Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
13 | g.39543931C>T | CA697959829 | LHFPL6 | c.385+56901G>A (n.385+56901G>A) | dbSNP gnomAD v3 gnomAD v4 |
13 | g.39543931C>A | CA13829612 | LHFPL6 | c.385+56901G>T (n.385+56901G>T) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
13 | g.39543931C= | CA2086018475 | LHFPL6 | c.385+56901G= (n.385+56901G=) | dbSNP |