Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
10 | g.76151274A>T | CA13195251 | LRMDA | c.516+92491A>T (n.516+92491A>T) c.432+92491A>T (n.432+92491A>T) n.870+92491A>T n.783+92491A>T | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
10 | g.76151274A>G | CA1920786930 | LRMDA | c.516+92491A>G (n.516+92491A>G) c.432+92491A>G (n.432+92491A>G) n.870+92491A>G n.783+92491A>G | dbSNP |