Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
15 | g.50490450C>G | CA174941 | USP8 | c.2159C>G (p.Pro720Arg) c.1841C>G (p.Pro614Arg) c.2072C>G (p.Pro691Arg) c.1487C>G (p.Pro496Arg) c.1589C>G (p.Pro530Arg) | ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC |
15 | g.50490450C>T | CA392399160 | USP8 | c.2159C>T (p.Pro720Leu) c.1841C>T (p.Pro614Leu) c.2072C>T (p.Pro691Leu) c.1487C>T (p.Pro496Leu) c.1589C>T (p.Pro530Leu) | dbSNP gnomAD v4 COSMIC |