Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
22 | g.25777694T>C | CA10160021 | MYO18B | c.1981T>C (p.Trp661Arg) n.552T>C c.2107T>C (p.Trp703Arg) c.1624T>C (p.Trp542Arg) c.-413T>C (n.-413T>C) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
22 | g.25777694T>G | CA410992844 | MYO18B | c.1981T>G (p.Trp661Gly) n.552T>G c.2107T>G (p.Trp703Gly) c.1624T>G (p.Trp542Gly) c.-413T>G (n.-413T>G) | dbSNP |
22 | g.25777694T>A | CA410992843 | MYO18B | c.1981T>A (p.Trp661Arg) n.552T>A c.2107T>A (p.Trp703Arg) c.1624T>A (p.Trp542Arg) c.-413T>A (n.-413T>A) | dbSNP |