Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
3 | g.64719689C>T | CA248428 | ADAMTS9-AS2 | n.469+34351C>T | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
3 | g.64719689C>G | CA909332713 | ADAMTS9-AS2 | n.469+34351C>G | dbSNP |
3 | g.64719689C>A | CA909332715 | ADAMTS9-AS2 | n.469+34351C>A | dbSNP |
3 | g.64719689C= | CA1370818778 | ADAMTS9-AS2 | n.469+34351C= | dbSNP |