Chr Mutation (hg38) CAid Gene Transcript Linkouts
9g.94606867C>GCA374106775FBP1c.813G>C (n.813G>C)
c.653G>C (p.Arg218Thr)
c.458G>C (p.Arg153Thr)
c.401G>C (p.Arg134Thr)
c.407G>C (p.Arg136Thr)
dbSNP
9g.94606867C>ACA374106773FBP1c.813G>T (n.813G>T)
c.653G>T (p.Arg218Met)
c.458G>T (p.Arg153Met)
c.401G>T (p.Arg134Met)
c.407G>T (p.Arg136Met)
dbSNP
9g.94606867C>TCA5136172FBP1c.813G>A (n.813G>A)
c.653G>A (p.Arg218Lys)
c.458G>A (p.Arg153Lys)
c.401G>A (p.Arg134Lys)
c.407G>A (p.Arg136Lys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4

Number of alleles fetched