Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
19 | g.48756272A>T | CA508274906 | FGF21 | c.36A>T (p.Gly12=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.48756272A>C | CA508274905 | FGF21 | c.36A>C (p.Gly12=) | dbSNP |
19 | g.48756272A>G | CA9557881 | FGF21 | c.36A>G (p.Gly12=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.48756272A= | CA2340055560 | FGF21 | c.36A= (p.Gly12=) | dbSNP |