Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
7 | g.27198258C>G | CA367069657 | HOXA13 | c.1107G>C (p.Trp369Cys) | dbSNP |
7 | g.27198258C>T | CA257393 | HOXA13 | c.1107G>A (p.Trp369Ter) | ClinVar dbSNP |
7 | g.27198258C>A | CA367069656 | HOXA13 | c.1107G>T (p.Trp369Cys) | dbSNP |