Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
14 | g.70672562G>C | CA2145308974 | TTC9 | c.*1407G>C (n.*1407G>C) | dbSNP |
14 | g.70672562G>T | CA13994751 | TTC9 | c.*1407G>T (n.*1407G>T) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.70672562G= | CA2145308971 | TTC9 | c.*1407G= (n.*1407G=) | dbSNP |