Chr Mutation (hg38) CAid Gene Transcript Linkouts
10g.121498562C>ACA16602619FGFR2c.1608G>T (p.Met536Ile)
c.1599G>T (p.Met533Ile)
c.429G>T (p.Met143Ile)
n.947G>T
c.1254G>T (p.Met418Ile)
n.425G>T
c.*307G>T (n.*307G>T)
n.3946G>T
n.2618G>T
c.1605G>T (p.Met535Ile)
c.1332G>T (p.Met444Ile)
c.1338G>T (p.Met446Ile)
c.1341G>T (p.Met447Ile)
c.1263G>T (p.Met421Ile)
c.1257G>T (p.Met419Ile)
c.1269G>T (p.Met423Ile)
c.381G>T (p.Met127Ile)
c.921G>T (p.Met307Ile)
c.*652G>T (n.*652G>T)
c.1260G>T (p.Met420Ile)
n.2055G>T
c.1659G>T (p.Met553Ile)
c.1656G>T (p.Met552Ile)
c.1665G>T (p.Met555Ile)
c.1398G>T (p.Met466Ile)
c.1320G>T (p.Met440Ile)
c.1662G>T (p.Met554Ile)
c.1317G>T (p.Met439Ile)
c.1311G>T (p.Met437Ile)
c.1395G>T (p.Met465Ile)
c.1392G>T (p.Met464Ile)
c.1389G>T (p.Met463Ile)
c.435G>T (p.Met145Ile)
n.2041G>T
ClinVar dbSNP
10g.121498562C>GCA16602620FGFR2c.1608G>C (p.Met536Ile)
c.1599G>C (p.Met533Ile)
c.429G>C (p.Met143Ile)
n.947G>C
c.1254G>C (p.Met418Ile)
n.425G>C
c.*307G>C (n.*307G>C)
n.3946G>C
n.2618G>C
c.1605G>C (p.Met535Ile)
c.1332G>C (p.Met444Ile)
c.1338G>C (p.Met446Ile)
c.1341G>C (p.Met447Ile)
c.1263G>C (p.Met421Ile)
c.1257G>C (p.Met419Ile)
c.1269G>C (p.Met423Ile)
c.381G>C (p.Met127Ile)
c.921G>C (p.Met307Ile)
c.*652G>C (n.*652G>C)
c.1260G>C (p.Met420Ile)
n.2055G>C
c.1659G>C (p.Met553Ile)
c.1656G>C (p.Met552Ile)
c.1665G>C (p.Met555Ile)
c.1398G>C (p.Met466Ile)
c.1320G>C (p.Met440Ile)
c.1662G>C (p.Met554Ile)
c.1317G>C (p.Met439Ile)
c.1311G>C (p.Met437Ile)
c.1395G>C (p.Met465Ile)
c.1392G>C (p.Met464Ile)
c.1389G>C (p.Met463Ile)
c.435G>C (p.Met145Ile)
n.2041G>C
ClinVar dbSNP
10g.121498562C>TCA16602621FGFR2c.1608G>A (p.Met536Ile)
c.1599G>A (p.Met533Ile)
c.429G>A (p.Met143Ile)
n.947G>A
c.1254G>A (p.Met418Ile)
n.425G>A
c.*307G>A (n.*307G>A)
n.3946G>A
n.2618G>A
c.1605G>A (p.Met535Ile)
c.1332G>A (p.Met444Ile)
c.1338G>A (p.Met446Ile)
c.1341G>A (p.Met447Ile)
c.1263G>A (p.Met421Ile)
c.1257G>A (p.Met419Ile)
c.1269G>A (p.Met423Ile)
c.381G>A (p.Met127Ile)
c.921G>A (p.Met307Ile)
c.*652G>A (n.*652G>A)
c.1260G>A (p.Met420Ile)
n.2055G>A
c.1659G>A (p.Met553Ile)
c.1656G>A (p.Met552Ile)
c.1665G>A (p.Met555Ile)
c.1398G>A (p.Met466Ile)
c.1320G>A (p.Met440Ile)
c.1662G>A (p.Met554Ile)
c.1317G>A (p.Met439Ile)
c.1311G>A (p.Met437Ile)
c.1395G>A (p.Met465Ile)
c.1392G>A (p.Met464Ile)
c.1389G>A (p.Met463Ile)
c.435G>A (p.Met145Ile)
n.2041G>A
ClinVar dbSNP gnomAD v4

Number of alleles fetched