Chr Mutation (hg38) CAid Gene Transcript Linkouts
10g.121488063A>TCA16602761FGFR2c.1917T>A (p.Asn639Lys)
c.1908T>A (p.Asn636Lys)
c.738T>A (p.Asn246Lys)
n.1256T>A
c.1563T>A (p.Asn521Lys)
n.734T>A
n.326T>A
c.*616T>A (n.*616T>A)
n.4255T>A
n.2927T>A
c.1914T>A (p.Asn638Lys)
c.1641T>A (p.Asn547Lys)
c.1647T>A (p.Asn549Lys)
c.1650T>A (p.Asn550Lys)
c.1572T>A (p.Asn524Lys)
c.1566T>A (p.Asn522Lys)
c.1578T>A (p.Asn526Lys)
c.690T>A (p.Asn230Lys)
c.1230T>A (p.Asn410Lys)
c.*961T>A (n.*961T>A)
c.1569T>A (p.Asn523Lys)
n.2364T>A
c.1968T>A (p.Asn656Lys)
c.1965T>A (p.Asn655Lys)
c.1974T>A (p.Asn658Lys)
c.1707T>A (p.Asn569Lys)
c.1629T>A (p.Asn543Lys)
c.1971T>A (p.Asn657Lys)
c.1626T>A (p.Asn542Lys)
c.1620T>A (p.Asn540Lys)
c.1704T>A (p.Asn568Lys)
c.1701T>A (p.Asn567Lys)
c.1698T>A (p.Asn566Lys)
c.744T>A (p.Asn248Lys)
n.2350T>A
ClinVar dbSNP
10g.121488063A>GCA471647326FGFR2c.1917T>C (p.Asn639=)
c.1908T>C (p.Asn636=)
c.738T>C (p.Asn246=)
n.1256T>C
c.1563T>C (p.Asn521=)
n.734T>C
n.326T>C
c.*616T>C (n.*616T>C)
n.4255T>C
n.2927T>C
c.1914T>C (p.Asn638=)
c.1641T>C (p.Asn547=)
c.1647T>C (p.Asn549=)
c.1650T>C (p.Asn550=)
c.1572T>C (p.Asn524=)
c.1566T>C (p.Asn522=)
c.1578T>C (p.Asn526=)
c.690T>C (p.Asn230=)
c.1230T>C (p.Asn410=)
c.*961T>C (n.*961T>C)
c.1569T>C (p.Asn523=)
n.2364T>C
c.1968T>C (p.Asn656=)
c.1965T>C (p.Asn655=)
c.1974T>C (p.Asn658=)
c.1707T>C (p.Asn569=)
c.1629T>C (p.Asn543=)
c.1971T>C (p.Asn657=)
c.1626T>C (p.Asn542=)
c.1620T>C (p.Asn540=)
c.1704T>C (p.Asn568=)
c.1701T>C (p.Asn567=)
c.1698T>C (p.Asn566=)
c.744T>C (p.Asn248=)
n.2350T>C
dbSNP gnomAD v4
10g.121488063A=CA1941012762FGFR2c.1917T= (p.Asn639=)
c.1908T= (p.Asn636=)
c.738T= (p.Asn246=)
n.1256T=
c.1563T= (p.Asn521=)
n.734T=
n.326T=
c.*616T= (n.*616T=)
n.4255T=
n.2927T=
c.1914T= (p.Asn638=)
c.1641T= (p.Asn547=)
c.1647T= (p.Asn549=)
c.1650T= (p.Asn550=)
c.1572T= (p.Asn524=)
c.1566T= (p.Asn522=)
c.1578T= (p.Asn526=)
c.690T= (p.Asn230=)
c.1230T= (p.Asn410=)
c.*961T= (n.*961T=)
c.1569T= (p.Asn523=)
n.2364T=
c.1968T= (p.Asn656=)
c.1965T= (p.Asn655=)
c.1974T= (p.Asn658=)
c.1707T= (p.Asn569=)
c.1629T= (p.Asn543=)
c.1971T= (p.Asn657=)
c.1626T= (p.Asn542=)
c.1620T= (p.Asn540=)
c.1704T= (p.Asn568=)
c.1701T= (p.Asn567=)
c.1698T= (p.Asn566=)
c.744T= (p.Asn248=)
n.2350T=
dbSNP

Number of alleles fetched