Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
2 | g.233672714C>A | CA351081013 | UGT1A10,UGT1A8,UGT1A9 | c.855+35337C>A (n.855+35337C>A) c.855+54152C>A (n.855+54152C>A) c.780C>A (p.Asp260Glu) | |
2 | g.233672714C= | CA1335852785 | UGT1A10,UGT1A8,UGT1A9 | c.855+35337C= (n.855+35337C=) c.855+54152C= (n.855+54152C=) c.780C= (p.Asp260=) | |
2 | g.233672714C>G | CA2178126 | UGT1A10,UGT1A8,UGT1A9 | c.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 |
2 | g.233672714C>T | CA431856970 | UGT1A10,UGT1A8,UGT1A9 | c.855+35337C>T (n.855+35337C>T) c.855+54152C>T (n.855+54152C>T) c.780C>T (p.Asp260=) | dbSNP |
2 | g.233672715T>A | CA351081015 | UGT1A10,UGT1A8,UGT1A9 | c.855+35338T>A (n.855+35338T>A) c.855+54153T>A (n.855+54153T>A) c.781T>A (p.Tyr261Asn) | |
2 | g.233672715T>C | CA2178127 | UGT1A10,UGT1A8,UGT1A9 | c.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 |
2 | g.233672715T>G | CA351081017 | UGT1A10,UGT1A8,UGT1A9 | c.855+35338T>G (n.855+35338T>G) c.855+54153T>G (n.855+54153T>G) c.781T>G (p.Tyr261Asp) | |
2 | g.233672715T= | CA1335852789 | UGT1A10,UGT1A8,UGT1A9 | c.855+35338T= (n.855+35338T=) c.855+54153T= (n.855+54153T=) c.781T= (p.Tyr261=) | |
2 | g.233672716A= | CA1335852791 | UGT1A10,UGT1A8,UGT1A9 | c.855+35339A= (n.855+35339A=) c.855+54154A= (n.855+54154A=) c.782A= (p.Tyr261=) | |
2 | g.233672716A>C | CA351081020 | UGT1A10,UGT1A8,UGT1A9 | c.855+35339A>C (n.855+35339A>C) c.855+54154A>C (n.855+54154A>C) c.782A>C (p.Tyr261Ser) | |
2 | g.233672716A>G | CA351081025 | UGT1A10,UGT1A8,UGT1A9 | c.855+35339A>G (n.855+35339A>G) c.855+54154A>G (n.855+54154A>G) c.782A>G (p.Tyr261Cys) | dbSNP gnomAD v4 |
2 | g.233672716A>T | CA351081023 | UGT1A10,UGT1A8,UGT1A9 | c.855+35339A>T (n.855+35339A>T) c.855+54154A>T (n.855+54154A>T) c.782A>T (p.Tyr261Phe) | |
2 | g.233672717T>A | CA351081027 | UGT1A10,UGT1A8,UGT1A9 | c.855+35340T>A (n.855+35340T>A) c.855+54155T>A (n.855+54155T>A) c.783T>A (p.Tyr261Ter) | |
2 | g.233672717T>C | CA431856984 | UGT1A10,UGT1A8,UGT1A9 | c.855+35340T>C (n.855+35340T>C) c.855+54155T>C (n.855+54155T>C) c.783T>C (p.Tyr261=) | gnomAD v4 |
2 | g.233672717T>G | CA351081029 | UGT1A10,UGT1A8,UGT1A9 | c.855+35340T>G (n.855+35340T>G) c.855+54155T>G (n.855+54155T>G) c.783T>G (p.Tyr261Ter) | |
2 | g.233672718C>A | CA351081032 | UGT1A10,UGT1A8,UGT1A9 | c.855+35341C>A (n.855+35341C>A) c.855+54156C>A (n.855+54156C>A) c.784C>A (p.Pro262Thr) | gnomAD v4 |
2 | g.233672718C= | CA1335852794 | UGT1A10,UGT1A8,UGT1A9 | c.855+35341C= (n.855+35341C=) c.855+54156C= (n.855+54156C=) c.784C= (p.Pro262=) | |
2 | g.233672718C>G | CA351081034 | UGT1A10,UGT1A8,UGT1A9 | c.855+35341C>G (n.855+35341C>G) c.855+54156C>G (n.855+54156C>G) c.784C>G (p.Pro262Ala) | |
2 | g.233672718C>T | CA351081033 | UGT1A10,UGT1A8,UGT1A9 | c.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 |
2 | g.233672719C>A | CA351081035 | UGT1A10,UGT1A8,UGT1A9 | c.855+35342C>A (n.855+35342C>A) c.855+54157C>A (n.855+54157C>A) c.785C>A (p.Pro262His) | |
2 | g.233672719C>G | CA351081037 | UGT1A10,UGT1A8,UGT1A9 | c.855+35342C>G (n.855+35342C>G) c.855+54157C>G (n.855+54157C>G) c.785C>G (p.Pro262Arg) | |
2 | g.233672719C>T | CA351081036 | UGT1A10,UGT1A8,UGT1A9 | c.855+35342C>T (n.855+35342C>T) c.855+54157C>T (n.855+54157C>T) c.785C>T (p.Pro262Leu) | gnomAD v4 |
2 | g.233672720C>A | CA431856993 | UGT1A10,UGT1A8,UGT1A9 | c.855+35343C>A (n.855+35343C>A) c.855+54158C>A (n.855+54158C>A) c.786C>A (p.Pro262=) | |
2 | g.233672720C>G | CA431857005 | UGT1A10,UGT1A8,UGT1A9 | c.855+35343C>G (n.855+35343C>G) c.855+54158C>G (n.855+54158C>G) c.786C>G (p.Pro262=) | |
2 | g.233672720C>T | CA431857007 | UGT1A10,UGT1A8,UGT1A9 | c.855+35343C>T (n.855+35343C>T) c.855+54158C>T (n.855+54158C>T) c.786C>T (p.Pro262=) | |
2 | g.233672721A>C | CA351081038 | UGT1A10,UGT1A8,UGT1A9 | c.855+35344A>C (n.855+35344A>C) c.855+54159A>C (n.855+54159A>C) c.787A>C (p.Lys263Gln) | |
2 | g.233672721A>G | CA351081042 | UGT1A10,UGT1A8,UGT1A9 | c.855+35344A>G (n.855+35344A>G) c.855+54159A>G (n.855+54159A>G) c.787A>G (p.Lys263Glu) | COSMIC |
2 | g.233672721A>T | CA351081039 | UGT1A10,UGT1A8,UGT1A9 | c.855+35344A>T (n.855+35344A>T) c.855+54159A>T (n.855+54159A>T) c.787A>T (p.Lys263Ter) | |
2 | g.233672722A>C | CA351081051 | UGT1A10,UGT1A8,UGT1A9 | c.855+35345A>C (n.855+35345A>C) c.855+54160A>C (n.855+54160A>C) c.788A>C (p.Lys263Thr) | |
2 | g.233672722A>G | CA351081054 | UGT1A10,UGT1A8,UGT1A9 | c.855+35345A>G (n.855+35345A>G) c.855+54160A>G (n.855+54160A>G) c.788A>G (p.Lys263Arg) | |
2 | g.233672722A>T | CA351081053 | UGT1A10,UGT1A8,UGT1A9 | c.855+35345A>T (n.855+35345A>T) c.855+54160A>T (n.855+54160A>T) c.788A>T (p.Lys263Ile) | |
2 | g.233672723A= | CA1335852800 | UGT1A10,UGT1A8,UGT1A9 | c.855+35346A= (n.855+35346A=) c.855+54161A= (n.855+54161A=) c.789A= (p.Lys263=) | |
2 | g.233672723A>C | CA351081055 | UGT1A10,UGT1A8,UGT1A9 | c.855+35346A>C (n.855+35346A>C) c.855+54161A>C (n.855+54161A>C) c.789A>C (p.Lys263Asn) | |
2 | g.233672723A>G | CA431857018 | UGT1A10,UGT1A8,UGT1A9 | c.855+35346A>G (n.855+35346A>G) c.855+54161A>G (n.855+54161A>G) c.789A>G (p.Lys263=) | |
2 | g.233672723A>T | CA67608900 | UGT1A10,UGT1A8,UGT1A9 | c.855+35346A>T (n.855+35346A>T) c.855+54161A>T (n.855+54161A>T) c.789A>T (p.Lys263Asn) | dbSNP |
2 | g.233672724C>A | CA351081059 | UGT1A10,UGT1A8,UGT1A9 | c.855+35347C>A (n.855+35347C>A) c.855+54162C>A (n.855+54162C>A) c.790C>A (p.Pro264Thr) | dbSNP |
2 | g.233672724C= | CA1335852803 | UGT1A10,UGT1A8,UGT1A9 | c.855+35347C= (n.855+35347C=) c.855+54162C= (n.855+54162C=) c.790C= (p.Pro264=) | |
2 | g.233672724C>G | CA351081060 | UGT1A10,UGT1A8,UGT1A9 | c.855+35347C>G (n.855+35347C>G) c.855+54162C>G (n.855+54162C>G) c.790C>G (p.Pro264Ala) | |
2 | g.233672724C>T | CA351081061 | UGT1A10,UGT1A8,UGT1A9 | c.855+35347C>T (n.855+35347C>T) c.855+54162C>T (n.855+54162C>T) c.790C>T (p.Pro264Ser) | gnomAD v4 |
2 | g.233672725C>A | CA351081062 | UGT1A10,UGT1A8,UGT1A9 | c.855+35348C>A (n.855+35348C>A) c.855+54163C>A (n.855+54163C>A) c.791C>A (p.Pro264His) | |
2 | g.233672725C= | CA1335852806 | UGT1A10,UGT1A8,UGT1A9 | c.855+35348C= (n.855+35348C=) c.855+54163C= (n.855+54163C=) c.791C= (p.Pro264=) | |
2 | g.233672725C>G | CA351081063 | UGT1A10,UGT1A8,UGT1A9 | c.855+35348C>G (n.855+35348C>G) c.855+54163C>G (n.855+54163C>G) c.791C>G (p.Pro264Arg) | dbSNP |
2 | g.233672725C>T | CA351081065 | UGT1A10,UGT1A8,UGT1A9 | c.855+35348C>T (n.855+35348C>T) c.855+54163C>T (n.855+54163C>T) c.791C>T (p.Pro264Leu) | dbSNP gnomAD v4 |
2 | g.233672725_233672726insAAACA | CA2754690889 | UGT1A10,UGT1A8,UGT1A9 | c.855+35348_855+35349insAAACA (n.855+35348_855+35349insAAACA) c.855+54163_855+54164insAAACA (n.855+54163_855+54164insAAACA) c.791_792insAAACA (p.Val265AsnfsTer3) | |
2 | g.233672726C>A | CA431857033 | UGT1A10,UGT1A8,UGT1A9 | c.855+35349C>A (n.855+35349C>A) c.855+54164C>A (n.855+54164C>A) c.792C>A (p.Pro264=) | |
2 | g.233672726C= | CA1335852810 | UGT1A10,UGT1A8,UGT1A9 | c.855+35349C= (n.855+35349C=) c.855+54164C= (n.855+54164C=) c.792C= (p.Pro264=) | |
2 | g.233672726C>G | CA431857041 | UGT1A10,UGT1A8,UGT1A9 | c.855+35349C>G (n.855+35349C>G) c.855+54164C>G (n.855+54164C>G) c.792C>G (p.Pro264=) | gnomAD v4 |
2 | g.233672726C>T | CA2178128 | UGT1A10,UGT1A8,UGT1A9 | c.855+35349C>T (n.855+35349C>T) c.855+54164C>T (n.855+54164C>T) c.792C>T (p.Pro264=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.233672727G>A | CA2178129 | UGT1A10,UGT1A8,UGT1A9 | c.855+35350G>A (n.855+35350G>A) c.855+54165G>A (n.855+54165G>A) c.793G>A (p.Val265Met) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.233672727G>C | CA351081070 | UGT1A10,UGT1A8,UGT1A9 | c.855+35350G>C (n.855+35350G>C) c.855+54165G>C (n.855+54165G>C) c.793G>C (p.Val265Leu) |