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.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
20g.46725605A>CCA409267268SLC2A10c.569A>C (p.Asp190Ala)
c.632A>C (p.Asp211Ala)
c.578A>C (p.Asp193Ala)
n.768A>C
n.755A>C
20g.46725605A>GCA409267269SLC2A10c.569A>G (p.Asp190Gly)
c.632A>G (p.Asp211Gly)
c.578A>G (p.Asp193Gly)
n.768A>G
n.755A>G
20g.46725605A>TCA409267270SLC2A10c.569A>T (p.Asp190Val)
c.632A>T (p.Asp211Val)
c.578A>T (p.Asp193Val)
n.768A>T
n.755A>T
20g.46725606T>ACA409267271SLC2A10c.570T>A (p.Asp190Glu)
c.633T>A (p.Asp211Glu)
c.579T>A (p.Asp193Glu)
n.769T>A
n.756T>A
dbSNP gnomAD v3 gnomAD v4
20g.46725606T>CCA510847735SLC2A10c.570T>C (p.Asp190=)
c.633T>C (p.Asp211=)
c.579T>C (p.Asp193=)
n.769T>C
n.756T>C
20g.46725606T>GCA409267272SLC2A10c.570T>G (p.Asp190Glu)
c.633T>G (p.Asp211Glu)
c.579T>G (p.Asp193Glu)
n.769T>G
n.756T>G
dbSNP
20g.46725606T=CA2366796276SLC2A10c.570T= (p.Asp190=)
c.633T= (p.Asp211=)
c.579T= (p.Asp193=)
n.769T=
n.756T=
20g.46725607G>ACA409267273SLC2A10c.571G>A (p.Glu191Lys)
c.634G>A (p.Glu212Lys)
c.580G>A (p.Glu194Lys)
n.770G>A
n.757G>A
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
20g.46725607G>CCA409267275SLC2A10c.571G>C (p.Glu191Gln)
c.634G>C (p.Glu212Gln)
c.580G>C (p.Glu194Gln)
n.770G>C
n.757G>C
20g.46725607G=CA2366796277SLC2A10c.571G= (p.Glu191=)
c.634G= (p.Glu212=)
c.580G= (p.Glu194=)
n.770G=
n.757G=
20g.46725607G>TCA409267274SLC2A10c.571G>T (p.Glu191Ter)
c.634G>T (p.Glu212Ter)
c.580G>T (p.Glu194Ter)
n.770G>T
n.757G>T
20g.46725608A>CCA409267276SLC2A10c.572A>C (p.Glu191Ala)
c.635A>C (p.Glu212Ala)
c.581A>C (p.Glu194Ala)
n.771A>C
n.758A>C
20g.46725608A>GCA409267277SLC2A10c.572A>G (p.Glu191Gly)
c.635A>G (p.Glu212Gly)
c.581A>G (p.Glu194Gly)
n.771A>G
n.758A>G
20g.46725608A>TCA409267278SLC2A10c.572A>T (p.Glu191Val)
c.635A>T (p.Glu212Val)
c.581A>T (p.Glu194Val)
n.771A>T
n.758A>T
20g.46725609G>ACA510847736SLC2A10c.573G>A (p.Glu191=)
c.636G>A (p.Glu212=)
c.582G>A (p.Glu194=)
n.772G>A
n.759G>A
20g.46725609G>CCA409267279SLC2A10c.573G>C (p.Glu191Asp)
c.636G>C (p.Glu212Asp)
c.582G>C (p.Glu194Asp)
n.772G>C
n.759G>C
20g.46725609G>TCA409267281SLC2A10c.573G>T (p.Glu191Asp)
c.636G>T (p.Glu212Asp)
c.582G>T (p.Glu194Asp)
n.772G>T
n.759G>T
gnomAD v4
20g.46725610A>CCA409267282SLC2A10c.574A>C (p.Thr192Pro)
c.637A>C (p.Thr213Pro)
c.583A>C (p.Thr195Pro)
n.773A>C
n.760A>C
20g.46725610A>GCA409267283SLC2A10c.574A>G (p.Thr192Ala)
c.637A>G (p.Thr213Ala)
c.583A>G (p.Thr195Ala)
n.773A>G
n.760A>G
20g.46725610A>TCA409267284SLC2A10c.574A>T (p.Thr192Ser)
c.637A>T (p.Thr213Ser)
c.583A>T (p.Thr195Ser)
n.773A>T
n.760A>T
20g.46725611C>ACA409267285SLC2A10c.575C>A (p.Thr192Asn)
c.638C>A (p.Thr213Asn)
c.584C>A (p.Thr195Asn)
n.774C>A
n.761C>A
dbSNP
20g.46725611C=CA2366796278SLC2A10c.575C= (p.Thr192=)
c.638C= (p.Thr213=)
c.584C= (p.Thr195=)
n.774C=
n.761C=
20g.46725611C>GCA409267286SLC2A10c.575C>G (p.Thr192Ser)
c.638C>G (p.Thr213Ser)
c.584C>G (p.Thr195Ser)
n.774C>G
n.761C>G
20g.46725611C>TCA409267287SLC2A10c.575C>T (p.Thr192Ile)
c.638C>T (p.Thr213Ile)
c.584C>T (p.Thr195Ile)
n.774C>T
n.761C>T
20g.46725612T>ACA510847737SLC2A10c.576T>A (p.Thr192=)
c.639T>A (p.Thr213=)
c.585T>A (p.Thr195=)
n.775T>A
n.762T>A
20g.46725612T>CCA510847738SLC2A10c.576T>C (p.Thr192=)
c.639T>C (p.Thr213=)
c.585T>C (p.Thr195=)
n.775T>C
n.762T>C
20g.46725612T>GCA510847739SLC2A10c.576T>G (p.Thr192=)
c.639T>G (p.Thr213=)
c.585T>G (p.Thr195=)
n.775T>G
n.762T>G
20g.46725613G>ACA315755821SLC2A10c.577G>A (p.Ala193Thr)
c.640G>A (p.Ala214Thr)
c.586G>A (p.Ala196Thr)
n.776G>A
n.763G>A
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
20g.46725613G>CCA409267289SLC2A10c.577G>C (p.Ala193Pro)
c.640G>C (p.Ala214Pro)
c.586G>C (p.Ala196Pro)
n.776G>C
n.763G>C
20g.46725613G=CA2366796279SLC2A10c.577G= (p.Ala193=)
c.640G= (p.Ala214=)
c.586G= (p.Ala196=)
n.776G=
n.763G=
20g.46725613G>TCA409267288SLC2A10c.577G>T (p.Ala193Ser)
c.640G>T (p.Ala214Ser)
c.586G>T (p.Ala196Ser)
n.776G>T
n.763G>T
20g.46725614C>ACA409267290SLC2A10c.578C>A (p.Ala193Glu)
c.641C>A (p.Ala214Glu)
c.587C>A (p.Ala196Glu)
n.777C>A
n.764C>A
dbSNP
20g.46725614C=CA2366796280SLC2A10c.578C= (p.Ala193=)
c.641C= (p.Ala214=)
c.587C= (p.Ala196=)
n.777C=
n.764C=
20g.46725614C>GCA409267291SLC2A10c.578C>G (p.Ala193Gly)
c.641C>G (p.Ala214Gly)
c.587C>G (p.Ala196Gly)
n.777C>G
n.764C>G
20g.46725614C>TCA409267292SLC2A10c.578C>T (p.Ala193Val)
c.641C>T (p.Ala214Val)
c.587C>T (p.Ala196Val)
n.777C>T
n.764C>T
dbSNP gnomAD v2
20g.46725615A>CCA510847740SLC2A10c.579A>C (p.Ala193=)
c.642A>C (p.Ala214=)
c.588A>C (p.Ala196=)
n.778A>C
n.765A>C
20g.46725615A>GCA510847741SLC2A10c.579A>G (p.Ala193=)
c.642A>G (p.Ala214=)
c.588A>G (p.Ala196=)
n.778A>G
n.765A>G
ClinVar gnomAD v4
20g.46725615A>TCA510847742SLC2A10c.579A>T (p.Ala193=)
c.642A>T (p.Ala214=)
c.588A>T (p.Ala196=)
n.778A>T
n.765A>T
20g.46725616A>CCA409267293SLC2A10c.580A>C (p.Thr194Pro)
c.643A>C (p.Thr215Pro)
c.589A>C (p.Thr197Pro)
n.779A>C
n.766A>C
20g.46725616A>GCA409267294SLC2A10c.580A>G (p.Thr194Ala)
c.643A>G (p.Thr215Ala)
c.589A>G (p.Thr197Ala)
n.779A>G
n.766A>G
dbSNP gnomAD v3 gnomAD v4
20g.46725616A>TCA409267295SLC2A10c.580A>T (p.Thr194Ser)
c.643A>T (p.Thr215Ser)
c.589A>T (p.Thr197Ser)
n.779A>T
n.766A>T
20g.46725617C>ACA409267296SLC2A10c.581C>A (p.Thr194Lys)
c.644C>A (p.Thr215Lys)
c.590C>A (p.Thr197Lys)
n.780C>A
n.767C>A
20g.46725617C=CA2366796281SLC2A10c.581C= (p.Thr194=)
c.644C= (p.Thr215=)
c.590C= (p.Thr197=)
n.780C=
n.767C=
20g.46725617C>GCA409267297SLC2A10c.581C>G (p.Thr194Arg)
c.644C>G (p.Thr215Arg)
c.590C>G (p.Thr197Arg)
n.780C>G
n.767C>G
20g.46725617C>TCA9892002SLC2A10c.581C>T (p.Thr194Ile)
c.644C>T (p.Thr215Ile)
c.590C>T (p.Thr197Ile)
n.780C>T
n.767C>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
20g.46725617_46725618insCCACAACCAAACACACCCACA2816531406SLC2A10c.581_582insCCACAACCAAACACACCCA (p.Lys196AsnfsTer16)
c.644_645insCCACAACCAAACACACCCA (p.Lys217AsnfsTer16)
c.590_591insCCACAACCAAACACACCCA (p.Lys199AsnfsTer16)
n.780_781insCCACAACCAAACACACCCA
n.767_768insCCACAACCAAACACACCCA
20g.46725618A>CCA510847743SLC2A10c.582A>C (p.Thr194=)
c.645A>C (p.Thr215=)
c.591A>C (p.Thr197=)
n.781A>C
n.768A>C
20g.46725618A>GCA510847744SLC2A10c.582A>G (p.Thr194=)
c.645A>G (p.Thr215=)
c.591A>G (p.Thr197=)
n.781A>G
n.768A>G
20g.46725618A>TCA510847745SLC2A10c.582A>T (p.Thr194=)
c.645A>T (p.Thr215=)
c.591A>T (p.Thr197=)
n.781A>T
n.768A>T
20g.46725619C>ACA409267298SLC2A10c.583C>A (p.His195Asn)
c.646C>A (p.His216Asn)
c.592C>A (p.His198Asn)
n.782C>A
n.769C>A
20g.46725619C>GCA409267299SLC2A10c.583C>G (p.His195Asp)
c.646C>G (p.His216Asp)
c.592C>G (p.His198Asp)
n.782C>G
n.769C>G
20g.46725619C>TCA409267300SLC2A10c.583C>T (p.His195Tyr)
c.646C>T (p.His216Tyr)
c.592C>T (p.His198Tyr)
n.782C>T
n.769C>T
20g.46725620A=CA2366796282SLC2A10c.584A= (p.His195=)
c.647A= (p.His216=)
c.593A= (p.His198=)
n.783A=
n.770A=
20g.46725620A>CCA409267301SLC2A10c.584A>C (p.His195Pro)
c.647A>C (p.His216Pro)
c.593A>C (p.His198Pro)
n.783A>C
n.770A>C
dbSNP gnomAD v3 gnomAD v4
20g.46725620A>GCA409267303SLC2A10c.584A>G (p.His195Arg)
c.647A>G (p.His216Arg)
c.593A>G (p.His198Arg)
n.783A>G
n.770A>G
20g.46725620A>TCA409267302SLC2A10c.584A>T (p.His195Leu)
c.647A>T (p.His216Leu)
c.593A>T (p.His198Leu)
n.783A>T
n.770A>T
20g.46725621C>ACA409267304SLC2A10c.585C>A (p.His195Gln)
c.648C>A (p.His216Gln)
c.594C>A (p.His198Gln)
n.784C>A
n.771C>A
gnomAD v4
20g.46725621C>GCA409267305SLC2A10c.585C>G (p.His195Gln)
c.648C>G (p.His216Gln)
c.594C>G (p.His198Gln)
n.784C>G
n.771C>G
20g.46725621C>TCA510847746SLC2A10c.585C>T (p.His195=)
c.648C>T (p.His216=)
c.594C>T (p.His198=)
n.784C>T
n.771C>T
ClinVar
20g.46725622A=CA2366796283SLC2A10c.586A= (p.Lys196=)
c.649A= (p.Lys217=)
c.595A= (p.Lys199=)
n.785A=
n.772A=
20g.46725622A>CCA409267308SLC2A10c.586A>C (p.Lys196Gln)
c.649A>C (p.Lys217Gln)
c.595A>C (p.Lys199Gln)
n.785A>C
n.772A>C
dbSNP gnomAD v2 gnomAD v4
20g.46725622A>GCA409267312SLC2A10c.586A>G (p.Lys196Glu)
c.649A>G (p.Lys217Glu)
c.595A>G (p.Lys199Glu)
n.785A>G
n.772A>G
dbSNP
20g.46725622A>TCA409267310SLC2A10c.586A>T (p.Lys196Ter)
c.649A>T (p.Lys217Ter)
c.595A>T (p.Lys199Ter)
n.785A>T
n.772A>T
20g.46725623A=CA2366796284SLC2A10c.587A= (p.Lys196=)
c.650A= (p.Lys217=)
c.596A= (p.Lys199=)
n.786A=
n.773A=
20g.46725623A>CCA409267315SLC2A10c.587A>C (p.Lys196Thr)
c.650A>C (p.Lys217Thr)
c.596A>C (p.Lys199Thr)
n.786A>C
n.773A>C
20g.46725623A>GCA409267318SLC2A10c.587A>G (p.Lys196Arg)
c.650A>G (p.Lys217Arg)
c.596A>G (p.Lys199Arg)
n.786A>G
n.773A>G
20g.46725623A>TCA320063SLC2A10c.587A>T (p.Lys196Met)
c.650A>T (p.Lys217Met)
c.596A>T (p.Lys199Met)
n.786A>T
n.773A>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
20g.46725624G>ACA510847747SLC2A10c.588G>A (p.Lys196=)
c.651G>A (p.Lys217=)
c.597G>A (p.Lys199=)
n.787G>A
n.774G>A
20g.46725624G>CCA409267319SLC2A10c.588G>C (p.Lys196Asn)
c.651G>C (p.Lys217Asn)
c.597G>C (p.Lys199Asn)
n.787G>C
n.774G>C
20g.46725624G>TCA409267321SLC2A10c.588G>T (p.Lys196Asn)
c.651G>T (p.Lys217Asn)
c.597G>T (p.Lys199Asn)
n.787G>T
n.774G>T
20g.46725625G>ACA409267323SLC2A10c.589G>A (p.Asp197Asn)
c.652G>A (p.Asp218Asn)
c.598G>A (p.Asp200Asn)
n.788G>A
n.775G>A
gnomAD v4 COSMIC
20g.46725625G>CCA409267326SLC2A10c.589G>C (p.Asp197His)
c.652G>C (p.Asp218His)
c.598G>C (p.Asp200His)
n.788G>C
n.775G>C
20g.46725625G=CA2366796285SLC2A10c.589G= (p.Asp197=)
c.652G= (p.Asp218=)
c.598G= (p.Asp200=)
n.788G=
n.775G=
20g.46725625G>TCA9892003SLC2A10c.589G>T (p.Asp197Tyr)
c.652G>T (p.Asp218Tyr)
c.598G>T (p.Asp200Tyr)
n.788G>T
n.775G>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
20g.46725626A=CA2366796286SLC2A10c.590A= (p.Asp197=)
c.653A= (p.Asp218=)
c.599A= (p.Asp200=)
n.789A=
n.776A=
20g.46725626A>CCA409267328SLC2A10c.590A>C (p.Asp197Ala)
c.653A>C (p.Asp218Ala)
c.599A>C (p.Asp200Ala)
n.789A>C
n.776A>C
20g.46725626A>GCA409267330SLC2A10c.590A>G (p.Asp197Gly)
c.653A>G (p.Asp218Gly)
c.599A>G (p.Asp200Gly)
n.789A>G
n.776A>G
ClinVar dbSNP
20g.46725626A>TCA409267331SLC2A10c.590A>T (p.Asp197Val)
c.653A>T (p.Asp218Val)
c.599A>T (p.Asp200Val)
n.789A>T
n.776A>T
gnomAD v4
20g.46725627C>ACA409267333SLC2A10c.591C>A (p.Asp197Glu)
c.654C>A (p.Asp218Glu)
c.600C>A (p.Asp200Glu)
n.790C>A
n.777C>A
gnomAD v4
20g.46725627C>GCA409267335SLC2A10c.591C>G (p.Asp197Glu)
c.654C>G (p.Asp218Glu)
c.600C>G (p.Asp200Glu)
n.790C>G
n.777C>G
20g.46725627C>TCA510847748SLC2A10c.591C>T (p.Asp197=)
c.654C>T (p.Asp218=)
c.600C>T (p.Asp200=)
n.790C>T
n.777C>T
20g.46725628C>ACA409267337SLC2A10c.592C>A (p.Leu198Ile)
c.655C>A (p.Leu219Ile)
c.601C>A (p.Leu201Ile)
n.791C>A
n.778C>A
20g.46725628C=CA2366796287SLC2A10c.592C= (p.Leu198=)
c.655C= (p.Leu219=)
c.601C= (p.Leu201=)
n.791C=
n.778C=
20g.46725628C>GCA409267338SLC2A10c.592C>G (p.Leu198Val)
c.655C>G (p.Leu219Val)
c.601C>G (p.Leu201Val)
n.791C>G
n.778C>G
20g.46725628C>TCA409267339SLC2A10c.592C>T (p.Leu198Phe)
c.655C>T (p.Leu219Phe)
c.601C>T (p.Leu201Phe)
n.791C>T
n.778C>T
dbSNP gnomAD v2 gnomAD v4
20g.46725629T>ACA409267342SLC2A10c.593T>A (p.Leu198His)
c.656T>A (p.Leu219His)
c.602T>A (p.Leu201His)
n.792T>A
n.779T>A
20g.46725629T>CCA409267344SLC2A10c.593T>C (p.Leu198Pro)
c.656T>C (p.Leu219Pro)
c.602T>C (p.Leu201Pro)
n.792T>C
n.779T>C
20g.46725629T>GCA409267345SLC2A10c.593T>G (p.Leu198Arg)
c.656T>G (p.Leu219Arg)
c.602T>G (p.Leu201Arg)
n.792T>G
n.779T>G
20g.46725630C>ACA510847750SLC2A10c.594C>A (p.Leu198=)
c.657C>A (p.Leu219=)
c.603C>A (p.Leu201=)
n.793C>A
n.780C>A
20g.46725630C>GCA510847751SLC2A10c.594C>G (p.Leu198=)
c.657C>G (p.Leu219=)
c.603C>G (p.Leu201=)
n.793C>G
n.780C>G
20g.46725630C>TCA510847749SLC2A10c.594C>T (p.Leu198=)
c.657C>T (p.Leu219=)
c.603C>T (p.Leu201=)
n.793C>T
n.780C>T
20g.46725631A>CCA409267353SLC2A10c.595A>C (p.Ile199Leu)
c.658A>C (p.Ile220Leu)
c.604A>C (p.Ile202Leu)
n.794A>C
n.781A>C
gnomAD v4
20g.46725631A>GCA409267348SLC2A10c.595A>G (p.Ile199Val)
c.658A>G (p.Ile220Val)
c.604A>G (p.Ile202Val)
n.794A>G
n.781A>G
ClinVar
20g.46725631A>TCA409267350SLC2A10c.595A>T (p.Ile199Phe)
c.658A>T (p.Ile220Phe)
c.604A>T (p.Ile202Phe)
n.794A>T
n.781A>T
20g.46725632T>ACA409267358SLC2A10c.596T>A (p.Ile199Asn)
c.659T>A (p.Ile220Asn)
c.605T>A (p.Ile202Asn)
n.795T>A
n.782T>A
20g.46725632T>CCA409267359SLC2A10c.596T>C (p.Ile199Thr)
c.659T>C (p.Ile220Thr)
c.605T>C (p.Ile202Thr)
n.795T>C
n.782T>C
20g.46725632T>GCA409267360SLC2A10c.596T>G (p.Ile199Ser)
c.659T>G (p.Ile220Ser)
c.605T>G (p.Ile202Ser)
n.795T>G
n.782T>G
20g.46725633C>ACA510847753SLC2A10c.597C>A (p.Ile199=)
c.660C>A (p.Ile220=)
c.606C>A (p.Ile202=)
n.796C>A
n.783C>A
20g.46725633C>GCA409267361SLC2A10c.597C>G (p.Ile199Met)
c.660C>G (p.Ile220Met)
c.606C>G (p.Ile202Met)
n.796C>G
n.783C>G
20g.46725633C>TCA510847752SLC2A10c.597C>T (p.Ile199=)
c.660C>T (p.Ile220=)
c.606C>T (p.Ile202=)
n.796C>T
n.783C>T
COSMIC
20g.46725635delCA2816531410SLC2A10c.599del (p.Pro200HisfsTer?)
c.662del (p.Pro221HisfsTer?)
c.608del (p.Pro203HisfsTer?)
n.798del
n.785del

Number of alleles fetched