Chr Mutation (hg38) CAid Gene Transcript Linkouts
2g.233672708T>ACA431856908UGT1A10,UGT1A8,UGT1A9c.855+35331T>A (n.855+35331T>A)
c.855+54146T>A (n.855+54146T>A)
c.774T>A (p.Val258=)
2g.233672708T>CCA431856912UGT1A10,UGT1A8,UGT1A9c.855+35331T>C (n.855+35331T>C)
c.855+54146T>C (n.855+54146T>C)
c.774T>C (p.Val258=)
2g.233672708T>GCA431856914UGT1A10,UGT1A8,UGT1A9c.855+35331T>G (n.855+35331T>G)
c.855+54146T>G (n.855+54146T>G)
c.774T>G (p.Val258=)
2g.233672709T>ACA351080992UGT1A10,UGT1A8,UGT1A9c.855+35332T>A (n.855+35332T>A)
c.855+54147T>A (n.855+54147T>A)
c.775T>A (p.Leu259Met)
 dbSNP gnomAD v3 gnomAD v4
2g.233672709T>CCA431856917UGT1A10,UGT1A8,UGT1A9c.855+35332T>C (n.855+35332T>C)
c.855+54147T>C (n.855+54147T>C)
c.775T>C (p.Leu259=)
2g.233672709T>GCA2178125UGT1A10,UGT1A8,UGT1A9c.855+35332T>G (n.855+35332T>G)
c.855+54147T>G (n.855+54147T>G)
c.775T>G (p.Leu259Val)
 dbSNP ExAC gnomAD v2 gnomAD v4
2g.233672709T=CA1335852771UGT1A10,UGT1A8,UGT1A9c.855+35332T= (n.855+35332T=)
c.855+54147T= (n.855+54147T=)
c.775T= (p.Leu259=)
2g.233672710T>ACA351080993UGT1A10,UGT1A8,UGT1A9c.855+35333T>A (n.855+35333T>A)
c.855+54148T>A (n.855+54148T>A)
c.776T>A (p.Leu259Ter)
2g.233672710T>CCA351080994UGT1A10,UGT1A8,UGT1A9c.855+35333T>C (n.855+35333T>C)
c.855+54148T>C (n.855+54148T>C)
c.776T>C (p.Leu259Ser)
 dbSNP gnomAD v2 gnomAD v4
2g.233672710T>GCA351080995UGT1A10,UGT1A8,UGT1A9c.855+35333T>G (n.855+35333T>G)
c.855+54148T>G (n.855+54148T>G)
c.776T>G (p.Leu259Trp)
 gnomAD v4
2g.233672710T=CA1335852775UGT1A10,UGT1A8,UGT1A9c.855+35333T= (n.855+35333T=)
c.855+54148T= (n.855+54148T=)
c.776T= (p.Leu259=)
2g.233672711G>ACA431856924UGT1A10,UGT1A8,UGT1A9c.855+35334G>A (n.855+35334G>A)
c.855+54149G>A (n.855+54149G>A)
c.777G>A (p.Leu259=)
2g.233672711G>CCA351080999UGT1A10,UGT1A8,UGT1A9c.855+35334G>C (n.855+35334G>C)
c.855+54149G>C (n.855+54149G>C)
c.777G>C (p.Leu259Phe)
2g.233672711G>TCA351081002UGT1A10,UGT1A8,UGT1A9c.855+35334G>T (n.855+35334G>T)
c.855+54149G>T (n.855+54149G>T)
c.777G>T (p.Leu259Phe)
2g.233672712G>ACA351081004UGT1A10,UGT1A8,UGT1A9c.855+35335G>A (n.855+35335G>A)
c.855+54150G>A (n.855+54150G>A)
c.778G>A (p.Asp260Asn)
2g.233672712G>CCA351081008UGT1A10,UGT1A8,UGT1A9c.855+35335G>C (n.855+35335G>C)
c.855+54150G>C (n.855+54150G>C)
c.778G>C (p.Asp260His)
2g.233672712G>TCA351081009UGT1A10,UGT1A8,UGT1A9c.855+35335G>T (n.855+35335G>T)
c.855+54150G>T (n.855+54150G>T)
c.778G>T (p.Asp260Tyr)
2g.233672713A=CA1335852779UGT1A10,UGT1A8,UGT1A9c.855+35336A= (n.855+35336A=)
c.855+54151A= (n.855+54151A=)
c.779A= (p.Asp260=)
2g.233672713A>CCA351081010UGT1A10,UGT1A8,UGT1A9c.855+35336A>C (n.855+35336A>C)
c.855+54151A>C (n.855+54151A>C)
c.779A>C (p.Asp260Ala)
2g.233672713A>GCA351081011UGT1A10,UGT1A8,UGT1A9c.855+35336A>G (n.855+35336A>G)
c.855+54151A>G (n.855+54151A>G)
c.779A>G (p.Asp260Gly)
 dbSNP gnomAD v2
2g.233672713A>TCA351081012UGT1A10,UGT1A8,UGT1A9c.855+35336A>T (n.855+35336A>T)
c.855+54151A>T (n.855+54151A>T)
c.779A>T (p.Asp260Val)
2g.233672714C>ACA351081013UGT1A10,UGT1A8,UGT1A9c.855+35337C>A (n.855+35337C>A)
c.855+54152C>A (n.855+54152C>A)
c.780C>A (p.Asp260Glu)
2g.233672714C=CA1335852785UGT1A10,UGT1A8,UGT1A9c.855+35337C= (n.855+35337C=)
c.855+54152C= (n.855+54152C=)
c.780C= (p.Asp260=)
2g.233672714C>GCA2178126UGT1A10,UGT1A8,UGT1A9c.855+35337C>G (n.855+35337C>G)
c.855+54152C>G (n.855+54152C>G)
c.780C>G (p.Asp260Glu)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.233672714C>TCA431856970UGT1A10,UGT1A8,UGT1A9c.855+35337C>T (n.855+35337C>T)
c.855+54152C>T (n.855+54152C>T)
c.780C>T (p.Asp260=)
 dbSNP
2g.233672715T>ACA351081015UGT1A10,UGT1A8,UGT1A9c.855+35338T>A (n.855+35338T>A)
c.855+54153T>A (n.855+54153T>A)
c.781T>A (p.Tyr261Asn)
2g.233672715T>CCA2178127UGT1A10,UGT1A8,UGT1A9c.855+35338T>C (n.855+35338T>C)
c.855+54153T>C (n.855+54153T>C)
c.781T>C (p.Tyr261His)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.233672715T>GCA351081017UGT1A10,UGT1A8,UGT1A9c.855+35338T>G (n.855+35338T>G)
c.855+54153T>G (n.855+54153T>G)
c.781T>G (p.Tyr261Asp)
2g.233672715T=CA1335852789UGT1A10,UGT1A8,UGT1A9c.855+35338T= (n.855+35338T=)
c.855+54153T= (n.855+54153T=)
c.781T= (p.Tyr261=)
2g.233672716A=CA1335852791UGT1A10,UGT1A8,UGT1A9c.855+35339A= (n.855+35339A=)
c.855+54154A= (n.855+54154A=)
c.782A= (p.Tyr261=)
2g.233672716A>CCA351081020UGT1A10,UGT1A8,UGT1A9c.855+35339A>C (n.855+35339A>C)
c.855+54154A>C (n.855+54154A>C)
c.782A>C (p.Tyr261Ser)
2g.233672716A>GCA351081025UGT1A10,UGT1A8,UGT1A9c.855+35339A>G (n.855+35339A>G)
c.855+54154A>G (n.855+54154A>G)
c.782A>G (p.Tyr261Cys)
 dbSNP gnomAD v4
2g.233672716A>TCA351081023UGT1A10,UGT1A8,UGT1A9c.855+35339A>T (n.855+35339A>T)
c.855+54154A>T (n.855+54154A>T)
c.782A>T (p.Tyr261Phe)
2g.233672717T>ACA351081027UGT1A10,UGT1A8,UGT1A9c.855+35340T>A (n.855+35340T>A)
c.855+54155T>A (n.855+54155T>A)
c.783T>A (p.Tyr261Ter)
2g.233672717T>CCA431856984UGT1A10,UGT1A8,UGT1A9c.855+35340T>C (n.855+35340T>C)
c.855+54155T>C (n.855+54155T>C)
c.783T>C (p.Tyr261=)
 gnomAD v4
2g.233672717T>GCA351081029UGT1A10,UGT1A8,UGT1A9c.855+35340T>G (n.855+35340T>G)
c.855+54155T>G (n.855+54155T>G)
c.783T>G (p.Tyr261Ter)
2g.233672718C>ACA351081032UGT1A10,UGT1A8,UGT1A9c.855+35341C>A (n.855+35341C>A)
c.855+54156C>A (n.855+54156C>A)
c.784C>A (p.Pro262Thr)
 gnomAD v4
2g.233672718C=CA1335852794UGT1A10,UGT1A8,UGT1A9c.855+35341C= (n.855+35341C=)
c.855+54156C= (n.855+54156C=)
c.784C= (p.Pro262=)
2g.233672718C>GCA351081034UGT1A10,UGT1A8,UGT1A9c.855+35341C>G (n.855+35341C>G)
c.855+54156C>G (n.855+54156C>G)
c.784C>G (p.Pro262Ala)
2g.233672718C>TCA351081033UGT1A10,UGT1A8,UGT1A9c.855+35341C>T (n.855+35341C>T)
c.855+54156C>T (n.855+54156C>T)
c.784C>T (p.Pro262Ser)
 dbSNP gnomAD v2 gnomAD v4
2g.233672719C>ACA351081035UGT1A10,UGT1A8,UGT1A9c.855+35342C>A (n.855+35342C>A)
c.855+54157C>A (n.855+54157C>A)
c.785C>A (p.Pro262His)
2g.233672719C>GCA351081037UGT1A10,UGT1A8,UGT1A9c.855+35342C>G (n.855+35342C>G)
c.855+54157C>G (n.855+54157C>G)
c.785C>G (p.Pro262Arg)
2g.233672719C>TCA351081036UGT1A10,UGT1A8,UGT1A9c.855+35342C>T (n.855+35342C>T)
c.855+54157C>T (n.855+54157C>T)
c.785C>T (p.Pro262Leu)
 gnomAD v4
2g.233672720C>ACA431856993UGT1A10,UGT1A8,UGT1A9c.855+35343C>A (n.855+35343C>A)
c.855+54158C>A (n.855+54158C>A)
c.786C>A (p.Pro262=)
2g.233672720C>GCA431857005UGT1A10,UGT1A8,UGT1A9c.855+35343C>G (n.855+35343C>G)
c.855+54158C>G (n.855+54158C>G)
c.786C>G (p.Pro262=)
2g.233672720C>TCA431857007UGT1A10,UGT1A8,UGT1A9c.855+35343C>T (n.855+35343C>T)
c.855+54158C>T (n.855+54158C>T)
c.786C>T (p.Pro262=)
2g.233672721A>CCA351081038UGT1A10,UGT1A8,UGT1A9c.855+35344A>C (n.855+35344A>C)
c.855+54159A>C (n.855+54159A>C)
c.787A>C (p.Lys263Gln)
2g.233672721A>GCA351081042UGT1A10,UGT1A8,UGT1A9c.855+35344A>G (n.855+35344A>G)
c.855+54159A>G (n.855+54159A>G)
c.787A>G (p.Lys263Glu)
 COSMIC
2g.233672721A>TCA351081039UGT1A10,UGT1A8,UGT1A9c.855+35344A>T (n.855+35344A>T)
c.855+54159A>T (n.855+54159A>T)
c.787A>T (p.Lys263Ter)
2g.233672722A>CCA351081051UGT1A10,UGT1A8,UGT1A9c.855+35345A>C (n.855+35345A>C)
c.855+54160A>C (n.855+54160A>C)
c.788A>C (p.Lys263Thr)

Number of alleles fetched