Chr Mutation (hg38) CAid Gene Transcript Linkouts
10g.121498597T>CCA16603155FGFR2c.1573A>G (p.Thr525Ala)
c.1564A>G (p.Thr522Ala)
c.394A>G (p.Thr132Ala)
n.912A>G
c.1219A>G (p.Thr407Ala)
n.390A>G
c.*272A>G (n.*272A>G)
n.3911A>G
n.2583A>G
c.1570A>G (p.Thr524Ala)
c.1297A>G (p.Thr433Ala)
c.1303A>G (p.Thr435Ala)
c.1306A>G (p.Thr436Ala)
c.1228A>G (p.Thr410Ala)
c.1222A>G (p.Thr408Ala)
c.1234A>G (p.Thr412Ala)
c.346A>G (p.Thr116Ala)
c.886A>G (p.Thr296Ala)
c.*617A>G (n.*617A>G)
c.1225A>G (p.Thr409Ala)
n.2020A>G
c.1624A>G (p.Thr542Ala)
c.1621A>G (p.Thr541Ala)
c.1630A>G (p.Thr544Ala)
c.1363A>G (p.Thr455Ala)
c.1285A>G (p.Thr429Ala)
c.1627A>G (p.Thr543Ala)
c.1282A>G (p.Thr428Ala)
c.1276A>G (p.Thr426Ala)
c.1360A>G (p.Thr454Ala)
c.1357A>G (p.Thr453Ala)
c.1354A>G (p.Thr452Ala)
c.400A>G (p.Thr134Ala)
n.2006A>G
ClinVar dbSNP
10g.121498597T>ACA378321786FGFR2c.1573A>T (p.Thr525Ser)
c.1564A>T (p.Thr522Ser)
c.394A>T (p.Thr132Ser)
n.912A>T
c.1219A>T (p.Thr407Ser)
n.390A>T
c.*272A>T (n.*272A>T)
n.3911A>T
n.2583A>T
c.1570A>T (p.Thr524Ser)
c.1297A>T (p.Thr433Ser)
c.1303A>T (p.Thr435Ser)
c.1306A>T (p.Thr436Ser)
c.1228A>T (p.Thr410Ser)
c.1222A>T (p.Thr408Ser)
c.1234A>T (p.Thr412Ser)
c.346A>T (p.Thr116Ser)
c.886A>T (p.Thr296Ser)
c.*617A>T (n.*617A>T)
c.1225A>T (p.Thr409Ser)
n.2020A>T
c.1624A>T (p.Thr542Ser)
c.1621A>T (p.Thr541Ser)
c.1630A>T (p.Thr544Ser)
c.1363A>T (p.Thr455Ser)
c.1285A>T (p.Thr429Ser)
c.1627A>T (p.Thr543Ser)
c.1282A>T (p.Thr428Ser)
c.1276A>T (p.Thr426Ser)
c.1360A>T (p.Thr454Ser)
c.1357A>T (p.Thr453Ser)
c.1354A>T (p.Thr452Ser)
c.400A>T (p.Thr134Ser)
n.2006A>T
dbSNP

Number of alleles fetched