Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
7 | g.44153435A>T | CA16609255 | GCK | c.*72T>A (n.*72T>A) c.74T>A (p.Leu25Gln) n.560T>A c.77T>A (p.Leu26Gln) c.71T>A (p.Leu24Gln) n.509T>A | ClinVar dbSNP gnomAD v4 |
7 | g.44153435A>C | CA213838 | GCK | c.*72T>G (n.*72T>G) c.74T>G (p.Leu25Arg) n.560T>G c.77T>G (p.Leu26Arg) c.71T>G (p.Leu24Arg) n.509T>G | ClinVar dbSNP |