| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 2 | g.233672700G>A | CA2178121 | UGT1A10,UGT1A8,UGT1A9 | c.855+35323G>A (n.855+35323G>A) c.855+54138G>A (n.855+54138G>A) c.766G>A (p.Asp256Asn) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 2 | g.233672700G>C | CA351080935 | UGT1A10,UGT1A8,UGT1A9 | c.855+35323G>C (n.855+35323G>C) c.855+54138G>C (n.855+54138G>C) c.766G>C (p.Asp256His) | |
| 2 | g.233672700G= | CA1335852752 | UGT1A10,UGT1A8,UGT1A9 | c.855+35323G= (n.855+35323G=) c.855+54138G= (n.855+54138G=) c.766G= (p.Asp256=) | |
| 2 | g.233672700G>T | CA351080941 | UGT1A10,UGT1A8,UGT1A9 | c.855+35323G>T (n.855+35323G>T) c.855+54138G>T (n.855+54138G>T) c.766G>T (p.Asp256Tyr) | |
| 2 | g.233672701A>C | CA351080945 | UGT1A10,UGT1A8,UGT1A9 | c.855+35324A>C (n.855+35324A>C) c.855+54139A>C (n.855+54139A>C) c.767A>C (p.Asp256Ala) | gnomAD v4 |
| 2 | g.233672701A>G | CA351080944 | UGT1A10,UGT1A8,UGT1A9 | c.855+35324A>G (n.855+35324A>G) c.855+54139A>G (n.855+54139A>G) c.767A>G (p.Asp256Gly) | |
| 2 | g.233672701A>T | CA351080943 | UGT1A10,UGT1A8,UGT1A9 | c.855+35324A>T (n.855+35324A>T) c.855+54139A>T (n.855+54139A>T) c.767A>T (p.Asp256Val) | |
| 2 | g.233672702C>A | CA351080947 | UGT1A10,UGT1A8,UGT1A9 | c.855+35325C>A (n.855+35325C>A) c.855+54140C>A (n.855+54140C>A) c.768C>A (p.Asp256Glu) | |
| 2 | g.233672702C>G | CA351080949 | UGT1A10,UGT1A8,UGT1A9 | c.855+35325C>G (n.855+35325C>G) c.855+54140C>G (n.855+54140C>G) c.768C>G (p.Asp256Glu) | |
| 2 | g.233672702C>T | CA431856873 | UGT1A10,UGT1A8,UGT1A9 | c.855+35325C>T (n.855+35325C>T) c.855+54140C>T (n.855+54140C>T) c.768C>T (p.Asp256=) | gnomAD v4 |
| 2 | g.233672703T>A | CA351080953 | UGT1A10,UGT1A8,UGT1A9 | c.855+35326T>A (n.855+35326T>A) c.855+54141T>A (n.855+54141T>A) c.769T>A (p.Phe257Ile) | |
| 2 | g.233672703T>C | CA351080956 | UGT1A10,UGT1A8,UGT1A9 | c.855+35326T>C (n.855+35326T>C) c.855+54141T>C (n.855+54141T>C) c.769T>C (p.Phe257Leu) | |
| 2 | g.233672703T>G | CA2178122 | UGT1A10,UGT1A8,UGT1A9 | c.855+35326T>G (n.855+35326T>G) c.855+54141T>G (n.855+54141T>G) c.769T>G (p.Phe257Val) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 2 | g.233672703T= | CA1335852755 | UGT1A10,UGT1A8,UGT1A9 | c.855+35326T= (n.855+35326T=) c.855+54141T= (n.855+54141T=) c.769T= (p.Phe257=) | |
| 2 | g.233672704T>A | CA351080962 | UGT1A10,UGT1A8,UGT1A9 | c.855+35327T>A (n.855+35327T>A) c.855+54142T>A (n.855+54142T>A) c.770T>A (p.Phe257Tyr) | |
| 2 | g.233672704T>C | CA351080963 | UGT1A10,UGT1A8,UGT1A9 | c.855+35327T>C (n.855+35327T>C) c.855+54142T>C (n.855+54142T>C) c.770T>C (p.Phe257Ser) | |
| 2 | g.233672704T>G | CA351080964 | UGT1A10,UGT1A8,UGT1A9 | c.855+35327T>G (n.855+35327T>G) c.855+54142T>G (n.855+54142T>G) c.770T>G (p.Phe257Cys) | |
| 2 | g.233672705T>A | CA351080967 | UGT1A10,UGT1A8,UGT1A9 | c.855+35328T>A (n.855+35328T>A) c.855+54143T>A (n.855+54143T>A) c.771T>A (p.Phe257Leu) | |
| 2 | g.233672705T>C | CA431856886 | UGT1A10,UGT1A8,UGT1A9 | c.855+35328T>C (n.855+35328T>C) c.855+54143T>C (n.855+54143T>C) c.771T>C (p.Phe257=) | gnomAD v4 |
| 2 | g.233672705T>G | CA351080970 | UGT1A10,UGT1A8,UGT1A9 | c.855+35328T>G (n.855+35328T>G) c.855+54143T>G (n.855+54143T>G) c.771T>G (p.Phe257Leu) | |
| 2 | g.233672706G>A | CA351080977 | UGT1A10,UGT1A8,UGT1A9 | c.855+35329G>A (n.855+35329G>A) c.855+54144G>A (n.855+54144G>A) c.772G>A (p.Val258Ile) | |
| 2 | g.233672706G>C | CA67608847 | UGT1A10,UGT1A8,UGT1A9 | c.855+35329G>C (n.855+35329G>C) c.855+54144G>C (n.855+54144G>C) c.772G>C (p.Val258Leu) | dbSNP |
| 2 | g.233672706G= | CA1335852760 | UGT1A10,UGT1A8,UGT1A9 | c.855+35329G= (n.855+35329G=) c.855+54144G= (n.855+54144G=) c.772G= (p.Val258=) | |
| 2 | g.233672706G>T | CA351080986 | UGT1A10,UGT1A8,UGT1A9 | c.855+35329G>T (n.855+35329G>T) c.855+54144G>T (n.855+54144G>T) c.772G>T (p.Val258Phe) | |
| 2 | g.233672707T>A | CA351080990 | UGT1A10,UGT1A8,UGT1A9 | c.855+35330T>A (n.855+35330T>A) c.855+54145T>A (n.855+54145T>A) c.773T>A (p.Val258Asp) | |
| 2 | g.233672707T>C | CA2178123 | UGT1A10,UGT1A8,UGT1A9 | c.855+35330T>C (n.855+35330T>C) c.855+54145T>C (n.855+54145T>C) c.773T>C (p.Val258Ala) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 2 | g.233672707T>G | CA2178124 | UGT1A10,UGT1A8,UGT1A9 | c.855+35330T>G (n.855+35330T>G) c.855+54145T>G (n.855+54145T>G) c.773T>G (p.Val258Gly) | dbSNP ExAC gnomAD v2 |
| 2 | g.233672707T= | CA1335852765 | UGT1A10,UGT1A8,UGT1A9 | c.855+35330T= (n.855+35330T=) c.855+54145T= (n.855+54145T=) c.773T= (p.Val258=) | |
| 2 | g.233672708T>A | CA431856908 | UGT1A10,UGT1A8,UGT1A9 | c.855+35331T>A (n.855+35331T>A) c.855+54146T>A (n.855+54146T>A) c.774T>A (p.Val258=) | |
| 2 | g.233672708T>C | CA431856912 | UGT1A10,UGT1A8,UGT1A9 | c.855+35331T>C (n.855+35331T>C) c.855+54146T>C (n.855+54146T>C) c.774T>C (p.Val258=) | |
| 2 | g.233672708T>G | CA431856914 | UGT1A10,UGT1A8,UGT1A9 | c.855+35331T>G (n.855+35331T>G) c.855+54146T>G (n.855+54146T>G) c.774T>G (p.Val258=) | |
| 2 | g.233672709T>A | CA351080992 | UGT1A10,UGT1A8,UGT1A9 | c.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 |
| 2 | g.233672709T>C | CA431856917 | UGT1A10,UGT1A8,UGT1A9 | c.855+35332T>C (n.855+35332T>C) c.855+54147T>C (n.855+54147T>C) c.775T>C (p.Leu259=) | |
| 2 | g.233672709T>G | CA2178125 | UGT1A10,UGT1A8,UGT1A9 | c.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 |
| 2 | g.233672709T= | CA1335852771 | UGT1A10,UGT1A8,UGT1A9 | c.855+35332T= (n.855+35332T=) c.855+54147T= (n.855+54147T=) c.775T= (p.Leu259=) | |
| 2 | g.233672710T>A | CA351080993 | UGT1A10,UGT1A8,UGT1A9 | c.855+35333T>A (n.855+35333T>A) c.855+54148T>A (n.855+54148T>A) c.776T>A (p.Leu259Ter) | |
| 2 | g.233672710T>C | CA351080994 | UGT1A10,UGT1A8,UGT1A9 | c.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 |
| 2 | g.233672710T>G | CA351080995 | UGT1A10,UGT1A8,UGT1A9 | c.855+35333T>G (n.855+35333T>G) c.855+54148T>G (n.855+54148T>G) c.776T>G (p.Leu259Trp) | gnomAD v4 |
| 2 | g.233672710T= | CA1335852775 | UGT1A10,UGT1A8,UGT1A9 | c.855+35333T= (n.855+35333T=) c.855+54148T= (n.855+54148T=) c.776T= (p.Leu259=) | |
| 2 | g.233672711G>A | CA431856924 | UGT1A10,UGT1A8,UGT1A9 | c.855+35334G>A (n.855+35334G>A) c.855+54149G>A (n.855+54149G>A) c.777G>A (p.Leu259=) | |
| 2 | g.233672711G>C | CA351080999 | UGT1A10,UGT1A8,UGT1A9 | c.855+35334G>C (n.855+35334G>C) c.855+54149G>C (n.855+54149G>C) c.777G>C (p.Leu259Phe) | |
| 2 | g.233672711G>T | CA351081002 | UGT1A10,UGT1A8,UGT1A9 | c.855+35334G>T (n.855+35334G>T) c.855+54149G>T (n.855+54149G>T) c.777G>T (p.Leu259Phe) | |
| 2 | g.233672712G>A | CA351081004 | UGT1A10,UGT1A8,UGT1A9 | c.855+35335G>A (n.855+35335G>A) c.855+54150G>A (n.855+54150G>A) c.778G>A (p.Asp260Asn) | |
| 2 | g.233672712G>C | CA351081008 | UGT1A10,UGT1A8,UGT1A9 | c.855+35335G>C (n.855+35335G>C) c.855+54150G>C (n.855+54150G>C) c.778G>C (p.Asp260His) | |
| 2 | g.233672712G>T | CA351081009 | UGT1A10,UGT1A8,UGT1A9 | c.855+35335G>T (n.855+35335G>T) c.855+54150G>T (n.855+54150G>T) c.778G>T (p.Asp260Tyr) | |
| 2 | g.233672713A= | CA1335852779 | UGT1A10,UGT1A8,UGT1A9 | c.855+35336A= (n.855+35336A=) c.855+54151A= (n.855+54151A=) c.779A= (p.Asp260=) | |
| 2 | g.233672713A>C | CA351081010 | UGT1A10,UGT1A8,UGT1A9 | c.855+35336A>C (n.855+35336A>C) c.855+54151A>C (n.855+54151A>C) c.779A>C (p.Asp260Ala) | |
| 2 | g.233672713A>G | CA351081011 | UGT1A10,UGT1A8,UGT1A9 | c.855+35336A>G (n.855+35336A>G) c.855+54151A>G (n.855+54151A>G) c.779A>G (p.Asp260Gly) | dbSNP gnomAD v2 |
| 2 | g.233672713A>T | CA351081012 | UGT1A10,UGT1A8,UGT1A9 | c.855+35336A>T (n.855+35336A>T) c.855+54151A>T (n.855+54151A>T) c.779A>T (p.Asp260Val) | |
| 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) |