Chr Mutation (hg38) CAid Gene Transcript Linkouts
10g.121496705C>GCA378320649FGFR2c.1693G>C (p.Val565Leu)
c.1684G>C (p.Val562Leu)
c.514G>C (p.Val172Leu)
n.1032G>C
c.1339G>C (p.Val447Leu)
n.510G>C
n.102G>C
c.*392G>C (n.*392G>C)
n.4031G>C
n.2703G>C
c.1690G>C (p.Val564Leu)
c.1417G>C (p.Val473Leu)
c.1423G>C (p.Val475Leu)
c.1426G>C (p.Val476Leu)
c.1348G>C (p.Val450Leu)
c.1342G>C (p.Val448Leu)
c.1354G>C (p.Val452Leu)
c.466G>C (p.Val156Leu)
c.1006G>C (p.Val336Leu)
c.*737G>C (n.*737G>C)
c.1345G>C (p.Val449Leu)
n.2140G>C
c.1744G>C (p.Val582Leu)
c.1741G>C (p.Val581Leu)
c.1750G>C (p.Val584Leu)
c.1483G>C (p.Val495Leu)
c.1405G>C (p.Val469Leu)
c.1747G>C (p.Val583Leu)
c.1402G>C (p.Val468Leu)
c.1396G>C (p.Val466Leu)
c.1480G>C (p.Val494Leu)
c.1477G>C (p.Val493Leu)
c.1474G>C (p.Val492Leu)
c.520G>C (p.Val174Leu)
n.2126G>C
ClinVar dbSNP
10g.121496705C>TCA16602612FGFR2c.1693G>A (p.Val565Ile)
c.1684G>A (p.Val562Ile)
c.514G>A (p.Val172Ile)
n.1032G>A
c.1339G>A (p.Val447Ile)
n.510G>A
n.102G>A
c.*392G>A (n.*392G>A)
n.4031G>A
n.2703G>A
c.1690G>A (p.Val564Ile)
c.1417G>A (p.Val473Ile)
c.1423G>A (p.Val475Ile)
c.1426G>A (p.Val476Ile)
c.1348G>A (p.Val450Ile)
c.1342G>A (p.Val448Ile)
c.1354G>A (p.Val452Ile)
c.466G>A (p.Val156Ile)
c.1006G>A (p.Val336Ile)
c.*737G>A (n.*737G>A)
c.1345G>A (p.Val449Ile)
n.2140G>A
c.1744G>A (p.Val582Ile)
c.1741G>A (p.Val581Ile)
c.1750G>A (p.Val584Ile)
c.1483G>A (p.Val495Ile)
c.1405G>A (p.Val469Ile)
c.1747G>A (p.Val583Ile)
c.1402G>A (p.Val468Ile)
c.1396G>A (p.Val466Ile)
c.1480G>A (p.Val494Ile)
c.1477G>A (p.Val493Ile)
c.1474G>A (p.Val492Ile)
c.520G>A (p.Val174Ile)
n.2126G>A
ClinVar dbSNP

Number of alleles fetched