Chr Mutation (hg38) CAid Gene Transcript Linkouts
20g.46725379_46725868delinsCCA2697547414SLC2A10c.343_832delinsC (p.Ser115_Ala278delinsPro)
c.406_895delinsC (p.Ser136_Ala299delinsPro)
c.352_841delinsC (p.Ser118_Ala281delinsPro)
n.542_1031delinsC
n.529_1018delinsC
 ClinVar
20g.46725504_46725505delCA2527029223SLC2A10c.468_469del (p.Leu157GlyfsTer?)
c.531_532del (p.Leu178GlyfsTer?)
c.477_478del (p.Leu160GlyfsTer?)
n.667_668del
n.654_655del
20g.46725504A>CCA510847661SLC2A10c.468A>C (p.Ala156=)
c.531A>C (p.Ala177=)
c.477A>C (p.Ala159=)
n.667A>C
n.654A>C
20g.46725504A>GCA510847662SLC2A10c.468A>G (p.Ala156=)
c.531A>G (p.Ala177=)
c.477A>G (p.Ala159=)
n.667A>G
n.654A>G
20g.46725504A>TCA510847663SLC2A10c.468A>T (p.Ala156=)
c.531A>T (p.Ala177=)
c.477A>T (p.Ala159=)
n.667A>T
n.654A>T
20g.46725505C>ACA409267067SLC2A10c.469C>A (p.Leu157Met)
c.532C>A (p.Leu178Met)
c.478C>A (p.Leu160Met)
n.668C>A
n.655C>A
20g.46725505C>GCA409267068SLC2A10c.469C>G (p.Leu157Val)
c.532C>G (p.Leu178Val)
c.478C>G (p.Leu160Val)
n.668C>G
n.655C>G
20g.46725505C>TCA510847664SLC2A10c.469C>T (p.Leu157=)
c.532C>T (p.Leu178=)
c.478C>T (p.Leu160=)
n.668C>T
n.655C>T
20g.46725509_46725512delCA2580615418SLC2A10c.473_476del (p.Ala158ValfsTer?)
c.536_539del (p.Ala179ValfsTer?)
c.482_485del (p.Ala161ValfsTer?)
n.672_675del
n.659_662del
 ClinVar dbSNP
20g.46725506T>ACA409267069SLC2A10c.470T>A (p.Leu157Gln)
c.533T>A (p.Leu178Gln)
c.479T>A (p.Leu160Gln)
n.669T>A
n.656T>A
20g.46725506T>CCA409267070SLC2A10c.470T>C (p.Leu157Pro)
c.533T>C (p.Leu178Pro)
c.479T>C (p.Leu160Pro)
n.669T>C
n.656T>C
20g.46725506T>GCA409267071SLC2A10c.470T>G (p.Leu157Arg)
c.533T>G (p.Leu178Arg)
c.479T>G (p.Leu160Arg)
n.669T>G
n.656T>G
20g.46725507G>ACA9891979SLC2A10c.471G>A (p.Leu157=)
c.534G>A (p.Leu178=)
c.480G>A (p.Leu160=)
n.670G>A
n.657G>A
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
20g.46725507G>CCA510847665SLC2A10c.471G>C (p.Leu157=)
c.534G>C (p.Leu178=)
c.480G>C (p.Leu160=)
n.670G>C
n.657G>C
20g.46725507G=CA2366796234SLC2A10c.471G= (p.Leu157=)
c.534G= (p.Leu178=)
c.480G= (p.Leu160=)
n.670G=
n.657G=
20g.46725507G>TCA510847666SLC2A10c.471G>T (p.Leu157=)
c.534G>T (p.Leu178=)
c.480G>T (p.Leu160=)
n.670G>T
n.657G>T
20g.46725508G>ACA409267072SLC2A10c.472G>A (p.Ala158Thr)
c.535G>A (p.Ala179Thr)
c.481G>A (p.Ala161Thr)
n.671G>A
n.658G>A
20g.46725508G>CCA409267073SLC2A10c.472G>C (p.Ala158Pro)
c.535G>C (p.Ala179Pro)
c.481G>C (p.Ala161Pro)
n.671G>C
n.658G>C
 dbSNP
20g.46725508G=CA2366796235SLC2A10c.472G= (p.Ala158=)
c.535G= (p.Ala179=)
c.481G= (p.Ala161=)
n.671G=
n.658G=
20g.46725508G>TCA409267074SLC2A10c.472G>T (p.Ala158Ser)
c.535G>T (p.Ala179Ser)
c.481G>T (p.Ala161Ser)
n.671G>T
n.658G>T
20g.46725509C>ACA409267076SLC2A10c.473C>A (p.Ala158Asp)
c.536C>A (p.Ala179Asp)
c.482C>A (p.Ala161Asp)
n.672C>A
n.659C>A
20g.46725509C>GCA409267077SLC2A10c.473C>G (p.Ala158Gly)
c.536C>G (p.Ala179Gly)
c.482C>G (p.Ala161Gly)
n.672C>G
n.659C>G
20g.46725509C>TCA409267075SLC2A10c.473C>T (p.Ala158Val)
c.536C>T (p.Ala179Val)
c.482C>T (p.Ala161Val)
n.672C>T
n.659C>T
 gnomAD v4
20g.46725510T>ACA510847667SLC2A10c.474T>A (p.Ala158=)
c.537T>A (p.Ala179=)
c.483T>A (p.Ala161=)
n.673T>A
n.660T>A
20g.46725510T>CCA510847668SLC2A10c.474T>C (p.Ala158=)
c.537T>C (p.Ala179=)
c.483T>C (p.Ala161=)
n.673T>C
n.660T>C
 gnomAD v4
20g.46725510T>GCA510847669SLC2A10c.474T>G (p.Ala158=)
c.537T>G (p.Ala179=)
c.483T>G (p.Ala161=)
n.673T>G
n.660T>G
20g.46725511G>ACA409267078SLC2A10c.475G>A (p.Gly159Ser)
c.538G>A (p.Gly180Ser)
c.484G>A (p.Gly162Ser)
n.674G>A
n.661G>A
20g.46725511G>CCA409267079SLC2A10c.475G>C (p.Gly159Arg)
c.538G>C (p.Gly180Arg)
c.484G>C (p.Gly162Arg)
n.674G>C
n.661G>C
20g.46725511G=CA2366796236SLC2A10c.475G= (p.Gly159=)
c.538G= (p.Gly180=)
c.484G= (p.Gly162=)
n.674G=
n.661G=
20g.46725511G>TCA9891980SLC2A10c.475G>T (p.Gly159Cys)
c.538G>T (p.Gly180Cys)
c.484G>T (p.Gly162Cys)
n.674G>T
n.661G>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
20g.46725512G>ACA409267080SLC2A10c.476G>A (p.Gly159Asp)
c.539G>A (p.Gly180Asp)
c.485G>A (p.Gly162Asp)
n.675G>A
n.662G>A
20g.46725512G>CCA315755686SLC2A10c.476G>C (p.Gly159Ala)
c.539G>C (p.Gly180Ala)
c.485G>C (p.Gly162Ala)
n.675G>C
n.662G>C
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
20g.46725512G=CA2366796237SLC2A10c.476G= (p.Gly159=)
c.539G= (p.Gly180=)
c.485G= (p.Gly162=)
n.675G=
n.662G=
20g.46725512G>TCA409267081SLC2A10c.476G>T (p.Gly159Val)
c.539G>T (p.Gly180Val)
c.485G>T (p.Gly162Val)
n.675G>T
n.662G>T
 ClinVar dbSNP gnomAD v2 gnomAD v4
20g.46725513T>ACA510847670SLC2A10c.477T>A (p.Gly159=)
c.540T>A (p.Gly180=)
c.486T>A (p.Gly162=)
n.676T>A
n.663T>A
20g.46725513T>CCA510847671SLC2A10c.477T>C (p.Gly159=)
c.540T>C (p.Gly180=)
c.486T>C (p.Gly162=)
n.676T>C
n.663T>C
 gnomAD v4
20g.46725513T>GCA9891981SLC2A10c.477T>G (p.Gly159=)
c.540T>G (p.Gly180=)
c.486T>G (p.Gly162=)
n.676T>G
n.663T>G
 dbSNP ExAC gnomAD v2 gnomAD v4
20g.46725513T=CA2366796238SLC2A10c.477T= (p.Gly159=)
c.540T= (p.Gly180=)
c.486T= (p.Gly162=)
n.676T=
n.663T=
20g.46725514A>CCA409267082SLC2A10c.478A>C (p.Thr160Pro)
c.541A>C (p.Thr181Pro)
c.487A>C (p.Thr163Pro)
n.677A>C
n.664A>C
20g.46725514A>GCA409267083SLC2A10c.478A>G (p.Thr160Ala)
c.541A>G (p.Thr181Ala)
c.487A>G (p.Thr163Ala)
n.677A>G
n.664A>G
20g.46725514A>TCA409267084SLC2A10c.478A>T (p.Thr160Ser)
c.541A>T (p.Thr181Ser)
c.487A>T (p.Thr163Ser)
n.677A>T
n.664A>T
 gnomAD v4
20g.46725515C>ACA409267085SLC2A10c.479C>A (p.Thr160Asn)
c.542C>A (p.Thr181Asn)
c.488C>A (p.Thr163Asn)
n.678C>A
n.665C>A
 dbSNP gnomAD v3 gnomAD v4
20g.46725515C=CA2366796239SLC2A10c.479C= (p.Thr160=)
c.542C= (p.Thr181=)
c.488C= (p.Thr163=)
n.678C=
n.665C=
20g.46725515C>GCA9891982SLC2A10c.479C>G (p.Thr160Ser)
c.542C>G (p.Thr181Ser)
c.488C>G (p.Thr163Ser)
n.678C>G
n.665C>G
 dbSNP ExAC gnomAD v2 gnomAD v4
20g.46725515C>TCA9891983SLC2A10c.479C>T (p.Thr160Ile)
c.542C>T (p.Thr181Ile)
c.488C>T (p.Thr163Ile)
n.678C>T
n.665C>T
 dbSNP ExAC gnomAD v2 gnomAD v4
20g.46725519dupCA2653170811SLC2A10c.483dup (p.Trp162LeufsTer30)
c.546dup (p.Trp183LeufsTer30)
c.492dup (p.Trp165LeufsTer30)
n.682dup
n.669dup
 gnomAD v4
20g.46725519delCA2573157155SLC2A10c.483del (p.Trp162GlyfsTer?)
c.546del (p.Trp183GlyfsTer?)
c.492del (p.Trp165GlyfsTer?)
n.682del
n.669del
 ClinVar dbSNP
20g.46725516C>ACA510847672SLC2A10c.480C>A (p.Thr160=)
c.543C>A (p.Thr181=)
c.489C>A (p.Thr163=)
n.679C>A
n.666C>A
20g.46725516C>GCA510847673SLC2A10c.480C>G (p.Thr160=)
c.543C>G (p.Thr181=)
c.489C>G (p.Thr163=)
n.679C>G
n.666C>G
 gnomAD v4
20g.46725516C>TCA510847674SLC2A10c.480C>T (p.Thr160=)
c.543C>T (p.Thr181=)
c.489C>T (p.Thr163=)
n.679C>T
n.666C>T
20g.46725517C>ACA409267086SLC2A10c.481C>A (p.Pro161Thr)
c.544C>A (p.Pro182Thr)
c.490C>A (p.Pro164Thr)
n.680C>A
n.667C>A
20g.46725517C=CA2366796240SLC2A10c.481C= (p.Pro161=)
c.544C= (p.Pro182=)
c.490C= (p.Pro164=)
n.680C=
n.667C=
20g.46725517C>GCA409267087SLC2A10c.481C>G (p.Pro161Ala)
c.544C>G (p.Pro182Ala)
c.490C>G (p.Pro164Ala)
n.680C>G
n.667C>G
 dbSNP gnomAD v2
20g.46725517C>TCA409267088SLC2A10c.481C>T (p.Pro161Ser)
c.544C>T (p.Pro182Ser)
c.490C>T (p.Pro164Ser)
n.680C>T
n.667C>T
 gnomAD v4
20g.46725518C>ACA9891984SLC2A10c.482C>A (p.Pro161His)
c.545C>A (p.Pro182His)
c.491C>A (p.Pro164His)
n.681C>A
n.668C>A
 dbSNP ExAC gnomAD v2 gnomAD v4
20g.46725518C=CA2366796241SLC2A10c.482C= (p.Pro161=)
c.545C= (p.Pro182=)
c.491C= (p.Pro164=)
n.681C=
n.668C=
20g.46725518C>GCA409267089SLC2A10c.482C>G (p.Pro161Arg)
c.545C>G (p.Pro182Arg)
c.491C>G (p.Pro164Arg)
n.681C>G
n.668C>G
20g.46725518C>TCA9891985SLC2A10c.482C>T (p.Pro161Leu)
c.545C>T (p.Pro182Leu)
c.491C>T (p.Pro164Leu)
n.681C>T
n.668C>T
 dbSNP ExAC gnomAD v2 gnomAD v4
20g.46725519C>ACA510847677SLC2A10c.483C>A (p.Pro161=)
c.546C>A (p.Pro182=)
c.492C>A (p.Pro164=)
n.682C>A
n.669C>A
 gnomAD v4
20g.46725519C>GCA510847676SLC2A10c.483C>G (p.Pro161=)
c.546C>G (p.Pro182=)
c.492C>G (p.Pro164=)
n.682C>G
n.669C>G
20g.46725519C>TCA510847675SLC2A10c.483C>T (p.Pro161=)
c.546C>T (p.Pro182=)
c.492C>T (p.Pro164=)
n.682C>T
n.669C>T
20g.46725519_46725520delinsCTCA2366796242SLC2A10c.483_484delinsCT (p.Pro161=)
c.546_547delinsCT (p.Pro182=)
c.492_493delinsCT (p.Pro164=)
n.682_683delinsCT
n.669_670delinsCT
20g.46725520delCA1017976908SLC2A10c.484del (p.Trp162GlyfsTer?)
c.547del (p.Trp183GlyfsTer?)
c.493del (p.Trp165GlyfsTer?)
n.683del
n.670del
 dbSNP gnomAD v3 gnomAD v4
20g.46725520T>ACA409267090SLC2A10c.484T>A (p.Trp162Arg)
c.547T>A (p.Trp183Arg)
c.493T>A (p.Trp165Arg)
n.683T>A
n.670T>A
20g.46725520T>CCA9891986SLC2A10c.484T>C (p.Trp162Arg)
c.547T>C (p.Trp183Arg)
c.493T>C (p.Trp165Arg)
n.683T>C
n.670T>C
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
20g.46725520T>GCA409267091SLC2A10c.484T>G (p.Trp162Gly)
c.547T>G (p.Trp183Gly)
c.493T>G (p.Trp165Gly)
n.683T>G
n.670T>G
20g.46725520T=CA2366796243SLC2A10c.484T= (p.Trp162=)
c.547T= (p.Trp183=)
c.493T= (p.Trp165=)
n.683T=
n.670T=
20g.46725521G>ACA409267092SLC2A10c.485G>A (p.Trp162Ter)
c.548G>A (p.Trp183Ter)
c.494G>A (p.Trp165Ter)
n.684G>A
n.671G>A
 ClinVar dbSNP
20g.46725521G>CCA409267093SLC2A10c.485G>C (p.Trp162Ser)
c.548G>C (p.Trp183Ser)
c.494G>C (p.Trp165Ser)
n.684G>C
n.671G>C
20g.46725521G>TCA409267094SLC2A10c.485G>T (p.Trp162Leu)
c.548G>T (p.Trp183Leu)
c.494G>T (p.Trp165Leu)
n.684G>T
n.671G>T
20g.46725522G>ACA409267095SLC2A10c.486G>A (p.Trp162Ter)
c.549G>A (p.Trp183Ter)
c.495G>A (p.Trp165Ter)
n.685G>A
n.672G>A
20g.46725522G>CCA409267096SLC2A10c.486G>C (p.Trp162Cys)
c.549G>C (p.Trp183Cys)
c.495G>C (p.Trp165Cys)
n.685G>C
n.672G>C
20g.46725522G>TCA409267097SLC2A10c.486G>T (p.Trp162Cys)
c.549G>T (p.Trp183Cys)
c.495G>T (p.Trp165Cys)
n.685G>T
n.672G>T
20g.46725523G>ACA409267098SLC2A10c.487G>A (p.Gly163Arg)
c.550G>A (p.Gly184Arg)
c.496G>A (p.Gly166Arg)
n.686G>A
n.673G>A
20g.46725523G>CCA409267099SLC2A10c.487G>C (p.Gly163Arg)
c.550G>C (p.Gly184Arg)
c.496G>C (p.Gly166Arg)
n.686G>C
n.673G>C
20g.46725523G>TCA409267100SLC2A10c.487G>T (p.Gly163Ter)
c.550G>T (p.Gly184Ter)
c.496G>T (p.Gly166Ter)
n.686G>T
n.673G>T
20g.46725524G>ACA409267103SLC2A10c.488G>A (p.Gly163Glu)
c.551G>A (p.Gly184Glu)
c.497G>A (p.Gly166Glu)
n.687G>A
n.674G>A
 gnomAD v4 COSMIC
20g.46725524G>CCA409267102SLC2A10c.488G>C (p.Gly163Ala)
c.551G>C (p.Gly184Ala)
c.497G>C (p.Gly166Ala)
n.687G>C
n.674G>C
20g.46725524G>TCA409267101SLC2A10c.488G>T (p.Gly163Val)
c.551G>T (p.Gly184Val)
c.497G>T (p.Gly166Val)
n.687G>T
n.674G>T
20g.46725525A=CA2366796244SLC2A10c.489A= (p.Gly163=)
c.552A= (p.Gly184=)
c.498A= (p.Gly166=)
n.688A=
n.675A=
20g.46725525A>CCA510847678SLC2A10c.489A>C (p.Gly163=)
c.552A>C (p.Gly184=)
c.498A>C (p.Gly166=)
n.688A>C
n.675A>C
20g.46725525A>GCA510847680SLC2A10c.489A>G (p.Gly163=)
c.552A>G (p.Gly184=)
c.498A>G (p.Gly166=)
n.688A>G
n.675A>G
 dbSNP
20g.46725525A>TCA510847679SLC2A10c.489A>T (p.Gly163=)
c.552A>T (p.Gly184=)
c.498A>T (p.Gly166=)
n.688A>T
n.675A>T
 dbSNP gnomAD v2 gnomAD v4
20g.46725526T>ACA409267104SLC2A10c.490T>A (p.Trp164Arg)
c.553T>A (p.Trp185Arg)
c.499T>A (p.Trp167Arg)
n.689T>A
n.676T>A
20g.46725526T>CCA409267105SLC2A10c.490T>C (p.Trp164Arg)
c.553T>C (p.Trp185Arg)
c.499T>C (p.Trp167Arg)
n.689T>C
n.676T>C
 gnomAD v4
20g.46725526T>GCA409267106SLC2A10c.490T>G (p.Trp164Gly)
c.553T>G (p.Trp185Gly)
c.499T>G (p.Trp167Gly)
n.689T>G
n.676T>G
20g.46725527G>ACA409267107SLC2A10c.491G>A (p.Trp164Ter)
c.554G>A (p.Trp185Ter)
c.500G>A (p.Trp167Ter)
n.690G>A
n.677G>A
20g.46725527G>CCA409267108SLC2A10c.491G>C (p.Trp164Ser)
c.554G>C (p.Trp185Ser)
c.500G>C (p.Trp167Ser)
n.690G>C
n.677G>C
20g.46725527G>TCA409267109SLC2A10c.491G>T (p.Trp164Leu)
c.554G>T (p.Trp185Leu)
c.500G>T (p.Trp167Leu)
n.690G>T
n.677G>T
20g.46725528G>ACA409267110SLC2A10c.492G>A (p.Trp164Ter)
c.555G>A (p.Trp185Ter)
c.501G>A (p.Trp167Ter)
n.691G>A
n.678G>A
20g.46725528G>CCA409267111SLC2A10c.492G>C (p.Trp164Cys)
c.555G>C (p.Trp185Cys)
c.501G>C (p.Trp167Cys)
n.691G>C
n.678G>C
 gnomAD v4
20g.46725528G>TCA409267112SLC2A10c.492G>T (p.Trp164Cys)
c.555G>T (p.Trp185Cys)
c.501G>T (p.Trp167Cys)
n.691G>T
n.678G>T
20g.46725529A>CCA510847681SLC2A10c.493A>C (p.Arg165=)
c.556A>C (p.Arg186=)
c.502A>C (p.Arg168=)
n.692A>C
n.679A>C
20g.46725529A>GCA409267113SLC2A10c.493A>G (p.Arg165Gly)
c.556A>G (p.Arg186Gly)
c.502A>G (p.Arg168Gly)
n.692A>G
n.679A>G
20g.46725529A>TCA409267114SLC2A10c.493A>T (p.Arg165Trp)
c.556A>T (p.Arg186Trp)
c.502A>T (p.Arg168Trp)
n.692A>T
n.679A>T
20g.46725530G>ACA409267117SLC2A10c.494G>A (p.Arg165Lys)
c.557G>A (p.Arg186Lys)
c.503G>A (p.Arg168Lys)
n.693G>A
n.680G>A
20g.46725530G>CCA409267116SLC2A10c.494G>C (p.Arg165Thr)
c.557G>C (p.Arg186Thr)
c.503G>C (p.Arg168Thr)
n.693G>C
n.680G>C
20g.46725530G>TCA409267115SLC2A10c.494G>T (p.Arg165Met)
c.557G>T (p.Arg186Met)
c.503G>T (p.Arg168Met)
n.693G>T
n.680G>T
20g.46725531G>ACA510847682SLC2A10c.495G>A (p.Arg165=)
c.558G>A (p.Arg186=)
c.504G>A (p.Arg168=)
n.694G>A
n.681G>A
20g.46725531G>CCA409267118SLC2A10c.495G>C (p.Arg165Ser)
c.558G>C (p.Arg186Ser)
c.504G>C (p.Arg168Ser)
n.694G>C
n.681G>C
20g.46725531G>TCA409267119SLC2A10c.495G>T (p.Arg165Ser)
c.558G>T (p.Arg186Ser)
c.504G>T (p.Arg168Ser)
n.694G>T
n.681G>T
20g.46725532C>ACA409267120SLC2A10c.496C>A (p.His166Asn)
c.559C>A (p.His187Asn)
c.505C>A (p.His169Asn)
n.695C>A
n.682C>A
20g.46725532C>GCA409267121SLC2A10c.496C>G (p.His166Asp)
c.559C>G (p.His187Asp)
c.505C>G (p.His169Asp)
n.695C>G
n.682C>G
20g.46725532C>TCA409267122SLC2A10c.496C>T (p.His166Tyr)
c.559C>T (p.His187Tyr)
c.505C>T (p.His169Tyr)
n.695C>T
n.682C>T
 gnomAD v4
20g.46725533A>CCA409267123SLC2A10c.497A>C (p.His166Pro)
c.560A>C (p.His187Pro)
c.506A>C (p.His169Pro)
n.696A>C
n.683A>C
20g.46725533A>GCA409267124SLC2A10c.497A>G (p.His166Arg)
c.560A>G (p.His187Arg)
c.506A>G (p.His169Arg)
n.696A>G
n.683A>G
 gnomAD v4
20g.46725533A>TCA409267125SLC2A10c.497A>T (p.His166Leu)
c.560A>T (p.His187Leu)
c.506A>T (p.His169Leu)
n.696A>T
n.683A>T
20g.46725534C>ACA409267126SLC2A10c.498C>A (p.His166Gln)
c.561C>A (p.His187Gln)
c.507C>A (p.His169Gln)
n.697C>A
n.684C>A
20g.46725534C>GCA409267127SLC2A10c.498C>G (p.His166Gln)
c.561C>G (p.His187Gln)
c.507C>G (p.His169Gln)
n.697C>G
n.684C>G
20g.46725534C>TCA510847683SLC2A10c.498C>T (p.His166=)
c.561C>T (p.His187=)
c.507C>T (p.His169=)
n.697C>T
n.684C>T
20g.46725535A>CCA409267128SLC2A10c.499A>C (p.Met167Leu)
c.562A>C (p.Met188Leu)
c.508A>C (p.Met170Leu)
n.698A>C
n.685A>C
20g.46725535A>GCA409267129SLC2A10c.499A>G (p.Met167Val)
c.562A>G (p.Met188Val)
c.508A>G (p.Met170Val)
n.698A>G
n.685A>G
 ClinVar
20g.46725535A>TCA409267130SLC2A10c.499A>T (p.Met167Leu)
c.562A>T (p.Met188Leu)
c.508A>T (p.Met170Leu)
n.698A>T
n.685A>T
 gnomAD v4
20g.46725535_46725536delinsATCA2366796245SLC2A10c.499_500delinsAT (p.Met167=)
c.562_563delinsAT (p.Met188=)
c.508_509delinsAT (p.Met170=)
n.698_699delinsAT
n.685_686delinsAT
20g.46725536delCA636177762SLC2A10c.500del (p.Met167SerfsTer?)
c.563del (p.Met188SerfsTer?)
c.509del (p.Met170SerfsTer?)
n.699del
n.686del
 dbSNP gnomAD v2 gnomAD v4
20g.46725536T>ACA409267133SLC2A10c.500T>A (p.Met167Lys)
c.563T>A (p.Met188Lys)
c.509T>A (p.Met170Lys)
n.699T>A
n.686T>A
20g.46725536T>CCA409267132SLC2A10c.500T>C (p.Met167Thr)
c.563T>C (p.Met188Thr)
c.509T>C (p.Met170Thr)
n.699T>C
n.686T>C
 gnomAD v4
20g.46725536T>GCA409267131SLC2A10c.500T>G (p.Met167Arg)
c.563T>G (p.Met188Arg)
c.509T>G (p.Met170Arg)
n.699T>G
n.686T>G
 gnomAD v4
20g.46725537G>ACA9891987SLC2A10c.501G>A (p.Met167Ile)
c.564G>A (p.Met188Ile)
c.510G>A (p.Met170Ile)
n.700G>A
n.687G>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
20g.46725537G>CCA409267134SLC2A10c.501G>C (p.Met167Ile)
c.564G>C (p.Met188Ile)
c.510G>C (p.Met170Ile)
n.700G>C
n.687G>C
20g.46725537G=CA2366796246SLC2A10c.501G= (p.Met167=)
c.564G= (p.Met188=)
c.510G= (p.Met170=)
n.700G=
n.687G=
20g.46725537G>TCA409267135SLC2A10c.501G>T (p.Met167Ile)
c.564G>T (p.Met188Ile)
c.510G>T (p.Met170Ile)
n.700G>T
n.687G>T
20g.46725538T>ACA409267136SLC2A10c.502T>A (p.Phe168Ile)
c.565T>A (p.Phe189Ile)
c.511T>A (p.Phe171Ile)
n.701T>A
n.688T>A
20g.46725538T>CCA409267137SLC2A10c.502T>C (p.Phe168Leu)
c.565T>C (p.Phe189Leu)
c.511T>C (p.Phe171Leu)
n.701T>C
n.688T>C
20g.46725538T>GCA409267138SLC2A10c.502T>G (p.Phe168Val)
c.565T>G (p.Phe189Val)
c.511T>G (p.Phe171Val)
n.701T>G
n.688T>G
20g.46725539T>ACA409267141SLC2A10c.503T>A (p.Phe168Tyr)
c.566T>A (p.Phe189Tyr)
c.512T>A (p.Phe171Tyr)
n.702T>A
n.689T>A
 gnomAD v4
20g.46725539T>CCA409267140SLC2A10c.503T>C (p.Phe168Ser)
c.566T>C (p.Phe189Ser)
c.512T>C (p.Phe171Ser)
n.702T>C
n.689T>C
20g.46725539T>GCA409267139SLC2A10c.503T>G (p.Phe168Cys)
c.566T>G (p.Phe189Cys)
c.512T>G (p.Phe171Cys)
n.702T>G
n.689T>G
20g.46725540C>ACA324019SLC2A10c.504C>A (p.Phe168Leu)
c.567C>A (p.Phe189Leu)
c.513C>A (p.Phe171Leu)
n.703C>A
n.690C>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
20g.46725540C=CA2366796247SLC2A10c.504C= (p.Phe168=)
c.567C= (p.Phe189=)
c.513C= (p.Phe171=)
n.703C=
n.690C=
20g.46725540C>GCA409267142SLC2A10c.504C>G (p.Phe168Leu)
c.567C>G (p.Phe189Leu)
c.513C>G (p.Phe171Leu)
n.703C>G
n.690C>G
20g.46725540C>TCA9891988SLC2A10c.504C>T (p.Phe168=)
c.567C>T (p.Phe189=)
c.513C>T (p.Phe171=)
n.703C>T
n.690C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
20g.46725541G>ACA9891989SLC2A10c.505G>A (p.Gly169Ser)
c.568G>A (p.Gly190Ser)
c.514G>A (p.Gly172Ser)
n.704G>A
n.691G>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
20g.46725541G>CCA409267143SLC2A10c.505G>C (p.Gly169Arg)
c.568G>C (p.Gly190Arg)
c.514G>C (p.Gly172Arg)
n.704G>C
n.691G>C
20g.46725541G=CA2366796248SLC2A10c.505G= (p.Gly169=)
c.568G= (p.Gly190=)
c.514G= (p.Gly172=)
n.704G=
n.691G=
20g.46725541G>TCA409267144SLC2A10c.505G>T (p.Gly169Cys)
c.568G>T (p.Gly190Cys)
c.514G>T (p.Gly172Cys)
n.704G>T
n.691G>T
 gnomAD v4
20g.46725542G>ACA9891990SLC2A10c.506G>A (p.Gly169Asp)
c.569G>A (p.Gly190Asp)
c.515G>A (p.Gly172Asp)
n.705G>A
n.692G>A
 dbSNP ExAC gnomAD v2 gnomAD v4
20g.46725542G>CCA409267145SLC2A10c.506G>C (p.Gly169Ala)
c.569G>C (p.Gly190Ala)
c.515G>C (p.Gly172Ala)
n.705G>C
n.692G>C
 ClinVar
20g.46725542G=CA2366796249SLC2A10c.506G= (p.Gly169=)
c.569G= (p.Gly190=)
c.515G= (p.Gly172=)
n.705G=
n.692G=
20g.46725542G>TCA409267146SLC2A10c.506G>T (p.Gly169Val)
c.569G>T (p.Gly190Val)
c.515G>T (p.Gly172Val)
n.705G>T
n.692G>T
 gnomAD v4
20g.46725543C>ACA510847684SLC2A10c.507C>A (p.Gly169=)
c.570C>A (p.Gly190=)
c.516C>A (p.Gly172=)
n.706C>A
n.693C>A
20g.46725543C=CA2366796250SLC2A10c.507C= (p.Gly169=)
c.570C= (p.Gly190=)
c.516C= (p.Gly172=)
n.706C=
n.693C=
20g.46725543C>GCA510847685SLC2A10c.507C>G (p.Gly169=)
c.570C>G (p.Gly190=)
c.516C>G (p.Gly172=)
n.706C>G
n.693C>G
20g.46725543C>TCA9891991SLC2A10c.507C>T (p.Gly169=)
c.570C>T (p.Gly190=)
c.516C>T (p.Gly172=)
n.706C>T
n.693C>T
 dbSNP ExAC gnomAD v2 gnomAD v4
20g.46725544T>ACA409267147SLC2A10c.508T>A (p.Trp170Arg)
c.571T>A (p.Trp191Arg)
c.517T>A (p.Trp173Arg)
n.707T>A
n.694T>A
20g.46725544T>CCA409267148SLC2A10c.508T>C (p.Trp170Arg)
c.571T>C (p.Trp191Arg)
c.517T>C (p.Trp173Arg)
n.707T>C
n.694T>C
20g.46725544T>GCA409267149SLC2A10c.508T>G (p.Trp170Gly)
c.571T>G (p.Trp191Gly)
c.517T>G (p.Trp173Gly)
n.707T>G
n.694T>G
20g.46725545G>ACA409267150SLC2A10c.509G>A (p.Trp170Ter)
c.572G>A (p.Trp191Ter)
c.518G>A (p.Trp173Ter)
n.708G>A
n.695G>A
 dbSNP gnomAD v2
20g.46725545G>CCA409267151SLC2A10c.509G>C (p.Trp170Ser)
c.572G>C (p.Trp191Ser)
c.518G>C (p.Trp173Ser)
n.708G>C
n.695G>C
20g.46725545G=CA2366796251SLC2A10c.509G= (p.Trp170=)
c.572G= (p.Trp191=)
c.518G= (p.Trp173=)
n.708G=
n.695G=
20g.46725545G>TCA409267152SLC2A10c.509G>T (p.Trp170Leu)
c.572G>T (p.Trp191Leu)
c.518G>T (p.Trp173Leu)
n.708G>T
n.695G>T
20g.46725546G>ACA340263SLC2A10c.510G>A (p.Trp170Ter)
c.573G>A (p.Trp191Ter)
c.519G>A (p.Trp173Ter)
n.709G>A
n.696G>A
 ClinVar dbSNP
20g.46725546G>CCA409267153SLC2A10c.510G>C (p.Trp170Cys)
c.573G>C (p.Trp191Cys)
c.519G>C (p.Trp173Cys)
n.709G>C
n.696G>C
20g.46725546G=CA2366796252SLC2A10c.510G= (p.Trp170=)
c.573G= (p.Trp191=)
c.519G= (p.Trp173=)
n.709G=
n.696G=
20g.46725546G>TCA409267154SLC2A10c.510G>T (p.Trp170Cys)
c.573G>T (p.Trp191Cys)
c.519G>T (p.Trp173Cys)
n.709G>T
n.696G>T
 dbSNP gnomAD v2 gnomAD v4
20g.46725547G>ACA409267155SLC2A10c.511G>A (p.Ala171Thr)
c.574G>A (p.Ala192Thr)
c.520G>A (p.Ala174Thr)
n.710G>A
n.697G>A
20g.46725547G>CCA409267156SLC2A10c.511G>C (p.Ala171Pro)
c.574G>C (p.Ala192Pro)
c.520G>C (p.Ala174Pro)
n.710G>C
n.697G>C
20g.46725547G>TCA409267157SLC2A10c.511G>T (p.Ala171Ser)
c.574G>T (p.Ala192Ser)
c.520G>T (p.Ala174Ser)
n.710G>T
n.697G>T
20g.46725548C>ACA409267158SLC2A10c.512C>A (p.Ala171Asp)
c.575C>A (p.Ala192Asp)
c.521C>A (p.Ala174Asp)
n.711C>A
n.698C>A
20g.46725548C>GCA409267160SLC2A10c.512C>G (p.Ala171Gly)
c.575C>G (p.Ala192Gly)
c.521C>G (p.Ala174Gly)
n.711C>G
n.698C>G
20g.46725548C>TCA409267159SLC2A10c.512C>T (p.Ala171Val)
c.575C>T (p.Ala192Val)
c.521C>T (p.Ala174Val)
n.711C>T
n.698C>T
 COSMIC
20g.46725549C>ACA510847686SLC2A10c.513C>A (p.Ala171=)
c.576C>A (p.Ala192=)
c.522C>A (p.Ala174=)
n.712C>A
n.699C>A
20g.46725549C>GCA510847687SLC2A10c.513C>G (p.Ala171=)
c.576C>G (p.Ala192=)
c.522C>G (p.Ala174=)
n.712C>G
n.699C>G
20g.46725549C>TCA510847688SLC2A10c.513C>T (p.Ala171=)
c.576C>T (p.Ala192=)
c.522C>T (p.Ala174=)
n.712C>T
n.699C>T
20g.46725550A>CCA409267161SLC2A10c.514A>C (p.Thr172Pro)
c.577A>C (p.Thr193Pro)
c.523A>C (p.Thr175Pro)
n.713A>C
n.700A>C
20g.46725550A>GCA409267162SLC2A10c.514A>G (p.Thr172Ala)
c.577A>G (p.Thr193Ala)
c.523A>G (p.Thr175Ala)
n.713A>G
n.700A>G
20g.46725550A>TCA409267163SLC2A10c.514A>T (p.Thr172Ser)
c.577A>T (p.Thr193Ser)
c.523A>T (p.Thr175Ser)
n.713A>T
n.700A>T
20g.46725551C>ACA409267164SLC2A10c.515C>A (p.Thr172Asn)
c.578C>A (p.Thr193Asn)
c.524C>A (p.Thr175Asn)
n.714C>A
n.701C>A
20g.46725551C=CA2366796253SLC2A10c.515C= (p.Thr172=)
c.578C= (p.Thr193=)
c.524C= (p.Thr175=)
n.714C=
n.701C=
20g.46725551C>GCA409267165SLC2A10c.515C>G (p.Thr172Ser)
c.578C>G (p.Thr193Ser)
c.524C>G (p.Thr175Ser)
n.714C>G
n.701C>G
20g.46725551C>TCA241805SLC2A10c.515C>T (p.Thr172Ile)
c.578C>T (p.Thr193Ile)
c.524C>T (p.Thr175Ile)
n.714C>T
n.701C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
20g.46725552T>ACA510847689SLC2A10c.516T>A (p.Thr172=)
c.579T>A (p.Thr193=)
c.525T>A (p.Thr175=)
n.715T>A
n.702T>A
 ClinVar
20g.46725552T>CCA510847690SLC2A10c.516T>C (p.Thr172=)
c.579T>C (p.Thr193=)
c.525T>C (p.Thr175=)
n.715T>C
n.702T>C
20g.46725552T>GCA510847691SLC2A10c.516T>G (p.Thr172=)
c.579T>G (p.Thr193=)
c.525T>G (p.Thr175=)
n.715T>G
n.702T>G
20g.46725553G>ACA16616241SLC2A10c.517G>A (p.Ala173Thr)
c.580G>A (p.Ala194Thr)
c.526G>A (p.Ala176Thr)
n.716G>A
n.703G>A
 ClinVar dbSNP gnomAD v3 gnomAD v4
20g.46725553G>CCA409267166SLC2A10c.517G>C (p.Ala173Pro)
c.580G>C (p.Ala194Pro)
c.526G>C (p.Ala176Pro)
n.716G>C
n.703G>C
20g.46725553G=CA2366796254SLC2A10c.517G= (p.Ala173=)
c.580G= (p.Ala194=)
c.526G= (p.Ala176=)
n.716G=
n.703G=
20g.46725553G>TCA409267167SLC2A10c.517G>T (p.Ala173Ser)
c.580G>T (p.Ala194Ser)
c.526G>T (p.Ala176Ser)
n.716G>T
n.703G>T
20g.46725554C>ACA409267168SLC2A10c.518C>A (p.Ala173Glu)
c.581C>A (p.Ala194Glu)
c.527C>A (p.Ala176Glu)
n.717C>A
n.704C>A
20g.46725554C>GCA409267169SLC2A10c.518C>G (p.Ala173Gly)
c.581C>G (p.Ala194Gly)
c.527C>G (p.Ala176Gly)
n.717C>G
n.704C>G
20g.46725554C>TCA409267170SLC2A10c.518C>T (p.Ala173Val)
c.581C>T (p.Ala194Val)
c.527C>T (p.Ala176Val)
n.717C>T
n.704C>T
20g.46725555A=CA2366796255SLC2A10c.519A= (p.Ala173=)
c.582A= (p.Ala194=)
c.528A= (p.Ala176=)
n.718A=
n.705A=
20g.46725555A>CCA510847692SLC2A10c.519A>C (p.Ala173=)
c.582A>C (p.Ala194=)
c.528A>C (p.Ala176=)
n.718A>C
n.705A>C
20g.46725555A>GCA9891992SLC2A10c.519A>G (p.Ala173=)
c.582A>G (p.Ala194=)
c.528A>G (p.Ala176=)
n.718A>G
n.705A>G
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
20g.46725555A>TCA510847693SLC2A10c.519A>T (p.Ala173=)
c.582A>T (p.Ala194=)
c.528A>T (p.Ala176=)
n.718A>T
n.705A>T
20g.46725556C>ACA409267173SLC2A10c.520C>A (p.Pro174Thr)
c.583C>A (p.Pro195Thr)
c.529C>A (p.Pro177Thr)
n.719C>A
n.706C>A
20g.46725556C=CA2366796256SLC2A10c.520C= (p.Pro174=)
c.583C= (p.Pro195=)
c.529C= (p.Pro177=)
n.719C=
n.706C=
20g.46725556C>GCA409267171SLC2A10c.520C>G (p.Pro174Ala)
c.583C>G (p.Pro195Ala)
c.529C>G (p.Pro177Ala)
n.719C>G
n.706C>G
 ClinVar dbSNP gnomAD v2 gnomAD v4
20g.46725556C>TCA409267172SLC2A10c.520C>T (p.Pro174Ser)
c.583C>T (p.Pro195Ser)
c.529C>T (p.Pro177Ser)
n.719C>T
n.706C>T
20g.46725557C>ACA409267174SLC2A10c.521C>A (p.Pro174His)
c.584C>A (p.Pro195His)
c.530C>A (p.Pro177His)
n.720C>A
n.707C>A
20g.46725557C>GCA409267175SLC2A10c.521C>G (p.Pro174Arg)
c.584C>G (p.Pro195Arg)
c.530C>G (p.Pro177Arg)
n.720C>G
n.707C>G
20g.46725557C>TCA409267176SLC2A10c.521C>T (p.Pro174Leu)
c.584C>T (p.Pro195Leu)
c.530C>T (p.Pro177Leu)
n.720C>T
n.707C>T
20g.46725558T>ACA510847694SLC2A10c.522T>A (p.Pro174=)
c.585T>A (p.Pro195=)
c.531T>A (p.Pro177=)
n.721T>A
n.708T>A
20g.46725558T>CCA510847695SLC2A10c.522T>C (p.Pro174=)
c.585T>C (p.Pro195=)
c.531T>C (p.Pro177=)
n.721T>C
n.708T>C
 gnomAD v3 gnomAD v4
20g.46725558T>GCA510847696SLC2A10c.522T>G (p.Pro174=)
c.585T>G (p.Pro195=)
c.531T>G (p.Pro177=)
n.721T>G
n.708T>G
20g.46725559G>ACA409267177SLC2A10c.523G>A (p.Ala175Thr)
c.586G>A (p.Ala196Thr)
c.532G>A (p.Ala178Thr)
n.722G>A
n.709G>A
 gnomAD v4
20g.46725559G>CCA409267178SLC2A10c.523G>C (p.Ala175Pro)
c.586G>C (p.Ala196Pro)
c.532G>C (p.Ala178Pro)
n.722G>C
n.709G>C
20g.46725559G>TCA409267179SLC2A10c.523G>T (p.Ala175Ser)
c.586G>T (p.Ala196Ser)
c.532G>T (p.Ala178Ser)
n.722G>T
n.709G>T
20g.46725560C>ACA409267180SLC2A10c.524C>A (p.Ala175Asp)
c.587C>A (p.Ala196Asp)
c.533C>A (p.Ala178Asp)
n.723C>A
n.710C>A
20g.46725560C>GCA409267181SLC2A10c.524C>G (p.Ala175Gly)
c.587C>G (p.Ala196Gly)
c.533C>G (p.Ala178Gly)
n.723C>G
n.710C>G
20g.46725560C>TCA409267182SLC2A10c.524C>T (p.Ala175Val)
c.587C>T (p.Ala196Val)
c.533C>T (p.Ala178Val)
n.723C>T
n.710C>T
20g.46725561T>ACA510847699SLC2A10c.525T>A (p.Ala175=)
c.588T>A (p.Ala196=)
c.534T>A (p.Ala178=)
n.724T>A
n.711T>A
 gnomAD v4
20g.46725561T>CCA510847698SLC2A10c.525T>C (p.Ala175=)
c.588T>C (p.Ala196=)
c.534T>C (p.Ala178=)
n.724T>C
n.711T>C
20g.46725561T>GCA510847697SLC2A10c.525T>G (p.Ala175=)
c.588T>G (p.Ala196=)
c.534T>G (p.Ala178=)
n.724T>G
n.711T>G
20g.46725562delCA2653170833SLC2A10c.526del (p.Val176SerfsTer?)
c.589del (p.Val197SerfsTer?)
c.535del (p.Val179SerfsTer?)
n.725del
n.712del
 gnomAD v4
20g.46725562G>ACA9891993SLC2A10c.526G>A (p.Val176Ile)
c.589G>A (p.Val197Ile)
c.535G>A (p.Val179Ile)
n.725G>A
n.712G>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
20g.46725562G>CCA409267183SLC2A10c.526G>C (p.Val176Leu)
c.589G>C (p.Val197Leu)
c.535G>C (p.Val179Leu)
n.725G>C
n.712G>C
 ClinVar
20g.46725562G=CA2366796257SLC2A10c.526G= (p.Val176=)
c.589G= (p.Val197=)
c.535G= (p.Val179=)
n.725G=
n.712G=
20g.46725562G>TCA409267184SLC2A10c.526G>T (p.Val176Phe)
c.589G>T (p.Val197Phe)
c.535G>T (p.Val179Phe)
n.725G>T
n.712G>T
20g.46725563T>ACA409267186SLC2A10c.527T>A (p.Val176Asp)
c.590T>A (p.Val197Asp)
c.536T>A (p.Val179Asp)
n.726T>A
n.713T>A
20g.46725563T>CCA409267187SLC2A10c.527T>C (p.Val176Ala)
c.590T>C (p.Val197Ala)
c.536T>C (p.Val179Ala)
n.726T>C
n.713T>C
20g.46725563T>GCA409267185SLC2A10c.527T>G (p.Val176Gly)
c.590T>G (p.Val197Gly)
c.536T>G (p.Val179Gly)
n.726T>G
n.713T>G
20g.46725564C>ACA510847700SLC2A10c.528C>A (p.Val176=)
c.591C>A (p.Val197=)
c.537C>A (p.Val179=)
n.727C>A
n.714C>A
20g.46725564C>GCA510847701SLC2A10c.528C>G (p.Val176=)
c.591C>G (p.Val197=)
c.537C>G (p.Val179=)
n.727C>G
n.714C>G
20g.46725564C>TCA510847702SLC2A10c.528C>T (p.Val176=)
c.591C>T (p.Val197=)
c.537C>T (p.Val179=)
n.727C>T
n.714C>T
20g.46725565C>ACA409267188SLC2A10c.529C>A (p.Leu177Met)
c.592C>A (p.Leu198Met)
c.538C>A (p.Leu180Met)
n.728C>A
n.715C>A
20g.46725565C>GCA409267189SLC2A10c.529C>G (p.Leu177Val)
c.592C>G (p.Leu198Val)
c.538C>G (p.Leu180Val)
n.728C>G
n.715C>G
 gnomAD v4
20g.46725565C>TCA510847703SLC2A10c.529C>T (p.Leu177=)
c.592C>T (p.Leu198=)
c.538C>T (p.Leu180=)
n.728C>T
n.715C>T
 gnomAD v4
20g.46725566T>ACA409267190SLC2A10c.530T>A (p.Leu177Gln)
c.593T>A (p.Leu198Gln)
c.539T>A (p.Leu180Gln)
n.729T>A
n.716T>A
20g.46725566T>CCA9891994SLC2A10c.530T>C (p.Leu177Pro)
c.593T>C (p.Leu198Pro)
c.539T>C (p.Leu180Pro)
n.729T>C
n.716T>C
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
20g.46725566T>GCA409267191SLC2A10c.530T>G (p.Leu177Arg)
c.593T>G (p.Leu198Arg)
c.539T>G (p.Leu180Arg)
n.729T>G
n.716T>G
20g.46725566T=CA2366796258SLC2A10c.530T= (p.Leu177=)
c.593T= (p.Leu198=)
c.539T= (p.Leu180=)
n.729T=
n.716T=
20g.46725567G>ACA9891995SLC2A10c.531G>A (p.Leu177=)
c.594G>A (p.Leu198=)
c.540G>A (p.Leu180=)
n.730G>A
n.717G>A
 dbSNP ExAC
20g.46725567G>CCA510847705SLC2A10c.531G>C (p.Leu177=)
c.594G>C (p.Leu198=)
c.540G>C (p.Leu180=)
n.730G>C
n.717G>C
20g.46725567G=CA2366796259SLC2A10c.531G= (p.Leu177=)
c.594G= (p.Leu198=)
c.540G= (p.Leu180=)
n.730G=
n.717G=
20g.46725567G>TCA510847704SLC2A10c.531G>T (p.Leu177=)
c.594G>T (p.Leu198=)
c.540G>T (p.Leu180=)
n.730G>T
n.717G>T
20g.46725568C>ACA409267192SLC2A10c.532C>A (p.Gln178Lys)
c.595C>A (p.Gln199Lys)
c.541C>A (p.Gln181Lys)
n.731C>A
n.718C>A
20g.46725568C>GCA409267193SLC2A10c.532C>G (p.Gln178Glu)
c.595C>G (p.Gln199Glu)
c.541C>G (p.Gln181Glu)
n.731C>G
n.718C>G
20g.46725568C>TCA409267194SLC2A10c.532C>T (p.Gln178Ter)
c.595C>T (p.Gln199Ter)
c.541C>T (p.Gln181Ter)
n.731C>T
n.718C>T
 gnomAD v4
20g.46725569A=CA2366796260SLC2A10c.533A= (p.Gln178=)
c.596A= (p.Gln199=)
c.542A= (p.Gln181=)
n.732A=
n.719A=
20g.46725569A>CCA409267195SLC2A10c.533A>C (p.Gln178Pro)
c.596A>C (p.Gln199Pro)
c.542A>C (p.Gln181Pro)
n.732A>C
n.719A>C
20g.46725569A>GCA409267196SLC2A10c.533A>G (p.Gln178Arg)
c.596A>G (p.Gln199Arg)
c.542A>G (p.Gln181Arg)
n.732A>G
n.719A>G
 ClinVar dbSNP gnomAD v2 gnomAD v4
20g.46725569A>TCA409267197SLC2A10c.533A>T (p.Gln178Leu)
c.596A>T (p.Gln199Leu)
c.542A>T (p.Gln181Leu)
n.732A>T
n.719A>T
20g.46725570A=CA2366796261SLC2A10c.534A= (p.Gln178=)
c.597A= (p.Gln199=)
c.543A= (p.Gln181=)
n.733A=
n.720A=
20g.46725570A>CCA409267199SLC2A10c.534A>C (p.Gln178His)
c.597A>C (p.Gln199His)
c.543A>C (p.Gln181His)
n.733A>C
n.720A>C
20g.46725570A>GCA510847706SLC2A10c.534A>G (p.Gln178=)
c.597A>G (p.Gln199=)
c.543A>G (p.Gln181=)
n.733A>G
n.720A>G
 dbSNP gnomAD v3 gnomAD v4
20g.46725570A>TCA409267200SLC2A10c.534A>T (p.Gln178His)
c.597A>T (p.Gln199His)
c.543A>T (p.Gln181His)
n.733A>T
n.720A>T
 gnomAD v4
20g.46725571T>ACA409267202SLC2A10c.535T>A (p.Ser179Thr)
c.598T>A (p.Ser200Thr)
c.544T>A (p.Ser182Thr)
n.734T>A
n.721T>A
20g.46725571T>CCA9891996SLC2A10c.535T>C (p.Ser179Pro)
c.598T>C (p.Ser200Pro)
c.544T>C (p.Ser182Pro)
n.734T>C
n.721T>C
 dbSNP ExAC gnomAD v2 gnomAD v4
20g.46725571T>GCA409267201SLC2A10c.535T>G (p.Ser179Ala)
c.598T>G (p.Ser200Ala)
c.544T>G (p.Ser182Ala)
n.734T>G
n.721T>G
20g.46725571T=CA2366796262SLC2A10c.535T= (p.Ser179=)
c.598T= (p.Ser200=)
c.544T= (p.Ser182=)
n.734T=
n.721T=
20g.46725572C>ACA409267203SLC2A10c.536C>A (p.Ser179Tyr)
c.599C>A (p.Ser200Tyr)
c.545C>A (p.Ser182Tyr)
n.735C>A
n.722C>A
20g.46725572C>GCA409267204SLC2A10c.536C>G (p.Ser179Cys)
c.599C>G (p.Ser200Cys)
c.545C>G (p.Ser182Cys)
n.735C>G
n.722C>G
20g.46725572C>TCA409267205SLC2A10c.536C>T (p.Ser179Phe)
c.599C>T (p.Ser200Phe)
c.545C>T (p.Ser182Phe)
n.735C>T
n.722C>T
 COSMIC
20g.46725573C>ACA510847707SLC2A10c.537C>A (p.Ser179=)
c.600C>A (p.Ser200=)
c.546C>A (p.Ser182=)
n.736C>A
n.723C>A
20g.46725573C>GCA510847708SLC2A10c.537C>G (p.Ser179=)
c.600C>G (p.Ser200=)
c.546C>G (p.Ser182=)
n.736C>G
n.723C>G
20g.46725573C>TCA510847709SLC2A10c.537C>T (p.Ser179=)
c.600C>T (p.Ser200=)
c.546C>T (p.Ser182=)
n.736C>T
n.723C>T
20g.46725574C>ACA409267206SLC2A10c.538C>A (p.Leu180Ile)
c.601C>A (p.Leu201Ile)
c.547C>A (p.Leu183Ile)
n.737C>A
n.724C>A
20g.46725574C=CA2366796263SLC2A10c.538C= (p.Leu180=)
c.601C= (p.Leu201=)
c.547C= (p.Leu183=)
n.737C=
n.724C=
20g.46725574C>GCA409267207SLC2A10c.538C>G (p.Leu180Val)
c.601C>G (p.Leu201Val)
c.547C>G (p.Leu183Val)
n.737C>G
n.724C>G
20g.46725574C>TCA9891997SLC2A10c.538C>T (p.Leu180Phe)
c.601C>T (p.Leu201Phe)
c.547C>T (p.Leu183Phe)
n.737C>T
n.724C>T
 dbSNP ExAC gnomAD v3 gnomAD v4
20g.46725575T>ACA409267208SLC2A10c.539T>A (p.Leu180His)
c.602T>A (p.Leu201His)
c.548T>A (p.Leu183His)
n.738T>A
n.725T>A
20g.46725575T>CCA409267209SLC2A10c.539T>C (p.Leu180Pro)
c.602T>C (p.Leu201Pro)
c.548T>C (p.Leu183Pro)
n.738T>C
n.725T>C
20g.46725575T>GCA409267210SLC2A10c.539T>G (p.Leu180Arg)
c.602T>G (p.Leu201Arg)
c.548T>G (p.Leu183Arg)
n.738T>G
n.725T>G
20g.46725576C>ACA510847710SLC2A10c.540C>A (p.Leu180=)
c.603C>A (p.Leu201=)
c.549C>A (p.Leu183=)
n.739C>A
n.726C>A
20g.46725576C>GCA510847711SLC2A10c.540C>G (p.Leu180=)
c.603C>G (p.Leu201=)
c.549C>G (p.Leu183=)
n.739C>G
n.726C>G
20g.46725576C>TCA510847712SLC2A10c.540C>T (p.Leu180=)
c.603C>T (p.Leu201=)
c.549C>T (p.Leu183=)
n.739C>T
n.726C>T
20g.46725577A>CCA409267211SLC2A10c.541A>C (p.Ser181Arg)
c.604A>C (p.Ser202Arg)
c.550A>C (p.Ser184Arg)
n.740A>C
n.727A>C
20g.46725577A>GCA409267212SLC2A10c.541A>G (p.Ser181Gly)
c.604A>G (p.Ser202Gly)
c.550A>G (p.Ser184Gly)
n.740A>G
n.727A>G
20g.46725577A>TCA409267213SLC2A10c.541A>T (p.Ser181Cys)
c.604A>T (p.Ser202Cys)
c.550A>T (p.Ser184Cys)
n.740A>T
n.727A>T
20g.46725578G>ACA409267216SLC2A10c.542G>A (p.Ser181Asn)
c.605G>A (p.Ser202Asn)
c.551G>A (p.Ser184Asn)
n.741G>A
n.728G>A
 dbSNP gnomAD v3 gnomAD v4
20g.46725578G>CCA409267215SLC2A10c.542G>C (p.Ser181Thr)
c.605G>C (p.Ser202Thr)
c.551G>C (p.Ser184Thr)
n.741G>C
n.728G>C
20g.46725578G=CA2366796264SLC2A10c.542G= (p.Ser181=)
c.605G= (p.Ser202=)
c.551G= (p.Ser184=)
n.741G=
n.728G=
20g.46725578G>TCA409267214SLC2A10c.542G>T (p.Ser181Ile)
c.605G>T (p.Ser202Ile)
c.551G>T (p.Ser184Ile)
n.741G>T
n.728G>T
20g.46725579C>ACA409267218SLC2A10c.543C>A (p.Ser181Arg)
c.606C>A (p.Ser202Arg)
c.552C>A (p.Ser184Arg)
n.742C>A
n.729C>A
 gnomAD v4
20g.46725579C>GCA409267217SLC2A10c.543C>G (p.Ser181Arg)
c.606C>G (p.Ser202Arg)
c.552C>G (p.Ser184Arg)
n.742C>G
n.729C>G
20g.46725579C>TCA510847713SLC2A10c.543C>T (p.Ser181=)
c.606C>T (p.Ser202=)
c.552C>T (p.Ser184=)
n.742C>T
n.729C>T
 gnomAD v4
20g.46725580C>ACA409267219SLC2A10c.544C>A (p.Leu182Ile)
c.607C>A (p.Leu203Ile)
c.553C>A (p.Leu185Ile)
n.743C>A
n.730C>A
20g.46725580C>GCA409267220SLC2A10c.544C>G (p.Leu182Val)
c.607C>G (p.Leu203Val)
c.553C>G (p.Leu185Val)
n.743C>G
n.730C>G
20g.46725580C>TCA409267221SLC2A10c.544C>T (p.Leu182Phe)
c.607C>T (p.Leu203Phe)
c.553C>T (p.Leu185Phe)
n.743C>T
n.730C>T
20g.46725581T>ACA409267222SLC2A10c.545T>A (p.Leu182His)
c.608T>A (p.Leu203His)
c.554T>A (p.Leu185His)
n.744T>A
n.731T>A
20g.46725581T>CCA409267223SLC2A10c.545T>C (p.Leu182Pro)
c.608T>C (p.Leu203Pro)
c.554T>C (p.Leu185Pro)
n.744T>C
n.731T>C
20g.46725581T>GCA409267224SLC2A10c.545T>G (p.Leu182Arg)
c.608T>G (p.Leu203Arg)
c.554T>G (p.Leu185Arg)
n.744T>G
n.731T>G
20g.46725582C>ACA510847714SLC2A10c.546C>A (p.Leu182=)
c.609C>A (p.Leu203=)
c.555C>A (p.Leu185=)
n.745C>A
n.732C>A
 ClinVar dbSNP gnomAD v4
20g.46725582C=CA2366796265SLC2A10c.546C= (p.Leu182=)
c.609C= (p.Leu203=)
c.555C= (p.Leu185=)
n.745C=
n.732C=
20g.46725582C>GCA510847715SLC2A10c.546C>G (p.Leu182=)
c.609C>G (p.Leu203=)
c.555C>G (p.Leu185=)
n.745C>G
n.732C>G
20g.46725582C>TCA9891998SLC2A10c.546C>T (p.Leu182=)
c.609C>T (p.Leu203=)
c.555C>T (p.Leu185=)
n.745C>T
n.732C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
20g.46725583C>ACA409267225SLC2A10c.547C>A (p.Leu183Ile)
c.610C>A (p.Leu204Ile)
c.556C>A (p.Leu186Ile)
n.746C>A
n.733C>A
20g.46725583C=CA2366796266SLC2A10c.547C= (p.Leu183=)
c.610C= (p.Leu204=)
c.556C= (p.Leu186=)
n.746C=
n.733C=
20g.46725583C>GCA409267226SLC2A10c.547C>G (p.Leu183Val)
c.610C>G (p.Leu204Val)
c.556C>G (p.Leu186Val)
n.746C>G
n.733C>G
20g.46725583C>TCA409267227SLC2A10c.547C>T (p.Leu183Phe)
c.610C>T (p.Leu204Phe)
c.556C>T (p.Leu186Phe)
n.746C>T
n.733C>T
 ClinVar dbSNP gnomAD v2 gnomAD v4
20g.46725584T>ACA409267228SLC2A10c.548T>A (p.Leu183His)
c.611T>A (p.Leu204His)
c.557T>A (p.Leu186His)
n.747T>A
n.734T>A
20g.46725584T>CCA409267229SLC2A10c.548T>C (p.Leu183Pro)
c.611T>C (p.Leu204Pro)
c.557T>C (p.Leu186Pro)
n.747T>C
n.734T>C
20g.46725584T>GCA409267230SLC2A10c.548T>G (p.Leu183Arg)
c.611T>G (p.Leu204Arg)
c.557T>G (p.Leu186Arg)
n.747T>G
n.734T>G
20g.46725585C>ACA510847716SLC2A10c.549C>A (p.Leu183=)
c.612C>A (p.Leu204=)
c.558C>A (p.Leu186=)
n.748C>A
n.735C>A
20g.46725585C=CA2366796267SLC2A10c.549C= (p.Leu183=)
c.612C= (p.Leu204=)
c.558C= (p.Leu186=)
n.748C=
n.735C=
20g.46725585C>GCA510847717SLC2A10c.549C>G (p.Leu183=)
c.612C>G (p.Leu204=)
c.558C>G (p.Leu186=)
n.748C>G
n.735C>G
 dbSNP
20g.46725585C>TCA510847718SLC2A10c.549C>T (p.Leu183=)
c.612C>T (p.Leu204=)
c.558C>T (p.Leu186=)
n.748C>T
n.735C>T
20g.46725586T>ACA409267231SLC2A10c.550T>A (p.Phe184Ile)
c.613T>A (p.Phe205Ile)
c.559T>A (p.Phe187Ile)
n.749T>A
n.736T>A
20g.46725586T>CCA409267233SLC2A10c.550T>C (p.Phe184Leu)
c.613T>C (p.Phe205Leu)
c.559T>C (p.Phe187Leu)
n.749T>C
n.736T>C
20g.46725586T>GCA409267232SLC2A10c.550T>G (p.Phe184Val)
c.613T>G (p.Phe205Val)
c.559T>G (p.Phe187Val)
n.749T>G
n.736T>G
20g.46725587T>ACA409267234SLC2A10c.551T>A (p.Phe184Tyr)
c.614T>A (p.Phe205Tyr)
c.560T>A (p.Phe187Tyr)
n.750T>A
n.737T>A
20g.46725587T>CCA409267235SLC2A10c.551T>C (p.Phe184Ser)
c.614T>C (p.Phe205Ser)
c.560T>C (p.Phe187Ser)
n.750T>C
n.737T>C
20g.46725587T>GCA409267236SLC2A10c.551T>G (p.Phe184Cys)
c.614T>G (p.Phe205Cys)
c.560T>G (p.Phe187Cys)
n.750T>G
n.737T>G
20g.46725588C>ACA409267237SLC2A10c.552C>A (p.Phe184Leu)
c.615C>A (p.Phe205Leu)
c.561C>A (p.Phe187Leu)
n.751C>A
n.738C>A
20g.46725588C=CA2366796268SLC2A10c.552C= (p.Phe184=)
c.615C= (p.Phe205=)
c.561C= (p.Phe187=)
n.751C=
n.738C=
20g.46725588C>GCA409267238SLC2A10c.552C>G (p.Phe184Leu)
c.615C>G (p.Phe205Leu)
c.561C>G (p.Phe187Leu)
n.751C>G
n.738C>G
20g.46725588C>TCA510847719SLC2A10c.552C>T (p.Phe184=)
c.615C>T (p.Phe205=)
c.561C>T (p.Phe187=)
n.751C>T
n.738C>T
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
20g.46725589C>ACA409267239SLC2A10c.553C>A (p.Leu185Ile)
c.616C>A (p.Leu206Ile)
c.562C>A (p.Leu188Ile)
n.752C>A
n.739C>A
20g.46725589C>GCA409267240SLC2A10c.553C>G (p.Leu185Val)
c.616C>G (p.Leu206Val)
c.562C>G (p.Leu188Val)
n.752C>G
n.739C>G
20g.46725589C>TCA409267241SLC2A10c.553C>T (p.Leu185Phe)
c.616C>T (p.Leu206Phe)
c.562C>T (p.Leu188Phe)
n.752C>T
n.739C>T
 gnomAD v4
20g.46725590T>ACA409267242SLC2A10c.554T>A (p.Leu185His)
c.617T>A (p.Leu206His)
c.563T>A (p.Leu188His)
n.753T>A
n.740T>A
 COSMIC
20g.46725590T>CCA409267243SLC2A10c.554T>C (p.Leu185Pro)
c.617T>C (p.Leu206Pro)
c.563T>C (p.Leu188Pro)
n.753T>C
n.740T>C
20g.46725590T>GCA409267244SLC2A10c.554T>G (p.Leu185Arg)
c.617T>G (p.Leu206Arg)
c.563T>G (p.Leu188Arg)
n.753T>G
n.740T>G
20g.46725591C>ACA510847722SLC2A10c.555C>A (p.Leu185=)
c.618C>A (p.Leu206=)
c.564C>A (p.Leu188=)
n.754C>A
n.741C>A
20g.46725591C>GCA510847721SLC2A10c.555C>G (p.Leu185=)
c.618C>G (p.Leu206=)
c.564C>G (p.Leu188=)
n.754C>G
n.741C>G
20g.46725591C>TCA510847720SLC2A10c.555C>T (p.Leu185=)
c.618C>T (p.Leu206=)
c.564C>T (p.Leu188=)
n.754C>T
n.741C>T
20g.46725592C>ACA409267246SLC2A10c.556C>A (p.Pro186Thr)
c.619C>A (p.Pro207Thr)
c.565C>A (p.Pro189Thr)
n.755C>A
n.742C>A
20g.46725592C=CA2366796269SLC2A10c.556C= (p.Pro186=)
c.619C= (p.Pro207=)
c.565C= (p.Pro189=)
n.755C=
n.742C=
20g.46725592C>GCA409267247SLC2A10c.556C>G (p.Pro186Ala)
c.619C>G (p.Pro207Ala)
c.565C>G (p.Pro189Ala)
n.755C>G
n.742C>G
20g.46725592C>TCA409267245SLC2A10c.556C>T (p.Pro186Ser)
c.619C>T (p.Pro207Ser)
c.565C>T (p.Pro189Ser)
n.755C>T
n.742C>T
 dbSNP gnomAD v3 gnomAD v4 COSMIC
20g.46725593C>ACA409267248SLC2A10c.557C>A (p.Pro186His)
c.620C>A (p.Pro207His)
c.566C>A (p.Pro189His)
n.756C>A
n.743C>A
20g.46725593C=CA2366796270SLC2A10c.557C= (p.Pro186=)
c.620C= (p.Pro207=)
c.566C= (p.Pro189=)
n.756C=
n.743C=
20g.46725593C>GCA409267249SLC2A10c.557C>G (p.Pro186Arg)
c.620C>G (p.Pro207Arg)
c.566C>G (p.Pro189Arg)
n.756C>G
n.743C>G
20g.46725593C>TCA9891999SLC2A10c.557C>T (p.Pro186Leu)
c.620C>T (p.Pro207Leu)
c.566C>T (p.Pro189Leu)
n.756C>T
n.743C>T
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
20g.46725594T>ACA510847723SLC2A10c.558T>A (p.Pro186=)
c.621T>A (p.Pro207=)
c.567T>A (p.Pro189=)
n.757T>A
n.744T>A
20g.46725594T>CCA510847725SLC2A10c.558T>C (p.Pro186=)
c.621T>C (p.Pro207=)
c.567T>C (p.Pro189=)
n.757T>C
n.744T>C
20g.46725594T>GCA510847724SLC2A10c.558T>G (p.Pro186=)
c.621T>G (p.Pro207=)
c.567T>G (p.Pro189=)
n.757T>G
n.744T>G
20g.46725595G>ACA409267250SLC2A10c.559G>A (p.Ala187Thr)
c.622G>A (p.Ala208Thr)
c.568G>A (p.Ala190Thr)
n.758G>A
n.745G>A
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
20g.46725595G>CCA409267251SLC2A10c.559G>C (p.Ala187Pro)
c.622G>C (p.Ala208Pro)
c.568G>C (p.Ala190Pro)
n.758G>C
n.745G>C
20g.46725595G=CA2366796271SLC2A10c.559G= (p.Ala187=)
c.622G= (p.Ala208=)
c.568G= (p.Ala190=)
n.758G=
n.745G=
20g.46725595G>TCA409267252SLC2A10c.559G>T (p.Ala187Ser)
c.622G>T (p.Ala208Ser)
c.568G>T (p.Ala190Ser)
n.758G>T
n.745G>T
20g.46725595_46725596delinsGCCA2366796272SLC2A10c.559_560delinsGC (p.Ala187=)
c.622_623delinsGC (p.Ala208=)
c.568_569delinsGC (p.Ala190=)
n.758_759delinsGC
n.745_746delinsGC
20g.46725596delCA636177764SLC2A10c.560del (p.Ala187ValfsTer?)
c.623del (p.Ala208ValfsTer?)
c.569del (p.Ala190ValfsTer?)
n.759del
n.746del
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
20g.46725596C>ACA9892000SLC2A10c.560C>A (p.Ala187Asp)
c.623C>A (p.Ala208Asp)
c.569C>A (p.Ala190Asp)
n.759C>A
n.746C>A
 dbSNP ExAC gnomAD v2 gnomAD v4
20g.46725596C=CA2366796273SLC2A10c.560C= (p.Ala187=)
c.623C= (p.Ala208=)
c.569C= (p.Ala190=)
n.759C=
n.746C=
20g.46725596C>GCA409267254SLC2A10c.560C>G (p.Ala187Gly)
c.623C>G (p.Ala208Gly)
c.569C>G (p.Ala190Gly)
n.759C>G
n.746C>G
20g.46725596C>TCA409267253SLC2A10c.560C>T (p.Ala187Val)
c.623C>T (p.Ala208Val)
c.569C>T (p.Ala190Val)
n.759C>T
n.746C>T
 ClinVar dbSNP gnomAD v4
20g.46725597T>ACA510847726SLC2A10c.561T>A (p.Ala187=)
c.624T>A (p.Ala208=)
c.570T>A (p.Ala190=)
n.760T>A
n.747T>A
20g.46725597T>CCA510847727SLC2A10c.561T>C (p.Ala187=)
c.624T>C (p.Ala208=)
c.570T>C (p.Ala190=)
n.760T>C
n.747T>C
20g.46725597T>GCA510847728SLC2A10c.561T>G (p.Ala187=)
c.624T>G (p.Ala208=)
c.570T>G (p.Ala190=)
n.760T>G
n.747T>G
20g.46725598G>ACA409267255SLC2A10c.562G>A (p.Gly188Ser)
c.625G>A (p.Gly209Ser)
c.571G>A (p.Gly191Ser)
n.761G>A
n.748G>A
 gnomAD v4
20g.46725598G>CCA315755801SLC2A10c.562G>C (p.Gly188Arg)
c.625G>C (p.Gly209Arg)
c.571G>C (p.Gly191Arg)
n.761G>C
n.748G>C
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
20g.46725598G=CA2366796274SLC2A10c.562G= (p.Gly188=)
c.625G= (p.Gly209=)
c.571G= (p.Gly191=)
n.761G=
n.748G=
20g.46725598G>TCA409267256SLC2A10c.562G>T (p.Gly188Cys)
c.625G>T (p.Gly209Cys)
c.571G>T (p.Gly191Cys)
n.761G>T
n.748G>T
20g.46725599G>ACA409267257SLC2A10c.563G>A (p.Gly188Asp)
c.626G>A (p.Gly209Asp)
c.572G>A (p.Gly191Asp)
n.762G>A
n.749G>A
20g.46725599G>CCA409267258SLC2A10c.563G>C (p.Gly188Ala)
c.626G>C (p.Gly209Ala)
c.572G>C (p.Gly191Ala)
n.762G>C
n.749G>C
20g.46725599G>TCA409267259SLC2A10c.563G>T (p.Gly188Val)
c.626G>T (p.Gly209Val)
c.572G>T (p.Gly191Val)
n.762G>T
n.749G>T
20g.46725600T>ACA510847729SLC2A10c.564T>A (p.Gly188=)
c.627T>A (p.Gly209=)
c.573T>A (p.Gly191=)
n.763T>A
n.750T>A
20g.46725600T>CCA510847730SLC2A10c.564T>C (p.Gly188=)
c.627T>C (p.Gly209=)
c.573T>C (p.Gly191=)
n.763T>C
n.750T>C
20g.46725600T>GCA510847731SLC2A10c.564T>G (p.Gly188=)
c.627T>G (p.Gly209=)
c.573T>G (p.Gly191=)
n.763T>G
n.750T>G
 gnomAD v4
20g.46725601A>CCA409267260SLC2A10c.565A>C (p.Thr189Pro)
c.628A>C (p.Thr210Pro)
c.574A>C (p.Thr192Pro)
n.764A>C
n.751A>C
20g.46725601A>GCA409267262SLC2A10c.565A>G (p.Thr189Ala)
c.628A>G (p.Thr210Ala)
c.574A>G (p.Thr192Ala)
n.764A>G
n.751A>G
20g.46725601A>TCA409267261SLC2A10c.565A>T (p.Thr189Ser)
c.628A>T (p.Thr210Ser)
c.574A>T (p.Thr192Ser)
n.764A>T
n.751A>T
20g.46725602C>ACA409267263SLC2A10c.566C>A (p.Thr189Lys)
c.629C>A (p.Thr210Lys)
c.575C>A (p.Thr192Lys)
n.765C>A
n.752C>A
20g.46725602C>GCA409267264SLC2A10c.566C>G (p.Thr189Arg)
c.629C>G (p.Thr210Arg)
c.575C>G (p.Thr192Arg)
n.765C>G
n.752C>G
20g.46725602C>TCA409267265SLC2A10c.566C>T (p.Thr189Ile)
c.629C>T (p.Thr210Ile)
c.575C>T (p.Thr192Ile)
n.765C>T
n.752C>T
 ClinVar gnomAD v4
20g.46725603A>CCA510847732SLC2A10c.567A>C (p.Thr189=)
c.630A>C (p.Thr210=)
c.576A>C (p.Thr192=)
n.766A>C
n.753A>C
20g.46725603A>GCA510847733SLC2A10c.567A>G (p.Thr189=)
c.630A>G (p.Thr210=)
c.576A>G (p.Thr192=)
n.766A>G
n.753A>G
20g.46725603A>TCA510847734SLC2A10c.567A>T (p.Thr189=)
c.630A>T (p.Thr210=)
c.576A>T (p.Thr192=)
n.766A>T
n.753A>T
20g.46725604G>ACA409267266SLC2A10c.568G>A (p.Asp190Asn)
c.631G>A (p.Asp211Asn)
c.577G>A (p.Asp193Asn)
n.767G>A
n.754G>A
20g.46725604G>CCA409267267SLC2A10c.568G>C (p.Asp190His)
c.631G>C (p.Asp211His)
c.577G>C (p.Asp193His)
n.767G>C
n.754G>C
20g.46725604G=CA2366796275SLC2A10c.568G= (p.Asp190=)
c.631G= (p.Asp211=)
c.577G= (p.Asp193=)
n.767G=
n.754G=
20g.46725604G>TCA9892001SLC2A10c.568G>T (p.Asp190Tyr)
c.631G>T (p.Asp211Tyr)
c.577G>T (p.Asp193Tyr)
n.767G>T
n.754G>T
 dbSNP ExAC gnomAD v2 gnomAD v4

Number of alleles fetched