Chr Mutation (hg38) CAid Gene Transcript Linkouts
10g.121488003T>CCA471647212FGFR2c.1977A>G (p.Lys659=)
c.1968A>G (p.Lys656=)
c.798A>G (p.Lys266=)
n.1316A>G
c.1623A>G (p.Lys541=)
n.794A>G
n.386A>G
c.*676A>G (n.*676A>G)
n.4315A>G
n.2987A>G
c.1974A>G (p.Lys658=)
c.1701A>G (p.Lys567=)
c.1707A>G (p.Lys569=)
c.1710A>G (p.Lys570=)
c.1632A>G (p.Lys544=)
c.1626A>G (p.Lys542=)
c.1638A>G (p.Lys546=)
c.750A>G (p.Lys250=)
c.1290A>G (p.Lys430=)
c.*1021A>G (n.*1021A>G)
c.1629A>G (p.Lys543=)
n.2424A>G
c.2028A>G (p.Lys676=)
c.2025A>G (p.Lys675=)
c.2034A>G (p.Lys678=)
c.1767A>G (p.Lys589=)
c.1689A>G (p.Lys563=)
c.2031A>G (p.Lys677=)
c.1686A>G (p.Lys562=)
c.1680A>G (p.Lys560=)
c.1764A>G (p.Lys588=)
c.1761A>G (p.Lys587=)
c.1758A>G (p.Lys586=)
c.804A>G (p.Lys268=)
n.2410A>G
dbSNP
10g.121488003T>ACA16603135FGFR2c.1977A>T (p.Lys659Asn)
c.1968A>T (p.Lys656Asn)
c.798A>T (p.Lys266Asn)
n.1316A>T
c.1623A>T (p.Lys541Asn)
n.794A>T
n.386A>T
c.*676A>T (n.*676A>T)
n.4315A>T
n.2987A>T
c.1974A>T (p.Lys658Asn)
c.1701A>T (p.Lys567Asn)
c.1707A>T (p.Lys569Asn)
c.1710A>T (p.Lys570Asn)
c.1632A>T (p.Lys544Asn)
c.1626A>T (p.Lys542Asn)
c.1638A>T (p.Lys546Asn)
c.750A>T (p.Lys250Asn)
c.1290A>T (p.Lys430Asn)
c.*1021A>T (n.*1021A>T)
c.1629A>T (p.Lys543Asn)
n.2424A>T
c.2028A>T (p.Lys676Asn)
c.2025A>T (p.Lys675Asn)
c.2034A>T (p.Lys678Asn)
c.1767A>T (p.Lys589Asn)
c.1689A>T (p.Lys563Asn)
c.2031A>T (p.Lys677Asn)
c.1686A>T (p.Lys562Asn)
c.1680A>T (p.Lys560Asn)
c.1764A>T (p.Lys588Asn)
c.1761A>T (p.Lys587Asn)
c.1758A>T (p.Lys586Asn)
c.804A>T (p.Lys268Asn)
n.2410A>T
ClinVar dbSNP

Number of alleles fetched