Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
7 | g.121339035C>G | CA369024784 | WNT16 | c.788C>G (p.Thr263Arg) c.758C>G (p.Thr253Arg) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.121339035C>T | CA4455799 | WNT16 | c.788C>T (p.Thr263Ile) c.758C>T (p.Thr253Ile) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.121339035C= | CA1739111349 | WNT16 | c.788C= (p.Thr263=) c.758C= (p.Thr253=) | dbSNP |
7 | g.121339035C>A | CA369024779 | WNT16 | c.788C>A (p.Thr263Lys) c.758C>A (p.Thr253Lys) | dbSNP |