UGT1A10 Y483N - GET-Evidence

Note: This variant has not been sufficiently evaluated by a GET-Evidence editor.

To be considered sufficiently evaluated a variant must have both "variant evidence" and "clinical importance" scores filled in.

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UGT1A10 Y483N

(UGT1A10 Tyr483Asn)

Short summary


Variant evidence
Computational -
Functional -
Case/Control -
Familial -
Clinical importance
Severity -
Treatability -
Penetrance -


Insufficiently evaluated not reviewed

(The "insufficiently evaluated" qualifier is assigned automatically based on the above evidence and importance scores.)

Inheritance pattern


Summary of published research, and additional commentary


Allele frequency

  • None available.



Other external references

    Web search results (2 hits -- see all)
  • Assay ID Availability Assay Type
    UGT1A1,UGT1A9,UGT1A6,UGT1A4,UGT1A10,UGT1A5,UGT1A3,UGT1A8,LOC339766,UGT1A7 ... rs34993780. LOC339766,UGT1A9,UGT1A5,UGT1A6,UGT1A10,UGT1A4,UGT1A8,UGT1A3,UGT1A1,UGT1A7 ...
  • Submission PS203281 [PharmGKB]
    rs34993780. UGT1A7. T. plus. Exon1. Tyr. 100%. 86. 129. Pyrosequencing. View. chr2:234345798 ... rs34993780. UGT1A10. T. plus. Exon1. Tyr. 100%. 86. 129. Pyrosequencing. View ...

Other in silico analyses

  • NBLOSUM100 score = 5
  • GET-Evidence autoscore = 2

Edit history

Gene search

"GENE" or "GENE A123C":

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