Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
5 | g.33879687C>A | CA810023075 | ADAMTS12 | c.489+1432G>T (n.489+1432G>T) | dbSNP |
5 | g.33879687C>T | CA11925775 | ADAMTS12 | c.489+1432G>A (n.489+1432G>A) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
5 | g.33879687C= | CA1538170557 | ADAMTS12 | c.489+1432G= (n.489+1432G=) | dbSNP |