Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
11 | g.620599G>T | CA13369098 | CDHR5 | c.790-213C>A (n.790-213C>A) c.*622-213C>A (n.*622-213C>A) n.750-213C>A n.59-213C>A | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.620599G>C | CA934285460 | CDHR5 | c.790-213C>G (n.790-213C>G) c.*622-213C>G (n.*622-213C>G) n.750-213C>G n.59-213C>G | dbSNP gnomAD v3 gnomAD v4 |