674T>G (p.Val225Gly)
c.578T>G (p.Val193Gly)
n.602T>G
9g.136673915A>GCA5342857AGPAT2c.674T>C (p.Val225Ala)
c.578T>C (p.Val193Ala)
n.602T>C
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
9g.136673915A>TCA375577750AGPAT2c.674T>A (p.Val225Glu)
c.578T>A (p.Val193Glu)
n.602T>A
9g.136673916C>ACA375577751AGPAT2c.673G>T (p.Val225Leu)
c.577G>T (p.Val193Leu)
n.601G>T
 gnomAD v4
9g.136673916C>GCA375577753AGPAT2c.673G>C (p.Val225Leu)
c.577G>C (p.Val193Leu)
n.601G>C
 gnomAD v4
9g.136673916C>TCA375577759AGPAT2c.673G>A (p.Val225Met)
c.577G>A (p.Val193Met)
n.601G>A
 gnomAD v4
9g.136673917T>ACA467737228AGPAT2c.672A>T (p.Thr224=)
c.576A>T (p.Thr192=)
n.600A>T
9g.136673917T>CCA467737235AGPAT2c.672A>G (p.Thr224=)
c.576A>G (p.Thr192=)
n.600A>G
9g.136673917T>GCA467737231AGPAT2c.672A>C (p.Thr224=)
c.576A>C (p.Thr192=)
n.600A>C
9g.136673918G>ACA375577763AGPAT2c.671C>T (p.Thr224Ile)
c.575C>T (p.Thr192Ile)
n.599C>T
 gnomAD v4
9g.136673918G>CCA201626932AGPAT2c.671C>G (p.Thr224Arg)
c.575C>G (p.Thr192Arg)
n.599C>G
 dbSNP
9g.136673918G>TCA375577767AGPAT2c.671C>A (p.Thr224Lys)
c.575C>A (p.Thr192Lys)
n.599C>A
 gnomAD v4
9g.136673919T>ACA375577768AGPAT2c.670A>T (p.Thr224Ser)
c.574A>T (p.Thr192Ser)
n.598A>T
9g.136673919T>CCA375577769AGPAT2c.670A>G (p.Thr224Ala)
c.574A>G (p.Thr192Ala)
n.598A>G
 gnomAD v4
9g.136673919T>GCA375577770AGPAT2c.670A>C (p.Thr224Pro)
c.574A>C (p.Thr192Pro)
n.598A>C
9g.136673920G>ACA201626936AGPAT2c.669C>T (p.Val223=)
c.573C>T (p.Val191=)
n.597C>T
 dbSNP gnomAD v2 gnomAD v4
9g.136673920G>CCA467737257AGPAT2c.669C>G (p.Val223=)
c.573C>G (p.Val191=)
n.597C>G
9g.136673920G>TCA467737260AGPAT2c.669C>A (p.Val223=)
c.573C>A (p.Val191=)
n.597C>A
 gnomAD v4
9g.136673921A>CCA375577778AGPAT2c.668T>G (p.Val223Gly)
c.572T>G (p.Val191Gly)
n.596T>G
9g.136673921A>GCA375577775AGPAT2c.668T>C (p.Val223Ala)
c.572T>C (p.Val191Ala)
n.596T>C
 dbSNP gnomAD v4
9g.136673921A>TCA375577773AGPAT2c.668T>A (p.Val223Asp)
c.572T>A (p.Val191Asp)
n.596T>A
 gnomAD v4
9g.136673922C>ACA375577781AGPAT2c.667G>T (p.Val223Phe)
c.571G>T (p.Val191Phe)
n.595G>T
 gnomAD v4
9g.136673922C>GCA201626941AGPAT2c.667G>C (p.Val223Leu)
c.571G>C (p.Val191Leu)
n.595G>C
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
9g.136673922C>TCA375577791AGPAT2c.667G>A (p.Val223Ile)
c.571G>A (p.Val191Ile)
n.595G>A
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
9g.136673923T>ACA467737289AGPAT2c.666A>T (p.Thr222=)
c.570A>T (p.Thr190=)
n.594A>T
 gnomAD v4
9g.136673923T>CCA467737292AGPAT2c.666A>G (p.Thr222=)
c.570A>G (p.Thr190=)
n.594A>G
 gnomAD v4
9g.136673923T>GCA467737294AGPAT2c.666A>C (p.Thr222=)
c.570A>C (p.Thr190=)
n.594A>C
9g.136673924_136673925delCA2692653773AGPAT2c.665_666del (p.Thr222SerfsTer?)
c.569_570del (p.Thr190SerfsTer?)
n.593_594del
 gnomAD v4
9g.136673924G>ACA375577795AGPAT2c.665C>T (p.Thr222Ile)
c.569C>T (p.Thr190Ile)
n.593C>T
 dbSNP gnomAD v4
9g.136673924G>CCA375577796AGPAT2c.665C>G (p.Thr222Arg)
c.569C>G (p.Thr190Arg)
n.593C>G
 gnomAD v4
9g.136673924G>TCA375577797AGPAT2c.665C>A (p.Thr222Lys)
c.569C>A (p.Thr190Lys)
n.593C>A
 gnomAD v4
9g.136673925T>ACA375577802AGPAT2c.664A>T (p.Thr222Ser)
c.568A>T (p.Thr190Ser)
n.592A>T
 gnomAD v4
9g.136673925T>CCA375577809AGPAT2c.664A>G (p.Thr222Ala)
c.568A>G (p.Thr190Ala)
n.592A>G
9g.136673925T>GCA375577811AGPAT2c.664A>C (p.Thr222Pro)
c.568A>C (p.Thr190Pro)
n.592A>C
9g.136673926T>ACA467737313AGPAT2c.663A>T (p.Gly221=)
c.567A>T (p.Gly189=)
n.591A>T
9g.136673926T>CCA467737314AGPAT2c.663A>G (p.Gly221=)
c.567A>G (p.Gly189=)
n.591A>G
9g.136673926T>GCA467737317AGPAT2c.663A>C (p.Gly221=)
c.567A>C (p.Gly189=)
n.591A>C
9g.136673927C>ACA375577813AGPAT2c.662G>T (p.Gly221Val)
c.566G>T (p.Gly189Val)
n.590G>T
 gnomAD v4
9g.136673927C>GCA375577816AGPAT2c.662G>C (p.Gly221Ala)
c.566G>C (p.Gly189Ala)
n.590G>C
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
9g.136673927C>TCA375577822AGPAT2c.662G>A (p.Gly221Glu)
c.566G>A (p.Gly189Glu)
n.590G>A
 gnomAD v4
9g.136673928delCA5342858AGPAT2c.662del
c.566del
n.590del
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
9g.136673928C>ACA375577829AGPAT2c.662-1G>T (n.662-1G>T)
c.566-1G>T (n.566-1G>T)
n.590-1G>T
 gnomAD v4
9g.136673928C>GCA375577832AGPAT2c.662-1G>C (n.662-1G>C)
c.566-1G>C (n.566-1G>C)
n.590-1G>C
9g.136673928C>TCA375577839AGPAT2c.662-1G>A (n.662-1G>A)
c.566-1G>A (n.566-1G>A)
n.590-1G>A
 gnomAD v4
9g.136673929T>ACA375577842AGPAT2c.662-2A>T (n.662-2A>T)
c.566-2A>T (n.566-2A>T)
n.590-2A>T
9g.136673929T>CCA375577855AGPAT2c.662-2A>G (n.662-2A>G)
c.566-2A>G (n.566-2A>G)
n.590-2A>G
 gnomAD v4
9g.136673929T>GCA375577854AGPAT2c.662-2A>C (n.662-2A>C)
c.566-2A>C (n.566-2A>C)
n.590-2A>C
 ClinVar dbSNP gnomAD v4

Number of alleles fetched