Chr Mutation (hg38) CAid Gene Transcript Linkouts
10g.121498522T>GCA16043908FGFR2c.1648A>C (p.Asn550His)
c.1639A>C (p.Asn547His)
c.469A>C (p.Asn157His)
n.987A>C
c.1294A>C (p.Asn432His)
n.465A>C
c.*347A>C (n.*347A>C)
n.3986A>C
n.2658A>C
c.1645A>C (p.Asn549His)
c.1372A>C (p.Asn458His)
c.1378A>C (p.Asn460His)
c.1381A>C (p.Asn461His)
c.1303A>C (p.Asn435His)
c.1297A>C (p.Asn433His)
c.1309A>C (p.Asn437His)
c.421A>C (p.Asn141His)
c.961A>C (p.Asn321His)
c.*692A>C (n.*692A>C)
c.1300A>C (p.Asn434His)
n.2095A>C
c.1699A>C (p.Asn567His)
c.1696A>C (p.Asn566His)
c.1705A>C (p.Asn569His)
c.1438A>C (p.Asn480His)
c.1360A>C (p.Asn454His)
c.1702A>C (p.Asn568His)
c.1357A>C (p.Asn453His)
c.1351A>C (p.Asn451His)
c.1435A>C (p.Asn479His)
c.1432A>C (p.Asn478His)
c.1429A>C (p.Asn477His)
c.475A>C (p.Asn159His)
n.2081A>C
ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC
10g.121498522T>CCA378321436FGFR2c.1648A>G (p.Asn550Asp)
c.1639A>G (p.Asn547Asp)
c.469A>G (p.Asn157Asp)
n.987A>G
c.1294A>G (p.Asn432Asp)
n.465A>G
c.*347A>G (n.*347A>G)
n.3986A>G
n.2658A>G
c.1645A>G (p.Asn549Asp)
c.1372A>G (p.Asn458Asp)
c.1378A>G (p.Asn460Asp)
c.1381A>G (p.Asn461Asp)
c.1303A>G (p.Asn435Asp)
c.1297A>G (p.Asn433Asp)
c.1309A>G (p.Asn437Asp)
c.421A>G (p.Asn141Asp)
c.961A>G (p.Asn321Asp)
c.*692A>G (n.*692A>G)
c.1300A>G (p.Asn434Asp)
n.2095A>G
c.1699A>G (p.Asn567Asp)
c.1696A>G (p.Asn566Asp)
c.1705A>G (p.Asn569Asp)
c.1438A>G (p.Asn480Asp)
c.1360A>G (p.Asn454Asp)
c.1702A>G (p.Asn568Asp)
c.1357A>G (p.Asn453Asp)
c.1351A>G (p.Asn451Asp)
c.1435A>G (p.Asn479Asp)
c.1432A>G (p.Asn478Asp)
c.1429A>G (p.Asn477Asp)
c.475A>G (p.Asn159Asp)
n.2081A>G
dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC

Number of alleles fetched