Chr Mutation (hg38) CAid Gene Transcript Linkouts
9g.36234114C>ACA340505CLTA,GNEc.881G>T (p.Arg294Leu)
c.611G>T (p.Arg204Leu)
c.788G>T (p.Arg263Leu)
c.486-29084C>A (n.486-29084C>A)
c.458G>T (p.Arg153Leu)
c.773G>T (p.Arg258Leu)
c.728G>T (p.Arg243Leu)
c.635G>T (p.Arg212Leu)
ClinVar dbSNP
9g.36234114C=CA1846355748CLTA,GNEc.881G= (p.Arg294=)
c.611G= (p.Arg204=)
c.788G= (p.Arg263=)
c.486-29084C= (n.486-29084C=)
c.458G= (p.Arg153=)
c.773G= (p.Arg258=)
c.728G= (p.Arg243=)
c.635G= (p.Arg212=)
dbSNP
9g.36234114C>TCA373430875CLTA,GNEc.881G>A (p.Arg294Gln)
c.611G>A (p.Arg204Gln)
c.788G>A (p.Arg263Gln)
c.486-29084C>T (n.486-29084C>T)
c.458G>A (p.Arg153Gln)
c.773G>A (p.Arg258Gln)
c.728G>A (p.Arg243Gln)
c.635G>A (p.Arg212Gln)
ClinVar dbSNP COSMIC COSMIC COSMIC

Number of alleles fetched