Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|

19 | g.4717660A>T | CA304514604 | DPP9 | c.56+2191T>A (p.=) c.57-1508T>A (p.=) c.39+1829T>A (p.=) c.-229-1934T>A (p.=) c.-93-1934T>A (p.=) n.314-1508T>A n.313+2191T>A n.302-1508T>A c.-125+2263T>A (p.=) c.23T>A (p.Leu8His) n.364-1508T>A c.178+1543T>A (p.=) n.284+2191T>A | dbSNP |

19 | g.4717660A>G | CA9104515 | DPP9 | c.56+2191T>C (p.=) c.57-1508T>C (p.=) c.39+1829T>C (p.=) c.-229-1934T>C (p.=) c.-93-1934T>C (p.=) n.314-1508T>C n.313+2191T>C n.302-1508T>C c.-125+2263T>C (p.=) c.23T>C (p.Leu8Pro) n.364-1508T>C c.178+1543T>C (p.=) n.284+2191T>C | dbSNP ExAC gnomAD |