Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
11 | g.616865G>T | CA1947210978 | CDHR5 | c.*486C>A (n.*486C>A) c.*701C>A (n.*701C>A) | dbSNP gnomAD v4 |
11 | g.616865G>A | CA5784161 | CDHR5 | c.*486C>T (n.*486C>T) c.*701C>T (n.*701C>T) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.616865G= | CA1947210979 | CDHR5 | c.*486C= (n.*486C=) c.*701C= (n.*701C=) | dbSNP |