Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
12 | g.43536193A>C | CA236329611 | ADAMTS20 | c.454-3998T>G (n.454-3998T>G) c.456-4000T>G (n.456-4000T>G) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
12 | g.43536193A>T | CA2032423439 | ADAMTS20 | c.454-3998T>A (n.454-3998T>A) c.456-4000T>A (n.456-4000T>A) | dbSNP |