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Mutations

Gene nameGeneTranscriptAA syntaxCDS syntaxMutation typePubmed ID
RHOC ENSG00000155366 ENST00000285735 p.R122R c.366G>A Silent -
MYL4 ENSG00000198336 ENST00000354968 p.A22A c.66C>T Silent -
PRSS36 ENSG00000178226 ENST00000268281 p.A328V c.983C>T Missense_Mutation -
GPRIN1 ENSG00000169258 ENST00000303991 p.R951C c.2851C>T Missense_Mutation -
FAM71E1 ENSG00000142530 ENST00000600100 p.P55R c.164C>G Missense_Mutation -
TG ENSG00000042832 ENST00000220616 p.T491I c.1472C>T Missense_Mutation -
FAM169A ENSG00000198780 ENST00000510496 p.S529S c.1587T>C Silent -
CCDC106 ENSG00000173581 ENST00000586790 p.V61V c.183C>A Silent -
ASF1A ENSG00000111875 ENST00000229595 p.E52G c.155A>G Missense_Mutation -
CPLANE1 ENSG00000197603 ENST00000508244 p.S792C c.2374A>T Missense_Mutation -