Chr Mutation (hg38) CAid Gene Transcript Linkouts
10g.121498556C>GCA16602617FGFR2c.1614G>C (p.Met538Ile)
c.1605G>C (p.Met535Ile)
c.435G>C (p.Met145Ile)
n.953G>C
c.1260G>C (p.Met420Ile)
n.431G>C
c.*313G>C (n.*313G>C)
n.3952G>C
n.2624G>C
c.1611G>C (p.Met537Ile)
c.1338G>C (p.Met446Ile)
c.1344G>C (p.Met448Ile)
c.1347G>C (p.Met449Ile)
c.1269G>C (p.Met423Ile)
c.1263G>C (p.Met421Ile)
c.1275G>C (p.Met425Ile)
c.387G>C (p.Met129Ile)
c.927G>C (p.Met309Ile)
c.*658G>C (n.*658G>C)
c.1266G>C (p.Met422Ile)
n.2061G>C
c.1665G>C (p.Met555Ile)
c.1662G>C (p.Met554Ile)
c.1671G>C (p.Met557Ile)
c.1404G>C (p.Met468Ile)
c.1326G>C (p.Met442Ile)
c.1668G>C (p.Met556Ile)
c.1323G>C (p.Met441Ile)
c.1317G>C (p.Met439Ile)
c.1401G>C (p.Met467Ile)
c.1398G>C (p.Met466Ile)
c.1395G>C (p.Met465Ile)
c.441G>C (p.Met147Ile)
n.2047G>C
ClinVar dbSNP
10g.121498556C>ACA16602616FGFR2c.1614G>T (p.Met538Ile)
c.1605G>T (p.Met535Ile)
c.435G>T (p.Met145Ile)
n.953G>T
c.1260G>T (p.Met420Ile)
n.431G>T
c.*313G>T (n.*313G>T)
n.3952G>T
n.2624G>T
c.1611G>T (p.Met537Ile)
c.1338G>T (p.Met446Ile)
c.1344G>T (p.Met448Ile)
c.1347G>T (p.Met449Ile)
c.1269G>T (p.Met423Ile)
c.1263G>T (p.Met421Ile)
c.1275G>T (p.Met425Ile)
c.387G>T (p.Met129Ile)
c.927G>T (p.Met309Ile)
c.*658G>T (n.*658G>T)
c.1266G>T (p.Met422Ile)
n.2061G>T
c.1665G>T (p.Met555Ile)
c.1662G>T (p.Met554Ile)
c.1671G>T (p.Met557Ile)
c.1404G>T (p.Met468Ile)
c.1326G>T (p.Met442Ile)
c.1668G>T (p.Met556Ile)
c.1323G>T (p.Met441Ile)
c.1317G>T (p.Met439Ile)
c.1401G>T (p.Met467Ile)
c.1398G>T (p.Met466Ile)
c.1395G>T (p.Met465Ile)
c.441G>T (p.Met147Ile)
n.2047G>T
ClinVar dbSNP gnomAD v4 COSMIC COSMIC COSMIC COSMIC COSMIC
10g.121498556C>TCA16602618FGFR2c.1614G>A (p.Met538Ile)
c.1605G>A (p.Met535Ile)
c.435G>A (p.Met145Ile)
n.953G>A
c.1260G>A (p.Met420Ile)
n.431G>A
c.*313G>A (n.*313G>A)
n.3952G>A
n.2624G>A
c.1611G>A (p.Met537Ile)
c.1338G>A (p.Met446Ile)
c.1344G>A (p.Met448Ile)
c.1347G>A (p.Met449Ile)
c.1269G>A (p.Met423Ile)
c.1263G>A (p.Met421Ile)
c.1275G>A (p.Met425Ile)
c.387G>A (p.Met129Ile)
c.927G>A (p.Met309Ile)
c.*658G>A (n.*658G>A)
c.1266G>A (p.Met422Ile)
n.2061G>A
c.1665G>A (p.Met555Ile)
c.1662G>A (p.Met554Ile)
c.1671G>A (p.Met557Ile)
c.1404G>A (p.Met468Ile)
c.1326G>A (p.Met442Ile)
c.1668G>A (p.Met556Ile)
c.1323G>A (p.Met441Ile)
c.1317G>A (p.Met439Ile)
c.1401G>A (p.Met467Ile)
c.1398G>A (p.Met466Ile)
c.1395G>A (p.Met465Ile)
c.441G>A (p.Met147Ile)
n.2047G>A
ClinVar dbSNP

Number of alleles fetched