Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
2 | g.233681881T>A | CA766279967 | UGT1A10,UGT1A8,UGT1A9 | c.855+44504T>A (n.855+44504T>A) c.855+63319T>A (n.855+63319T>A) c.855+9092T>A (n.855+9092T>A) | dbSNP gnomAD v3 gnomAD v4 |
2 | g.233681881T>G | CA11102067 | UGT1A10,UGT1A8,UGT1A9 | c.855+44504T>G (n.855+44504T>G) c.855+63319T>G (n.855+63319T>G) c.855+9092T>G (n.855+9092T>G) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |