Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
21 | g.46602317C>G | CA10083311 | S100B | c.99G>C (p.Leu33=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
21 | g.46602317C>T | CA512755612 | S100B | c.99G>A (p.Leu33=) | dbSNP |
21 | g.46602317C>A | CA322004931 | S100B | c.99G>T (p.Leu33=) | dbSNP |