Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
16 | g.55486666C>A | CA977553057 | MMP2 | c.832+889C>A (n.832+889C>A) c.682+889C>A (n.682+889C>A) c.604+889C>A (n.604+889C>A) | dbSNP gnomAD v3 gnomAD v4 |
16 | g.55486666C>G | CA281397602 | MMP2 | c.832+889C>G (n.832+889C>G) c.682+889C>G (n.682+889C>G) c.604+889C>G (n.604+889C>G) | dbSNP gnomAD v3 gnomAD v4 |
16 | g.55486666C>T | CA14247543 | MMP2 | c.832+889C>T (n.832+889C>T) c.682+889C>T (n.682+889C>T) c.604+889C>T (n.604+889C>T) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |