Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
9 | g.36234114C>A | CA340505 | CLTA,GNE | c.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 |
9 | g.36234114C= | CA1846355748 | CLTA,GNE | c.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 |
9 | g.36234114C>T | CA373430875 | CLTA,GNE | c.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 |