Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
16 | g.2496469T>A | CA16608138 | TBC1D24 | c.321T>A (p.Asn107Lys) n.503T>A | ClinVar dbSNP gnomAD v4 |
16 | g.2496469T= | CA2202259807 | TBC1D24 | c.321T= (p.Asn107=) n.503T= | dbSNP |
16 | g.2496469T>C | CA493366700 | TBC1D24 | c.321T>C (p.Asn107=) n.503T>C | ClinVar dbSNP |