Chr Mutation (hg38) CAid Gene Transcript Linkouts
15g.50490450C>GCA174941USP8c.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
15g.50490450C>TCA392399160USP8c.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

Number of alleles fetched