Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
5 | g.76731998A>C | CA11972665 | F2R | c.89-316A>C (n.89-316A>C) c.-275-316A>C (n.-275-316A>C) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
5 | g.76731998A>T | CA814109080 | F2R | c.89-316A>T (n.89-316A>T) c.-275-316A>T (n.-275-316A>T) | dbSNP |