Unique variants in the RANBP2 gene

Information The variants shown are described using the NM_006267.5 transcript reference sequence.

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Effect     

Reported     

Exon     

AscendingDNA change (cDNA)     

Published as     

RNA change     

Protein     

Clinical classification     

DNA change (genomic) (hg38)     

Published as     

Reference     

DB-ID     

dbSNP ID     

Frequency     

Variant remarks     

Owner     
+/. 3 - c.1754C>T - r.(?) p.(Thr585Met) Conflicting interpretations of pathogenicity g.108751993C>T - H B Chew et al.(2020) RANBP2_000001 rs121434502 - - Nur Aisyah Athirah
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