Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
8 | g.120623156C>T | CA1815240376 | SNTB1 | c.996+9288G>A (n.996+9288G>A) n.716+9288G>A | dbSNP |
8 | g.120623156C>A | CA184997379 | SNTB1 | c.996+9288G>T (n.996+9288G>T) n.716+9288G>T | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |