Chr Mutation (hg38) CAid Gene Transcript Linkouts
21g.44286431_44288165delCA2580618164AIREc.133-126_539-180del
n.294-126_1083-180del
n.302-126_1091-180del
ClinVar
21g.44286691_44286699delCA2695230255AIREc.267_275del (p.Tyr90_Arg92del)
n.428_436del
n.436_444del
21g.44286698C>ACA512490237AIREc.274C>A (p.Arg92=)
n.435C>A
n.443C>A
21g.44286698C=CA2391565234AIREc.274C= (p.Arg92=)
n.435C=
n.443C=
21g.44286698C>GCA410423492AIREc.274C>G (p.Arg92Gly)
n.435C>G
n.443C>G
21g.44286698C>TCA16608527AIREc.274C>T (p.Arg92Trp)
n.435C>T
n.443C>T
ClinVar dbSNP gnomAD v3 gnomAD v4
21g.44286699G>ACA410423495AIREc.275G>A (p.Arg92Gln)
n.436G>A
n.444G>A
ClinVar dbSNP gnomAD v3 gnomAD v4
21g.44286699G>CCA410423494AIREc.275G>C (p.Arg92Pro)
n.436G>C
n.444G>C
21g.44286699G=CA2391565235AIREc.275G= (p.Arg92=)
n.436G=
n.444G=
21g.44286699G>TCA410423493AIREc.275G>T (p.Arg92Leu)
n.436G>T
n.444G>T
21g.44286700G>ACA10051507AIREc.276G>A (p.Arg92=)
n.437G>A
n.445G>A
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
21g.44286700G>CCA512490238AIREc.276G>C (p.Arg92=)
n.437G>C
n.445G>C
21g.44286700G=CA2391565236AIREc.276G= (p.Arg92=)
n.437G=
n.445G=
21g.44286700G>TCA512490239AIREc.276G>T (p.Arg92=)
n.437G>T
n.445G>T
dbSNP gnomAD v2 gnomAD v4
21g.44286701C>ACA410423496AIREc.277C>A (p.Leu93Met)
n.438C>A
n.446C>A
21g.44286701C>GCA410423497AIREc.277C>G (p.Leu93Val)
n.438C>G
n.446C>G
21g.44286701C>TCA512490240AIREc.277C>T (p.Leu93=)
n.438C>T
n.446C>T
ClinVar
21g.44286702T>ACA410423498AIREc.278T>A (p.Leu93Gln)
n.439T>A
n.447T>A
ClinVar gnomAD v4
21g.44286702T>CCA10051508AIREc.278T>C (p.Leu93Pro)
n.439T>C
n.447T>C
dbSNP ExAC gnomAD v4 COSMIC
21g.44286702T>GCA219203AIREc.278T>G (p.Leu93Arg)
n.439T>G
n.447T>G
ClinVar dbSNP
21g.44286702T=CA2391565237AIREc.278T= (p.Leu93=)
n.439T=
n.447T=
21g.44286703G>ACA512490241AIREc.279G>A (p.Leu93=)
n.440G>A
n.448G>A
21g.44286703G>CCA512490243AIREc.279G>C (p.Leu93=)
n.440G>C
n.448G>C
21g.44286703G>TCA512490244AIREc.279G>T (p.Leu93=)
n.440G>T
n.448G>T
21g.44286704C>ACA410423500AIREc.280C>A (p.Gln94Lys)
n.441C>A
n.449C>A
gnomAD v4
21g.44286704C=CA2391565238AIREc.280C= (p.Gln94=)
n.441C=
n.449C=
21g.44286704C>GCA410423499AIREc.280C>G (p.Gln94Glu)
n.441C>G
n.449C>G
21g.44286704C>TCA10051509AIREc.280C>T (p.Gln94Ter)
n.441C>T
n.449C>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
21g.44286705A>CCA410423501AIREc.281A>C (p.Gln94Pro)
n.442A>C
n.450A>C
gnomAD v4
21g.44286705A>GCA410423502AIREc.281A>G (p.Gln94Arg)
n.442A>G
n.450A>G
21g.44286705A>TCA410423503AIREc.281A>T (p.Gln94Leu)
n.442A>T
n.450A>T
21g.44286706G>ACA10051510AIREc.282G>A (p.Gln94=)
n.443G>A
n.451G>A
ClinVar dbSNP ExAC gnomAD v4
21g.44286706G>CCA410423504AIREc.282G>C (p.Gln94His)
n.443G>C
n.451G>C
21g.44286706G=CA2391565239AIREc.282G= (p.Gln94=)
n.443G=
n.451G=
21g.44286706G>TCA410423505AIREc.282G>T (p.Gln94His)
n.443G>T
n.451G>T
21g.44286707C>ACA410423506AIREc.283C>A (p.Pro95Thr)
n.444C>A
n.452C>A
21g.44286707C>GCA410423508AIREc.283C>G (p.Pro95Ala)
n.444C>G
n.452C>G
21g.44286707C>TCA410423507AIREc.283C>T (p.Pro95Ser)
n.444C>T
n.452C>T
ClinVar gnomAD v4
21g.44286708C>ACA410423509AIREc.284C>A (p.Pro95His)
n.445C>A
n.453C>A
21g.44286708C=CA2391565240AIREc.284C= (p.Pro95=)
n.445C=
n.453C=
21g.44286708C>GCA410423510AIREc.284C>G (p.Pro95Arg)
n.445C>G
n.453C>G
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
21g.44286708C>TCA410423511AIREc.284C>T (p.Pro95Leu)
n.445C>T
n.453C>T
21g.44286709C>ACA512490245AIREc.285C>A (p.Pro95=)
n.446C>A
n.454C>A
21g.44286709C>GCA512490247AIREc.285C>G (p.Pro95=)
n.446C>G
n.454C>G
21g.44286709C>TCA512490246AIREc.285C>T (p.Pro95=)
n.446C>T
n.454C>T
ClinVar
21g.44286710A>CCA410423512AIREc.286A>C (p.Ile96Leu)
n.447A>C
n.455A>C
ClinVar dbSNP
21g.44286710A>GCA410423513AIREc.286A>G (p.Ile96Val)
n.447A>G
n.455A>G
21g.44286710A>TCA410423514AIREc.286A>T (p.Ile96Phe)
n.447A>T
n.455A>T
21g.44286711T>ACA410423515AIREc.287T>A (p.Ile96Asn)
n.448T>A
n.456T>A
21g.44286711T>CCA410423516AIREc.287T>C (p.Ile96Thr)
n.448T>C
n.456T>C

Number of alleles fetched