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
20g.46725430C>ACA510847603SLC2A10c.394C>A (p.Arg132=)
n.546C>A
c.457C>A (p.Arg153=)
c.403C>A (p.Arg135=)
n.593C>A
n.580C>A
20g.46725430C=CA2366796201SLC2A10c.394C= (p.Arg132=)
n.546C=
c.457C= (p.Arg153=)
c.403C= (p.Arg135=)
n.593C=
n.580C=
20g.46725430C>GCA409266926SLC2A10c.394C>G (p.Arg132Gly)
n.546C>G
c.457C>G (p.Arg153Gly)
c.403C>G (p.Arg135Gly)
n.593C>G
n.580C>G
20g.46725430C>TCA340267SLC2A10c.394C>T (p.Arg132Trp)
n.546C>T
c.457C>T (p.Arg153Trp)
c.403C>T (p.Arg135Trp)
n.593C>T
n.580C>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
20g.46725431G>ACA9891969SLC2A10c.395G>A (p.Arg132Gln)
n.547G>A
c.458G>A (p.Arg153Gln)
c.404G>A (p.Arg135Gln)
n.594G>A
n.581G>A
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
20g.46725431G>CCA409266927SLC2A10c.395G>C (p.Arg132Pro)
n.547G>C
c.458G>C (p.Arg153Pro)
c.404G>C (p.Arg135Pro)
n.594G>C
n.581G>C
dbSNP gnomAD v2 gnomAD v4
20g.46725431G=CA2366796202SLC2A10c.395G= (p.Arg132=)
n.547G=
c.458G= (p.Arg153=)
c.404G= (p.Arg135=)
n.594G=
n.581G=
20g.46725431G>TCA409266928SLC2A10c.395G>T (p.Arg132Leu)
n.547G>T
c.458G>T (p.Arg153Leu)
c.404G>T (p.Arg135Leu)
n.594G>T
n.581G>T
ClinVar dbSNP
20g.46725432G>ACA510847604SLC2A10c.396G>A (p.Arg132=)
n.548G>A
c.459G>A (p.Arg153=)
c.405G>A (p.Arg135=)
n.595G>A
n.582G>A
20g.46725432G>CCA510847605SLC2A10c.396G>C (p.Arg132=)
n.548G>C
c.459G>C (p.Arg153=)
c.405G>C (p.Arg135=)
n.595G>C
n.582G>C
20g.46725432G>TCA510847606SLC2A10c.396G>T (p.Arg132=)
n.548G>T
c.459G>T (p.Arg153=)
c.405G>T (p.Arg135=)
n.595G>T
n.582G>T
20g.46725433G>ACA409266929SLC2A10c.397G>A (p.Gly133Arg)
n.549G>A
c.460G>A (p.Gly154Arg)
c.406G>A (p.Gly136Arg)
n.596G>A
n.583G>A
ClinVar dbSNP COSMIC
20g.46725433G>CCA409266930SLC2A10c.397G>C (p.Gly133Arg)
n.549G>C
c.460G>C (p.Gly154Arg)
c.406G>C (p.Gly136Arg)
n.596G>C
n.583G>C
20g.46725433G=CA2366796203SLC2A10c.397G= (p.Gly133=)
n.549G=
c.460G= (p.Gly154=)
c.406G= (p.Gly136=)
n.596G=
n.583G=
20g.46725433G>TCA409266931SLC2A10c.397G>T (p.Gly133Ter)
n.549G>T
c.460G>T (p.Gly154Ter)
c.406G>T (p.Gly136Ter)
n.596G>T
n.583G>T
20g.46725434G>ACA409266932SLC2A10c.398G>A (p.Gly133Glu)
n.550G>A
c.461G>A (p.Gly154Glu)
c.407G>A (p.Gly136Glu)
n.597G>A
n.584G>A
20g.46725434G>CCA409266933SLC2A10c.398G>C (p.Gly133Ala)
n.550G>C
c.461G>C (p.Gly154Ala)
c.407G>C (p.Gly136Ala)
n.597G>C
n.584G>C
20g.46725434G>TCA409266934SLC2A10c.398G>T (p.Gly133Val)
n.550G>T
c.461G>T (p.Gly154Val)
c.407G>T (p.Gly136Val)
n.597G>T
n.584G>T
20g.46725435A>CCA510847607SLC2A10c.399A>C (p.Gly133=)
n.551A>C
c.462A>C (p.Gly154=)
c.408A>C (p.Gly136=)
n.598A>C
n.585A>C
20g.46725435A>GCA510847608SLC2A10c.399A>G (p.Gly133=)
n.551A>G
c.462A>G (p.Gly154=)
c.408A>G (p.Gly136=)
n.598A>G
n.585A>G
20g.46725435A>TCA510847609SLC2A10c.399A>T (p.Gly133=)
n.551A>T
c.462A>T (p.Gly154=)
c.408A>T (p.Gly136=)
n.598A>T
n.585A>T
20g.46725436G>ACA409266936SLC2A10c.400G>A (p.Val134Met)
n.552G>A
c.463G>A (p.Val155Met)
c.409G>A (p.Val137Met)
n.599G>A
n.586G>A
20g.46725436G>CCA409266937SLC2A10c.400G>C (p.Val134Leu)
n.552G>C
c.463G>C (p.Val155Leu)
c.409G>C (p.Val137Leu)
n.599G>C
n.586G>C
20g.46725436G>TCA409266935SLC2A10c.400G>T (p.Val134Leu)
n.552G>T
c.463G>T (p.Val155Leu)
c.409G>T (p.Val137Leu)
n.599G>T
n.586G>T
20g.46725437T>ACA409266938SLC2A10c.401T>A (p.Val134Glu)
n.553T>A
c.464T>A (p.Val155Glu)
c.410T>A (p.Val137Glu)
n.600T>A
n.587T>A
20g.46725437T>CCA409266939SLC2A10c.401T>C (p.Val134Ala)
n.553T>C
c.464T>C (p.Val155Ala)
c.410T>C (p.Val137Ala)
n.600T>C
n.587T>C
20g.46725437T>GCA409266940SLC2A10c.401T>G (p.Val134Gly)
n.553T>G
c.464T>G (p.Val155Gly)
c.410T>G (p.Val137Gly)
n.600T>G
n.587T>G
gnomAD v4
20g.46725438G>ACA510847610SLC2A10c.402G>A (p.Val134=)
n.554G>A
c.465G>A (p.Val155=)
c.411G>A (p.Val137=)
n.601G>A
n.588G>A
COSMIC
20g.46725438G>CCA510847611SLC2A10c.402G>C (p.Val134=)
n.554G>C
c.465G>C (p.Val155=)
c.411G>C (p.Val137=)
n.601G>C
n.588G>C
20g.46725438G>TCA510847612SLC2A10c.402G>T (p.Val134=)
n.554G>T
c.465G>T (p.Val155=)
c.411G>T (p.Val137=)
n.601G>T
n.588G>T
20g.46725439C>ACA409266941SLC2A10c.403C>A (p.Leu135Met)
n.555C>A
c.466C>A (p.Leu156Met)
c.412C>A (p.Leu138Met)
n.602C>A
n.589C>A
20g.46725439C=CA2366796204SLC2A10c.403C= (p.Leu135=)
n.555C=
c.466C= (p.Leu156=)
c.412C= (p.Leu138=)
n.602C=
n.589C=
20g.46725439C>GCA409266942SLC2A10c.403C>G (p.Leu135Val)
n.555C>G
c.466C>G (p.Leu156Val)
c.412C>G (p.Leu138Val)
n.602C>G
n.589C>G
dbSNP gnomAD v2 gnomAD v4
20g.46725439C>TCA510847613SLC2A10c.403C>T (p.Leu135=)
n.555C>T
c.466C>T (p.Leu156=)
c.412C>T (p.Leu138=)
n.602C>T
n.589C>T
dbSNP
20g.46725440T>ACA409266945SLC2A10c.404T>A (p.Leu135Gln)
n.556T>A
c.467T>A (p.Leu156Gln)
c.413T>A (p.Leu138Gln)
n.603T>A
n.590T>A
20g.46725440T>CCA409266944SLC2A10c.404T>C (p.Leu135Pro)
n.556T>C
c.467T>C (p.Leu156Pro)
c.413T>C (p.Leu138Pro)
n.603T>C
n.590T>C
20g.46725440T>GCA409266943SLC2A10c.404T>G (p.Leu135Arg)
n.556T>G
c.467T>G (p.Leu156Arg)
c.413T>G (p.Leu138Arg)
n.603T>G
n.590T>G
20g.46725441G>ACA510847614SLC2A10c.405G>A (p.Leu135=)
n.557G>A
c.468G>A (p.Leu156=)
c.414G>A (p.Leu138=)
n.604G>A
n.591G>A
gnomAD v4
20g.46725441G>CCA510847616SLC2A10c.405G>C (p.Leu135=)
n.557G>C
c.468G>C (p.Leu156=)
c.414G>C (p.Leu138=)
n.604G>C
n.591G>C
20g.46725441G>TCA510847615SLC2A10c.405G>T (p.Leu135=)
n.557G>T
c.468G>T (p.Leu156=)
c.414G>T (p.Leu138=)
n.604G>T
n.591G>T
dbSNP
20g.46725442G>ACA409266946SLC2A10c.406G>A (p.Val136Met)
n.558G>A
c.469G>A (p.Val157Met)
c.415G>A (p.Val139Met)
n.605G>A
n.592G>A
20g.46725442G>CCA409266947SLC2A10c.406G>C (p.Val136Leu)
n.558G>C
c.469G>C (p.Val157Leu)
c.415G>C (p.Val139Leu)
n.605G>C
n.592G>C
dbSNP
20g.46725442G=CA2366796205SLC2A10c.406G= (p.Val136=)
n.558G=
c.469G= (p.Val157=)
c.415G= (p.Val139=)
n.605G=
n.592G=
20g.46725442G>TCA409266948SLC2A10c.406G>T (p.Val136Leu)
n.558G>T
c.469G>T (p.Val157Leu)
c.415G>T (p.Val139Leu)
n.605G>T
n.592G>T
gnomAD v4
20g.46725443T>ACA409266949SLC2A10c.407T>A (p.Val136Glu)
n.559T>A
c.470T>A (p.Val157Glu)
c.416T>A (p.Val139Glu)
n.606T>A
n.593T>A
20g.46725443T>CCA409266950SLC2A10c.407T>C (p.Val136Ala)
n.559T>C
c.470T>C (p.Val157Ala)
c.416T>C (p.Val139Ala)
n.606T>C
n.593T>C
20g.46725443T>GCA409266951SLC2A10c.407T>G (p.Val136Gly)
n.559T>G
c.470T>G (p.Val157Gly)
c.416T>G (p.Val139Gly)
n.606T>G
n.593T>G
20g.46725444G>ACA510847617SLC2A10c.408G>A (p.Val136=)
n.560G>A
c.471G>A (p.Val157=)
c.417G>A (p.Val139=)
n.607G>A
n.594G>A
20g.46725444G>CCA510847618SLC2A10c.408G>C (p.Val136=)
n.560G>C
c.471G>C (p.Val157=)
c.417G>C (p.Val139=)
n.607G>C
n.594G>C

Number of alleles fetched