Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
11 | g.113946934T>A | CA15710492 | HTR3B | c.*797T>A (n.*797T>A) n.2163T>A | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.113946934T>C | CA2001404784 | HTR3B | c.*797T>C (n.*797T>C) n.2163T>C | dbSNP |
11 | g.113946934T= | CA2001404783 | HTR3B | c.*797T= (n.*797T=) n.2163T= | dbSNP |