Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
13 | g.110308365A>T | CA2118797615 | COL4A2 | c.99+242A>T (n.99+242A>T) n.405+242A>T | dbSNP |
13 | g.110308365A>G | CA13801887 | COL4A2 | c.99+242A>G (n.99+242A>G) n.405+242A>G | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |