Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
5 | g.159920474C>G | CA1595294873 | ADRA1B | c.949+2620C>G (n.949+2620C>G) | dbSNP |
5 | g.159920474C>A | CA11950140 | ADRA1B | c.949+2620C>A (n.949+2620C>A) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
5 | g.159920474C= | CA1595294872 | ADRA1B | c.949+2620C= (n.949+2620C=) | dbSNP |