Chr Mutation (hg38) CAid Gene Transcript Linkouts
10g.121498520A>CCA16602613FGFR2c.1650T>G (p.Asn550Lys)
c.1641T>G (p.Asn547Lys)
c.471T>G (p.Asn157Lys)
n.989T>G
c.1296T>G (p.Asn432Lys)
n.467T>G
c.*349T>G (n.*349T>G)
n.3988T>G
n.2660T>G
c.1647T>G (p.Asn549Lys)
c.1374T>G (p.Asn458Lys)
c.1380T>G (p.Asn460Lys)
c.1383T>G (p.Asn461Lys)
c.1305T>G (p.Asn435Lys)
c.1299T>G (p.Asn433Lys)
c.1311T>G (p.Asn437Lys)
c.423T>G (p.Asn141Lys)
c.963T>G (p.Asn321Lys)
c.*694T>G (n.*694T>G)
c.1302T>G (p.Asn434Lys)
n.2097T>G
c.1701T>G (p.Asn567Lys)
c.1698T>G (p.Asn566Lys)
c.1707T>G (p.Asn569Lys)
c.1440T>G (p.Asn480Lys)
c.1362T>G (p.Asn454Lys)
c.1704T>G (p.Asn568Lys)
c.1359T>G (p.Asn453Lys)
c.1353T>G (p.Asn451Lys)
c.1437T>G (p.Asn479Lys)
c.1434T>G (p.Asn478Lys)
c.1431T>G (p.Asn477Lys)
c.477T>G (p.Asn159Lys)
n.2083T>G
ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC
10g.121498520A>TCA16602614FGFR2c.1650T>A (p.Asn550Lys)
c.1641T>A (p.Asn547Lys)
c.471T>A (p.Asn157Lys)
n.989T>A
c.1296T>A (p.Asn432Lys)
n.467T>A
c.*349T>A (n.*349T>A)
n.3988T>A
n.2660T>A
c.1647T>A (p.Asn549Lys)
c.1374T>A (p.Asn458Lys)
c.1380T>A (p.Asn460Lys)
c.1383T>A (p.Asn461Lys)
c.1305T>A (p.Asn435Lys)
c.1299T>A (p.Asn433Lys)
c.1311T>A (p.Asn437Lys)
c.423T>A (p.Asn141Lys)
c.963T>A (p.Asn321Lys)
c.*694T>A (n.*694T>A)
c.1302T>A (p.Asn434Lys)
n.2097T>A
c.1701T>A (p.Asn567Lys)
c.1698T>A (p.Asn566Lys)
c.1707T>A (p.Asn569Lys)
c.1440T>A (p.Asn480Lys)
c.1362T>A (p.Asn454Lys)
c.1704T>A (p.Asn568Lys)
c.1359T>A (p.Asn453Lys)
c.1353T>A (p.Asn451Lys)
c.1437T>A (p.Asn479Lys)
c.1434T>A (p.Asn478Lys)
c.1431T>A (p.Asn477Lys)
c.477T>A (p.Asn159Lys)
n.2083T>A
ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC

Number of alleles fetched