Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.139561710C>TCA255381F9c.1025C>T (p.Thr342Met)
n.1692C>T
c.911C>T (p.Thr304Met)
c.896C>T (p.Thr299Met)
ClinVar dbSNP gnomAD v4 COSMIC
Xg.139561710C>GCA414445449F9c.1025C>G (p.Thr342Arg)
n.1692C>G
c.911C>G (p.Thr304Arg)
c.896C>G (p.Thr299Arg)
dbSNP
Xg.139561710C>ACA414445446F9c.1025C>A (p.Thr342Lys)
n.1692C>A
c.911C>A (p.Thr304Lys)
c.896C>A (p.Thr299Lys)
dbSNP

Number of alleles fetched