Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
16 | g.58588274G>A | CA14221847 | CNOT1 | c.211-396C>T (n.211-396C>T) n.544-396C>T n.484-396C>T | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.58588274G>C | CA2225144406 | CNOT1 | c.211-396C>G (n.211-396C>G) n.544-396C>G n.484-396C>G | dbSNP |