Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
6 | g.11012626G>A | CA12315018 | ELOVL2 | c.4-1817C>T (n.4-1817C>T) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.11012626G>C | CA817075657 | ELOVL2 | c.4-1817C>G (n.4-1817C>G) | dbSNP |
6 | g.11012626G= | CA1610255009 | ELOVL2 | c.4-1817C= (n.4-1817C=) | dbSNP |