Chr Mutation (hg38) CAid Gene Transcript Linkouts
10g.121538644T>ACA5721071FGFR2c.696A>T (p.Val232=)
c.429A>T (p.Val143=)
c.351A>T (p.Val117=)
n.998A>T
c.753A>T (p.Val251=)
c.486A>T (p.Val162=)
c.408A>T (p.Val136=)
n.957A>T
dbSNP ExAC gnomAD
10g.121538644T>CCA5721070FGFR2c.696A>G (p.Val232=)
c.429A>G (p.Val143=)
c.351A>G (p.Val117=)
n.998A>G
c.753A>G (p.Val251=)
c.486A>G (p.Val162=)
c.408A>G (p.Val136=)
n.957A>G
ClinVar dbSNP ExAC gnomAD

Number of alleles fetched