Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.154896103G>ACA255011F8c.6403C>T (p.Arg2135Ter)
c.6298C>T (p.Arg2100Ter)
ClinVar dbSNP COSMIC COSMIC
Xg.154896103G>CCA414899439F8c.6403C>G (p.Arg2135Gly)
c.6298C>G (p.Arg2100Gly)
dbSNP
Xg.154896103G>TCA519352452F8c.6403C>A (p.Arg2135=)
c.6298C>A (p.Arg2100=)
dbSNP gnomAD v4

Number of alleles fetched