Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
4 | g.55432133G>A | CA11646873 | CLOCK,TMEM165 | c.*3282C>T (n.*3282C>T) c.352+7490G>A c.408+7490G>A c.898+7490G>A (n.898+7490G>A) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.55432133G= | CA1459095797 | CLOCK,TMEM165 | c.*3282C= (n.*3282C=) c.352+7490G= c.408+7490G= c.898+7490G= (n.898+7490G=) | dbSNP |